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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2009-04-06 16:21:08 UTC

Update Date

2021-09-14 15:37:14 UTC

HMDB ID

HMDB0012214

Secondary Accession Numbers

HMDB12214

Metabolite Identification

Common Name

Dihydrozeatin-O-glucoside

Description

Dihydrozeatin-O-glucoside belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol, a phosphorylated alcohol (phosphoprenol), or a hydroxy fatty acid, or to one carboxyl group of a fatty acid (ester linkage) or an amino alcohol. Dihydrozeatin-O-glucoside is an extremely weak basic (essentially neutral) compound (based on its pKa). Dihydrozeatin-O-glucoside is the product of the O-glucosylation of dihydrozeatin in the cytokinin O-glucosylation. The O-glucosylation is reversible and resistant to beta-glucosidases. This reaction only shuts the physiological activity of the molecule temporarily, and is a way to store a molecule.

Structure

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


  Mrv1652306222023382D          

 33 35  0  0  1  0            999 V2000
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9920    0.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1715   -0.0180    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3276   -0.6855    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  8  1  1  1  0  0  0
  8  2  1  0  0  0  0
  8  5  1  0  0  0  0
  9  4  1  1  0  0  0
 11  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 10  2  0  0  0  0
 15 10  1  0  0  0  0
 16 13  1  0  0  0  0
 17  3  1  0  0  0  0
 17 14  1  0  0  0  0
 18  6  2  0  0  0  0
 18 10  1  0  0  0  0
 19  6  1  0  0  0  0
 19 15  2  0  0  0  0
 20  7  2  0  0  0  0
 20 14  1  0  0  0  0
 21  7  1  0  0  0  0
 21 15  1  0  0  0  0
 22  4  1  0  0  0  0
 11 23  1  6  0  0  0
 12 24  1  6  0  0  0
 13 25  1  6  0  0  0
 26  5  1  0  0  0  0
 16 26  1  1  0  0  0
 27  9  1  0  0  0  0
 27 16  1  0  0  0  0
  8 28  1  6  0  0  0
  9 29  1  6  0  0  0
 11 30  1  1  0  0  0
 12 31  1  6  0  0  0
 13 32  1  1  0  0  0
 16 33  1  6  0  0  0
M  END

HMDB0012214
     RDKit          3D
Dihydrozeatin-O-glucoside
 52 54  0  0  0  0  0  0  0  0999 V2000
   -0.0097    2.5838    0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5607    1.2266    0.7776 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8142    1.5958    1.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5020    0.3577    2.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9147   -0.5453    1.0508 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9794   -0.3299    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8007    0.7099    0.1343 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261    0.8573   -0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0805   -0.0579   -1.6899 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2940   -1.1361   -1.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2711   -2.2310   -2.5411 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2726   -3.0473   -2.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -2.4824   -1.1295 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2025   -1.3160   -0.8121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142    0.5991    1.7288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6739    0.3786    1.1784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6813   -0.4690    0.0891 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0729    0.2361   -1.0145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4044    0.5499   -1.0735 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9077    1.4236    0.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2431    2.6251    0.0272 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1786   -0.7374   -1.2088 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9163   -1.2589   -2.4743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588   -1.7276   -0.1348 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8189   -1.5605    0.8867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4760   -1.7061    0.3708 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7714   -2.8389   -0.0598 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5710    2.5008   -0.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8463    3.2925    0.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6320    3.0370    1.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8149    0.6367   -0.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975    2.2060    0.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5274    2.1796    2.4864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4577    0.6408    2.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8750   -0.1952    2.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3488   -1.4447    0.9798 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6767    1.4612    0.8423 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4733    1.7300   -0.7236 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9800   -4.0069   -2.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0054   -0.3336    2.1845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5614    1.3117    2.5661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178   -0.7836   -0.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5645    1.1092   -2.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9397    0.9283    1.0118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9858    1.6547   -0.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6940    3.3455   -0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2644   -0.4673   -1.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6591   -1.8637   -2.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0822   -2.7495   -0.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7055   -1.3646    0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5162   -1.8080    1.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147   -2.7161   -0.9882 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  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  2 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 14  6  2  0
 26 17  1  0
 14 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  6
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  7 37  1  0
  8 38  1  0
 12 39  1  0
 15 40  1  0
 15 41  1  0
 17 42  1  6
 19 43  1  6
 20 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  6
 23 48  1  0
 24 49  1  6
 25 50  1  0
 26 51  1  1
 27 52  1  0
M  END


  Mrv1652306222023382D          

 33 35  0  0  1  0            999 V2000
    3.5724   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9920    0.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.1447   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1715   -0.0180    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3276   -0.6855    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  8  1  1  1  0  0  0
  8  2  1  0  0  0  0
  8  5  1  0  0  0  0
  9  4  1  1  0  0  0
 11  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 10  2  0  0  0  0
 15 10  1  0  0  0  0
 16 13  1  0  0  0  0
 17  3  1  0  0  0  0
 17 14  1  0  0  0  0
 18  6  2  0  0  0  0
 18 10  1  0  0  0  0
 19  6  1  0  0  0  0
 19 15  2  0  0  0  0
 20  7  2  0  0  0  0
 20 14  1  0  0  0  0
 21  7  1  0  0  0  0
 21 15  1  0  0  0  0
 22  4  1  0  0  0  0
 11 23  1  6  0  0  0
 12 24  1  6  0  0  0
 13 25  1  6  0  0  0
 26  5  1  0  0  0  0
 16 26  1  1  0  0  0
 27  9  1  0  0  0  0
 27 16  1  0  0  0  0
  8 28  1  6  0  0  0
  9 29  1  6  0  0  0
 11 30  1  1  0  0  0
 12 31  1  6  0  0  0
 13 32  1  1  0  0  0
 16 33  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0012214

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@](C)(CCNC1=C2N=CN=C2NC=N1)CO[C@]1([H])O[C@]([H])(CO)[C@@]([H])(O)[C@]([H])(O)[C@@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C16H25N5O6/c1-8(2-3-17-14-10-15(19-6-18-10)21-7-20-14)5-26-16-13(25)12(24)11(23)9(4-22)27-16/h6-9,11-13,16,22-25H,2-5H2,1H3,(H2,17,18,19,20,21)/t8-,9+,11+,12-,13+,16+/m0/s1

> <INCHI_KEY>
QRZHDHJUYBONQQ-CBGBLGFFSA-N

> <FORMULA>
C16H25N5O6

> <MOLECULAR_WEIGHT>
383.405

> <EXACT_MASS>
383.180483545

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.529054064947594

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2S)-2-methyl-4-[(3H-purin-6-yl)amino]butoxy]oxane-3,4,5-triol

> <ALOGPS_LOGP>
-1.43

> <JCHEM_LOGP>
-1.7479510699999987

> <ALOGPS_LOGS>
-2.81

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.210974071736148

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.552529813299208

> <JCHEM_PKA_STRONGEST_BASIC>
3.0286256189920744

> <JCHEM_POLAR_SURFACE_AREA>
165.87

> <JCHEM_REFRACTIVITY>
94.7799

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.95e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2S)-2-methyl-4-(3H-purin-6-ylamino)butoxy]oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0012214
     RDKit          3D
Dihydrozeatin-O-glucoside
 52 54  0  0  0  0  0  0  0  0999 V2000
   -0.0097    2.5838    0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5607    1.2266    0.7776 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8142    1.5958    1.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5020    0.3577    2.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9147   -0.5453    1.0508 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9794   -0.3299    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8007    0.7099    0.1343 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261    0.8573   -0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0805   -0.0579   -1.6899 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2940   -1.1361   -1.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2711   -2.2310   -2.5411 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2726   -3.0473   -2.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -2.4824   -1.1295 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2025   -1.3160   -0.8121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142    0.5991    1.7288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6739    0.3786    1.1784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6813   -0.4690    0.0891 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0729    0.2361   -1.0145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4044    0.5499   -1.0735 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9077    1.4236    0.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2431    2.6251    0.0272 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1786   -0.7374   -1.2088 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9163   -1.2589   -2.4743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588   -1.7276   -0.1348 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8189   -1.5605    0.8867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4760   -1.7061    0.3708 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7714   -2.8389   -0.0598 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5710    2.5008   -0.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8463    3.2925    0.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6320    3.0370    1.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8149    0.6367   -0.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975    2.2060    0.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5274    2.1796    2.4864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4577    0.6408    2.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8750   -0.1952    2.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3488   -1.4447    0.9798 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6767    1.4612    0.8423 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4733    1.7300   -0.7236 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9800   -4.0069   -2.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0054   -0.3336    2.1845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5614    1.3117    2.5661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178   -0.7836   -0.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5645    1.1092   -2.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9397    0.9283    1.0118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9858    1.6547   -0.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6940    3.3455   -0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2644   -0.4673   -1.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6591   -1.8637   -2.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0822   -2.7495   -0.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7055   -1.3646    0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5162   -1.8080    1.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147   -2.7161   -0.9882 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  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  2 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 14  6  2  0
 26 17  1  0
 14 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  6
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  7 37  1  0
  8 38  1  0
 12 39  1  0
 15 40  1  0
 15 41  1  0
 17 42  1  6
 19 43  1  6
 20 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  6
 23 48  1  0
 24 49  1  6
 25 50  1  0
 26 51  1  1
 27 52  1  0
M  END

HEADER    PROTEIN                                 22-JUN-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-JUN-20         0                                  
HETATM    1  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.671  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.852   0.127   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.337  -1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       2.667  -1.540   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0      -0.320  -0.034   0.000  0.00  0.00           N+0
HETATM   19  N   UNK     0      -2.478  -1.280   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0       1.334  -3.850   0.000  0.00  0.00           N+0
HETATM   21  N   UNK     0      -1.334  -3.850   0.000  0.00  0.00           N+0
HETATM   22  O   UNK     0      16.004  -1.540   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      14.671   0.770   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      12.003   2.310   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       9.336   0.770   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      12.003  -2.310   0.000  0.00  0.00           O+0
HETATM   28  H   UNK     0       5.335  -3.080   0.000  0.00  0.00           H+0
HETATM   29  H   UNK     0      14.671  -0.770   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0      13.337   1.540   0.000  0.00  0.00           H+0
HETATM   31  H   UNK     0      12.003  -0.770   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0      10.669   1.540   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       9.336  -0.770   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2    3    8                                                       
CONECT    3    2   17                                                       
CONECT    4    9   22                                                       
CONECT    5    8   26                                                       
CONECT    6   18   19                                                       
CONECT    7   20   21                                                       
CONECT    8    1    2    5   28                                             
CONECT    9    4   11   27   29                                             
CONECT   10   14   15   18                                                  
CONECT   11    9   12   23   30                                             
CONECT   12   11   13   24   31                                             
CONECT   13   12   16   25   32                                             
CONECT   14   10   17   20                                                  
CONECT   15   10   19   21                                                  
CONECT   16   13   26   27   33                                             
CONECT   17    3   14                                                       
CONECT   18    6   10                                                       
CONECT   19    6   15                                                       
CONECT   20    7   14                                                       
CONECT   21    7   15                                                       
CONECT   22    4                                                            
CONECT   23   11                                                            
CONECT   24   12                                                            
CONECT   25   13                                                            
CONECT   26    5   16                                                       
CONECT   27    9   16                                                       
CONECT   28    8                                                            
CONECT   29    9                                                            
CONECT   30   11                                                            
CONECT   31   12                                                            
CONECT   32   13                                                            
CONECT   33   16                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

COMPND    HMDB0012214
HETATM    1  C1  UNL     1      -0.010   2.584   0.326  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.561   1.227   0.778  1.00  0.00           C  
HETATM    3  C3  UNL     1       1.814   1.596   1.576  1.00  0.00           C  
HETATM    4  C4  UNL     1       2.502   0.358   2.089  1.00  0.00           C  
HETATM    5  N1  UNL     1       2.915  -0.545   1.051  1.00  0.00           N  
HETATM    6  C5  UNL     1       3.979  -0.330   0.148  1.00  0.00           C  
HETATM    7  N2  UNL     1       4.801   0.710   0.134  1.00  0.00           N  
HETATM    8  C6  UNL     1       5.826   0.857  -0.752  1.00  0.00           C  
HETATM    9  N3  UNL     1       6.080  -0.058  -1.690  1.00  0.00           N  
HETATM   10  C7  UNL     1       5.294  -1.136  -1.738  1.00  0.00           C  
HETATM   11  N4  UNL     1       5.271  -2.231  -2.541  1.00  0.00           N  
HETATM   12  C8  UNL     1       4.273  -3.047  -2.185  1.00  0.00           C  
HETATM   13  N5  UNL     1       3.625  -2.482  -1.130  1.00  0.00           N  
HETATM   14  C9  UNL     1       4.203  -1.316  -0.812  1.00  0.00           C  
HETATM   15  C10 UNL     1      -0.414   0.599   1.729  1.00  0.00           C  
HETATM   16  O1  UNL     1      -1.674   0.379   1.178  1.00  0.00           O  
HETATM   17  C11 UNL     1      -1.681  -0.469   0.089  1.00  0.00           C  
HETATM   18  O2  UNL     1      -2.073   0.236  -1.015  1.00  0.00           O  
HETATM   19  C12 UNL     1      -3.404   0.550  -1.074  1.00  0.00           C  
HETATM   20  C13 UNL     1      -3.908   1.424   0.024  1.00  0.00           C  
HETATM   21  O3  UNL     1      -3.243   2.625   0.027  1.00  0.00           O  
HETATM   22  C14 UNL     1      -4.179  -0.737  -1.209  1.00  0.00           C  
HETATM   23  O4  UNL     1      -3.916  -1.259  -2.474  1.00  0.00           O  
HETATM   24  C15 UNL     1      -3.859  -1.728  -0.135  1.00  0.00           C  
HETATM   25  O5  UNL     1      -4.819  -1.561   0.887  1.00  0.00           O  
HETATM   26  C16 UNL     1      -2.476  -1.706   0.371  1.00  0.00           C  
HETATM   27  O6  UNL     1      -1.771  -2.839  -0.060  1.00  0.00           O  
HETATM   28  H1  UNL     1      -0.571   2.501  -0.607  1.00  0.00           H  
HETATM   29  H2  UNL     1       0.846   3.292   0.155  1.00  0.00           H  
HETATM   30  H3  UNL     1      -0.632   3.037   1.124  1.00  0.00           H  
HETATM   31  H4  UNL     1       0.815   0.637  -0.103  1.00  0.00           H  
HETATM   32  H5  UNL     1       2.497   2.206   0.995  1.00  0.00           H  
HETATM   33  H6  UNL     1       1.527   2.180   2.486  1.00  0.00           H  
HETATM   34  H7  UNL     1       3.458   0.641   2.626  1.00  0.00           H  
HETATM   35  H8  UNL     1       1.875  -0.195   2.817  1.00  0.00           H  
HETATM   36  H9  UNL     1       2.349  -1.445   0.980  1.00  0.00           H  
HETATM   37  H10 UNL     1       4.677   1.461   0.842  1.00  0.00           H  
HETATM   38  H11 UNL     1       6.473   1.730  -0.724  1.00  0.00           H  
HETATM   39  H12 UNL     1       3.980  -4.007  -2.624  1.00  0.00           H  
HETATM   40  H13 UNL     1      -0.005  -0.334   2.185  1.00  0.00           H  
HETATM   41  H14 UNL     1      -0.561   1.312   2.566  1.00  0.00           H  
HETATM   42  H15 UNL     1      -0.618  -0.784  -0.084  1.00  0.00           H  
HETATM   43  H16 UNL     1      -3.565   1.109  -2.037  1.00  0.00           H  
HETATM   44  H17 UNL     1      -3.940   0.928   1.012  1.00  0.00           H  
HETATM   45  H18 UNL     1      -4.986   1.655  -0.219  1.00  0.00           H  
HETATM   46  H19 UNL     1      -3.694   3.346  -0.487  1.00  0.00           H  
HETATM   47  H20 UNL     1      -5.264  -0.467  -1.194  1.00  0.00           H  
HETATM   48  H21 UNL     1      -4.659  -1.864  -2.751  1.00  0.00           H  
HETATM   49  H22 UNL     1      -4.082  -2.749  -0.559  1.00  0.00           H  
HETATM   50  H23 UNL     1      -5.705  -1.365   0.467  1.00  0.00           H  
HETATM   51  H24 UNL     1      -2.516  -1.808   1.496  1.00  0.00           H  
HETATM   52  H25 UNL     1      -1.415  -2.716  -0.988  1.00  0.00           H  
CONECT    1    2   28   29   30
CONECT    2    3   15   31
CONECT    3    4   32   33
CONECT    4    5   34   35
CONECT    5    6   36
CONECT    6    7   14   14
CONECT    7    8   37
CONECT    8    9    9   38
CONECT    9   10
CONECT   10   11   11   14
CONECT   11   12
CONECT   12   13   13   39
CONECT   13   14
CONECT   15   16   40   41
CONECT   16   17
CONECT   17   18   26   42
CONECT   18   19
CONECT   19   20   22   43
CONECT   20   21   44   45
CONECT   21   46
CONECT   22   23   24   47
CONECT   23   48
CONECT   24   25   26   49
CONECT   25   50
CONECT   26   27   51
CONECT   27   52
END

HMDB0012214
     RDKit          3D
Dihydrozeatin-O-glucoside
 52 54  0  0  0  0  0  0  0  0999 V2000
   -0.0097    2.5838    0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5607    1.2266    0.7776 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8142    1.5958    1.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5020    0.3577    2.0893 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9147   -0.5453    1.0508 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9794   -0.3299    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8007    0.7099    0.1343 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8261    0.8573   -0.7522 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0805   -0.0579   -1.6899 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2940   -1.1361   -1.7379 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2711   -2.2310   -2.5411 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2726   -3.0473   -2.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6248   -2.4824   -1.1295 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2025   -1.3160   -0.8121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4142    0.5991    1.7288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6739    0.3786    1.1784 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6813   -0.4690    0.0891 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0729    0.2361   -1.0145 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4044    0.5499   -1.0735 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9077    1.4236    0.0240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2431    2.6251    0.0272 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1786   -0.7374   -1.2088 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9163   -1.2589   -2.4743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8588   -1.7276   -0.1348 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8189   -1.5605    0.8867 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4760   -1.7061    0.3708 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7714   -2.8389   -0.0598 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5710    2.5008   -0.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8463    3.2925    0.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6320    3.0370    1.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8149    0.6367   -0.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4975    2.2060    0.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5274    2.1796    2.4864 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4577    0.6408    2.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8750   -0.1952    2.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3488   -1.4447    0.9798 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6767    1.4612    0.8423 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4733    1.7300   -0.7236 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9800   -4.0069   -2.6243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0054   -0.3336    2.1845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5614    1.3117    2.5661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178   -0.7836   -0.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5645    1.1092   -2.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9397    0.9283    1.0118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9858    1.6547   -0.2194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6940    3.3455   -0.4867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2644   -0.4673   -1.1939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6591   -1.8637   -2.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0822   -2.7495   -0.5592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7055   -1.3646    0.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5162   -1.8080    1.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4147   -2.7161   -0.9882 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  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
  2 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 14  6  2  0
 26 17  1  0
 14 10  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  6
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  7 37  1  0
  8 38  1  0
 12 39  1  0
 15 40  1  0
 15 41  1  0
 17 42  1  6
 19 43  1  6
 20 44  1  0
 20 45  1  0
 21 46  1  0
 22 47  1  6
 23 48  1  0
 24 49  1  6
 25 50  1  0
 26 51  1  1
 27 52  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-Methyl-4-(1H-purin-6-ylamino)butyl beta-D-glucopyranoside	HMDB
2-Methyl-4-(1H-purin-6-ylamino)butyl β-D-glucopyranoside	HMDB
Dihydrozeatin O-beta-D-glucoside	HMDB
Dihydrozeatin O-glucoside	HMDB
Dihydrozeatin O-β-D-glucoside	HMDB
O-beta-D-Glucopyranosyldihydrozeatin	HMDB
O-Β-D-glucopyranosyldihydrozeatin	HMDB

Chemical Formula

C₁₆H₂₅N₅O₆

Average Molecular Weight

383.405

Monoisotopic Molecular Weight

383.180483545

IUPAC Name

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2S)-2-methyl-4-[(3H-purin-6-yl)amino]butoxy]oxane-3,4,5-triol

Traditional Name

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2S)-2-methyl-4-(3H-purin-6-ylamino)butoxy]oxane-3,4,5-triol

CAS Registry Number

62512-96-3

SMILES

C[C@@H](CCNC1=C2N=CN=C2N=CN1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C16H25N5O6/c1-8(2-3-17-14-10-15(19-6-18-10)21-7-20-14)5-26-16-13(25)12(24)11(23)9(4-22)27-16/h6-9,11-13,16,22-25H,2-5H2,1H3,(H2,17,18,19,20,21)/t8-,9+,11+,12-,13+,16+/m0/s1

InChI Key

QRZHDHJUYBONQQ-CBGBLGFFSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl glycosides

Direct Parent

Fatty acyl glycosides of mono- and disaccharides

Alternative Parents

Substituents

Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
6-alkylaminopurine
O-glycosyl compound
Glycosyl compound
6-aminopurine
Purine
Imidazopyrimidine
Secondary aliphatic/aromatic amine
Aminopyrimidine
Imidolactam
Pyrimidine
Oxane
Monosaccharide
Heteroaromatic compound
Imidazole
Azole
Secondary alcohol
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary amine
Polyol
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0012214)
Cell membrane (HMDB: HMDB0012214)

Biofluid or Excreta

Urine (HMDB: HMDB0012214)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0012214)

Source

Endogenous

Endogenous (HMDB: HMDB0012214)

Plant

Animal

Animal (HMDB: HMDB0012214)

Exogenous

Food

Food (HMDB: HMDB0012214)

Animal origin

Poultry

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Herb and spice mixture

Curry powder (FooDB: FOOD00678)

Herbs and Spices (FooDB: FOOD00866)

Vegetable

Cabbage

Onion-family vegetable

Allium (FooDB: FOOD00005)
Garden onion (FooDB: FOOD00006)
Leek (FooDB: FOOD00007)
Garden onion (var.) (FooDB: FOOD00226)
Shallot (FooDB: FOOD00243)
Wild leek (FooDB: FOOD00396)
Red onion (FooDB: FOOD00962)
Green onion (FooDB: FOOD00963)
Onion-family vegetables (FooDB: FOOD00855)

Root vegetable

Shoot vegetable

Leaf vegetable

Common beet (FooDB: FOOD00025)
Endive (FooDB: FOOD00048)
Rocket salad (ssp.) (FooDB: FOOD00077)
Swamp cabbage (FooDB: FOOD00091)
Lettuce (FooDB: FOOD00095)
Garden cress (FooDB: FOOD00099)
Spinach (FooDB: FOOD00178)
Swiss chard (FooDB: FOOD00237)
Chicory leaves (FooDB: FOOD00250)
Garland chrysanthemum (FooDB: FOOD00333)
Corn salad (FooDB: FOOD00340)
Jute (FooDB: FOOD00389)
Lambsquarters (FooDB: FOOD00394)
Malabar spinach (FooDB: FOOD00404)
New Zealand spinach (FooDB: FOOD00415)
Yautia (FooDB: FOOD00510)
Ostrich fern (FooDB: FOOD00556)
Romaine lettuce (FooDB: FOOD00888)
Iceberg lettuce (FooDB: FOOD00973)
Pea shoots (FooDB: FOOD00975)
Yau choy (FooDB: FOOD00976)
Water spinach (FooDB: FOOD00977)
Rocket salad (FooDB: FOOD00244)
Green vegetables (FooDB: FOOD00872)

Fruit vegetable

Pepper (FooDB: FOOD00040)
Olive (FooDB: FOOD00121)
Avocado (FooDB: FOOD00130)
Garden tomato (FooDB: FOOD00171)
Cherry tomato (FooDB: FOOD00172)
Garden tomato (var.) (FooDB: FOOD00173)
Eggplant (FooDB: FOOD00174)
Pepper (C. baccatum) (FooDB: FOOD00231)
Pepper (C. chinense) (FooDB: FOOD00232)
Pepper (Capsicum) (FooDB: FOOD00233)
Groundcherry (FooDB: FOOD00371)
Pepper (C. frutescens) (FooDB: FOOD00428)
Mexican groundcherry (FooDB: FOOD00491)
Pepper (C. pubescens) (FooDB: FOOD00849)
Green bell pepper (FooDB: FOOD00877)
Yellow bell pepper (FooDB: FOOD00878)
Orange bell pepper (FooDB: FOOD00879)
Red bell pepper (FooDB: FOOD00880)
Italian sweet red pepper (FooDB: FOOD00881)
Jalapeno pepper (FooDB: FOOD00955)
Cubanelle pepper (FooDB: FOOD00971)

Tuber

Stalk vegetable

Other vegetable

Giant butterbur (FooDB: FOOD00314)
Carob (FooDB: FOOD00321)
Chinese water chestnut (FooDB: FOOD00332)
Horseradish tree (FooDB: FOOD00379)
Sacred lotus (FooDB: FOOD00402)
Nopal (FooDB: FOOD00416)
Okra (FooDB: FOOD00420)
Sesbania flower (FooDB: FOOD00469)
Agave (FooDB: FOOD00563)
Narrowleaf cattail (FooDB: FOOD00564)
Heart of palm (FooDB: FOOD00718)
Tree fern (FooDB: FOOD00797)

Mushroom

Castanospermum australe (FooDB: FOOD00893)
Gentiana lutea (FooDB: FOOD00894)
Juniperus communis (FooDB: FOOD00895)
Albizia gummifera (FooDB: FOOD00896)

Brassica

Brassicas (FooDB: FOOD00857)

Fruit

Tropical fruit

Citrus

Lime (FooDB: FOOD00053)
Lemon (FooDB: FOOD00054)
Pummelo (FooDB: FOOD00055)
Mandarin orange (Clementine, Tangerine) (FooDB: FOOD00056)
Sweet orange (FooDB: FOOD00057)
Grapefruit/Pummelo hybrid (FooDB: FOOD00255)
Grapefruit (FooDB: FOOD00256)
Persian lime (FooDB: FOOD00543)
Sour orange (FooDB: FOOD00918)
Mikan (FooDB: FOOD00932)
Clementine (FooDB: FOOD00959)
Citrus (FooDB: FOOD00859)

Pome

Berry

Black crowberry (FooDB: FOOD00075)
Strawberry (FooDB: FOOD00083)
Black huckleberry (FooDB: FOOD00084)
Sea-buckthornberry (FooDB: FOOD00087)
Mulberry (FooDB: FOOD00116)
Black mulberry (FooDB: FOOD00117)
Black chokeberry (FooDB: FOOD00136)
Blackcurrant (FooDB: FOOD00155)
Redcurrant (FooDB: FOOD00156)
Gooseberry (FooDB: FOOD00157)
Cloudberry (FooDB: FOOD00161)
Red raspberry (FooDB: FOOD00162)
Black raspberry (FooDB: FOOD00163)
Black elderberry (FooDB: FOOD00166)
Rowanberry (FooDB: FOOD00176)
Vaccinium (Blueberry, Cranberry, Huckleberry) (FooDB: FOOD00188)
Lowbush blueberry (FooDB: FOOD00189)
Sparkleberry (FooDB: FOOD00190)
Highbush blueberry (FooDB: FOOD00191)
American cranberry (FooDB: FOOD00192)
Bilberry (FooDB: FOOD00193)
Lingonberry (FooDB: FOOD00194)
Muscadine grape (FooDB: FOOD00203)
Common grape (FooDB: FOOD00204)
Arctic blackberry (FooDB: FOOD00207)
Bayberry (FooDB: FOOD00209)
Elliott's blueberry (FooDB: FOOD00210)
Canada blueberry (FooDB: FOOD00211)
Bog bilberry (FooDB: FOOD00212)
Buffalo currant (FooDB: FOOD00213)
European cranberry (FooDB: FOOD00217)
Deerberry (FooDB: FOOD00218)
Cascade huckleberry (FooDB: FOOD00220)
Oval-leaf huckleberry (FooDB: FOOD00221)
Evergreen huckleberry (FooDB: FOOD00222)
Red huckleberry (FooDB: FOOD00223)
Summer grape (FooDB: FOOD00227)
Fox grape (FooDB: FOOD00228)
Half-highbush blueberry (FooDB: FOOD00248)
Jostaberry (FooDB: FOOD00257)
Sweet rowanberry (FooDB: FOOD00265)
Skunk currant (FooDB: FOOD00267)
Squashberry (FooDB: FOOD00344)
Elderberry (FooDB: FOOD00358)
Grape (FooDB: FOOD00369)
Alaska blueberry (FooDB: FOOD00380)
Loganberry (FooDB: FOOD00400)
Ohelo berry (FooDB: FOOD00419)
Salmonberry (FooDB: FOOD00456)
Strawberry guava (FooDB: FOOD00482)
Boysenberry (FooDB: FOOD00542)
Chinese bayberry (FooDB: FOOD00852)
Saskatoon berry (FooDB: FOOD00884)
Nanking cherry (FooDB: FOOD00885)
Rabbiteye blueberry (FooDB: FOOD00898)
Blackberry (FooDB: FOOD00906)
Partridge berry (FooDB: FOOD00931)
Green grape (FooDB: FOOD00964)
Red grape (FooDB: FOOD00965)
Black plum (FooDB: FOOD00966)
Black raisin (FooDB: FOOD00968)
Chinese plum (FooDB: FOOD00978)
Green plum (FooDB: FOOD00979)
Wampee (FooDB: FOOD00980)
Goji (FooDB: FOOD00982)
Monk fruit (FooDB: FOOD00983)
Hawthorn (FooDB: FOOD00985)
Lantern fruit (FooDB: FOOD00986)
Cape gooseberry (FooDB: FOOD00988)
Rubus (Blackberry, Raspberry) (FooDB: FOOD00160)

Other fruit

Fig (FooDB: FOOD00081)
Date (FooDB: FOOD00135)
Jujube (FooDB: FOOD00388)

Drupe

Prunus (Cherry, Plum) (FooDB: FOOD00143)
Apricot (FooDB: FOOD00144)
Sweet cherry (FooDB: FOOD00145)
Sour cherry (FooDB: FOOD00146)
European plum (FooDB: FOOD00147)
Peach (FooDB: FOOD00149)
Nectarine (FooDB: FOOD00229)
Peach (var.) (FooDB: FOOD00230)
Common chokecherry (FooDB: FOOD00562)

Fruits (FooDB: FOOD00871)

Nut

Cashew nut (FooDB: FOOD00011)
Peanut (FooDB: FOOD00016)
Brazil nut (FooDB: FOOD00024)
Pecan nut (FooDB: FOOD00044)
Chestnut (FooDB: FOOD00045)
Common hazelnut (FooDB: FOOD00062)
Black walnut (FooDB: FOOD00093)
Common walnut (FooDB: FOOD00094)
Pine nut (FooDB: FOOD00138)
Pistachio (FooDB: FOOD00140)
Almond (FooDB: FOOD00148)
Macadamia nut (M. tetraphylla) (FooDB: FOOD00225)
Japanese walnut (FooDB: FOOD00240)
Acorn (FooDB: FOOD00282)
Beech nut (FooDB: FOOD00299)
Butternut (FooDB: FOOD00316)
Chinese chestnut (FooDB: FOOD00331)
European chestnut (FooDB: FOOD00363)
Hazelnut (FooDB: FOOD00376)
Hickory nut (FooDB: FOOD00377)
Japanese chestnut (FooDB: FOOD00385)
Pili nut (FooDB: FOOD00432)
Colorado pinyon (FooDB: FOOD00433)
Macadamia nut (FooDB: FOOD00525)
Walnut (FooDB: FOOD00608)
Mixed nuts (FooDB: FOOD00771)
Nuts (FooDB: FOOD00869)

Cereal and cereal product

Cereal

Cereal product

Dough

Sourdough (FooDB: FOOD00275)

Leavened bread

Flat bread

Other bread

Potato bread (FooDB: FOOD00811)
Other bread (FooDB: FOOD00269)

Sweet bread

Raisin bread (FooDB: FOOD00817)

Cereals and cereal products (FooDB: FOOD00858)

Pulse

Pea

Lentil

Lentils (FooDB: FOOD00098)

Other pulse

Lupine (FooDB: FOOD00104)
White lupine (FooDB: FOOD00403)

Bean

Green lentil (FooDB: FOOD00970)
Pulses (FooDB: FOOD00867)

Gourd

Watermelon (FooDB: FOOD00052)
Muskmelon (FooDB: FOOD00064)
Cucumber (FooDB: FOOD00065)
Cucurbita (FooDB: FOOD00066)
Bitter gourd (FooDB: FOOD00115)
Winter squash (FooDB: FOOD00283)
Butternut squash (FooDB: FOOD00317)
Calabash (FooDB: FOOD00318)
Chayote (FooDB: FOOD00325)
Towel gourd (FooDB: FOOD00492)
Wax gourd (FooDB: FOOD00499)
Tinda (FooDB: FOOD00559)
Horned melon (FooDB: FOOD00761)
Sunburst squash (pattypan squash) (FooDB: FOOD00874)
Green zucchini (FooDB: FOOD00875)
Yellow zucchini (FooDB: FOOD00876)
Japanese pumpkin (FooDB: FOOD00886)
Acorn squash (FooDB: FOOD00972)
Cantaloupe melon (FooDB: FOOD00984)

Coffee and coffee product

Coffee

Arabica coffee (FooDB: FOOD00059)
Robusta coffee (FooDB: FOOD00060)

Soy

Soy bean (FooDB: FOOD00085)

Soy product

Dish

Other dish

Taco shell (FooDB: FOOD00991)
Tostada shell (FooDB: FOOD00992)

Tea

Herbal tea

Hibiscus tea (FooDB: FOOD00723)
Greenthread tea (FooDB: FOOD00820)

Baking good

Wrapper

Wonton wrapper (FooDB: FOOD00818)

Abalone (FooDB: FOOD00279)
Conch (FooDB: FOOD00611)

Cocoa and cocoa product

Cocoa

Cocoa bean (FooDB: FOOD00182)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0012214)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0012214)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0012214)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0012214)

Nutrient

Nutrient (HMDB: HMDB0012214)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	4.96 g/L	ALOGPS
logP	-1.4	ALOGPS
logP	-1.7	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	5.55	ChemAxon
pKa (Strongest Basic)	3.03	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	165.87 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	94.78 m³·mol⁻¹	ChemAxon
Polarizability	38.53 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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]+	180.519	30932474
DeepCCS	[M-H]-	178.123	30932474
DeepCCS	[M-2H]-	211.682	30932474
DeepCCS	[M+Na]+	186.431	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Dihydrozeatin-O-glucoside	C[C@@H](CCNC1=C2N=CN=C2N=CN1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3878.5	Standard polar	33892256
Dihydrozeatin-O-glucoside	C[C@@H](CCNC1=C2N=CN=C2N=CN1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3254.1	Standard non polar	33892256
Dihydrozeatin-O-glucoside	C[C@@H](CCNC1=C2N=CN=C2N=CN1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3629.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Dihydrozeatin-O-glucoside,1TMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3457.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3436.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TMS,isomer #3	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3429.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TMS,isomer #4	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3430.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TMS,isomer #5	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3374.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TMS,isomer #6	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3484.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3381.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #10	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3350.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #11	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3314.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #12	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3423.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #13	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3308.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #14	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3410.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #15	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3384.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3362.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #3	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3361.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #4	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3318.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #5	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3427.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #6	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3341.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #7	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3345.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #8	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3305.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TMS,isomer #9	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3415.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3339.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #10	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3338.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #11	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3327.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #12	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3271.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #13	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3378.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #14	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3281.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #15	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3369.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #16	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3326.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #17	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3282.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #18	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3385.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #19	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3326.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3341.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #20	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3326.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #3	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3298.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #4	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3405.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #5	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3330.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #6	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3286.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #7	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3386.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #8	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3289.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TMS,isomer #9	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3381.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3348.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #10	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C	3326.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #11	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3305.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #12	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3398.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #13	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3317.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #14	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3315.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #15	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3326.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #2	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3302.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #3	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3396.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #4	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3302.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #5	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3391.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #6	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O	3341.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #7	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3298.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #8	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3389.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TMS,isomer #9	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O	3326.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #1	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3343.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #1	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3229.9	Standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #1	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4016.9	Standard polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3407.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3405.2	Standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4310.6	Standard polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #3	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3360.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #3	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	3346.2	Standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #3	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O	4110.7	Standard polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #4	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3369.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #4	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	3363.8	Standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #4	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C	4091.5	Standard polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #5	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3355.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #5	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3355.4	Standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #5	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4141.8	Standard polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #6	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3360.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #6	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3334.9	Standard non polar	33892256
Dihydrozeatin-O-glucoside,5TMS,isomer #6	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	4075.2	Standard polar	33892256
Dihydrozeatin-O-glucoside,6TMS,isomer #1	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3428.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,6TMS,isomer #1	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3313.0	Standard non polar	33892256
Dihydrozeatin-O-glucoside,6TMS,isomer #1	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C)[Si](C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C	3906.1	Standard polar	33892256
Dihydrozeatin-O-glucoside,1TBDMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3670.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TBDMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3659.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TBDMS,isomer #3	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3647.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TBDMS,isomer #4	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3648.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TBDMS,isomer #5	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3595.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,1TBDMS,isomer #6	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3721.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3757.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #10	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3693.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #11	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3670.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #12	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3796.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #13	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3675.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #14	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3791.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #15	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O	3790.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3731.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #3	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3740.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #4	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3703.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #5	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3821.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #6	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3679.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #7	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3681.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #8	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3674.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,2TBDMS,isomer #9	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3799.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3806.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #10	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O	3900.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #11	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3775.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #12	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3761.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #13	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3881.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #14	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3765.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #15	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3877.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #16	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3893.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #17	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3775.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #18	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3890.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #19	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3877.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #2	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3829.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #20	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3886.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #3	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3810.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #4	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	3933.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #5	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3800.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #6	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3783.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #7	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3911.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #8	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3805.3	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,3TBDMS,isomer #9	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3917.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #1	C[C@@H](CCNC1=C2N=CN=C2N=C[NH]1)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3981.1	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #10	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4042.4	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #11	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3904.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #12	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4007.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #13	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4004.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #14	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4005.8	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #15	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4013.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #2	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	3927.2	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #3	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4039.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #4	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	3949.5	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #5	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C	4063.6	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #6	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O	4054.0	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #7	C[C@@H](CCN(C1=C2N=CN=C2N=C[NH]1)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	3924.7	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #8	C[C@@H](CCNC1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C	4034.9	Semi standard non polar	33892256
Dihydrozeatin-O-glucoside,4TBDMS,isomer #9	C[C@@H](CCN(C1=C2N=CN=C2N=CN1[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)CO[C@@H]1O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O	4027.2	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 - Dihydrozeatin-O-glucoside GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - Dihydrozeatin-O-glucoside 10V, Positive-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 20V, Positive-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 40V, Positive-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 10V, Negative-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 20V, Negative-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 40V, Negative-QTOF	Not Available	2020-06-30	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 10V, Positive-QTOF	splash10-001i-0029000000-1d4fa4568269c5513fe1	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 20V, Positive-QTOF	splash10-0udr-1590000000-bedae57f5163cce0bf56	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 40V, Positive-QTOF	splash10-053l-3950000000-1df2011698a703ebaa47	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 10V, Negative-QTOF	splash10-001i-0219000000-d5479b5efb688910d114	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 20V, Negative-QTOF	splash10-05ai-8169000000-8026572c94303a33a5ae	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Dihydrozeatin-O-glucoside 40V, Negative-QTOF	splash10-001i-6911000000-0b8ca0c247125649df48	2021-09-25	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

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB028859

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

CPD-4617

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Dihydrozeatin-O-glucoside (HMDB0012214)

MOL for HMDB0012214 (Dihydrozeatin-O-glucoside)

3D MOL for HMDB0012214 (Dihydrozeatin-O-glucoside)

3D SDF for HMDB0012214 (Dihydrozeatin-O-glucoside)

3D-SDF for HMDB0012214 (Dihydrozeatin-O-glucoside)

PDB for HMDB0012214 (Dihydrozeatin-O-glucoside)

3D PDB for HMDB0012214 (Dihydrozeatin-O-glucoside)

SMILES for HMDB0012214 (Dihydrozeatin-O-glucoside)

INCHI for HMDB0012214 (Dihydrozeatin-O-glucoside)

Structure for HMDB0012214 (Dihydrozeatin-O-glucoside)

3D Structure for HMDB0012214 (Dihydrozeatin-O-glucoside)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra