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Cyclotrichosantol

PubChem CID: 101306800

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Compound Synonyms Cyclotrichosantol, 41507-26-0, 4alpha,14alpha-Dimethyl-24-ethyl-9,19-cyclocholest-25-ene-3beta-ol, (1S,3R,6S,7S,8S,11S,12S,15R,16R)-15-((2R,5R)-5-ethyl-6-methylhept-6-en-2-yl)-7,12,16-trimethylpentacyclo(9.7.0.01,3.03,8.012,16)octadecan-6-ol, (1S,3R,6S,7S,8S,11S,12S,15R,16R)-15-[(2R,5R)-5-ethyl-6-methylhept-6-en-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol, 4 alpha,14 alpha-dimethyl-24-ethyl-9,19-cyclocholest-25-ene-3 beta-ol
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 20.2
Hydrogen Bond Donor Count 1.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CC2CCC34CC35CCCCC5CCC4C2C1
Np Classifier Class Cycloartane triterpenoids
Deep Smiles CC[C@@H]C=C)C))CC[C@H][C@H]CC[C@@][C@]5C)CC[C@][C@H]6CC[C@@H][C@]6C7)CC[C@@H][C@H]6C))O)))))))))))))C)))))C
Heavy Atom Count 32.0
Classyfire Class Steroids and steroid derivatives
Scaffold Graph Node Level C1CC2CCC34CC35CCCCC5CCC4C2C1
Classyfire Subclass Cycloartanols and derivatives
Isotope Atom Count 0.0
Molecular Complexity 756.0
Database Name imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 11.0
Iupac Name (1S,3R,6S,7S,8S,11S,12S,15R,16R)-15-[(2R,5R)-5-ethyl-6-methylhept-6-en-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 10.6
Gsk 4 400 Rule False
Molecular Formula C31H52O
Scaffold Graph Node Bond Level C1CC2CCC34CC35CCCCC5CCC4C2C1
Inchi Key IGSHUKWRIPUVMM-QWGGAANJSA-N
Silicos It Class Poorly soluble
Rotatable Bond Count 6.0
Synonyms cyclotrichosantol
Esol Class Poorly soluble
Functional Groups C=C(C)C, CO
Compound Name Cyclotrichosantol
Exact Mass 440.402
Formal Charge 0.0
Monoisotopic Mass 440.402
Hydrogen Bond Acceptor Count 1.0
Molecular Weight 440.7
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 11.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C31H52O/c1-8-23(20(2)3)10-9-21(4)24-13-15-29(7)27-12-11-25-22(5)26(32)14-16-30(25)19-31(27,30)18-17-28(24,29)6/h21-27,32H,2,8-19H2,1,3-7H3/t21-,22+,23-,24-,25+,26+,27+,28-,29+,30-,31+/m1/s1
Smiles CC[C@H](CC[C@@H](C)[C@H]1CC[C@@]2([C@@]1(CC[C@]34[C@H]2CC[C@@H]5[C@]3(C4)CC[C@@H]([C@H]5C)O)C)C)C(=C)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Triterpenoids