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(1R)-1-[(2S,4aS,4bR,8aR,10aS)-2,4a,8,8a-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol

PubChem CID: 101277377

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Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 40.5
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC2C(C1)CCC1CCCCC12
Np Classifier Class Erythroxylane diterpenoids
Deep Smiles OC[C@@H][C@@]C)CC[C@][C@H]C6)CC[C@@][C@@H]6CCC=C6C))))))C)))))C)))))O
Heavy Atom Count 22.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CCC2C(C1)CCC1CCCCC12
Classyfire Subclass Diterpenoids
Isotope Atom Count 0.0
Molecular Complexity 470.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 6.0
Iupac Name (1R)-1-[(2S,4aS,4bR,8aR,10aS)-2,4a,8,8a-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 4.6
Gsk 4 400 Rule False
Molecular Formula C20H34O2
Scaffold Graph Node Bond Level C1=CC2CCC3CCCCC3C2CC1
Inchi Key IRRXAUMIYZICTI-RABCQHRBSA-N
Silicos It Class Soluble
Rotatable Bond Count 2.0
Synonyms erythroxydiol z
Esol Class Moderately soluble
Functional Groups CC=C(C)C, CO
Compound Name (1R)-1-[(2S,4aS,4bR,8aR,10aS)-2,4a,8,8a-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol
Exact Mass 306.256
Formal Charge 0.0
Monoisotopic Mass 306.256
Hydrogen Bond Acceptor Count 2.0
Molecular Weight 306.5
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/C20H34O2/c1-14-6-5-7-16-19(14,3)9-8-15-12-18(2,17(22)13-21)10-11-20(15,16)4/h6,15-17,21-22H,5,7-13H2,1-4H3/t15-,16-,17-,18-,19-,20-/m0/s1
Smiles CC1=CCC[C@H]2[C@]1(CC[C@@H]3[C@@]2(CC[C@](C3)(C)[C@H](CO)O)C)C
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Diterpenoids