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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 15:16:52 UTC

Update Date

2022-03-07 02:52:00 UTC

HMDB ID

HMDB0015490

Secondary Accession Numbers

HMDB15490

Metabolite Identification

Common Name

Paromomycin

Description

Paromomycin is only found in individuals that have used or taken this drug. It is an oligosaccharide antibiotic produced by various streptomyces. [PubChem]Paromomycin inhibits protein synthesis by binding to 16S ribosomal RNA. Bacterial proteins are synthesized by ribosomal RNA complexes which are composed of 2 subunits, a large subunit (50s) and small (30s) subunit, which forms a 70s ribosomal subunit. tRNA binds to the top of this ribosomal structure. Paramomycin binds to the A site, which causes defective polypeptide chains to be produced. Continuous production of defective proteins eventually leads to bacterial death.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

1421
  Mrv0541 02231215292D          

 42 45  0  0  1  0            999 V2000
    6.6349   -0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2059   -1.1857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 42  1  6  0  0  0
M  END

HMDB0015490
     RDKit          3D
Paromomycin
 87 90  0  0  0  0  0  0  0  0999 V2000
    9.1625   -1.4899    1.4700 N   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

1421
  Mrv0541 02231215292D          

 42 45  0  0  1  0            999 V2000
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   12.0095    0.7213    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.6349   -1.1857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9203   -1.5982    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9203   -2.4232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3493   -1.5982    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3493   -2.4232    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6349   -2.8358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3493    0.0518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2426    1.0438    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4356    0.8723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.6551    0.3293    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3808   -1.1857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9684   -0.4712    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1433   -0.4712    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.3986    1.8838    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7308   -1.1857    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7341    2.6375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1433   -1.9002    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.5547    2.7237    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.4756    0.2431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0397    2.0563    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7040    1.3025    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7308   -2.6147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1890    0.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 20  1  1  6  0  0  0
 26  1  1  1  0  0  0
 21  2  1  1  0  0  0
 30  2  1  1  0  0  0
  3 26  1  0  0  0  0
  3 29  1  0  0  0  0
 27  4  1  6  0  0  0
 33  4  1  6  0  0  0
 23  5  1  1  0  0  0
  6 30  1  0  0  0  0
  6 36  1  0  0  0  0
  7 33  1  0  0  0  0
  7 40  1  0  0  0  0
 28  8  1  6  0  0  0
 32  9  1  6  0  0  0
 34 10  1  1  0  0  0
 37 11  1  1  0  0  0
 12 38  1  0  0  0  0
 39 13  1  6  0  0  0
 14 41  1  0  0  0  0
 22 15  1  6  0  0  0
 24 16  1  6  0  0  0
 31 17  1  1  0  0  0
 35 18  1  6  0  0  0
 19 42  1  0  0  0  0
 20 21  1  0  0  0  0
 20 23  1  0  0  0  0
 21 22  1  0  0  0  0
 22 25  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 26 28  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 38  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 34  1  0  0  0  0
 33 35  1  0  0  0  0
 34 36  1  0  0  0  0
 35 37  1  0  0  0  0
 36 41  1  6  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 42  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0015490

> <DATABASE_NAME>
hmdb

> <SMILES>
NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C23H45N5O14/c24-2-7-13(32)15(34)10(27)21(37-7)41-19-9(4-30)39-23(17(19)36)42-20-12(31)5(25)1-6(26)18(20)40-22-11(28)16(35)14(33)8(3-29)38-22/h5-23,29-36H,1-4,24-28H2/t5-,6+,7+,8-,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23+/m1/s1

> <INCHI_KEY>
UOZODPSAJZTQNH-LSWIJEOBSA-N

> <FORMULA>
C23H45N5O14

> <MOLECULAR_WEIGHT>
615.6285

> <EXACT_MASS>
615.296301173

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_AVERAGE_POLARIZABILITY>
60.40275856764997

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-{[(2R,3S,4R,5S)-5-{[(1R,2R,3S,5R,6S)-3,5-diamino-2-{[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-hydroxycyclohexyl]oxy}-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy}oxane-3,4-diol

> <ALOGPS_LOGP>
-2.92

> <JCHEM_LOGP>
-8.308295949333333

> <ALOGPS_LOGS>
-0.89

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
5

> <JCHEM_PKA>
12.902517812527407

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.227454691752135

> <JCHEM_PKA_STRONGEST_BASIC>
9.938207381101218

> <JCHEM_POLAR_SURFACE_AREA>
347.31999999999994

> <JCHEM_REFRACTIVITY>
134.2427999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.97e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
paromomycin

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0015490
     RDKit          3D
Paromomycin
 87 90  0  0  0  0  0  0  0  0999 V2000
    9.1625   -1.4899    1.4700 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0063   -1.7974    0.6703 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0396   -0.6177    0.7737 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8971   -0.8625    0.0151 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9511    0.0831    0.3361 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7529   -0.2558   -0.2842 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7017   -0.3435    0.6263 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0401   -1.6921    0.4778 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5046   -2.6642    1.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2292   -2.0768    2.7815 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6829   -1.4986    0.6610 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3617   -0.2496    0.1634 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7539    0.3169    0.7391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7982    0.5203   -0.1459 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2345    1.9702   -0.1828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4221    2.0690   -0.9100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4437    2.4590    1.2285 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1439    2.6027    1.8725 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3725    1.6009    2.0230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1670    0.1290    1.8269 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0504   -0.3621    2.5964 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9822   -0.2672    0.3783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1610    0.0368   -0.2935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7659   -1.1065   -0.7945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0223   -1.3442   -0.2942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9898   -0.4472   -0.6738 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.3255   -1.0032   -0.1598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2922   -1.1299    1.2166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1536   -0.3725   -2.1936 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.1058    0.5732   -2.4952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8050   -0.0797   -2.8208 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9569   -0.2497   -4.1936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8378   -1.1040   -2.3027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5261   -0.9770   -2.9072 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5897    0.5956    0.2117 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8984    1.2029   -1.0051 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4107    1.4037   -0.2709 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4990    1.1958   -1.7095 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7824    1.7781    0.2287 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7472    2.2881    1.5236 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7272    0.5981    0.2413 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2861    0.3811   -1.0235 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8968   -1.1219    2.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7890   -0.8217    0.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2676   -1.9055   -0.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5442   -2.7219    1.0766 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8056   -0.4687    1.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7582    0.1972    1.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0282   -0.1274    1.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2125   -2.1564   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8791   -3.5776    1.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5732   -2.9274    1.4264 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4226   -2.7566    3.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1121   -0.4030   -0.9280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5152    0.1761   -1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078    2.6350   -0.6576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1729    1.9788   -1.8604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8842    3.4747    1.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4590    3.0338    1.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2337    3.2374    2.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4321    1.8837    1.8856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1539    1.8091    3.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0906   -0.3758    2.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2895   -1.2111    3.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6264    0.3941    3.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689   -1.3573    0.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1294   -1.9748   -0.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8956    0.5521   -0.2446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5813   -1.9402   -0.6903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0806   -0.2372   -0.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6385   -0.5395    1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4321   -1.3987   -2.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4484    0.4956   -3.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4516    0.9206   -2.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9835   -1.2416   -4.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2421   -2.1120   -2.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8253   -1.5087   -2.3548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5947   -1.2564   -3.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4963    1.4285    0.9497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4816    0.7492   -1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7153    2.2043   -0.0245 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8372    2.0785   -2.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6113    0.8376   -2.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1736    2.5745   -0.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8003    1.5970    2.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5851    0.8307    0.9166 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4873    1.2395   -1.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
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 12 35  1  0
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  5 37  1  0
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 41  3  1  0
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 22 14  1  0
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  1 43  1  0
  1 44  1  0
  2 45  1  0
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  3 47  1  1
  5 48  1  1
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  8 50  1  6
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 42 87  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: 1421                                              
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      12.385  -0.673   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0       9.718  -2.213   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      15.126  -0.530   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      16.012   3.355   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      15.052  -2.213   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       7.407  -3.547   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      18.449   2.270   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      12.735   2.659   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       5.098   0.454   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       3.557  -2.213   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      20.328   6.491   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      18.314  -0.953   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      22.139   3.999   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       5.868  -6.215   0.000  0.00  0.00           O+0
HETATM   15  N   UNK     0      10.281  -5.857   0.000  0.00  0.00           N+0
HETATM   16  N   UNK     0      15.052  -5.293   0.000  0.00  0.00           N+0
HETATM   17  N   UNK     0       8.177   0.454   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0      17.265   6.169   0.000  0.00  0.00           N+0
HETATM   19  N   UNK     0      22.418   1.346   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      12.385  -2.213   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.051  -2.983   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.051  -4.523   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.719  -2.983   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      13.719  -4.523   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.385  -5.293   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.719   0.097   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      15.386   1.948   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.880   1.628   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.156   0.615   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.177  -2.213   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.408  -0.880   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.867  -0.880   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      17.544   3.516   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.097  -2.213   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      18.170   4.923   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.867  -3.547   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      19.702   5.084   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      17.688   0.454   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      20.607   3.838   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      19.981   2.431   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       5.097  -4.881   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      20.886   1.186   0.000  0.00  0.00           C+0
CONECT    1   20   26                                                       
CONECT    2   21   30                                                       
CONECT    3   26   29                                                       
CONECT    4   27   33                                                       
CONECT    5   23                                                            
CONECT    6   30   36                                                       
CONECT    7   33   40                                                       
CONECT    8   28                                                            
CONECT    9   32                                                            
CONECT   10   34                                                            
CONECT   11   37                                                            
CONECT   12   38                                                            
CONECT   13   39                                                            
CONECT   14   41                                                            
CONECT   15   22                                                            
CONECT   16   24                                                            
CONECT   17   31                                                            
CONECT   18   35                                                            
CONECT   19   42                                                            
CONECT   20    1   21   23                                                  
CONECT   21    2   20   22                                                  
CONECT   22   15   21   25                                                  
CONECT   23    5   20   24                                                  
CONECT   24   16   23   25                                                  
CONECT   25   22   24                                                       
CONECT   26    1    3   28                                                  
CONECT   27    4   28   29                                                  
CONECT   28    8   26   27                                                  
CONECT   29    3   27   38                                                  
CONECT   30    2    6   31                                                  
CONECT   31   17   30   32                                                  
CONECT   32    9   31   34                                                  
CONECT   33    4    7   35                                                  
CONECT   34   10   32   36                                                  
CONECT   35   18   33   37                                                  
CONECT   36    6   34   41                                                  
CONECT   37   11   35   39                                                  
CONECT   38   12   29                                                       
CONECT   39   13   37   40                                                  
CONECT   40    7   39   42                                                  
CONECT   41   14   36                                                       
CONECT   42   19   40                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

COMPND    HMDB0015490
HETATM    1  N1  UNL     1       9.163  -1.490   1.470  1.00  0.00           N  
HETATM    2  C1  UNL     1       8.006  -1.797   0.670  1.00  0.00           C  
HETATM    3  C2  UNL     1       7.040  -0.618   0.774  1.00  0.00           C  
HETATM    4  O1  UNL     1       5.897  -0.863   0.015  1.00  0.00           O  
HETATM    5  C3  UNL     1       4.951   0.083   0.336  1.00  0.00           C  
HETATM    6  O2  UNL     1       3.753  -0.256  -0.284  1.00  0.00           O  
HETATM    7  C4  UNL     1       2.702  -0.344   0.626  1.00  0.00           C  
HETATM    8  C5  UNL     1       2.040  -1.692   0.478  1.00  0.00           C  
HETATM    9  C6  UNL     1       2.505  -2.664   1.543  1.00  0.00           C  
HETATM   10  O3  UNL     1       2.229  -2.077   2.782  1.00  0.00           O  
HETATM   11  O4  UNL     1       0.683  -1.499   0.661  1.00  0.00           O  
HETATM   12  C7  UNL     1       0.362  -0.250   0.163  1.00  0.00           C  
HETATM   13  O5  UNL     1      -0.754   0.317   0.739  1.00  0.00           O  
HETATM   14  C8  UNL     1      -1.798   0.520  -0.146  1.00  0.00           C  
HETATM   15  C9  UNL     1      -2.235   1.970  -0.183  1.00  0.00           C  
HETATM   16  O6  UNL     1      -3.422   2.069  -0.910  1.00  0.00           O  
HETATM   17  C10 UNL     1      -2.444   2.459   1.229  1.00  0.00           C  
HETATM   18  N2  UNL     1      -1.144   2.603   1.872  1.00  0.00           N  
HETATM   19  C11 UNL     1      -3.372   1.601   2.023  1.00  0.00           C  
HETATM   20  C12 UNL     1      -3.167   0.129   1.827  1.00  0.00           C  
HETATM   21  N3  UNL     1      -2.050  -0.362   2.596  1.00  0.00           N  
HETATM   22  C13 UNL     1      -2.982  -0.267   0.378  1.00  0.00           C  
HETATM   23  O7  UNL     1      -4.161   0.037  -0.294  1.00  0.00           O  
HETATM   24  C14 UNL     1      -4.766  -1.107  -0.795  1.00  0.00           C  
HETATM   25  O8  UNL     1      -6.022  -1.344  -0.294  1.00  0.00           O  
HETATM   26  C15 UNL     1      -6.990  -0.447  -0.674  1.00  0.00           C  
HETATM   27  C16 UNL     1      -8.326  -1.003  -0.160  1.00  0.00           C  
HETATM   28  O9  UNL     1      -8.292  -1.130   1.217  1.00  0.00           O  
HETATM   29  C17 UNL     1      -7.154  -0.372  -2.194  1.00  0.00           C  
HETATM   30  O10 UNL     1      -8.106   0.573  -2.495  1.00  0.00           O  
HETATM   31  C18 UNL     1      -5.805  -0.080  -2.821  1.00  0.00           C  
HETATM   32  O11 UNL     1      -5.957  -0.250  -4.194  1.00  0.00           O  
HETATM   33  C19 UNL     1      -4.838  -1.104  -2.303  1.00  0.00           C  
HETATM   34  N4  UNL     1      -3.526  -0.977  -2.907  1.00  0.00           N  
HETATM   35  C20 UNL     1       1.590   0.596   0.212  1.00  0.00           C  
HETATM   36  O12 UNL     1       1.898   1.203  -1.005  1.00  0.00           O  
HETATM   37  C21 UNL     1       5.411   1.404  -0.271  1.00  0.00           C  
HETATM   38  N5  UNL     1       5.499   1.196  -1.710  1.00  0.00           N  
HETATM   39  C22 UNL     1       6.782   1.778   0.229  1.00  0.00           C  
HETATM   40  O13 UNL     1       6.747   2.288   1.524  1.00  0.00           O  
HETATM   41  C23 UNL     1       7.727   0.598   0.241  1.00  0.00           C  
HETATM   42  O14 UNL     1       8.286   0.381  -1.024  1.00  0.00           O  
HETATM   43  H1  UNL     1       8.897  -1.122   2.392  1.00  0.00           H  
HETATM   44  H2  UNL     1       9.789  -0.822   0.991  1.00  0.00           H  
HETATM   45  H3  UNL     1       8.268  -1.905  -0.406  1.00  0.00           H  
HETATM   46  H4  UNL     1       7.544  -2.722   1.077  1.00  0.00           H  
HETATM   47  H5  UNL     1       6.806  -0.469   1.836  1.00  0.00           H  
HETATM   48  H6  UNL     1       4.758   0.197   1.406  1.00  0.00           H  
HETATM   49  H7  UNL     1       3.028  -0.127   1.656  1.00  0.00           H  
HETATM   50  H8  UNL     1       2.212  -2.156  -0.504  1.00  0.00           H  
HETATM   51  H9  UNL     1       1.879  -3.578   1.461  1.00  0.00           H  
HETATM   52  H10 UNL     1       3.573  -2.927   1.426  1.00  0.00           H  
HETATM   53  H11 UNL     1       2.423  -2.757   3.463  1.00  0.00           H  
HETATM   54  H12 UNL     1       0.112  -0.403  -0.928  1.00  0.00           H  
HETATM   55  H13 UNL     1      -1.515   0.176  -1.166  1.00  0.00           H  
HETATM   56  H14 UNL     1      -1.508   2.635  -0.658  1.00  0.00           H  
HETATM   57  H15 UNL     1      -3.173   1.979  -1.860  1.00  0.00           H  
HETATM   58  H16 UNL     1      -2.884   3.475   1.162  1.00  0.00           H  
HETATM   59  H17 UNL     1      -0.459   3.034   1.220  1.00  0.00           H  
HETATM   60  H18 UNL     1      -1.234   3.237   2.694  1.00  0.00           H  
HETATM   61  H19 UNL     1      -4.432   1.884   1.886  1.00  0.00           H  
HETATM   62  H20 UNL     1      -3.154   1.809   3.112  1.00  0.00           H  
HETATM   63  H21 UNL     1      -4.091  -0.376   2.239  1.00  0.00           H  
HETATM   64  H22 UNL     1      -2.290  -1.211   3.117  1.00  0.00           H  
HETATM   65  H23 UNL     1      -1.626   0.394   3.178  1.00  0.00           H  
HETATM   66  H24 UNL     1      -2.769  -1.357   0.376  1.00  0.00           H  
HETATM   67  H25 UNL     1      -4.129  -1.975  -0.516  1.00  0.00           H  
HETATM   68  H26 UNL     1      -6.896   0.552  -0.245  1.00  0.00           H  
HETATM   69  H27 UNL     1      -8.581  -1.940  -0.690  1.00  0.00           H  
HETATM   70  H28 UNL     1      -9.081  -0.237  -0.410  1.00  0.00           H  
HETATM   71  H29 UNL     1      -7.638  -0.539   1.644  1.00  0.00           H  
HETATM   72  H30 UNL     1      -7.432  -1.399  -2.515  1.00  0.00           H  
HETATM   73  H31 UNL     1      -8.448   0.496  -3.417  1.00  0.00           H  
HETATM   74  H32 UNL     1      -5.452   0.921  -2.544  1.00  0.00           H  
HETATM   75  H33 UNL     1      -5.984  -1.242  -4.365  1.00  0.00           H  
HETATM   76  H34 UNL     1      -5.242  -2.112  -2.592  1.00  0.00           H  
HETATM   77  H35 UNL     1      -2.825  -1.509  -2.355  1.00  0.00           H  
HETATM   78  H36 UNL     1      -3.595  -1.256  -3.901  1.00  0.00           H  
HETATM   79  H37 UNL     1       1.496   1.428   0.950  1.00  0.00           H  
HETATM   80  H38 UNL     1       1.482   0.749  -1.779  1.00  0.00           H  
HETATM   81  H39 UNL     1       4.715   2.204  -0.025  1.00  0.00           H  
HETATM   82  H40 UNL     1       5.837   2.079  -2.177  1.00  0.00           H  
HETATM   83  H41 UNL     1       4.611   0.838  -2.119  1.00  0.00           H  
HETATM   84  H42 UNL     1       7.174   2.575  -0.431  1.00  0.00           H  
HETATM   85  H43 UNL     1       6.800   1.597   2.217  1.00  0.00           H  
HETATM   86  H44 UNL     1       8.585   0.831   0.917  1.00  0.00           H  
HETATM   87  H45 UNL     1       8.487   1.240  -1.464  1.00  0.00           H  
CONECT    1    2   43   44
CONECT    2    3   45   46
CONECT    3    4   41   47
CONECT    4    5
CONECT    5    6   37   48
CONECT    6    7
CONECT    7    8   35   49
CONECT    8    9   11   50
CONECT    9   10   51   52
CONECT   10   53
CONECT   11   12
CONECT   12   13   35   54
CONECT   13   14
CONECT   14   15   22   55
CONECT   15   16   17   56
CONECT   16   57
CONECT   17   18   19   58
CONECT   18   59   60
CONECT   19   20   61   62
CONECT   20   21   22   63
CONECT   21   64   65
CONECT   22   23   66
CONECT   23   24
CONECT   24   25   33   67
CONECT   25   26
CONECT   26   27   29   68
CONECT   27   28   69   70
CONECT   28   71
CONECT   29   30   31   72
CONECT   30   73
CONECT   31   32   33   74
CONECT   32   75
CONECT   33   34   76
CONECT   34   77   78
CONECT   35   36   79
CONECT   36   80
CONECT   37   38   39   81
CONECT   38   82   83
CONECT   39   40   41   84
CONECT   40   85
CONECT   41   42   86
CONECT   42   87
END

HMDB0015490
     RDKit          3D
Paromomycin
 87 90  0  0  0  0  0  0  0  0999 V2000
    9.1625   -1.4899    1.4700 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.0063   -1.7974    0.6703 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0396   -0.6177    0.7737 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8971   -0.8625    0.0151 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9511    0.0831    0.3361 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7529   -0.2558   -0.2842 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7017   -0.3435    0.6263 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0401   -1.6921    0.4778 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5046   -2.6642    1.5426 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2292   -2.0768    2.7815 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6829   -1.4986    0.6610 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3617   -0.2496    0.1634 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7539    0.3169    0.7391 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7982    0.5203   -0.1459 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2345    1.9702   -0.1828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4221    2.0690   -0.9100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4437    2.4590    1.2285 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1439    2.6027    1.8725 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3725    1.6009    2.0230 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1670    0.1290    1.8269 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0504   -0.3621    2.5964 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9822   -0.2672    0.3783 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1610    0.0368   -0.2935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7659   -1.1065   -0.7945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0223   -1.3442   -0.2942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9898   -0.4472   -0.6738 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.3255   -1.0032   -0.1598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2922   -1.1299    1.2166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1536   -0.3725   -2.1936 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.1058    0.5732   -2.4952 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8050   -0.0797   -2.8208 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9569   -0.2497   -4.1936 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8378   -1.1040   -2.3027 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5261   -0.9770   -2.9072 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5897    0.5956    0.2117 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8984    1.2029   -1.0051 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4107    1.4037   -0.2709 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4990    1.1958   -1.7095 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7824    1.7781    0.2287 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7472    2.2881    1.5236 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7272    0.5981    0.2413 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2861    0.3811   -1.0235 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8968   -1.1219    2.3920 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7890   -0.8217    0.9907 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2676   -1.9055   -0.4057 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5442   -2.7219    1.0766 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8056   -0.4687    1.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7582    0.1972    1.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0282   -0.1274    1.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2125   -2.1564   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8791   -3.5776    1.4613 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5732   -2.9274    1.4264 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4226   -2.7566    3.4634 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1121   -0.4030   -0.9280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5152    0.1761   -1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078    2.6350   -0.6576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1729    1.9788   -1.8604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8842    3.4747    1.1616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4590    3.0338    1.2195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2337    3.2374    2.6943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4321    1.8837    1.8856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1539    1.8091    3.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0906   -0.3758    2.2390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2895   -1.2111    3.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6264    0.3941    3.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689   -1.3573    0.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1294   -1.9748   -0.5155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8956    0.5521   -0.2446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5813   -1.9402   -0.6903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0806   -0.2372   -0.4102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6385   -0.5395    1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4321   -1.3987   -2.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4484    0.4956   -3.4168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4516    0.9206   -2.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9835   -1.2416   -4.3651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2421   -2.1120   -2.5922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8253   -1.5087   -2.3548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5947   -1.2564   -3.9009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4963    1.4285    0.9497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4816    0.7492   -1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7153    2.2043   -0.0245 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8372    2.0785   -2.1774 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6113    0.8376   -2.1193 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1736    2.5745   -0.4313 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8003    1.5970    2.2166 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5851    0.8307    0.9166 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4873    1.2395   -1.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
  8 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
 31 33  1  0
 33 34  1  0
 12 35  1  0
 35 36  1  0
  5 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 41  3  1  0
 35  7  1  0
 22 14  1  0
 33 24  1  0
  1 43  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  1
  5 48  1  1
  7 49  1  1
  8 50  1  6
  9 51  1  0
  9 52  1  0
 10 53  1  0
 12 54  1  6
 14 55  1  6
 15 56  1  6
 16 57  1  0
 17 58  1  6
 18 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 20 63  1  1
 21 64  1  0
 21 65  1  0
 22 66  1  1
 24 67  1  6
 26 68  1  1
 27 69  1  0
 27 70  1  0
 28 71  1  0
 29 72  1  6
 30 73  1  0
 31 74  1  6
 32 75  1  0
 33 76  1  6
 34 77  1  0
 34 78  1  0
 35 79  1  1
 36 80  1  0
 37 81  1  6
 38 82  1  0
 38 83  1  0
 39 84  1  6
 40 85  1  0
 41 86  1  1
 42 87  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(1R,2R,3S,4R,6S)-4,6-Diamino-2-{[3-O-(2,6-diamino-2,6-dideoxy-beta-L-idopyranosyl)-beta-D-ribofuranosyl]oxy}-3-hydroxycyclohexyl 2-amino-2-deoxy-alpha-D-glucopyranoside	ChEBI
Aminosidin	ChEBI
Aminosidine	ChEBI
Catenulin	ChEBI
Crestomycin	ChEBI
Estomycin	ChEBI
Hydroxymycin	ChEBI
Monomycin a	ChEBI
Neomycin e	ChEBI
Paromomicina	ChEBI
Paromomycin I	ChEBI
Paromomycine	ChEBI
Paromomycinum	ChEBI
Paucimycin	ChEBI
Paucimycinum	ChEBI
R 400	ChEBI
R-400	ChEBI
Zygomycin a1	ChEBI
(1R,2R,3S,4R,6S)-4,6-Diamino-2-{[3-O-(2,6-diamino-2,6-dideoxy-b-L-idopyranosyl)-b-D-ribofuranosyl]oxy}-3-hydroxycyclohexyl 2-amino-2-deoxy-a-D-glucopyranoside	Generator
(1R,2R,3S,4R,6S)-4,6-Diamino-2-{[3-O-(2,6-diamino-2,6-dideoxy-β-L-idopyranosyl)-β-D-ribofuranosyl]oxy}-3-hydroxycyclohexyl 2-amino-2-deoxy-α-D-glucopyranoside	Generator
PRM	HMDB
Paramomycin sulfate	HMDB
Paramomycin sulphate	HMDB
Gabbromycin	HMDB
Parke davis brand OF paromomycin sulfate	HMDB
Paromomycin, beta-D-glucopyranosyl-isomer	HMDB
Sulfate, paromomycin	HMDB
Humatin	HMDB
Phosphate, paromomycin	HMDB
Cheminova brand OF paromomycin sulfate	HMDB
Paromomycin sulfate (1:1)	HMDB
Pfizer brand OF paromomycin sulfate	HMDB
beta-D-Glucopyranosyl-isomer paromomycin	HMDB
Monarch brand OF paromomycin sulfate	HMDB
Paramomycin	HMDB
Paromomycin phosphate	HMDB
Paromomycin sulfate	HMDB
Paromomycin sulfate (2:5)	HMDB
Paromomycin, beta D glucopyranosyl isomer	HMDB

Chemical Formula

C₂₃H₄₅N₅O₁₄

Average Molecular Weight

615.6285

Monoisotopic Molecular Weight

615.296301173

IUPAC Name

(2S,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-{[(2R,3S,4R,5S)-5-{[(1R,2R,3S,5R,6S)-3,5-diamino-2-{[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-hydroxycyclohexyl]oxy}-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy}oxane-3,4-diol

Traditional Name

paromomycin

CAS Registry Number

1263-89-4

SMILES

NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C23H45N5O14/c24-2-7-13(32)15(34)10(27)21(37-7)41-19-9(4-30)39-23(17(19)36)42-20-12(31)5(25)1-6(26)18(20)40-22-11(28)16(35)14(33)8(3-29)38-22/h5-23,29-36H,1-4,24-28H2/t5-,6+,7+,8-,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23+/m1/s1

InChI Key

UOZODPSAJZTQNH-LSWIJEOBSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 4,5-disubstituted 2-deoxystreptamines. These are 2-deoxystreptamine aminoglycosides that are glycosidically linked to a pyranose of furanose unit at the C4- and C5-positions.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

4,5-disubstituted 2-deoxystreptamines

Alternative Parents

Substituents

4,5-disubstituted 2-deoxystreptamine
Disaccharide
Glycosyl compound
O-glycosyl compound
Aminocyclitol or derivatives
Cyclohexanol
Cyclohexylamine
Cyclitol or derivatives
Oxane
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
1,2-aminoalcohol
Acetal
Organoheterocyclic compound
Oxacycle
Primary alcohol
Hydrocarbon derivative
Organopnictogen compound
Primary aliphatic amine
Organonitrogen compound
Organic nitrogen compound
Amine
Alcohol
Primary amine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

aminoglycoside antibiotic (CHEBI:7934 )
amino cyclitol glycoside (CHEBI:7934 )

Ontology

Not Available

Urine (PMID: 21059682)

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 21059682)

Cellular substructure

Cytoplasm (HMDB: HMDB0015490)

Process

Naturally occurring process

Biological process

Biochemical pathway

Drug action pathway

Paromomycin Action Pathway (PathBank: SMP0000714)

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	79.7 g/L	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	79.7 g/L	ALOGPS
logP	-2.9	ALOGPS
logP	-8.3	ChemAxon
logS	-0.89	ALOGPS
pKa (Strongest Acidic)	12.23	ChemAxon
pKa (Strongest Basic)	9.94	ChemAxon
Physiological Charge	5	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	347.32 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	134.24 m³·mol⁻¹	ChemAxon
Polarizability	60.4 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	236.308	30932474
DeepCCS	[M-H]-	234.544	30932474
DeepCCS	[M-2H]-	268.577	30932474
DeepCCS	[M+Na]+	242.535	30932474
AllCCS	[M+H]+	235.0	32859911
AllCCS	[M+H-H2O]+	234.2	32859911
AllCCS	[M+NH4]+	235.6	32859911
AllCCS	[M+Na]+	235.8	32859911
AllCCS	[M-H]-	209.9	32859911
AllCCS	[M+Na-2H]-	210.4	32859911
AllCCS	[M+HCOO]-	211.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Paromomycin	NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	3268.7	Standard polar	33892256
Paromomycin	NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5506.2	Standard non polar	33892256
Paromomycin	NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5325.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Paromomycin,1TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5043.9	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #10	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5102.6	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #11	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5093.9	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #12	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5092.0	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #13	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5085.6	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #2	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	5025.6	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5053.6	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #4	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	5027.8	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #5	C[Si](C)(C)O[C@@H]1[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@H]1O	5017.6	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #6	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5038.4	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #7	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@@H]1N	5011.7	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #8	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	5016.2	Semi standard non polar	33892256
Paromomycin,1TMS,isomer #9	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5116.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4891.6	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #10	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4960.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #11	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4974.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #12	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4951.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #13	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4864.6	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #14	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4868.9	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #15	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4896.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4902.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #17	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4878.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #18	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@@H](N)C[C@H]1N	4872.5	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #19	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4944.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4925.5	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #20	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4934.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #21	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4941.6	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #22	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4975.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #23	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4980.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4891.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4893.4	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4915.9	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4897.5	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4913.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #29	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4996.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4898.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #30	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5023.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #31	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4988.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #32	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4971.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #33	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O	4960.4	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #34	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	4866.6	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #35	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	4868.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #36	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@H]1O	4894.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #37	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O[Si](C)(C)C	4878.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #38	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4964.5	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #39	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4986.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4891.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #40	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4952.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #41	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4941.4	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #42	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	4951.5	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #43	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	4863.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #44	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@@H]1N	4868.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #45	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4887.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #46	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4944.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #47	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4953.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #48	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4975.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #49	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4936.4	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4903.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #50	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4927.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #51	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@H]1O	4878.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #52	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4883.4	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #53	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4996.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #54	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4977.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #55	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	4949.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #56	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4958.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #57	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O	4938.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #58	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O[Si](C)(C)C	4863.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #59	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4938.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4883.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #60	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	4968.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #61	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4947.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #62	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4929.9	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #63	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C	4934.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #64	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4959.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #65	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4974.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #66	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4953.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #67	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4934.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #68	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O	4936.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #69	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5063.5	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4886.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #70	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5040.9	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #71	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5021.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #72	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	5003.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #73	C[Si](C)(C)N(C[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O)[Si](C)(C)C	5191.2	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #74	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5061.9	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #75	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5058.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #76	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	5049.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #77	C[Si](C)(C)N([C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O)[Si](C)(C)C	5076.1	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #78	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5024.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #79	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	5032.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #8	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5000.8	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #80	C[Si](C)(C)N([C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N)[Si](C)(C)C	5061.5	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #81	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5002.0	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #82	C[Si](C)(C)N([C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C	5089.3	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #83	C[Si](C)(C)N([C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O)[Si](C)(C)C	5072.7	Semi standard non polar	33892256
Paromomycin,2TMS,isomer #9	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4979.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4785.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #10	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4803.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #100	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4781.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #101	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4848.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #102	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4851.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #103	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4821.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #104	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4825.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #105	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O	4815.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #106	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2N)[C@@H](N)C[C@H]1N	4752.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #107	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4795.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #108	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4801.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #109	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	4812.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #11	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4802.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #110	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4827.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #111	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4828.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #112	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4795.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #113	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4804.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #114	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4811.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #115	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4825.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #116	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4827.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #117	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4882.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #118	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4882.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #119	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4857.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4793.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #120	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4841.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #121	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	5056.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #122	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O[Si](C)(C)C	4893.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #123	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4888.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #124	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4858.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #125	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4937.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #126	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4894.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #127	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4903.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #128	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N([Si](C)(C)C)[Si](C)(C)C)[C@@H](N)C[C@H]1N	4952.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #129	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4923.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #13	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4786.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #130	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@H]1N	4922.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #131	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N([Si](C)(C)C)[Si](C)(C)C	4943.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #132	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4759.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #133	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4766.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #134	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4759.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #135	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4762.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #136	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4827.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #137	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4853.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #138	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4823.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #139	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O	4818.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4780.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #140	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O	4801.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #141	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4780.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #142	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4770.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #143	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4773.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #144	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4828.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #145	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	4855.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #146	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4815.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #147	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C	4819.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #148	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O	4809.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #149	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4782.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4772.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #150	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4786.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #151	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4851.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #152	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4874.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #153	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4821.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #154	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O	4820.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #155	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O	4809.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #156	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4786.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #157	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4835.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #158	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4861.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #159	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4814.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4785.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #160	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4821.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #161	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4819.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #162	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4842.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #163	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4865.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #164	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4820.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #165	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4825.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #166	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4819.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #167	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4953.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #168	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4901.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #169	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4903.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #17	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4879.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #170	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4889.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #171	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4940.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #172	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4921.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #173	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4929.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #174	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	4935.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #175	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4946.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #176	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4865.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #177	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4868.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #178	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5089.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #179	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O	4860.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #18	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	4853.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #180	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4966.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #181	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	4971.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #182	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	4735.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #183	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@H]1O	4741.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #184	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	4735.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #185	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4801.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #186	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4825.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #187	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4798.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #188	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O	4793.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #189	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	4796.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #19	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O	4823.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #190	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@H]1O	4758.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #191	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@@H]1N	4746.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #192	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4801.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #193	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	4829.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #194	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4792.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #195	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C	4795.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #196	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	4804.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #197	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4756.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #198	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4824.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #199	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4846.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4759.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #20	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4835.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #200	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4798.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #201	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O	4796.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #202	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	4809.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #203	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1N	4817.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #204	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4839.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #205	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4794.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #206	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4797.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #207	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4799.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #208	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4923.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #209	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4871.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #21	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4834.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #210	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4875.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #211	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N[Si](C)(C)C	4889.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #212	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	4920.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #213	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4918.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #214	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4896.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #215	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	4903.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #216	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	4923.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #217	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4861.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #218	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4843.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #219	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	5059.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #22	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4757.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #220	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	4860.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #221	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O)[C@H](N)[C@H]1O	4933.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #222	C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]1O	4936.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #223	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@H]1O	4746.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #224	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O[Si](C)(C)C	4735.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #225	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4798.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #226	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4827.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #227	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4800.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #228	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4793.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #229	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O	4796.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4757.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #230	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4762.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #231	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4794.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #232	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	4832.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #233	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4803.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #234	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4804.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #235	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C	4800.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #236	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4846.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #237	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4823.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #238	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4807.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #239	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4797.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #24	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4745.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #240	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O	4798.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #241	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N[Si](C)(C)C	4887.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #242	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4915.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #243	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4857.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #244	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4860.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #245	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1N([Si](C)(C)C)[Si](C)(C)C	4957.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #246	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4916.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #247	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4866.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #248	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4871.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #249	C[Si](C)(C)O[C@@H]1[C@@H](N)[C@@H](O[C@@H]2[C@@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@H]1O	4908.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4761.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #250	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4892.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #251	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	4900.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #252	C[Si](C)(C)O[C@@H]1[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@H]1O	4916.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #253	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4835.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #254	C[Si](C)(C)O[C@@H]1[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@H]1O	5055.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #255	C[Si](C)(C)O[C@@H]1[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@H]1O	4926.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #256	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1N	4743.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #257	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4800.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #258	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4834.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #259	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4811.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #26	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4844.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #260	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	4793.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #261	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O	4792.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #262	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4843.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #263	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4818.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #264	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	4804.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #265	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4797.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #266	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C	4799.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #267	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4931.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #268	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4908.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #269	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4893.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #27	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4822.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #270	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@H]1O	4894.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #271	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4931.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #272	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4872.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #273	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4869.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #274	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4880.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #275	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4929.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #276	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4849.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #277	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	4839.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #278	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4954.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #279	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4833.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #28	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	4813.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #280	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	5061.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #281	C[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N([Si](C)(C)C)[Si](C)(C)C	4946.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #282	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4794.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #283	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	4827.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #284	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4804.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #285	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4795.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #286	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4787.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #287	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4891.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #288	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4865.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #289	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4850.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #29	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4804.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #290	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4846.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #291	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@@H]1N	5052.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #292	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4910.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #293	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	4902.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #294	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	4902.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #295	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@@H]1N	4912.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #296	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4874.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #297	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4871.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #298	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@@H]1N	4905.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #299	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4857.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4762.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #30	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4804.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #300	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)[C@@H]1N	4938.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #301	C[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@@H]1N([Si](C)(C)C)[Si](C)(C)C	4941.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #302	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4897.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #303	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4874.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #304	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4857.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #305	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4851.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #306	C[Si](C)(C)O[C@@H]1[C@H](CN([Si](C)(C)C)[Si](C)(C)C)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	5064.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #307	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4913.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #308	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4904.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #309	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	4905.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4761.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #310	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	4906.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #311	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4876.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #312	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4873.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #313	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	4903.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #314	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4855.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #315	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@H]1O	4933.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #316	C[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]1O	4915.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #317	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4987.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #318	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4972.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #319	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4949.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4751.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #320	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5158.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #321	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5012.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #322	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4937.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #323	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4917.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #324	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5136.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #325	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5000.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #326	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4892.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #327	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5121.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #328	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5035.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #329	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	5115.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4766.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #330	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	5021.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #331	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4988.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #332	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4994.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #333	C[Si](C)(C)N[C@@H]1C[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5034.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #334	C[Si](C)(C)N[C@H]1C[C@@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5036.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #335	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	4977.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #336	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5001.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #337	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5061.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #338	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4989.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #339	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O)[C@H]1O	5046.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #34	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4845.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #340	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4936.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #341	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4980.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #342	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5024.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #343	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4988.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #344	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N([Si](C)(C)C)[Si](C)(C)C	5036.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #345	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5007.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #346	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5003.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #35	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4824.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #36	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	4813.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #37	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4804.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #38	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	4809.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #39	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4740.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4754.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #40	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4760.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #41	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O	4849.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #42	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4824.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #43	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	4803.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #44	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4802.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #45	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O	4792.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #46	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1N	4742.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #47	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4833.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #48	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4810.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #49	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4801.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1N	4745.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #50	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4808.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #51	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O	4798.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #52	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	4840.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #53	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4815.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #54	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4811.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #55	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4800.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #56	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C	4806.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #57	C[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4925.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #58	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	4915.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #59	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4903.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1N	4758.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #60	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@H]1O	4905.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #61	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N([Si](C)(C)C)[Si](C)(C)C)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4929.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #62	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4876.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #63	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4875.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #64	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C	4884.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #65	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N([Si](C)(C)C)[Si](C)(C)C)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4926.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #66	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4859.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #67	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4853.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #68	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	4955.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #69	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C)[C@@H](O)[C@@H]1O	4842.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #7	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4830.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #70	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	5071.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #71	C[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N([Si](C)(C)C)[Si](C)(C)C	4942.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #72	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4737.5	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #73	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4746.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #74	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4762.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #75	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4741.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #76	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@@H](N)C[C@H]1N	4745.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #77	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C	4798.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #78	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@@H]1O	4796.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #79	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4800.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #8	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4832.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #80	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4818.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #81	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4818.1	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #82	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4760.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #83	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	4774.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #84	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4755.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #85	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@@H](N)C[C@H]1N	4756.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #86	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4794.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #87	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C	4800.3	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #88	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4808.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #89	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4819.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #9	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	4813.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #90	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C	4821.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #91	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4786.6	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #92	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	4761.9	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #93	C[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]2N)[C@@H](N)C[C@H]1N	4764.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #94	C[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	4806.2	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #95	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O	4803.8	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #96	C[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	4816.4	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #97	C[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	4844.0	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #98	C[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4845.7	Semi standard non polar	33892256
Paromomycin,3TMS,isomer #99	C[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C)[C@@H]1O	4776.8	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5249.5	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5332.5	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5313.3	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5322.4	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5317.7	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	5240.9	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5258.1	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	5239.2	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](N)[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@H]1O	5241.5	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5249.7	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@@H]1N	5228.9	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #8	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	5233.1	Semi standard non polar	33892256
Paromomycin,1TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5346.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5287.8	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5336.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5369.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5329.0	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	5239.9	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	5243.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	5270.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5295.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2N)[C@@H](N)C[C@H]1N	5248.7	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2N)[C@@H](N)C[C@H]1N	5250.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5343.0	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5331.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5304.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5311.7	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5323.2	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #23	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O[Si](C)(C)C(C)(C)C	5334.2	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5279.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5275.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	5309.7	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	5286.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	5288.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #29	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1N	5350.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5280.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #30	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5367.7	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #31	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5383.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5343.9	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #33	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	5336.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #34	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	5226.7	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #35	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O	5227.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #36	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H](N)[C@H]1O	5260.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #37	CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H](N)[C@H]1O[Si](C)(C)C(C)(C)C	5250.2	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1N	5301.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #39	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5322.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5278.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #40	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5338.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #41	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5294.8	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #42	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	5309.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #43	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O	5229.8	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #44	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@@H]2O)[C@@H]1N	5229.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #45	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5264.0	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #46	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	5308.0	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #47	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1N	5304.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #48	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5324.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #49	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5333.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]1N	5294.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #50	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O	5296.2	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #51	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](N)[C@H]1O	5250.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #52	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1N	5253.9	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #53	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C(C)(C)C)[C@H]1O	5341.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #54	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C(C)(C)C)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5319.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #55	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	5314.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #56	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@H](N)[C@@H](O)[C@@H]1O	5348.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #57	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O[Si](C)(C)C(C)(C)C)O[C@@H](CN)[C@@H](O)[C@@H]1O	5303.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #58	CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](CN)O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@H]1O[Si](C)(C)C(C)(C)C	5238.7	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #59	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	5333.2	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1N	5269.0	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #60	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@H]2O)[C@H]1O	5311.9	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #61	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5290.8	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #62	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5291.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #63	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	5295.1	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #64	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	5342.8	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #65	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5316.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #66	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5294.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #67	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5295.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #68	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	5297.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #69	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5424.0	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](N)C[C@H](N)[C@H]2O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O)[C@@H]1O[C@H]1O[C@@H](CN)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1N	5268.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #70	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N[Si](C)(C)C(C)(C)C)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5400.9	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #71	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O	5398.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #72	CC(C)(C)[Si](C)(C)NC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	5385.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #73	CC(C)(C)[Si](C)(C)N(C[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	5544.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #74	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5391.9	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #75	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N[Si](C)(C)C(C)(C)C)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5397.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #76	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C(C)(C)C)[C@H]2O)[C@H]1O	5393.8	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #77	CC(C)(C)[Si](C)(C)N([C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O)[Si](C)(C)C(C)(C)C	5473.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #78	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C(C)(C)C)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5368.7	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #79	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N[Si](C)(C)C(C)(C)C	5371.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)[C@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@H]1O	5352.5	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #80	CC(C)(C)[Si](C)(C)N([C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N)[Si](C)(C)C(C)(C)C	5447.9	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #81	CC(C)(C)[Si](C)(C)N[C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N[Si](C)(C)C(C)(C)C)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O	5363.4	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #82	CC(C)(C)[Si](C)(C)N([C@H]1[C@@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]2O[C@H](CO)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	5498.6	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #83	CC(C)(C)[Si](C)(C)N([C@H]1[C@@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)O[C@@H](CN)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	5482.3	Semi standard non polar	33892256
Paromomycin,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N[C@H]1C[C@@H](N)[C@H](O)[C@@H](O[C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[C@H]3O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@H]2O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1N	5334.3	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (Non-derivatized) - 70eV, Positive	splash10-001i-9342160000-31e82797142b42a04602	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (1 TMS) - 70eV, Positive	splash10-05ai-9224006000-5f0d0b615d31a6175503	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_12) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_1_13) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Paromomycin GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-16	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 10V, Positive-QTOF	splash10-059t-0219482000-de54ecf4533aaf593cb7	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 20V, Positive-QTOF	splash10-08mr-0928620000-164caf74a05e11da1b90	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 40V, Positive-QTOF	splash10-074j-4916000000-9889a128fd12e51aa810	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 10V, Negative-QTOF	splash10-01p9-9014352000-7b4651a85addb05e31c8	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 20V, Negative-QTOF	splash10-0ff1-7928450000-0a6e638198c9d0cc1aa6	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 40V, Negative-QTOF	splash10-0fmi-5948010000-45dae05f691e7d1970ae	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 10V, Positive-QTOF	splash10-014l-0900448000-7d8ab098df904222341e	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 20V, Positive-QTOF	splash10-01ox-0900211000-56e8bf3a166490deef7f	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 40V, Positive-QTOF	splash10-0007-9812840000-4d2d1f05533b960d578a	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 10V, Negative-QTOF	splash10-03di-0101119000-a82209ef657383b76b04	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 20V, Negative-QTOF	splash10-03dl-4435198000-344c98991aa4d3444989	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Paromomycin 40V, Negative-QTOF	splash10-0fkc-5696400000-b9ad849333b79fa33235	2021-10-11	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
Paromomycin Action Pathway		Not Available

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry DB01421	21059682	details
Urine	Expected but not Quantified	Not Quantified	Not Available	Not Available	Taking drug identified by DrugBank entry DB01421	21059682	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB01421

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

C00018808

Chemspider ID

145115

KEGG Compound ID

C00832

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Paromomycin

METLIN ID

Not Available

PubChem Compound

165580

PDB ID

PAR

ChEBI ID

7934

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Vicens Q, Westhof E: Crystal structure of paromomycin docked into the eubacterial ribosomal decoding A site. Structure. 2001 Aug;9(8):647-58. [PubMed:11587639 ]

Showing metabocard for Paromomycin (HMDB0015490)

MOL for HMDB0015490 (Paromomycin)

3D MOL for HMDB0015490 (Paromomycin)

3D SDF for HMDB0015490 (Paromomycin)

3D-SDF for HMDB0015490 (Paromomycin)

PDB for HMDB0015490 (Paromomycin)

3D PDB for HMDB0015490 (Paromomycin)

SMILES for HMDB0015490 (Paromomycin)

INCHI for HMDB0015490 (Paromomycin)

Structure for HMDB0015490 (Paromomycin)

3D Structure for HMDB0015490 (Paromomycin)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra