Hmdb loader

Showing metabocard for Mangiferin (HMDB0034410)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 19:15:05 UTC
Update Date2022-03-07 02:54:05 UTC
HMDB IDHMDB0034410
Secondary Accession Numbers
  • HMDB34410
Metabolite Identification
Common NameMangiferin
DescriptionMangiferin belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. Mangiferin has been detected, but not quantified in, fruits and mangos (Mangifera indica). This could make mangiferin a potential biomarker for the consumption of these foods. Based on a literature review a small amount of articles have been published on Mangiferin.
Structure
Data?1563862559
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0034410 (Mangiferin)


  Mrv0541 05061307482D          

 30 33  0  0  0  0            999 V2000
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    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
    2.1434    1.2375    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
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  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
   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  1  2  0  0  0  0
  7  2  2  0  0  0  0
  7  6  1  0  0  0  0
  8  3  2  0  0  0  0
  9  2  1  0  0  0  0
  9  5  2  0  0  0  0
 10  3  1  0  0  0  0
 11  4  1  0  0  0  0
 12  8  1  0  0  0  0
 13 10  2  0  0  0  0
 14  5  1  0  0  0  0
 14 13  1  0  0  0  0
 15 11  1  0  0  0  0
 16 12  2  0  0  0  0
 16 13  1  0  0  0  0
 17 15  1  0  0  0  0
 18 17  1  0  0  0  0
 19 12  1  0  0  0  0
 19 18  1  0  0  0  0
 20  4  1  0  0  0  0
 21  6  1  0  0  0  0
 22  7  1  0  0  0  0
 23  8  1  0  0  0  0
 24 14  2  0  0  0  0
 25 15  1  0  0  0  0
 26 16  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29  9  1  0  0  0  0
 29 10  1  0  0  0  0
 30 11  1  0  0  0  0
 30 19  1  0  0  0  0
M  END
Download

3D MOL for HMDB0034410 (Mangiferin)

HMDB0034410
     RDKit          3D
Mangiferin
 48 51  0  0  0  0  0  0  0  0999 V2000
    2.8724    1.6395    0.6500 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8715    0.4850    0.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0882   -0.1366   -0.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2874    0.4840    0.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5207   -0.1286   -0.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6863    0.5483    0.2016 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5549   -1.3912   -0.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7426   -2.0598   -0.8938 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3400   -2.0242   -0.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1224   -1.4010   -0.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9702   -1.9886   -0.8678 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8098   -1.4238   -0.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6398   -2.1123   -0.9105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5852   -1.5579   -0.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7576   -2.2886   -0.9737 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7169   -0.2448   -0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0549    0.1794    0.1410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -0.5734   -0.5593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2217   -0.5661    0.1606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4543   -0.5185   -0.7334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4659   -1.6524   -1.5503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3211    0.4113    1.2625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7028    0.7345    1.3913 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6187    1.7054    1.1263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9886    2.0174    2.3353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4884    1.5704    0.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    2.6012    0.1619 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4387    0.4475    0.1563 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3710    1.7023    0.6904 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6647   -0.1517   -0.0978 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2101    1.4828    0.5858 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5979    0.1962    0.0587 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6421   -1.6505   -0.7117 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3693   -3.0272   -1.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7132   -3.1269   -1.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6538   -3.1961   -1.3538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2629   -0.2112    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2768   -1.6049    0.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3832   -0.5825   -0.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5290    0.4283   -1.2901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6328   -1.7296   -2.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0961   -0.1111    2.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8831    1.6542    1.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2567    2.5817    0.8800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3800    1.2786    2.6537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9898    1.7056   -0.9474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0785    3.4412    0.3844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9361    2.3929    1.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  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
 16 28  1  0
 28 29  1  0
 28 30  2  0
 30  2  1  0
 10  3  1  0
 30 12  1  0
 26 17  1  0
  4 31  1  0
  6 32  1  0
  8 33  1  0
  9 34  1  0
 13 35  1  0
 15 36  1  0
 17 37  1  0
 19 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 25 45  1  0
 26 46  1  0
 27 47  1  0
 29 48  1  0
M  END
Download

3D SDF for HMDB0034410 (Mangiferin)


  Mrv0541 05061307482D          

 30 33  0  0  0  0            999 V2000
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    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
    2.1434    1.2375    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
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  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
   -2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  1  2  0  0  0  0
  7  2  2  0  0  0  0
  7  6  1  0  0  0  0
  8  3  2  0  0  0  0
  9  2  1  0  0  0  0
  9  5  2  0  0  0  0
 10  3  1  0  0  0  0
 11  4  1  0  0  0  0
 12  8  1  0  0  0  0
 13 10  2  0  0  0  0
 14  5  1  0  0  0  0
 14 13  1  0  0  0  0
 15 11  1  0  0  0  0
 16 12  2  0  0  0  0
 16 13  1  0  0  0  0
 17 15  1  0  0  0  0
 18 17  1  0  0  0  0
 19 12  1  0  0  0  0
 19 18  1  0  0  0  0
 20  4  1  0  0  0  0
 21  6  1  0  0  0  0
 22  7  1  0  0  0  0
 23  8  1  0  0  0  0
 24 14  2  0  0  0  0
 25 15  1  0  0  0  0
 26 16  1  0  0  0  0
 27 17  1  0  0  0  0
 28 18  1  0  0  0  0
 29  9  1  0  0  0  0
 29 10  1  0  0  0  0
 30 11  1  0  0  0  0
 30 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0034410

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC3=C(C=C(O)C(O)=C3)C2=O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H18O11/c20-4-11-15(25)17(27)18(28)19(30-11)12-8(23)3-10-13(16(12)26)14(24)5-1-6(21)7(22)2-9(5)29-10/h1-3,11,15,17-23,25-28H,4H2

> <INCHI_KEY>
AEDDIBAIWPIIBD-UHFFFAOYSA-N

> <FORMULA>
C19H18O11

> <MOLECULAR_WEIGHT>
422.3396

> <EXACT_MASS>
422.084911418

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
40.0030531428138

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,3,6,7-tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H-xanthen-9-one

> <ALOGPS_LOGP>
-0.09

> <JCHEM_LOGP>
-0.3619419713333333

> <ALOGPS_LOGS>
-1.92

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.705292920734624

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.0200909635825255

> <JCHEM_PKA_STRONGEST_BASIC>
-2.979192626943851

> <JCHEM_POLAR_SURFACE_AREA>
197.36999999999998

> <JCHEM_REFRACTIVITY>
97.8582

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.02e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
mangiferin

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0034410 (Mangiferin)

HMDB0034410
     RDKit          3D
Mangiferin
 48 51  0  0  0  0  0  0  0  0999 V2000
    2.8724    1.6395    0.6500 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8715    0.4850    0.1665 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0882   -0.1366   -0.0946 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2874    0.4840    0.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5207   -0.1286   -0.0868 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6863    0.5483    0.2016 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5549   -1.3912   -0.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7426   -2.0598   -0.8938 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3400   -2.0242   -0.8857 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1224   -1.4010   -0.6244 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9702   -1.9886   -0.8678 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8098   -1.4238   -0.6291 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6398   -2.1123   -0.9105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5852   -1.5579   -0.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7576   -2.2886   -0.9737 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7169   -0.2448   -0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0549    0.1794    0.1410 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -0.5734   -0.5593 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2217   -0.5661    0.1606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4543   -0.5185   -0.7334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4659   -1.6524   -1.5503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3211    0.4113    1.2625 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7028    0.7345    1.3913 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6187    1.7054    1.1263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9886    2.0174    2.3353 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4884    1.5704    0.1004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    2.6012    0.1619 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4387    0.4475    0.1563 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3710    1.7023    0.6904 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6647   -0.1517   -0.0978 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2101    1.4828    0.5858 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5979    0.1962    0.0587 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6421   -1.6505   -0.7117 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3693   -3.0272   -1.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7132   -3.1269   -1.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6538   -3.1961   -1.3538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2629   -0.2112    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2768   -1.6049    0.6207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3832   -0.5825   -0.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5290    0.4283   -1.2901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6328   -1.7296   -2.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0961   -0.1111    2.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8831    1.6542    1.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2567    2.5817    0.8800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3800    1.2786    2.6537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9898    1.7056   -0.9474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0785    3.4412    0.3844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9361    2.3929    1.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 14 16  2  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
 16 28  1  0
 28 29  1  0
 28 30  2  0
 30  2  1  0
 10  3  1  0
 30 12  1  0
 26 17  1  0
  4 31  1  0
  6 32  1  0
  8 33  1  0
  9 34  1  0
 13 35  1  0
 15 36  1  0
 17 37  1  0
 19 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 25 45  1  0
 26 46  1  0
 27 47  1  0
 29 48  1  0
M  END
Download

PDB for HMDB0034410 (Mangiferin)

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -5.335   1.540   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      10.669   4.620   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    5    6                                                       
CONECT    2    7    9                                                       
CONECT    3    8   10                                                       
CONECT    4   11   20                                                       
CONECT    5    1    9   14                                                  
CONECT    6    1    7   21                                                  
CONECT    7    2    6   22                                                  
CONECT    8    3   12   23                                                  
CONECT    9    2    5   29                                                  
CONECT   10    3   13   29                                                  
CONECT   11    4   15   30                                                  
CONECT   12    8   16   19                                                  
CONECT   13   10   14   16                                                  
CONECT   14    5   13   24                                                  
CONECT   15   11   17   25                                                  
CONECT   16   12   13   26                                                  
CONECT   17   15   18   27                                                  
CONECT   18   17   19   28                                                  
CONECT   19   12   18   30                                                  
CONECT   20    4                                                            
CONECT   21    6                                                            
CONECT   22    7                                                            
CONECT   23    8                                                            
CONECT   24   14                                                            
CONECT   25   15                                                            
CONECT   26   16                                                            
CONECT   27   17                                                            
CONECT   28   18                                                            
CONECT   29    9   10                                                       
CONECT   30   11   19                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END
Download

3D PDB for HMDB0034410 (Mangiferin)

COMPND    HMDB0034410
HETATM    1  O1  UNL     1       2.872   1.639   0.650  1.00  0.00           O  
HETATM    2  C1  UNL     1       2.871   0.485   0.167  1.00  0.00           C  
HETATM    3  C2  UNL     1       4.088  -0.137  -0.095  1.00  0.00           C  
HETATM    4  C3  UNL     1       5.287   0.484   0.168  1.00  0.00           C  
HETATM    5  C4  UNL     1       6.521  -0.129  -0.087  1.00  0.00           C  
HETATM    6  O2  UNL     1       7.686   0.548   0.202  1.00  0.00           O  
HETATM    7  C5  UNL     1       6.555  -1.391  -0.617  1.00  0.00           C  
HETATM    8  O3  UNL     1       7.743  -2.060  -0.894  1.00  0.00           O  
HETATM    9  C6  UNL     1       5.340  -2.024  -0.886  1.00  0.00           C  
HETATM   10  C7  UNL     1       4.122  -1.401  -0.624  1.00  0.00           C  
HETATM   11  O4  UNL     1       2.970  -1.989  -0.868  1.00  0.00           O  
HETATM   12  C8  UNL     1       1.810  -1.424  -0.629  1.00  0.00           C  
HETATM   13  C9  UNL     1       0.640  -2.112  -0.911  1.00  0.00           C  
HETATM   14  C10 UNL     1      -0.585  -1.558  -0.676  1.00  0.00           C  
HETATM   15  O5  UNL     1      -1.758  -2.289  -0.974  1.00  0.00           O  
HETATM   16  C11 UNL     1      -0.717  -0.245  -0.131  1.00  0.00           C  
HETATM   17  C12 UNL     1      -2.055   0.179   0.141  1.00  0.00           C  
HETATM   18  O6  UNL     1      -3.032  -0.573  -0.559  1.00  0.00           O  
HETATM   19  C13 UNL     1      -4.222  -0.566   0.161  1.00  0.00           C  
HETATM   20  C14 UNL     1      -5.454  -0.518  -0.733  1.00  0.00           C  
HETATM   21  O7  UNL     1      -5.466  -1.652  -1.550  1.00  0.00           O  
HETATM   22  C15 UNL     1      -4.321   0.411   1.262  1.00  0.00           C  
HETATM   23  O8  UNL     1      -5.703   0.735   1.391  1.00  0.00           O  
HETATM   24  C16 UNL     1      -3.619   1.705   1.126  1.00  0.00           C  
HETATM   25  O9  UNL     1      -2.989   2.017   2.335  1.00  0.00           O  
HETATM   26  C17 UNL     1      -2.488   1.570   0.100  1.00  0.00           C  
HETATM   27  O10 UNL     1      -1.619   2.601   0.162  1.00  0.00           O  
HETATM   28  C18 UNL     1       0.439   0.447   0.156  1.00  0.00           C  
HETATM   29  O11 UNL     1       0.371   1.702   0.690  1.00  0.00           O  
HETATM   30  C19 UNL     1       1.665  -0.152  -0.098  1.00  0.00           C  
HETATM   31  H1  UNL     1       5.210   1.483   0.586  1.00  0.00           H  
HETATM   32  H2  UNL     1       8.598   0.196   0.059  1.00  0.00           H  
HETATM   33  H3  UNL     1       8.642  -1.651  -0.712  1.00  0.00           H  
HETATM   34  H4  UNL     1       5.369  -3.027  -1.304  1.00  0.00           H  
HETATM   35  H5  UNL     1       0.713  -3.127  -1.327  1.00  0.00           H  
HETATM   36  H6  UNL     1      -1.654  -3.196  -1.354  1.00  0.00           H  
HETATM   37  H7  UNL     1      -2.263  -0.211   1.246  1.00  0.00           H  
HETATM   38  H8  UNL     1      -4.277  -1.605   0.621  1.00  0.00           H  
HETATM   39  H9  UNL     1      -6.383  -0.583  -0.101  1.00  0.00           H  
HETATM   40  H10 UNL     1      -5.529   0.428  -1.290  1.00  0.00           H  
HETATM   41  H11 UNL     1      -4.633  -1.730  -2.096  1.00  0.00           H  
HETATM   42  H12 UNL     1      -4.096  -0.111   2.242  1.00  0.00           H  
HETATM   43  H13 UNL     1      -5.883   1.654   1.077  1.00  0.00           H  
HETATM   44  H14 UNL     1      -4.257   2.582   0.880  1.00  0.00           H  
HETATM   45  H15 UNL     1      -2.380   1.279   2.654  1.00  0.00           H  
HETATM   46  H16 UNL     1      -2.990   1.706  -0.947  1.00  0.00           H  
HETATM   47  H17 UNL     1      -2.078   3.441   0.384  1.00  0.00           H  
HETATM   48  H18 UNL     1       0.936   2.393   1.003  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   30
CONECT    3    4    4   10
CONECT    4    5   31
CONECT    5    6    7    7
CONECT    6   32
CONECT    7    8    9
CONECT    8   33
CONECT    9   10   10   34
CONECT   10   11
CONECT   11   12
CONECT   12   13   13   30
CONECT   13   14   35
CONECT   14   15   16   16
CONECT   15   36
CONECT   16   17   28
CONECT   17   18   26   37
CONECT   18   19
CONECT   19   20   22   38
CONECT   20   21   39   40
CONECT   21   41
CONECT   22   23   24   42
CONECT   23   43
CONECT   24   25   26   44
CONECT   25   45
CONECT   26   27   46
CONECT   27   47
CONECT   28   29   30   30
CONECT   29   48
END
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SMILES for HMDB0034410 (Mangiferin)

OCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC3=C(C=C(O)C(O)=C3)C2=O)C=C1O
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INCHI for HMDB0034410 (Mangiferin)

InChI=1S/C19H18O11/c20-4-11-15(25)17(27)18(28)19(30-11)12-8(23)3-10-13(16(12)26)14(24)5-1-6(21)7(22)2-9(5)29-10/h1-3,11,15,17-23,25-28H,4H2
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
1,3,6,7-Tetrahydroxyxanthone C2-beta-D-glucosideHMDB
2-b-D-Glucopyranosyl-1,3,6,7-tetrahydroxy-9H-xanthen-9-one, 9ciHMDB
AlpizarinHMDB
AlpizarineHMDB
AphloiolHMDB
ChedisarideHMDB
ChinoininHMDB
ChinominHMDB
ChinomineHMDB
EuxanthogenHMDB
HedysaridHMDB
HedysarideHMDB
Mangiferin from mangifera indica barkHMDB
MannipherinHMDB
Chemical FormulaC19H18O11
Average Molecular Weight422.3396
Monoisotopic Molecular Weight422.084911418
IUPAC Name1,3,6,7-tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H-xanthen-9-one
Traditional Namemangiferin
CAS Registry Number4773-96-0
SMILES
OCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC3=C(C=C(O)C(O)=C3)C2=O)C=C1O
InChI Identifier
InChI=1S/C19H18O11/c20-4-11-15(25)17(27)18(28)19(30-11)12-8(23)3-10-13(16(12)26)14(24)5-1-6(21)7(22)2-9(5)29-10/h1-3,11,15,17-23,25-28H,4H2
InChI KeyAEDDIBAIWPIIBD-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassBenzopyrans
Sub Class1-benzopyrans
Direct ParentXanthones
Alternative Parents
Substituents
  • Phenolic glycoside
  • Xanthone
  • Hexose monosaccharide
  • C-glycosyl compound
  • Chromone
  • Glycosyl compound
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Pyranone
  • Benzenoid
  • Pyran
  • Oxane
  • Monosaccharide
  • Heteroaromatic compound
  • Vinylogous acid
  • Secondary alcohol
  • Oxacycle
  • Polyol
  • Dialkyl ether
  • Ether
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Organic oxide
  • Organooxygen compound
  • Primary alcohol
  • Alcohol
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
ProcessNot Available
Role
Biological roleIndustrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point278 - 280 °CNot Available
Boiling Point842.70 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility467.8 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP0.130 (est)The Good Scents Company Information System
Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct TypeData SourceCCS Value (Å2)Reference
[M-H]-Baker195.81430932474
[M+H]+Baker196.61830932474
Predicted Molecular Properties
PropertyValueSource
Water Solubility5.02 g/LALOGPS
logP-0.09ALOGPS
logP-0.36ChemAxon
logS-1.9ALOGPS
pKa (Strongest Acidic)7.02ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area197.37 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity97.86 m³·mol⁻¹ChemAxon
Polarizability40 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+190.4630932474
DeepCCS[M-H]-188.08930932474
DeepCCS[M-2H]-221.50530932474
DeepCCS[M+Na]+196.68830932474
AllCCS[M+H]+198.332859911
AllCCS[M+H-H2O]+195.632859911
AllCCS[M+NH4]+200.732859911
AllCCS[M+Na]+201.432859911
AllCCS[M-H]-196.032859911
AllCCS[M+Na-2H]-196.332859911
AllCCS[M+HCOO]-196.732859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.3.26 minutes32390414
Predicted by Siyang on May 30, 202211.546 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20226.34 minutes32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid183.9 seconds40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid1369.2 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid199.3 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid71.8 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid145.4 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid72.3 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid346.9 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid378.5 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)745.8 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid624.0 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid136.8 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid1365.6 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid203.1 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid232.0 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate533.9 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA336.8 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water369.5 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
MangiferinOCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC3=C(C=C(O)C(O)=C3)C2=O)C=C1O5402.6Standard polar33892256
MangiferinOCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC3=C(C=C(O)C(O)=C3)C2=O)C=C1O3450.7Standard non polar33892256
MangiferinOCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC3=C(C=C(O)C(O)=C3)C2=O)C=C1O4240.8Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Mangiferin,1TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O4154.9Semi standard non polar33892256
Mangiferin,1TMS,isomer #2C[Si](C)(C)OC1C(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)OC(CO)C(O)C1O4165.4Semi standard non polar33892256
Mangiferin,1TMS,isomer #3C[Si](C)(C)OC1C(O)C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C1O4209.4Semi standard non polar33892256
Mangiferin,1TMS,isomer #4C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C1O4185.6Semi standard non polar33892256
Mangiferin,1TMS,isomer #5C[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24151.0Semi standard non polar33892256
Mangiferin,1TMS,isomer #6C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O)C(O)=C1C2=O4178.4Semi standard non polar33892256
Mangiferin,1TMS,isomer #7C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O24181.5Semi standard non polar33892256
Mangiferin,1TMS,isomer #8C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O24166.0Semi standard non polar33892256
Mangiferin,2TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O4055.5Semi standard non polar33892256
Mangiferin,2TMS,isomer #10C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)=C1C2=O4054.9Semi standard non polar33892256
Mangiferin,2TMS,isomer #11C[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24041.1Semi standard non polar33892256
Mangiferin,2TMS,isomer #12C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C1O4050.9Semi standard non polar33892256
Mangiferin,2TMS,isomer #13C[Si](C)(C)OC1C(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)OC(CO)C(O)C1O[Si](C)(C)C4078.0Semi standard non polar33892256
Mangiferin,2TMS,isomer #14C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C1O[Si](C)(C)C4079.0Semi standard non polar33892256
Mangiferin,2TMS,isomer #15C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O24068.0Semi standard non polar33892256
Mangiferin,2TMS,isomer #16C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O)C=C1O24046.2Semi standard non polar33892256
Mangiferin,2TMS,isomer #17C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)=C1C2=O4048.5Semi standard non polar33892256
Mangiferin,2TMS,isomer #18C[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24043.3Semi standard non polar33892256
Mangiferin,2TMS,isomer #19C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O24061.2Semi standard non polar33892256
Mangiferin,2TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O4065.6Semi standard non polar33892256
Mangiferin,2TMS,isomer #20C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O)C=C1O24051.9Semi standard non polar33892256
Mangiferin,2TMS,isomer #21C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)=C1C2=O4051.6Semi standard non polar33892256
Mangiferin,2TMS,isomer #22C[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24040.2Semi standard non polar33892256
Mangiferin,2TMS,isomer #23C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O24112.5Semi standard non polar33892256
Mangiferin,2TMS,isomer #24C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O24092.7Semi standard non polar33892256
Mangiferin,2TMS,isomer #25C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)=C1C2=O4095.7Semi standard non polar33892256
Mangiferin,2TMS,isomer #26C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O)C3O)C(O)=C1C2=O4093.7Semi standard non polar33892256
Mangiferin,2TMS,isomer #27C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O24102.7Semi standard non polar33892256
Mangiferin,2TMS,isomer #28C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C)C=C1O24088.3Semi standard non polar33892256
Mangiferin,2TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O4063.5Semi standard non polar33892256
Mangiferin,2TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O4024.9Semi standard non polar33892256
Mangiferin,2TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O4045.9Semi standard non polar33892256
Mangiferin,2TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O4064.8Semi standard non polar33892256
Mangiferin,2TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C4049.1Semi standard non polar33892256
Mangiferin,2TMS,isomer #8C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24063.8Semi standard non polar33892256
Mangiferin,2TMS,isomer #9C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O)C=C1O24055.6Semi standard non polar33892256
Mangiferin,3TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O3924.1Semi standard non polar33892256
Mangiferin,3TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3922.2Semi standard non polar33892256
Mangiferin,3TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3936.9Semi standard non polar33892256
Mangiferin,3TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O3899.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3915.7Semi standard non polar33892256
Mangiferin,3TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3915.8Semi standard non polar33892256
Mangiferin,3TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3929.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3900.4Semi standard non polar33892256
Mangiferin,3TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3908.9Semi standard non polar33892256
Mangiferin,3TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3908.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3948.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O3925.1Semi standard non polar33892256
Mangiferin,3TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3949.5Semi standard non polar33892256
Mangiferin,3TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3956.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #22C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23909.8Semi standard non polar33892256
Mangiferin,3TMS,isomer #23C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)=C1C2=O3915.4Semi standard non polar33892256
Mangiferin,3TMS,isomer #24C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O23964.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #25C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O23937.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #26C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O23952.6Semi standard non polar33892256
Mangiferin,3TMS,isomer #27C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O)C=C1O23921.8Semi standard non polar33892256
Mangiferin,3TMS,isomer #28C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23941.9Semi standard non polar33892256
Mangiferin,3TMS,isomer #29C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O)C=C1O23906.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O3940.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #30C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O)C=C1O23989.9Semi standard non polar33892256
Mangiferin,3TMS,isomer #31C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3902.8Semi standard non polar33892256
Mangiferin,3TMS,isomer #32C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)=C1C2=O3914.7Semi standard non polar33892256
Mangiferin,3TMS,isomer #33C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)=C1C2=O3937.6Semi standard non polar33892256
Mangiferin,3TMS,isomer #34C[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O23922.1Semi standard non polar33892256
Mangiferin,3TMS,isomer #35C[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O23930.2Semi standard non polar33892256
Mangiferin,3TMS,isomer #36C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4010.5Semi standard non polar33892256
Mangiferin,3TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O23960.5Semi standard non polar33892256
Mangiferin,3TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O)C=C1O23948.9Semi standard non polar33892256
Mangiferin,3TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)=C1C2=O3942.4Semi standard non polar33892256
Mangiferin,3TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3928.9Semi standard non polar33892256
Mangiferin,3TMS,isomer #40C[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O23940.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #41C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23889.2Semi standard non polar33892256
Mangiferin,3TMS,isomer #42C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)=C1C2=O3897.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #43C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O23941.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #44C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O)C=C1O23871.8Semi standard non polar33892256
Mangiferin,3TMS,isomer #45C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O)C=C1O23969.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #46C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)=C1C2=O3870.2Semi standard non polar33892256
Mangiferin,3TMS,isomer #47C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O[Si](C)(C)C)C=C1O23908.2Semi standard non polar33892256
Mangiferin,3TMS,isomer #48C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)=C1C2=O3911.7Semi standard non polar33892256
Mangiferin,3TMS,isomer #49C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O23959.8Semi standard non polar33892256
Mangiferin,3TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3933.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #50C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O)C=C1O23901.3Semi standard non polar33892256
Mangiferin,3TMS,isomer #51C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O)C=C1O23980.7Semi standard non polar33892256
Mangiferin,3TMS,isomer #52C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O[Si](C)(C)C)=C1C2=O3897.6Semi standard non polar33892256
Mangiferin,3TMS,isomer #53C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C)C=C1O23957.7Semi standard non polar33892256
Mangiferin,3TMS,isomer #54C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C)=C1C2=O3963.5Semi standard non polar33892256
Mangiferin,3TMS,isomer #55C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O23991.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #56C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C)C=C1O24011.5Semi standard non polar33892256
Mangiferin,3TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3937.0Semi standard non polar33892256
Mangiferin,3TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O3980.6Semi standard non polar33892256
Mangiferin,3TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O3903.4Semi standard non polar33892256
Mangiferin,3TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3923.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O3859.5Semi standard non polar33892256
Mangiferin,4TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3830.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3805.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3835.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3856.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3869.4Semi standard non polar33892256
Mangiferin,4TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3874.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O3828.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3858.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3843.7Semi standard non polar33892256
Mangiferin,4TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3860.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O3763.7Semi standard non polar33892256
Mangiferin,4TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3729.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3724.7Semi standard non polar33892256
Mangiferin,4TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3748.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3810.8Semi standard non polar33892256
Mangiferin,4TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3826.0Semi standard non polar33892256
Mangiferin,4TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3830.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3735.0Semi standard non polar33892256
Mangiferin,4TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3733.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3753.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3810.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3759.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3826.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3829.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3815.5Semi standard non polar33892256
Mangiferin,4TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3833.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3838.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3911.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #36C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23765.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23775.0Semi standard non polar33892256
Mangiferin,4TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23778.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23853.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3763.7Semi standard non polar33892256
Mangiferin,4TMS,isomer #40C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3785.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #41C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)=C1C2=O3773.7Semi standard non polar33892256
Mangiferin,4TMS,isomer #42C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)=C1C2=O3783.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #43C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O23835.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #44C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O23843.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #45C[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O23898.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #46C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23861.4Semi standard non polar33892256
Mangiferin,4TMS,isomer #47C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O)C=C1O23732.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #48C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O)C=C1O23858.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #49C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23736.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3778.5Semi standard non polar33892256
Mangiferin,4TMS,isomer #50C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23867.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #51C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O)C=C1O23828.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #52C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3738.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #53C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3742.7Semi standard non polar33892256
Mangiferin,4TMS,isomer #54C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)=C1C2=O3861.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #55C[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O23856.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #56C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23780.5Semi standard non polar33892256
Mangiferin,4TMS,isomer #57C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)=C1C2=O3788.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #58C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O23837.6Semi standard non polar33892256
Mangiferin,4TMS,isomer #59C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O)C=C1O23741.5Semi standard non polar33892256
Mangiferin,4TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O3768.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #60C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O)C=C1O23868.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #61C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)=C1C2=O3749.3Semi standard non polar33892256
Mangiferin,4TMS,isomer #62C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23785.8Semi standard non polar33892256
Mangiferin,4TMS,isomer #63C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23822.0Semi standard non polar33892256
Mangiferin,4TMS,isomer #64C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)=C1C2=O3786.9Semi standard non polar33892256
Mangiferin,4TMS,isomer #65C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O)C=C1O23789.7Semi standard non polar33892256
Mangiferin,4TMS,isomer #66C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O[Si](C)(C)C)C=C1O23763.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #67C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O[Si](C)(C)C)C=C1O23846.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #68C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O[Si](C)(C)C)=C1C2=O3769.1Semi standard non polar33892256
Mangiferin,4TMS,isomer #69C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O)C=C1O23819.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3765.2Semi standard non polar33892256
Mangiferin,4TMS,isomer #70C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C)C=C1O23892.0Semi standard non polar33892256
Mangiferin,4TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3770.4Semi standard non polar33892256
Mangiferin,4TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3784.2Semi standard non polar33892256
Mangiferin,5TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O3736.3Semi standard non polar33892256
Mangiferin,5TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3723.1Semi standard non polar33892256
Mangiferin,5TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3668.0Semi standard non polar33892256
Mangiferin,5TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3734.6Semi standard non polar33892256
Mangiferin,5TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3677.0Semi standard non polar33892256
Mangiferin,5TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3711.0Semi standard non polar33892256
Mangiferin,5TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3716.9Semi standard non polar33892256
Mangiferin,5TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3722.2Semi standard non polar33892256
Mangiferin,5TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3743.2Semi standard non polar33892256
Mangiferin,5TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3761.2Semi standard non polar33892256
Mangiferin,5TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3754.0Semi standard non polar33892256
Mangiferin,5TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O3755.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3828.5Semi standard non polar33892256
Mangiferin,5TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3711.0Semi standard non polar33892256
Mangiferin,5TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3712.8Semi standard non polar33892256
Mangiferin,5TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3720.4Semi standard non polar33892256
Mangiferin,5TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3792.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3804.5Semi standard non polar33892256
Mangiferin,5TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3806.4Semi standard non polar33892256
Mangiferin,5TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3669.1Semi standard non polar33892256
Mangiferin,5TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3680.4Semi standard non polar33892256
Mangiferin,5TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3685.9Semi standard non polar33892256
Mangiferin,5TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O3758.4Semi standard non polar33892256
Mangiferin,5TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3787.0Semi standard non polar33892256
Mangiferin,5TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3672.3Semi standard non polar33892256
Mangiferin,5TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3685.2Semi standard non polar33892256
Mangiferin,5TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3689.6Semi standard non polar33892256
Mangiferin,5TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3786.6Semi standard non polar33892256
Mangiferin,5TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3804.3Semi standard non polar33892256
Mangiferin,5TMS,isomer #36C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23743.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #37C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23705.3Semi standard non polar33892256
Mangiferin,5TMS,isomer #38C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23779.3Semi standard non polar33892256
Mangiferin,5TMS,isomer #39C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23714.8Semi standard non polar33892256
Mangiferin,5TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C3764.1Semi standard non polar33892256
Mangiferin,5TMS,isomer #40C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23779.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #41C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23779.6Semi standard non polar33892256
Mangiferin,5TMS,isomer #42C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3705.2Semi standard non polar33892256
Mangiferin,5TMS,isomer #43C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3716.3Semi standard non polar33892256
Mangiferin,5TMS,isomer #44C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)=C1C2=O3746.4Semi standard non polar33892256
Mangiferin,5TMS,isomer #45C[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O23774.1Semi standard non polar33892256
Mangiferin,5TMS,isomer #46C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23698.8Semi standard non polar33892256
Mangiferin,5TMS,isomer #47C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23830.3Semi standard non polar33892256
Mangiferin,5TMS,isomer #48C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O)C=C1O23737.4Semi standard non polar33892256
Mangiferin,5TMS,isomer #49C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23735.8Semi standard non polar33892256
Mangiferin,5TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3671.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #50C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3705.0Semi standard non polar33892256
Mangiferin,5TMS,isomer #51C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23709.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #52C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23786.5Semi standard non polar33892256
Mangiferin,5TMS,isomer #53C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O[Si](C)(C)C)=C1C2=O3710.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #54C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O)C=C1O23740.6Semi standard non polar33892256
Mangiferin,5TMS,isomer #55C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23776.8Semi standard non polar33892256
Mangiferin,5TMS,isomer #56C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C(O[Si](C)(C)C)C=C1O23771.8Semi standard non polar33892256
Mangiferin,5TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3739.7Semi standard non polar33892256
Mangiferin,5TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3680.8Semi standard non polar33892256
Mangiferin,5TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3711.9Semi standard non polar33892256
Mangiferin,5TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3716.7Semi standard non polar33892256
Mangiferin,6TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3708.1Semi standard non polar33892256
Mangiferin,6TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3711.4Semi standard non polar33892256
Mangiferin,6TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3670.9Semi standard non polar33892256
Mangiferin,6TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3685.7Semi standard non polar33892256
Mangiferin,6TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3671.5Semi standard non polar33892256
Mangiferin,6TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3705.3Semi standard non polar33892256
Mangiferin,6TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3717.4Semi standard non polar33892256
Mangiferin,6TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3696.7Semi standard non polar33892256
Mangiferin,6TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3719.8Semi standard non polar33892256
Mangiferin,6TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3702.2Semi standard non polar33892256
Mangiferin,6TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3793.7Semi standard non polar33892256
Mangiferin,6TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3730.1Semi standard non polar33892256
Mangiferin,6TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3691.6Semi standard non polar33892256
Mangiferin,6TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3684.8Semi standard non polar33892256
Mangiferin,6TMS,isomer #22C[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23688.4Semi standard non polar33892256
Mangiferin,6TMS,isomer #23C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23761.5Semi standard non polar33892256
Mangiferin,6TMS,isomer #24C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23731.9Semi standard non polar33892256
Mangiferin,6TMS,isomer #25C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C1O23722.1Semi standard non polar33892256
Mangiferin,6TMS,isomer #26C[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C2=O3684.3Semi standard non polar33892256
Mangiferin,6TMS,isomer #27C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C(O)C=C1O23727.9Semi standard non polar33892256
Mangiferin,6TMS,isomer #28C[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C)C(=O)C1=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C(O[Si](C)(C)C)C=C1O23719.0Semi standard non polar33892256
Mangiferin,6TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3707.0Semi standard non polar33892256
Mangiferin,6TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3736.1Semi standard non polar33892256
Mangiferin,6TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3748.3Semi standard non polar33892256
Mangiferin,6TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3736.2Semi standard non polar33892256
Mangiferin,6TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3677.6Semi standard non polar33892256
Mangiferin,6TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3693.6Semi standard non polar33892256
Mangiferin,6TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC4=CC(O[Si](C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3679.2Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O4415.1Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1C(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)OC(CO)C(O)C1O4468.9Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C1O4495.6Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C1O4465.9Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24424.4Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O)C(O)=C1C2=O4420.6Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O24426.1Semi standard non polar33892256
Mangiferin,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O24412.8Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O4533.1Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)=C1C2=O4540.7Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24552.6Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C1O4560.1Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1C(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C4581.1Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C1O[Si](C)(C)C(C)(C)C4566.9Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O24541.5Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C=C1O24540.4Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)=C1C2=O4537.7Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24550.2Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O24532.3Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O4533.6Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O)C=C1O24525.4Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)=C1C2=O4523.6Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24538.5Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O24598.4Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O24561.5Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4559.5Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O)C(O)C3O)C(O)=C1C2=O4550.9Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O24549.9Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24548.2Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O4534.0Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4541.1Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4538.0Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4556.7Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4518.9Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24544.5Semi standard non polar33892256
Mangiferin,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24542.8Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O4624.6Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4609.5Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4584.4Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4589.3Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4597.3Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4614.0Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4589.7Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4580.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4594.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4575.5Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4604.3Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O4629.2Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4621.9Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4607.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C1O24623.2Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)=C1C2=O4629.3Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24648.7Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24605.9Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24609.2Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24589.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24602.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24592.6Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4627.6Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24640.0Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4597.6Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)=C1C2=O4589.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)=C1C2=O4599.9Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24590.6Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24585.3Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4628.3Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O24592.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C=C1O24587.7Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)=C1C2=O4585.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4610.2Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24572.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24614.7Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)=C1C2=O4621.8Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O24637.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C=C1O24588.4Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C=C1O24628.8Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4591.5Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24603.3Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)=C1C2=O4608.4Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O)C(=O)C1=CC(O)=C(O)C=C1O24624.9Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4621.9Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O)C=C1O24574.8Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #51CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O)C=C1O24608.2Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #52CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4577.5Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24688.0Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #54CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4694.0Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O)C=C1O24674.2Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24693.8Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4603.6Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O4636.1Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4583.8Semi standard non polar33892256
Mangiferin,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4592.3Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O4749.8Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4671.5Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4700.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4664.5Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4684.7Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4697.8Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4686.3Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4669.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4713.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4726.3Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4698.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4680.7Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4608.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4662.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4608.7Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4670.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4676.1Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4670.1Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4605.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4661.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4605.5Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4672.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4673.0Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4678.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4669.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4632.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4649.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4639.3Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC4=CC(O)=C(O)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4709.8Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C1O24678.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C1O24688.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C1O24706.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O[Si](C)(C)C(C)(C)C)C=C1O24747.1Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4728.0Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4711.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)=C1C2=O4684.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)=C1C2=O4692.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24680.7Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24683.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C)C(=O)C1=CC(O)=C(O)C=C1O24672.3Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24673.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24626.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24705.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24633.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O[Si](C)(C)C(C)(C)C)=C(O)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4672.0Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24710.8Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #51CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C(O)C=C1O24682.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #52CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4629.0Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #53CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4633.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #54CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)=C1C2=O4673.8Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #55CC(C)(C)[Si](C)(C)OC1=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)=CC2=C1C(=O)C1=CC(O)=C(O)C=C1O24630.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #56CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24688.1Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #57CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)=C1C2=O4691.0Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #58CC(C)(C)[Si](C)(C)OC1=CC2=C(C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O)C(=O)C1=CC(O)=C(O)C=C1O24662.7Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #59CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C=C1O24632.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4682.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #60CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C=C1O24696.7Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #61CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4632.3Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #62CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24739.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #63CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24738.2Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #64CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4742.4Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #65CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C(O)C=C1O24677.5Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #66CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24692.5Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #67CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24724.3Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #68CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O[Si](C)(C)C(C)(C)C)=C1C2=O4693.9Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #69CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C(O)C=C1O24661.8Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4676.6Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #70CC(C)(C)[Si](C)(C)OC1=CC2=C(C=C1O[Si](C)(C)C(C)(C)C)C(=O)C1=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C(O[Si](C)(C)C(C)(C)C)C=C1O24776.7Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4731.5Semi standard non polar33892256
Mangiferin,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC4=CC(O)=C(O[Si](C)(C)C(C)(C)C)C=C4C(=O)C3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4673.9Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (Non-derivatized) - 70eV, Positivesplash10-00di-4369200000-758a8c37611a4a7f8cbb2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (3 TMS) - 70eV, Positivesplash10-00di-2500559000-5d3358daf4e39fc9144e2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (TMS_4_44) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (TMS_5_43) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (TMS_5_45) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (TMS_6_26) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (TBDMS_4_44) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS (TBDMS_4_49) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mangiferin GC-MS ("Mangiferin,4TMS,#44" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Mangiferin LC-ESI-qTof , Positive-QTOFsplash10-00di-0293000000-2addce902839fbc003172017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Mangiferin , positive-QTOFsplash10-00di-0293000000-2addce902839fbc003172017-09-14HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 10V, Positive-QTOFsplash10-05fr-0001900000-7e039093fc42c12265a72015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 20V, Positive-QTOFsplash10-05fr-5434900000-c6fdaad6c039bb9da77b2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 40V, Positive-QTOFsplash10-05tr-2091000000-17854a2e630e3479b4af2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 10V, Negative-QTOFsplash10-00di-0012900000-6f9ea5579c6507c5227c2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 20V, Negative-QTOFsplash10-0fk9-9467600000-db194aa8dbd21e8b7e232015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 40V, Negative-QTOFsplash10-052f-9361000000-8b32c733e44c1b73dbab2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 10V, Positive-QTOFsplash10-00di-0010900000-d25c0a3b3a1a7dd3f9552021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 20V, Positive-QTOFsplash10-00di-0192400000-77f0d8f1633f0093a85a2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 40V, Positive-QTOFsplash10-00di-3292000000-763751747c4de0e22fc82021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 10V, Negative-QTOFsplash10-00di-0013900000-92c719952c2fc11a9eb42021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 20V, Negative-QTOFsplash10-0pi3-0059300000-49f10ed9e69fe7ca88252021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mangiferin 40V, Negative-QTOFsplash10-0ab9-4194000000-36db5d0560a3e108b1902021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB012803
KNApSAcK IDC00002962
Chemspider ID4513535
KEGG Compound IDC10077
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkMangiferin
METLIN IDNot Available
PubChem Compound5358385
PDB IDNot Available
ChEBI ID6682
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1699751
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Zheng MS, Lu ZY: Antiviral effect of mangiferin and isomangiferin on herpes simplex virus. Chin Med J (Engl). 1990 Feb;103(2):160-5. [PubMed:2167819 ]
  2. Gottlieb M, Leal-Campanario R, Campos-Esparza MR, Sanchez-Gomez MV, Alberdi E, Arranz A, Delgado-Garcia JM, Gruart A, Matute C: Neuroprotection by two polyphenols following excitotoxicity and experimental ischemia. Neurobiol Dis. 2006 Aug;23(2):374-86. Epub 2006 Jun 27. [PubMed:16806951 ]
  3. Muruganandan S, Srinivasan K, Gupta S, Gupta PK, Lal J: Effect of mangiferin on hyperglycemia and atherogenicity in streptozotocin diabetic rats. J Ethnopharmacol. 2005 Mar 21;97(3):497-501. [PubMed:15740886 ]
  4. Pardo-Andreu GL, Cavalheiro RA, Dorta DJ, Naal Z, Delgado R, Vercesi AE, Curti C: Fe(III) shifts the mitochondria permeability transition-eliciting capacity of mangiferin to protection of organelle. J Pharmacol Exp Ther. 2007 Feb;320(2):646-53. Epub 2006 Oct 26. [PubMed:17068204 ]
  5. Prabhu S, Jainu M, Sabitha KE, Devi CS: Cardioprotective effect of mangiferin on isoproterenol induced myocardial infarction in rats. Indian J Exp Biol. 2006 Mar;44(3):209-15. [PubMed:16538859 ]
  6. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .