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Camelliagenin C

PubChem CID: 12302286

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Compound Synonyms Camelliagenin C, 14440-27-8, 4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8,9-triol, (3S,4R,4Ar,6aR,6bS,8R,8aS,9S,12aS,14aR,14bR)-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8,9-triol, Theasapogenol C, CHEBI:173217
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 101.0
Hydrogen Bond Donor Count 5.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2C(C1)CCC1C2CCC2C3CCCCC3CCC21
Np Classifier Class Oleanane triterpenoids
Deep Smiles OCCCO)CCCC6C=CCCCC6CC%14O)))C))C)CCCC6C)CCCC6C)CO)))O)))))))))))))))C)C
Heavy Atom Count 35.0
Classyfire Class Prenol lipids
Description Sapogenin from the seeds of Camellia japonica. Camelliagenin C is found in tea and fats and oils.
Scaffold Graph Node Level C1CCC2C(C1)CCC1C2CCC2C3CCCCC3CCC21
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 899.0
Database Name fooddb_chem_all;hmdb_chem_all;imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name 4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8,9-triol
Class Prenol lipids
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 5.1
Superclass Lipids and lipid-like molecules
Subclass Triterpenoids
Gsk 4 400 Rule False
Molecular Formula C30H50O5
Scaffold Graph Node Bond Level C1=C2C3CCCCC3CCC2C2CCC3CCCCC3C2C1
Inchi Key SPCSEMLFKVZFJN-UHFFFAOYSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 2.0
State Solid
Synonyms Camelliagenin C, Theasapogenol C, camelliagenin c
Esol Class Moderately soluble
Functional Groups CC=C(C)C, CO
Compound Name Camelliagenin C
Kingdom Organic compounds
Exact Mass 490.366
Formal Charge 0.0
Monoisotopic Mass 490.366
Hydrogen Bond Acceptor Count 5.0
Molecular Weight 490.7
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 11.0
Total Bond Stereocenter Count 0.0
Molecular Framework Aliphatic homopolycyclic compounds
Lipinski Rule Of 5 True
Inchi InChI=1S/C30H50O5/c1-25(2)13-19-18-7-8-21-26(3)11-10-22(33)27(4,16-31)20(26)9-12-28(21,5)29(18,6)15-24(35)30(19,17-32)23(34)14-25/h7,19-24,31-35H,8-17H2,1-6H3
Smiles CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)CO)O)C)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Taxonomy Direct Parent Triterpenoids
Np Classifier Superclass Triterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Camellia Japonica (Plant) Rel Props:Reference:ISBN:9788172360481