2-(4-Methyl-5-thiazolyl)ethyl Hexanoate

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: high

General Information

Common Name: 2-(4-Methyl-5-thiazolyl)ethyl Hexanoate
IUPAC Name: 2-(4-methyl-1,3-thiazol-5-yl)ethyl hexanoate
Molecular Formula: C13H24O2
SMILES: CCCCCC(=O)OCCC1=C(N=CS1)C
Inchi: 1S/C12H19NO2S/c1-3-4-5-6-12(14)15-8-7-11-10(2)13-9-16-11/h9H,3-8H2,1-2H3
Inchi Key: VJULDCZELAIZHC-UHFFFAOYSA-N
Cas No: 94159-32-7

Functional Group

Esters
Thiazoles

Drug Likeness

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

Cross References

PubChem: 3023839
Zinc: ZINC21999709
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 212.33
Mass (g/mol) 241.114
Molar Refractivity 63.78
Net Charge
HBD
HBA 2
Rt Bonds 7
Rings 1
TPSA 26.30
Hetero Atoms 4
Heavy Atoms 15
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 338.00 to 339.00
Vapor Pressure (mmHg@25.00 °C) 0.000101
Vapor Density (Air =1)
Fraction Csp3 0.92
LogP 3.118
iLOGP 3.15
XLOGP3 4.40
WLOGP 3.69
MLOGP 3.03
ESOL Log S -3.47
ESOL Solubility (mg/ml) 0.073
ESOL Solubility (mol/l) 0
ESOL Class: esol_class Soluble
Ali Log S -4.67
Ali Solubility (mg/ml) 0
Ali Solubility (mol/l) 0
Ali Class Moderately soluble
Silicos-IT LogSw -3.42
Silicos-IT Solubility (mg/ml) 0.08
Silicos-IT Solubility (mol/l) 0
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -4.47
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.802
CYP1A2 Inhibitor 1
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.703
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