(e,z)-2,6-Nonadienyl acetate

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: medium

General Information

Common Name: (e,z)-2,6-Nonadienyl acetate
IUPAC Name: [(2E,6Z)-nona-2,6-dienyl] acetate
Molecular Formula: C11H18O2
SMILES: CCC=CCCC=CCOC(=O)C
Inchi: 1S/C11H18O2/c1-3-4-5-6-7-8-9-10-13-11(2)12/h4-5,8-9H,3,6-7,10H2,1-2H3/b5-4-,9-8+
Inchi Key: UHONGPVFPQQOSO-FTGFODROSA-N
Cas No: 68555-65-7

Functional Group

Esters

Drug Likeness

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

Cross References

PubChem: 5363120
Zinc: ZINC25720288
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 182.26
Mass (g/mol) 182.131
Molar Refractivity 55.33
Net Charge
HBD
HBA 2
Rt Bonds 7
Rings
TPSA 26.30
Hetero Atoms 2
Heavy Atoms 13
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 231.00 
Vapor Pressure (mmHg@25.00 °C) 0.026
Vapor Density (Air =1) >1
Fraction Csp3 0.55
LogP 2.852
iLOGP 3.23
XLOGP3 2.66
WLOGP 2.85
MLOGP 2.67
ESOL Log S -2.18
ESOL Solubility (mg/ml) 1.19
ESOL Solubility (mol/l) 0.007
ESOL Class: esol_class Soluble
Ali Log S -2.86
Ali Solubility (mg/ml) 0.25
Ali Solubility (mol/l) 0
Ali Class Soluble
Silicos-IT LogSw -2.14
Silicos-IT Solubility (mg/ml) 1.31
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) -5.52
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.801
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.565
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