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Pterokaurene L3

PubChem CID: 26112861

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Compound Synonyms Pterokaurene L3, 77658-38-9, (1S,4S,5R,9R,10S,13R)-10-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid, AKOS040762241
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 57.5
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level CC1CC23CCC4CCCCC4C2CCC1C3
Np Classifier Class Kaurane and Phyllocladane diterpenoids, Tetracyclic diterpenoids
Deep Smiles C=CC[C@]C[C@H]5CC[C@@]6O)[C@][C@H]CC%10))[C@@]C)CCC6)))C=O)O))))C
Heavy Atom Count 23.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level CC1CC23CCC4CCCCC4C2CCC1C3
Classyfire Subclass Diterpenoids
Isotope Atom Count 0.0
Molecular Complexity 583.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 6.0
Iupac Name (1S,4S,5R,9R,10S,13R)-10-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 3.4
Gsk 4 400 Rule False
Molecular Formula C20H30O3
Scaffold Graph Node Bond Level C=C1CC23CCC4CCCCC4C2CCC1C3
Inchi Key GQFVICMVZLJUEP-ABWGISGVSA-N
Silicos It Class Soluble
Rotatable Bond Count 1.0
Synonyms pterokaurene l3
Esol Class Soluble
Functional Groups C=C(C)C, CC(=O)O, CO
Compound Name Pterokaurene L3
Exact Mass 318.219
Formal Charge 0.0
Monoisotopic Mass 318.219
Hydrogen Bond Acceptor Count 3.0
Molecular Weight 318.4
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 6.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C20H30O3/c1-13-11-19-9-6-15-17(2,16(21)22)7-4-8-18(15,3)20(19,23)10-5-14(13)12-19/h14-15,23H,1,4-12H2,2-3H3,(H,21,22)/t14-,15-,17-,18-,19-,20-/m1/s1
Smiles C[C@]1(CCC[C@@]2([C@@H]1CC[C@]34[C@]2(CC[C@H](C3)C(=C)C4)O)C)C(=O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Diterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Pteris Longipes (Plant) Rel Props:Reference:ISBN:9788185042114