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Gymnemic acid VIII

PubChem CID: 91617623

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Compound Synonyms Gymnemic acid VIII, (+)-Gymnemic acid VIII, Gymnemic acid viii, (+)-, UNII-O9N5N83DZZ, O9N5N83DZZ, 131653-19-5, beta-D-Glucopyranosiduronic acid, (3beta,4alpha,16beta,21beta-(S),22alpha)-16,22,23,28-tetrahydroxy-21-(2-methyl-1-oxobutoxy)olean-12-en-3-yl 3-o-beta-D-arabino-hexopyranos-2-ulos-1-yl-, GYMNEMIC ACID VIII (CONSTITUENT OF GYMNEMA) [DSC], .BETA.-D-GLUCOPYRANOSIDURONIC ACID, (3.BETA.,4.ALPHA.,16.BETA.,21.BETA.-(S),22.ALPHA.)-16,22,23,28-TETRAHYDROXY-21-(2-METHYL-1-OXOBUTOXY)OLEAN-12-EN-3-YL 3-O-.BETA.-D-ARABINO-HEXOPYRANOS-2-ULOS-1-YL-, Gymnemate VIII, (2S,3S,4S,5R,6R)-6-(((3S,4R,4aR,6aR,6bS,8S,8aR,9R,10R,12aS,14aR,14bR)-8,9-dihydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-10-((2S)-2-methylbutanoyl)oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy)-4-((2S,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-oxooxan-2-yl)oxy-3,5-dihydroxyoxane-2-carboxylic acid, (2S,3S,4S,5R,6R)-6-[[(3S,4R,4aR,6aR,6bS,8S,8aR,9R,10R,12aS,14aR,14bR)-8,9-dihydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-10-[(2S)-2-methylbutanoyl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-oxooxan-2-yl]oxy-3,5-dihydroxyoxane-2-carboxylic acid, GYMNEMIC ACID VIII (CONSTITUENT OF GYMNEMA), Q27285522
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 300.0
Hydrogen Bond Donor Count 10.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CCCCC1CC1CCCC(CC2CCC3C(CCC4C3CCC3C5CCCCC5CCC34)C2)C1
Np Classifier Class Oleanane triterpenoids
Deep Smiles OC[C@H]O[C@@H]O[C@@H][C@@H]O)[C@@H]O[C@@H][C@H]6O))C=O)O))))O[C@H]CC[C@][C@H][C@]6C)CO)))CC[C@@][C@@H]6CC=C[C@@]6C)C[C@@H][C@@][C@H]6CCC)C)[C@H][C@@H]6O))OC=O)[C@H]CC))C))))))))CO)))O))))))))C)))))C))))))))))C=O)[C@H][C@@H]6O))O
Heavy Atom Count 65.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level OC1CCCOC1OC1CCOC(OC2CCC3C(CCC4C3CCC3C5CCCCC5CCC34)C2)C1
Classyfire Subclass Terpene glycosides
Isotope Atom Count 0.0
Molecular Complexity 1840.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 22.0
Iupac Name (2S,3S,4S,5R,6R)-6-[[(3S,4R,4aR,6aR,6bS,8S,8aR,9R,10R,12aS,14aR,14bR)-8,9-dihydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-10-[(2S)-2-methylbutanoyl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-oxooxan-2-yl]oxy-3,5-dihydroxyoxane-2-carboxylic acid
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.9
Gsk 4 400 Rule False
Molecular Formula C47H74O18
Scaffold Graph Node Bond Level O=C1CCCOC1OC1CCOC(OC2CCC3C(CCC4C5CCC6CCCCC6C5=CCC34)C2)C1
Inchi Key KIFOYKWBRFBOHQ-XMNCZCGISA-N
Rotatable Bond Count 12.0
Synonyms gymnemic acid viii
Functional Groups CC(=O)O, CC(=O)OC, CC=C(C)C, CO, CO[C@@H](C)OC, CO[C@H](OC)C(C)=O
Compound Name Gymnemic acid VIII
Exact Mass 926.488
Formal Charge 0.0
Monoisotopic Mass 926.488
Hydrogen Bond Acceptor Count 18.0
Molecular Weight 927.1
Covalent Unit Count 1.0
Total Atom Stereocenter Count 22.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C47H74O18/c1-9-21(2)39(60)65-37-36(57)47(20-50)23(16-42(37,3)4)22-10-11-26-43(5)14-13-28(44(6,19-49)25(43)12-15-45(26,7)46(22,8)17-27(47)51)62-41-33(56)34(32(55)35(64-41)38(58)59)63-40-31(54)30(53)29(52)24(18-48)61-40/h10,21,23-30,32-37,40-41,48-53,55-57H,9,11-20H2,1-8H3,(H,58,59)/t21-,23-,24+,25+,26+,27-,28-,29+,30-,32-,33+,34-,35-,36-,37-,40-,41+,43-,44-,45+,46+,47-/m0/s1
Smiles CC[C@H](C)C(=O)O[C@H]1[C@@H]([C@@]2([C@H](C[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H]([C@@]5(C)CO)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)C(=O)O)O)O[C@H]7C(=O)[C@H]([C@@H]([C@H](O7)CO)O)O)O)C)C)[C@@H]2CC1(C)C)C)O)CO)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Triterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Gymnema Sylvestre (Plant) Rel Props:Reference:ISBN:9788185042145