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CID 171432

PubChem CID: 171432

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Compound Synonyms 55304-02-4, SCHEMBL25356272, DTXSID20970630, F82521, 22,23-Dihydroxyolean-12-en-3-yl 2-O-hexopyranosylhexopyranosiduronic acid, beta-D-Glucopyranosiduronic acid, (3beta,4beta,21alpha)-21,23-dihydroxyolean-12-en-3-yl 2-O-beta-D-galactopyranosyl
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 236.0
Hydrogen Bond Donor Count 9.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CCC(CC2CCCCC2CC2CCC3C(CCC4C3CCC3C5CCCCC5CCC34)C2)CC1
Np Classifier Class Oleanane triterpenoids
Deep Smiles OC[C@H]O[C@@H]O[C@H][C@@H]O[C@@H][C@@H][C@@H]6O))O))C=O)O))))OCCC[C@]CC6C)CO)))CC[C@@]C6CC=C[C@@]6C)CC[C@@][C@@H]6CCC)C)C[C@@H]6O))))))C)))))))))C)))))C)))))))))[C@@H][C@H][C@H]6O))O))O
Heavy Atom Count 56.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CCC(OC2CCCOC2OC2CCC3C(CCC4C3CCC3C5CCCCC5CCC34)C2)OC1
Classyfire Subclass Terpene glycosides
Isotope Atom Count 0.0
Molecular Complexity 1520.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 16.0
Iupac Name (2S,3R,4S,5R,6R)-6-[[(6aR,6bS,8aR,9S,12aR,14bR)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 3.5
Gsk 4 400 Rule False
Molecular Formula C42H68O14
Scaffold Graph Node Bond Level C1=C2C3CCCCC3CCC2C2CCC3CC(OC4OCCCC4OC4CCCCO4)CCC3C2C1
Inchi Key OKIHRVKXRCAJFQ-ZYNCYBBUSA-N
Silicos It Class Soluble
Rotatable Bond Count 7.0
Synonyms azukisaponin iis, soyasaponin iiis
Esol Class Poorly soluble
Functional Groups CC(=O)O, CC=C(C)C, CO, CO[C@@H](C)OC
Compound Name CID 171432
Exact Mass 796.461
Formal Charge 0.0
Monoisotopic Mass 796.461
Hydrogen Bond Acceptor Count 14.0
Molecular Weight 797.0
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 20.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C42H68O14/c1-37(2)16-21-20-8-9-24-39(4)12-11-26(40(5,19-44)23(39)10-13-42(24,7)41(20,6)15-14-38(21,3)25(45)17-37)54-36-33(30(49)29(48)32(55-36)34(51)52)56-35-31(50)28(47)27(46)22(18-43)53-35/h8,21-33,35-36,43-50H,9-19H2,1-7H3,(H,51,52)/t21-,22-,23?,24?,25+,26?,27+,28+,29-,30+,31-,32+,33-,35+,36-,38-,39+,40?,41-,42-/m1/s1
Smiles C[C@@]12CC[C@@]3(C(=CCC4[C@]3(CCC5[C@@]4(CCC(C5(C)CO)O[C@H]6[C@@H]([C@H]([C@H]([C@H](O6)C(=O)O)O)O)O[C@H]7[C@@H]([C@H]([C@H]([C@H](O7)CO)O)O)O)C)C)[C@H]1CC(C[C@@H]2O)(C)C)C
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 Glycine Max (Plant) Rel Props:Reference:https://www.ncbi.nlm.nih.gov/pubmed/16503561
  • 2. Outgoing r'ship FOUND_IN to/from Medicago Sativa (Plant) Rel Props:Reference:https://doi.org/10.2174/0929867033456729