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Paniculoside II

PubChem CID: 21593624

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Compound Synonyms Paniculoside II, 60129-64-8, [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,4S,5R,9R,10S,11S,13S,15R)-11,15-dihydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate, (4R,15R)-11beta,15-Dihydroxykaur-16-en-18-oic acid [beta-D-glucopyranosyl] ester, DTXSID801132161, HY-N3108, AKOS032962331, FS-8856, DA-59526, CS-0023251, [3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 11,15-dihydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate, Kaur-16-en-18-oic acid, 11,15-dihydroxy-, I(2)-D-glucopyranosyl ester, (4I+/-,11I(2),15I(2))-
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 157.0
Hydrogen Bond Donor Count 6.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC1CC23CCC4C(C(C)CC5CCCCC5)CCCC4C2CCC1C3
Np Classifier Class Kaurane and Phyllocladane diterpenoids
Deep Smiles OC[C@H]O[C@@H]OC=O)[C@]C)CCC[C@@][C@@H]6CC[C@][C@H]6[C@@H]O)C[C@H]C6)C=C)[C@H]7O)))))))))))C))))))))[C@@H][C@H][C@@H]6O))O))O
Heavy Atom Count 35.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level CC1CC23CCC4C(C(O)OC5CCCCO5)CCCC4C2CCC1C3
Classyfire Subclass Terpene glycosides
Isotope Atom Count 0.0
Molecular Complexity 879.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 13.0
Iupac Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,4S,5R,9R,10S,11S,13S,15R)-11,15-dihydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylate
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 0.8
Gsk 4 400 Rule False
Molecular Formula C26H40O9
Scaffold Graph Node Bond Level C=C1CC23CCC4C(C(=O)OC5CCCCO5)CCCC4C2CCC1C3
Inchi Key OHCCJDCXGVSWSO-WWXRUBGDSA-N
Silicos It Class Soluble
Rotatable Bond Count 4.0
Synonyms paniculosides ii
Esol Class Soluble
Functional Groups C=C(C)C, CO, CO[C@H](C)OC(C)=O
Compound Name Paniculoside II
Exact Mass 496.267
Formal Charge 0.0
Monoisotopic Mass 496.267
Hydrogen Bond Acceptor Count 9.0
Molecular Weight 496.6
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 13.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C26H40O9/c1-12-13-9-14(28)20-24(2)6-4-7-25(3,16(24)5-8-26(20,10-13)21(12)32)23(33)35-22-19(31)18(30)17(29)15(11-27)34-22/h13-22,27-32H,1,4-11H2,2-3H3/t13-,14+,15-,16+,17-,18+,19-,20+,21-,22+,24-,25-,26-/m1/s1
Smiles C[C@@]12CCC[C@@]([C@H]1CC[C@]34[C@H]2[C@H](C[C@H](C3)C(=C)[C@H]4O)O)(C)C(=O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Diterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Adenostemma Lavenia (Plant) Rel Props:Reference:ISBN:9788172362089