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Showing metabocard for Myricetin 3-arabinoside (HMDB0041635)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 03:19:44 UTC
Update Date2022-03-07 02:57:06 UTC
HMDB IDHMDB0041635
Secondary Accession Numbers
  • HMDB41635
Metabolite Identification
Common NameMyricetin 3-arabinoside
DescriptionMyricetin 3-arabinoside belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Myricetin 3-arabinoside has been detected, but not quantified in, american cranberries (Vaccinium macrocarpon). This could make myricetin 3-arabinoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Myricetin 3-arabinoside.
Structure
Data?1563863685
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0041635 (Myricetin 3-arabinoside)


  Mrv0541 02241222502D          

 32 35  0  0  1  0            999 V2000
   -0.9041   -0.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9041    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    0.9791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3330    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3330   -0.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185   -0.6709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185   -1.4959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0475   -0.6709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0475   -1.4959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7620   -0.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7620    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4764    0.9791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0475    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896    1.8041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5249    2.2166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5249    3.0416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2393    1.8041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9538    2.2166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2393    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9538    0.5666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5249    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9041   -1.9084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9041   -2.7334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896   -3.1459    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5249   -2.7334    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5249   -1.9084    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1896   -1.4959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1896   -0.6709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2393   -1.4959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2394   -3.1459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896   -3.9709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 29  1  1  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  4 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 14 22  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  1  0  0  0
 27 30  1  6  0  0  0
 26 31  1  1  0  0  0
 25 32  1  1  0  0  0
M  END
Download

3D MOL for HMDB0041635 (Myricetin 3-arabinoside)

HMDB0041635
     RDKit          3D
Myricetin 3-arabinoside
 50 53  0  0  0  0  0  0  0  0999 V2000
    0.5554    2.9189   -0.7778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3917    2.2118   -0.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4173    0.8354   -0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6486    0.2923   -1.1651 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8514   -0.0647   -0.4440 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6840    1.0723   -0.6830 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7897    1.0200    0.1715 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3104   -0.4227    0.2611 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6524   -0.4665    0.5455 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9844   -1.0418   -1.1041 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2215   -0.0697   -2.0629 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4617   -1.2594   -1.0889 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2300   -2.4321   -0.3546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4553    0.1215   -0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6127   -1.3180   -0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5784   -1.9462    0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8391   -3.3034    0.5742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8241   -3.8334    1.3950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1315   -4.1085   -0.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3642   -5.4737   -0.3809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1625   -3.5126   -1.0804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4526   -4.3161   -1.9457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9244   -2.1405   -0.9922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4262    0.7792    0.5937 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    2.0668    0.7702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4808    2.6862    1.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4966    4.0493    1.6231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5548    4.6695    2.2938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4437    4.8280    1.1411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3899    4.2313    0.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188    4.9836   -0.0197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4056    2.8665    0.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6726   -0.1405    0.6405 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5969    1.5992   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6039    1.4526    1.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6686   -0.9524    0.9929 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9486    0.4188    0.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5281   -1.9719   -1.2768 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0545    0.4307   -1.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0980   -1.3664   -2.1501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9436   -3.1299   -1.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1563   -1.3430    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0845   -4.7878    1.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0490   -5.9705    0.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6182   -5.3006   -2.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1925   -1.7479   -1.6456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2790    2.0437    1.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3305    4.9750    1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    5.8975    1.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2523    5.9701    0.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
  3 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
 14 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 12  5  1  0
 23 15  1  0
 32 25  1  0
  5 33  1  1
  7 34  1  0
  7 35  1  0
  8 36  1  1
  9 37  1  0
 10 38  1  6
 11 39  1  0
 12 40  1  6
 13 41  1  0
 16 42  1  0
 18 43  1  0
 20 44  1  0
 22 45  1  0
 23 46  1  0
 26 47  1  0
 28 48  1  0
 29 49  1  0
 31 50  1  0
M  END
Download

3D SDF for HMDB0041635 (Myricetin 3-arabinoside)


  Mrv0541 02241222502D          

 32 35  0  0  1  0            999 V2000
   -0.9041   -0.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9041    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185    0.9791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3330    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3330   -0.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185   -0.6709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6185   -1.4959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0475   -0.6709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0475   -1.4959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7620   -0.2584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7620    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4764    0.9791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0475    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896    1.8041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5249    2.2166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5249    3.0416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2393    1.8041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9538    2.2166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2393    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9538    0.5666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5249    0.5666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9041   -1.9084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9041   -2.7334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896   -3.1459    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5249   -2.7334    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5249   -1.9084    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1896   -1.4959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1896   -0.6709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2393   -1.4959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2394   -3.1459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1896   -3.9709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 29  1  1  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  2  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  4 13  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 14 22  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 23 28  1  0  0  0  0
 28 29  1  1  0  0  0
 27 30  1  6  0  0  0
 26 31  1  1  0  0  0
 25 32  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0041635

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@H]1CO[C@@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC(O)=C(O)C(O)=C2)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O12/c21-7-3-8(22)13-12(4-7)31-18(6-1-9(23)14(26)10(24)2-6)19(16(13)28)32-20-17(29)15(27)11(25)5-30-20/h1-4,11,15,17,20-27,29H,5H2/t11-,15-,17+,20-/m0/s1

> <INCHI_KEY>
SBEOEJNITMVWLK-KJCLSZHRSA-N

> <FORMULA>
C20H18O12

> <MOLECULAR_WEIGHT>
450.3497

> <EXACT_MASS>
450.07982604

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
41.67425553842691

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one

> <ALOGPS_LOGP>
0.69

> <JCHEM_LOGP>
0.18193432433333304

> <ALOGPS_LOGS>
-2.39

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.077437159089559

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.42809370258755

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265985532894106

> <JCHEM_POLAR_SURFACE_AREA>
206.59999999999997

> <JCHEM_REFRACTIVITY>
105.29389999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.83e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0041635 (Myricetin 3-arabinoside)

HMDB0041635
     RDKit          3D
Myricetin 3-arabinoside
 50 53  0  0  0  0  0  0  0  0999 V2000
    0.5554    2.9189   -0.7778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3917    2.2118   -0.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4173    0.8354   -0.5120 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6486    0.2923   -1.1651 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8514   -0.0647   -0.4440 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6840    1.0723   -0.6830 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7897    1.0200    0.1715 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3104   -0.4227    0.2611 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6524   -0.4665    0.5455 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9844   -1.0418   -1.1041 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2215   -0.0697   -2.0629 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4617   -1.2594   -1.0889 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2300   -2.4321   -0.3546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4553    0.1215   -0.0335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6127   -1.3180   -0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5784   -1.9462    0.6380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8391   -3.3034    0.5742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8241   -3.8334    1.3950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1315   -4.1085   -0.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3642   -5.4737   -0.3809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1625   -3.5126   -1.0804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4526   -4.3161   -1.9457 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9244   -2.1405   -0.9922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4262    0.7792    0.5937 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    2.0668    0.7702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4808    2.6862    1.4335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4966    4.0493    1.6231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5548    4.6695    2.2938 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4437    4.8280    1.1411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3899    4.2313    0.4760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3188    4.9836   -0.0197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4056    2.8665    0.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6726   -0.1405    0.6405 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5969    1.5992   -0.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6039    1.4526    1.1552 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6686   -0.9524    0.9929 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9486    0.4188    0.8379 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5281   -1.9719   -1.2768 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0545    0.4307   -1.9325 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0980   -1.3664   -2.1501 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9436   -3.1299   -1.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1563   -1.3430    1.3321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0845   -4.7878    1.4239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0490   -5.9705    0.1607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6182   -5.3006   -2.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1925   -1.7479   -1.6456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2790    2.0437    1.7920 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3305    4.9750    1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4358    5.8975    1.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2523    5.9701    0.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
  3 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 21 23  2  0
 14 24  1  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 32  2  1  0
 12  5  1  0
 23 15  1  0
 32 25  1  0
  5 33  1  1
  7 34  1  0
  7 35  1  0
  8 36  1  1
  9 37  1  0
 10 38  1  6
 11 39  1  0
 12 40  1  6
 13 41  1  0
 16 42  1  0
 18 43  1  0
 20 44  1  0
 22 45  1  0
 23 46  1  0
 26 47  1  0
 28 48  1  0
 29 49  1  0
 31 50  1  0
M  END
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PDB for HMDB0041635 (Myricetin 3-arabinoside)

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -1.688  -0.482   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.688   1.058   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -3.021   1.828   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -4.355   1.058   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.355  -0.482   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.021  -1.252   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -3.021  -2.792   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -5.689  -1.252   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.689  -2.792   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -7.022  -0.482   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -7.022   1.058   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -8.356   1.828   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -5.689   1.828   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.354   1.828   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.354   3.368   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.980   4.138   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.980   5.678   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.313   3.368   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.647   4.138   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.313   1.828   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.647   1.058   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.980   1.058   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.688  -3.562   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.688  -5.102   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.354  -5.872   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.980  -5.102   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.980  -3.562   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.354  -2.792   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -0.354  -1.252   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.313  -2.792   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       2.314  -5.872   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -0.354  -7.412   0.000  0.00  0.00           O+0
CONECT    1   29    2    6                                                  
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   13                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6                                                            
CONECT    8    5    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    4                                                       
CONECT   14    2   15   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   14                                                       
CONECT   23   24   28                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   32                                                  
CONECT   26   25   27   31                                                  
CONECT   27   26   28   30                                                  
CONECT   28   27   23   29                                                  
CONECT   29    1   28                                                       
CONECT   30   27                                                            
CONECT   31   26                                                            
CONECT   32   25                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END
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3D PDB for HMDB0041635 (Myricetin 3-arabinoside)

COMPND    HMDB0041635
HETATM    1  O1  UNL     1       0.555   2.919  -0.778  1.00  0.00           O  
HETATM    2  C1  UNL     1      -0.392   2.212  -0.345  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.417   0.835  -0.512  1.00  0.00           C  
HETATM    4  O2  UNL     1       0.649   0.292  -1.165  1.00  0.00           O  
HETATM    5  C3  UNL     1       1.851  -0.065  -0.444  1.00  0.00           C  
HETATM    6  O3  UNL     1       2.684   1.072  -0.683  1.00  0.00           O  
HETATM    7  C4  UNL     1       3.790   1.020   0.172  1.00  0.00           C  
HETATM    8  C5  UNL     1       4.310  -0.423   0.261  1.00  0.00           C  
HETATM    9  O4  UNL     1       5.652  -0.466   0.546  1.00  0.00           O  
HETATM   10  C6  UNL     1       3.984  -1.042  -1.104  1.00  0.00           C  
HETATM   11  O5  UNL     1       4.221  -0.070  -2.063  1.00  0.00           O  
HETATM   12  C7  UNL     1       2.462  -1.259  -1.089  1.00  0.00           C  
HETATM   13  O6  UNL     1       2.230  -2.432  -0.355  1.00  0.00           O  
HETATM   14  C8  UNL     1      -1.455   0.121  -0.034  1.00  0.00           C  
HETATM   15  C9  UNL     1      -1.613  -1.318  -0.141  1.00  0.00           C  
HETATM   16  C10 UNL     1      -2.578  -1.946   0.638  1.00  0.00           C  
HETATM   17  C11 UNL     1      -2.839  -3.303   0.574  1.00  0.00           C  
HETATM   18  O7  UNL     1      -3.824  -3.833   1.395  1.00  0.00           O  
HETATM   19  C12 UNL     1      -2.132  -4.108  -0.289  1.00  0.00           C  
HETATM   20  O8  UNL     1      -2.364  -5.474  -0.381  1.00  0.00           O  
HETATM   21  C13 UNL     1      -1.162  -3.513  -1.080  1.00  0.00           C  
HETATM   22  O9  UNL     1      -0.453  -4.316  -1.946  1.00  0.00           O  
HETATM   23  C14 UNL     1      -0.924  -2.140  -0.992  1.00  0.00           C  
HETATM   24  O10 UNL     1      -2.426   0.779   0.594  1.00  0.00           O  
HETATM   25  C15 UNL     1      -2.436   2.067   0.770  1.00  0.00           C  
HETATM   26  C16 UNL     1      -3.481   2.686   1.433  1.00  0.00           C  
HETATM   27  C17 UNL     1      -3.497   4.049   1.623  1.00  0.00           C  
HETATM   28  O11 UNL     1      -4.555   4.669   2.294  1.00  0.00           O  
HETATM   29  C18 UNL     1      -2.444   4.828   1.141  1.00  0.00           C  
HETATM   30  C19 UNL     1      -1.390   4.231   0.476  1.00  0.00           C  
HETATM   31  O12 UNL     1      -0.319   4.984  -0.020  1.00  0.00           O  
HETATM   32  C20 UNL     1      -1.406   2.867   0.304  1.00  0.00           C  
HETATM   33  H1  UNL     1       1.673  -0.140   0.640  1.00  0.00           H  
HETATM   34  H2  UNL     1       4.597   1.599  -0.323  1.00  0.00           H  
HETATM   35  H3  UNL     1       3.604   1.453   1.155  1.00  0.00           H  
HETATM   36  H4  UNL     1       3.669  -0.952   0.993  1.00  0.00           H  
HETATM   37  H5  UNL     1       5.949   0.419   0.838  1.00  0.00           H  
HETATM   38  H6  UNL     1       4.528  -1.972  -1.277  1.00  0.00           H  
HETATM   39  H7  UNL     1       5.054   0.431  -1.933  1.00  0.00           H  
HETATM   40  H8  UNL     1       2.098  -1.366  -2.150  1.00  0.00           H  
HETATM   41  H9  UNL     1       1.944  -3.130  -1.013  1.00  0.00           H  
HETATM   42  H10 UNL     1      -3.156  -1.343   1.332  1.00  0.00           H  
HETATM   43  H11 UNL     1      -4.085  -4.788   1.424  1.00  0.00           H  
HETATM   44  H12 UNL     1      -3.049  -5.971   0.161  1.00  0.00           H  
HETATM   45  H13 UNL     1      -0.618  -5.301  -2.014  1.00  0.00           H  
HETATM   46  H14 UNL     1      -0.192  -1.748  -1.646  1.00  0.00           H  
HETATM   47  H15 UNL     1      -4.279   2.044   1.792  1.00  0.00           H  
HETATM   48  H16 UNL     1      -5.331   4.975   1.742  1.00  0.00           H  
HETATM   49  H17 UNL     1      -2.436   5.897   1.279  1.00  0.00           H  
HETATM   50  H18 UNL     1      -0.252   5.970   0.074  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   32
CONECT    3    4   14   14
CONECT    4    5
CONECT    5    6   12   33
CONECT    6    7
CONECT    7    8   34   35
CONECT    8    9   10   36
CONECT    9   37
CONECT   10   11   12   38
CONECT   11   39
CONECT   12   13   40
CONECT   13   41
CONECT   14   15   24
CONECT   15   16   16   23
CONECT   16   17   42
CONECT   17   18   19   19
CONECT   18   43
CONECT   19   20   21
CONECT   20   44
CONECT   21   22   23   23
CONECT   22   45
CONECT   23   46
CONECT   24   25
CONECT   25   26   26   32
CONECT   26   27   47
CONECT   27   28   29   29
CONECT   28   48
CONECT   29   30   49
CONECT   30   31   32   32
CONECT   31   50
END
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SMILES for HMDB0041635 (Myricetin 3-arabinoside)

O[C@H]1CO[C@@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC(O)=C(O)C(O)=C2)[C@H](O)[C@H]1O
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INCHI for HMDB0041635 (Myricetin 3-arabinoside)

InChI=1S/C20H18O12/c21-7-3-8(22)13-12(4-7)31-18(6-1-9(23)14(26)10(24)2-6)19(16(13)28)32-20-17(29)15(27)11(25)5-30-20/h1-4,11,15,17,20-27,29H,5H2/t11-,15-,17+,20-/m0/s1
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View in JSmolView Stereo Labels
SynonymsNot Available
Chemical FormulaC20H18O12
Average Molecular Weight450.3497
Monoisotopic Molecular Weight450.07982604
IUPAC Name5,7-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one
Traditional Name5,7-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)chromen-4-one
CAS Registry Number132679-85-7
SMILES
O[C@H]1CO[C@@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC(O)=C(O)C(O)=C2)[C@H](O)[C@H]1O
InChI Identifier
InChI=1S/C20H18O12/c21-7-3-8(22)13-12(4-7)31-18(6-1-9(23)14(26)10(24)2-6)19(16(13)28)32-20-17(29)15(27)11(25)5-30-20/h1-4,11,15,17,20-27,29H,5H2/t11-,15-,17+,20-/m0/s1
InChI KeySBEOEJNITMVWLK-KJCLSZHRSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid-3-O-glycosides
Alternative Parents
Substituents
  • Flavonoid-3-o-glycoside
  • 3'-hydroxyflavonoid
  • 4'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Flavone
  • Hydroxyflavonoid
  • Chromone
  • Glycosyl compound
  • O-glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • Benzenetriol
  • Pyrogallol derivative
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Pyranone
  • Oxane
  • Pyran
  • Monocyclic benzene moiety
  • Monosaccharide
  • Benzenoid
  • Heteroaromatic compound
  • Vinylogous acid
  • Secondary alcohol
  • Oxacycle
  • Acetal
  • Polyol
  • Organoheterocyclic compound
  • Organooxygen compound
  • Hydrocarbon derivative
  • Alcohol
  • Organic oxygen compound
  • Organic oxide
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
ProcessNot Available
Role
Biological role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point203 - 205 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.83 g/LALOGPS
logP0.69ALOGPS
logP0.18ChemAxon
logS-2.4ALOGPS
pKa (Strongest Acidic)6.43ChemAxon
pKa (Strongest Basic)-3.5ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count8ChemAxon
Polar Surface Area206.6 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity105.29 m³·mol⁻¹ChemAxon
Polarizability41.67 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
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]+195.90130932474
DeepCCS[M-H]-193.50530932474
DeepCCS[M-2H]-226.6130932474
DeepCCS[M+Na]+201.81330932474
AllCCS[M+H]+201.432859911
AllCCS[M+H-H2O]+198.932859911
AllCCS[M+NH4]+203.732859911
AllCCS[M+Na]+204.432859911
AllCCS[M-H]-198.732859911
AllCCS[M+Na-2H]-198.832859911
AllCCS[M+HCOO]-199.132859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Myricetin 3-arabinosideO[C@H]1CO[C@@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC(O)=C(O)C(O)=C2)[C@H](O)[C@H]1O5884.7Standard polar33892256
Myricetin 3-arabinosideO[C@H]1CO[C@@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC(O)=C(O)C(O)=C2)[C@H](O)[C@H]1O4150.3Standard non polar33892256
Myricetin 3-arabinosideO[C@H]1CO[C@@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC(O)=C(O)C(O)=C2)[C@H](O)[C@H]1O4314.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Myricetin 3-arabinoside,1TMS,isomer #1C[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4308.8Semi standard non polar33892256
Myricetin 3-arabinoside,1TMS,isomer #2C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24271.6Semi standard non polar33892256
Myricetin 3-arabinoside,1TMS,isomer #3C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14333.2Semi standard non polar33892256
Myricetin 3-arabinoside,1TMS,isomer #4C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4263.1Semi standard non polar33892256
Myricetin 3-arabinoside,1TMS,isomer #5C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4259.5Semi standard non polar33892256
Myricetin 3-arabinoside,1TMS,isomer #6C[Si](C)(C)O[C@H]1[C@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)OC[C@H](O)[C@@H]1O4299.8Semi standard non polar33892256
Myricetin 3-arabinoside,1TMS,isomer #7C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O4301.2Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #1C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4163.0Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #10C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24190.7Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #11C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)=C(C1=CC(O)=C(O)C(O)=C1)O24195.0Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #12C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14219.2Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #13C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14232.3Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #14C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14183.1Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #15C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C14177.9Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #16C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4148.6Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #17C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4159.3Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #18C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4153.1Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #19C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4117.8Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #2C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4148.3Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #20C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4129.5Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #21C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4144.7Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #22C[Si](C)(C)O[C@H]1[C@@H](O)CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O[Si](C)(C)C4232.0Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #3C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14232.7Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #4C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24199.4Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #5C[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O4252.1Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #6C[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C4243.5Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #7C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14205.4Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #8C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4165.5Semi standard non polar33892256
Myricetin 3-arabinoside,2TMS,isomer #9C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O4170.0Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #1C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14080.5Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #10C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4096.9Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #11C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14128.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #12C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14139.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #13C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14167.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #14C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24126.2Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #15C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C)=C(C1=CC(O)=C(O)C(O)=C1)O24151.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #16C[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C4168.9Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #17C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14104.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #18C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14123.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #19C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14038.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #2C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4080.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #20C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C14045.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #21C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4066.2Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #22C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4079.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #23C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4037.2Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #24C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4010.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #25C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O4035.2Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #26C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O4048.9Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #27C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)=C(C1=CC(O)=C(O)C(O)=C1)O24121.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #28C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14140.5Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #29C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14065.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #3C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4090.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #30C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C14034.0Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #31C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14086.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #32C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C14051.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #33C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14040.5Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #34C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14018.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #35C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4088.0Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #36C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4067.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #37C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4034.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #38C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4082.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #39C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4049.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #4C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4113.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #40C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C4051.0Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #41C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4074.2Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #5C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4077.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #6C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4047.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #7C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C14051.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #8C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O4052.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TMS,isomer #9C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4074.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #1C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13961.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #10C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4073.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #11C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4011.1Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #12C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4000.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #13C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4032.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #14C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4026.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #15C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C4026.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #16C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13988.2Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #17C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13970.3Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #18C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13989.5Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #19C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3966.4Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #2C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14010.7Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #20C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3987.1Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #21C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4050.7Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #22C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14069.2Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #23C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14086.8Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #24C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14119.7Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #25C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)=C(C1=CC(O)=C(O)C(O)=C1)O24097.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #26C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14072.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #27C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13923.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #28C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13983.8Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #29C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13962.5Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #3C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14033.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #30C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13980.3Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #31C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13960.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #32C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13951.0Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #33C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4012.0Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #34C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3932.1Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #35C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3920.5Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #36C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3968.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #37C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3954.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #38C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3955.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #39C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3977.3Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #4C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13963.0Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #40C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C14024.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #41C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13975.5Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #42C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13933.8Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #43C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13928.4Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #44C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13973.6Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #45C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13962.8Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #46C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13976.0Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #47C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O4021.7Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #48C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C4010.4Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #49C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3994.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #5C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13956.0Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #50C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C4029.1Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #6C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4001.3Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #7C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4024.9Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #8C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3959.7Semi standard non polar33892256
Myricetin 3-arabinoside,4TMS,isomer #9C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3947.3Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #1C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13917.5Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #10C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13957.5Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #11C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O3981.2Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #12C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3908.1Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #13C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3912.3Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #14C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3910.1Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #15C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3918.2Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #16C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3936.8Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #17C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3993.0Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #18C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3991.8Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #19C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3972.9Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #2C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13923.4Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #20C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3988.2Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #21C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13974.8Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #22C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13972.0Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #23C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13968.8Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #24C[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3951.4Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #25C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14046.2Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #26C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13919.8Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #27C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13966.9Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #28C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13933.5Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #29C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13931.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #3C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13937.4Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #30C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13926.3Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #31C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13929.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #32C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13932.4Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #33C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3915.5Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #34C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3916.0Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #35C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3903.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #36C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3939.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #37C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13931.0Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #38C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13933.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #39C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13920.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #4C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13932.7Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #40C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13961.8Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #41C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3988.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #5C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13992.1Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #6C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13921.6Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #7C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13927.7Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #8C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13929.2Semi standard non polar33892256
Myricetin 3-arabinoside,5TMS,isomer #9C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13936.6Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #1C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13940.6Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #10C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13943.5Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #11C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O3939.8Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #12C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C3943.7Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #13C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3934.0Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #14C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3930.4Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #15C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3999.7Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #16C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O)=C3)OC2=C13971.0Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #17C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13942.6Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #18C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13935.1Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #19C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13923.0Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #2C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13947.8Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #20C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13925.5Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #21C[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C)=C1O[Si](C)(C)C3937.5Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #22C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13948.7Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #3C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13939.8Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #4C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13932.7Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #5C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13926.1Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #6C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13927.4Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #7C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O[Si](C)(C)C)=C(O)C(O[Si](C)(C)C)=C3)OC2=C13950.3Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #8C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13952.2Semi standard non polar33892256
Myricetin 3-arabinoside,6TMS,isomer #9C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC(O[Si](C)(C)C)=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13944.9Semi standard non polar33892256
Myricetin 3-arabinoside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4557.3Semi standard non polar33892256
Myricetin 3-arabinoside,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24556.7Semi standard non polar33892256
Myricetin 3-arabinoside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14583.3Semi standard non polar33892256
Myricetin 3-arabinoside,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4553.9Semi standard non polar33892256
Myricetin 3-arabinoside,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4559.6Semi standard non polar33892256
Myricetin 3-arabinoside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)OC[C@H](O)[C@@H]1O4543.3Semi standard non polar33892256
Myricetin 3-arabinoside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O4555.1Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4657.7Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24657.5Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)=C(C1=CC(O)=C(O)C(O)=C1)O24660.4Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14683.7Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14691.0Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14648.8Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14667.8Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4630.0Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4636.3Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C(C)(C)C)=C1O4640.9Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C(C)(C)C4617.6Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4663.9Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4642.1Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4642.8Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C4690.1Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14706.0Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24684.2Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4703.2Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4701.8Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14673.0Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4635.2Semi standard non polar33892256
Myricetin 3-arabinoside,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4651.9Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14749.9Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4738.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14783.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14796.9Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14800.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)=C(C1=CC(O)=C(O)C(O)=C1)O24772.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)=C(C1=CC(O)=C(O)C(O)=C1)O24772.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)O[C@H]1CO[C@@H](OC2=C(C3=CC(O)=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4814.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14757.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14767.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14733.5Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4730.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14790.5Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4703.2Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O4716.0Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC(O[Si](C)(C)C(C)(C)C)=C1O4717.9Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C(C)(C)C4710.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4739.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4737.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)=C(C1=CC(O)=C(O)C(O)=C1)O24761.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC(O)=C(O)C(O)=C3)OC2=C14785.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14721.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4747.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14754.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC(O)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14736.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14753.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O[Si](C)(C)C(C)(C)C)=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14738.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14730.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4736.4Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C(C)(C)C)=C1O4709.0Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C(C)(C)C4701.8Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C(C)(C)C)=C1O4720.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C(C)(C)C4714.0Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O4754.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C(C)(C)C)=C1O[Si](C)(C)C(C)(C)C4717.3Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4732.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O[Si](C)(C)C(C)(C)C)=C1O4735.1Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC(O)=C1O[Si](C)(C)C(C)(C)C4727.7Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)=C(C3=CC(O)=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14764.6Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4755.2Semi standard non polar33892256
Myricetin 3-arabinoside,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=C(O)C=C(C2=C(O[C@@H]3OC[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4736.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Myricetin 3-arabinoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-05ai-9405600000-7a3742ebe9fdf8c3cf592017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Myricetin 3-arabinoside GC-MS (3 TMS) - 70eV, Positivesplash10-0udi-4610039000-34e8e79ba557210e72482017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Myricetin 3-arabinoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 10V, Positive-QTOFsplash10-0gb9-0109600000-4f217d852feaa6b2db412017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 20V, Positive-QTOFsplash10-014i-0119100000-810e8c6eec6cfe2a9ba62017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 40V, Positive-QTOFsplash10-0udr-2924000000-99b787b1d3590d3ac8492017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 10V, Negative-QTOFsplash10-00kb-1115900000-e17e93d6c0cf282757892017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 20V, Negative-QTOFsplash10-014j-1339300000-a811ba6b36ca8af0b4b42017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 40V, Negative-QTOFsplash10-004l-6941000000-af2eb0873630419236d92017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 10V, Negative-QTOFsplash10-0002-0000900000-69a6df4817caa75dd5622021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 20V, Negative-QTOFsplash10-0f6t-0300900000-3166238da89a5bb719d92021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 40V, Negative-QTOFsplash10-0udl-1910200000-f97ab6e612a5c24dd1432021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 10V, Positive-QTOFsplash10-0udi-0000900000-a8b862d11b424a74dae12021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 20V, Positive-QTOFsplash10-0udi-0000900000-5794fb68ba4d07695a4d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Myricetin 3-arabinoside 40V, Positive-QTOFsplash10-0udi-1910400000-0e3d9459af73c4d8e8a32021-09-23Wishart 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 IDFDB021864
KNApSAcK IDNot Available
Chemspider ID10283343
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound21672568
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .