(3Z)-Hex-3-en-1-yl cyclopropanecarboxylate

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: medium

General Information

Common Name: (3Z)-Hex-3-en-1-yl cyclopropanecarboxylate
IUPAC Name: [(Z)-hex-3-enyl] cyclopropanecarboxylate
Molecular Formula: C14H20O2
SMILES: CCC=CCCOC(=O)C1CC1
Inchi: 1S/C10H16O2/c1-2-3-4-5-8-12-10(11)9-6-7-9/h3-4,9H,2,5-8H2,1H3/b4-3-
Inchi Key: AQALQDMWXUIMHX-ARJAWSKDSA-N
Cas No: 188570-78-7

Functional Group

Esters

Drug Likeness

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

Cross References

PubChem: 44152604
Zinc: ZINC96331732
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 220.31
Mass (g/mol) 168.115
Molar Refractivity 63.88
Net Charge
HBD
HBA 2
Rt Bonds 4
Rings 1
TPSA 26.30
Hetero Atoms 2
Heavy Atoms 16
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 225.00 to 226.00
Vapor Pressure (mmHg@25.00 °C) 0.086
Vapor Density (Air =1)
Fraction Csp3 0.79
LogP 2.296
iLOGP 3.19
XLOGP3 3.41
WLOGP 2.93
MLOGP 3.19
ESOL Log S -3.09
ESOL Solubility (mg/ml) 0.179
ESOL Solubility (mol/l) 0.001
ESOL Class: esol_class Soluble
Ali Log S -3.64
Ali Solubility (mg/ml) 0.05
Ali Solubility (mol/l) 0
Ali Class Soluble
Silicos-IT LogSw -1.92
Silicos-IT Solubility (mg/ml) 2.64
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) -5.22
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 1.104
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 1
CYP2C9 Inhibitor 1
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 2.189
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