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(1S,2S,5S,7S,8R)-2,6,6,7-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol

PubChem CID: 73950881

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Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 20.2
Hydrogen Bond Donor Count 1.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CC2CCC3CCC2(C1)C3
Np Classifier Class Prezizaane sesquiterpenoids
Deep Smiles C[C@H]CC[C@H][C@]5CC[C@H]C5)[C@]C7C)C))C)O
Heavy Atom Count 16.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CC2CCC3CCC2(C1)C3
Classyfire Subclass Sesquiterpenoids
Isotope Atom Count 0.0
Molecular Complexity 321.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 5.0
Iupac Name (1S,2S,5S,7S,8R)-2,6,6,7-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol
Veber Rule True
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 4.1
Gsk 4 400 Rule True
Molecular Formula C15H26O
Scaffold Graph Node Bond Level C1CC2CCC3CCC2(C1)C3
Inchi Key IJVXAOHQRPSJDV-HPYVJYLESA-N
Silicos It Class Soluble
Rotatable Bond Count 0.0
Synonyms jinkohol
Esol Class Soluble
Functional Groups CO
Compound Name (1S,2S,5S,7S,8R)-2,6,6,7-tetramethyltricyclo[6.2.1.01,5]undecan-7-ol
Exact Mass 222.198
Formal Charge 0.0
Monoisotopic Mass 222.198
Hydrogen Bond Acceptor Count 1.0
Molecular Weight 222.37
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 5.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C15H26O/c1-10-5-6-12-13(2,3)14(4,16)11-7-8-15(10,12)9-11/h10-12,16H,5-9H2,1-4H3/t10-,11+,12+,14-,15-/m0/s1
Smiles C[C@H]1CC[C@H]2[C@]13CC[C@H](C3)[C@](C2(C)C)(C)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Sesquiterpenoids

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