3-Cyclohexene-1-carboxylic acid, ethyl ester

Odors

Receptor Interaction

No receptors available

General Information

Common Name: 3-Cyclohexene-1-carboxylic acid, ethyl ester
IUPAC Name: ethyl cyclohex-3-ene-1-carboxylate
Molecular Formula: C9H14O2
SMILES: CCOC(=O)C1CCC=CC1
Inchi: 1S/C9H14O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-4,8H,2,5-7H2,1H3
Inchi Key: BYNLHLLOIZDKIC-UHFFFAOYSA-N
Cas No: 15111-56-5

Functional Group

Esters

Drug Likeness

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

Cross References

PubChem: 85803
Zinc: ZINC5650630
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 154.21
Mass (g/mol) 154.099
Molar Refractivity 44.07
Net Charge
HBD
HBA 2
Rt Bonds 3
Rings 1
TPSA 26.30
Hetero Atoms 2
Heavy Atoms 11
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 194.00 to 195.00
Vapor Pressure (mmHg@25.00 °C) 0.396
Vapor Density (Air =1)
Fraction Csp3 0.67
LogP 1.906
iLOGP 2.41
XLOGP3 1.96
WLOGP 1.91
MLOGP 1.78
ESOL Log S -1.83
ESOL Solubility (mg/ml) 2.27
ESOL Solubility (mol/l) 0.015
ESOL Class: esol_class Very soluble
Ali Log S -2.14
Ali Solubility (mg/ml) 1.12
Ali Solubility (mol/l) 0.01
Ali Class Soluble
Silicos-IT LogSw -1.31
Silicos-IT Solubility (mg/ml) 7.48
Silicos-IT Solubility (mol/l) 0.05
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -5.85
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.836
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.548
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