2-Acetyl-4-isopropylpyridine

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: high

General Information

Common Name: 2-Acetyl-4-isopropylpyridine
IUPAC Name: 1-(4-propan-2-ylpyridin-2-yl)ethanone
Molecular Formula: C10H13NO
SMILES: CC(C)C1=CC(=NC=C1)C(=O)C
Inchi: 1S/C10H13NO/c1-7(2)9-4-5-11-10(6-9)8(3)12/h4-7H,1-3H3
Inchi Key: BWJDKYNJXZATRV-UHFFFAOYSA-N
Cas No: 142896-09-1

Functional Group

Ketones
Pyridine

Drug Likeness

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

Cross References

PubChem: 529345
Zinc: ZINC32167294
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 163.22
Mass (g/mol) 163.1
Molar Refractivity 49.01
Net Charge
HBD
HBA 2
Rt Bonds 2
Rings 1
TPSA 29.96
Hetero Atoms 2
Heavy Atoms 12
Aromatic Heavy Atoms 6
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 245.00 to 247.00
Vapor Pressure (mmHg@25.00 °C) 0.028
Vapor Density (Air =1)
Fraction Csp3 0.40
LogP 2.408
iLOGP 2.29
XLOGP3 2.00
WLOGP 2.41
MLOGP 1.08
ESOL Log S -2.35
ESOL Solubility (mg/ml) 0.729
ESOL Solubility (mol/l) 0.004
ESOL Class: esol_class Soluble
Ali Log S -2.26
Ali Solubility (mg/ml) 0.91
Ali Solubility (mol/l) 0.01
Ali Class Soluble
Silicos-IT LogSw -3.17
Silicos-IT Solubility (mg/ml) 0.11
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) -5.88
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.77
CYP1A2 Inhibitor 1
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.719
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 1
Hepatotoxicity 1
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