1-(3,5,6-Trimethyl-3-cyclohexen-1-yl)ethanone

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: medium

General Information

Common Name: 1-(3,5,6-Trimethyl-3-cyclohexen-1-yl)ethanone
IUPAC Name: 1-(3,5,6-trimethylcyclohex-3-en-1-yl)ethanone
Molecular Formula: C11H18O
SMILES: CC1C=C(CC(C1C)C(=O)C)C
Inchi: 1S/C11H18O/c1-7-5-8(2)9(3)11(6-7)10(4)12/h5,8-9,11H,6H2,1-4H3
Inchi Key: KJJMTKOKFXURKM-UHFFFAOYSA-N
Cas No: 68480-14-8

Functional Group

Ketones

Drug Likeness

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

Cross References

PubChem: 109417
Zinc: ZINC6030580
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 166.26
Mass (g/mol) 166.136
Molar Refractivity 52.60
Net Charge
HBD
HBA 1
Rt Bonds 1
Rings 1
TPSA 17.07
Hetero Atoms 1
Heavy Atoms 12
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 223.00 to 224.00
Vapor Pressure (mmHg@25.00 °C) 0.096
Vapor Density (Air =1)
Fraction Csp3 0.73
LogP 2.814
iLOGP 2.48
XLOGP3 2.11
WLOGP 2.81
MLOGP 2.49
ESOL Log S -2.13
ESOL Solubility (mg/ml) 1.22
ESOL Solubility (mol/l) 0.007
ESOL Class: esol_class Soluble
Ali Log S -2.10
Ali Solubility (mg/ml) 1.32
Ali Solubility (mol/l) 0.01
Ali Class Soluble
Silicos-IT LogSw -2.10
Silicos-IT Solubility (mg/ml) 1.33
Silicos-IT Solubility (mol/l) 0.01
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -5.82
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.599
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.264
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