2-(4-Methylthiazol-5-yl)ethyl acetate

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: medium

General Information

Common Name: 2-(4-Methylthiazol-5-yl)ethyl acetate
IUPAC Name: 2-(4-methyl-1,3-thiazol-5-yl)ethyl acetate
Molecular Formula: C8H11NO2S
SMILES: CC1=C(SC=N1)CCOC(=O)C
Inchi: 1S/C8H11NO2S/c1-6-8(12-5-9-6)3-4-11-7(2)10/h5H,3-4H2,1-2H3
Inchi Key: CRTCWNPLKVVXIX-UHFFFAOYSA-N
Cas No: 656-53-1

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: 61192
Zinc: ZINC120539
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 185.24
Mass (g/mol) 185.051
Molar Refractivity 47.75
Net Charge
HBD
HBA 3
Rt Bonds 4
Rings 1
TPSA 67.43
Hetero Atoms 4
Heavy Atoms 12
Aromatic Heavy Atoms 5
Melting Point (°C) 131
Boiling Point (°C@760.00mm Hg) 259.00 to 260.00
Vapor Pressure (mmHg@25.00 °C) 0.012
Vapor Density (Air =1) 6.3
Fraction Csp3 0.50
LogP 1.557
iLOGP 2.23
XLOGP3 1.42
WLOGP 1.56
MLOGP 0.44
ESOL Log S -1.93
ESOL Solubility (mg/ml) 2.19
ESOL Solubility (mol/l) 0.012
ESOL Class: esol_class Very soluble
Ali Log S -2.44
Ali Solubility (mg/ml) 0.67
Ali Solubility (mol/l) 0
Ali Class Soluble
Silicos-IT LogSw -2.57
Silicos-IT Solubility (mg/ml) 0.5
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) -6.42
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.496
CYP1A2 Inhibitor 1
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 1
Acute Oral Toxicity 0.703
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 0
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