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[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aR,6aR,6aS,6bR,8aR,10R,11R,12aS,14bS)-1,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-4a-carboxylate

PubChem CID: 102117122

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Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 194.0
Hydrogen Bond Donor Count 7.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC2C(CCC3(C(C)CC4CCCCC4)CCCCC23)C2CCC3CCCCC3C12
Np Classifier Class Oleanane triterpenoids
Deep Smiles OC[C@H]O[C@@H]OC=O)[C@]CCC[C@H][C@H]6C=CC=O)[C@H][C@@][C@@]6CC%14))C))C)CC[C@@H][C@]6C)C[C@H][C@@H]C6C)C))O))O)))))))))))))O))C)C)))))))[C@@H][C@H][C@@H]6O))O))O
Heavy Atom Count 47.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level OC1CC2C(CCC3(C(O)OC4CCCCO4)CCCCC23)C2CCC3CCCCC3C12
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 1330.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 15.0
Iupac Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aR,6aR,6aS,6bR,8aR,10R,11R,12aS,14bS)-1,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-4a-carboxylate
Prediction Hob 0.0
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.3
Gsk 4 400 Rule False
Molecular Formula C36H56O11
Scaffold Graph Node Bond Level O=C1C=C2C(CCC3(C(=O)OC4CCCCO4)CCCCC23)C2CCC3CCCCC3C12
Prediction Swissadme 0.0
Inchi Key QRBQBRULJDJSSP-XTPLGFNASA-N
Silicos It Class Soluble
Fcsp3 0.8888888888888888
Logs -3.508
Rotatable Bond Count 4.0
Logd 1.206
Synonyms arjunglucoside iii
Esol Class Moderately soluble
Functional Groups CC(C)=CC(C)=O, CO, CO[C@H](C)OC(C)=O
Compound Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aR,6aR,6aS,6bR,8aR,10R,11R,12aS,14bS)-1,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-13-oxo-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picene-4a-carboxylate
Prediction Hob Swissadme 0.0
Exact Mass 664.382
Formal Charge 0.0
Monoisotopic Mass 664.382
Hydrogen Bond Acceptor Count 11.0
Molecular Weight 664.8
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 15.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Esol -5.146964600000002
Inchi InChI=1S/C36H56O11/c1-31(2)10-12-36(30(45)47-29-25(42)24(41)23(40)20(16-37)46-29)13-11-34(6)17(22(36)28(31)44)14-18(38)26-33(5)15-19(39)27(43)32(3,4)21(33)8-9-35(26,34)7/h14,19-29,37,39-44H,8-13,15-16H2,1-7H3/t19-,20-,21+,22-,23-,24+,25-,26-,27+,28+,29+,33+,34-,35-,36+/m1/s1
Smiles C[C@@]12CC[C@@H]3[C@@]([C@H]1C(=O)C=C4[C@]2(CC[C@@]5([C@H]4[C@@H](C(CC5)(C)C)O)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O)C)(C[C@H]([C@@H](C3(C)C)O)O)C
Nring 6.0
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 Terminalia Arjuna (Plant) Rel Props:Reference:ISBN:9788185042114
  • 2. Outgoing r'ship FOUND_IN to/from Terminalia Chebula (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all