cis-3,3,5-Trimethylcyclohexanol

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: medium

General Information

Common Name: cis-3,3,5-Trimethylcyclohexanol
IUPAC Name: (1S,5S)-3,3,5-trimethylcyclohexan-1-ol
Molecular Formula: C9H18O
SMILES: CC1CC(CC(C1)(C)C)O
Inchi: 1S/C9H18O/c1-7-4-8(10)6-9(2,3)5-7/h7-8,10H,4-6H2,1-3H3/t7-,8+/m1/s1
Inchi Key: BRRVXFOKWJKTGG-SFYZADRCSA-N
Cas No: 933-48-2

Functional Group

Alcohols

Drug Likeness

Name Value
Lipinski Violations 0
Ghose Violations 1
Veber Violations 0
Egan Violations 0
Muegge Violations 2

Cross References

PubChem: 101921
Zinc: ZINC1672941 
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 142.24
Mass (g/mol) 142.136
Molar Refractivity 44.16
Net Charge
HBD 1
HBA 1
Rt Bonds 0
Rings 1
TPSA 20.23
Hetero Atoms 1
Heavy Atoms 10
Aromatic Heavy Atoms 0
Melting Point (°C) 37.00 to 38.00
Boiling Point (°C@760.00mm Hg) 201.00 to 202.00
Vapor Pressure (mmHg@25.00 °C) 0.173
Vapor Density (Air =1)
Fraction Csp3 1.00
LogP 2.194
iLOGP 2.27
XLOGP3 2.62
WLOGP 2.19
MLOGP 2.15
ESOL Log S -2.37
ESOL Solubility (mg/ml) 0.603
ESOL Solubility (mol/l) 0.004
ESOL Class: esol_class Soluble
Ali Log S -2.69
Ali Solubility (mg/ml) 0.29
Ali Solubility (mol/l) 0
Ali Class Soluble
Silicos-IT LogSw -1.64
Silicos-IT Solubility (mg/ml) 3.29
Silicos-IT Solubility (mol/l) 0.02
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -5.31
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 1.067
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.562
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 1
Hepatotoxicity 0
Androgen Receptor Binding 0
Aromatase Binding 0
Estrogen Receptor Binding 0
Glucocorticoid Receptor Binding 0
Thyroid Receptor Binding 0
BRCP inhibitor 0
BSEP inhibitor 0
OATP1B1 inhibitor 1
OATP1B3 inhibitor 1
OATP2B1 inhibitor 0
OCT1 inhibitor 0
OCT2 inhibitor 0