2,3-Dimethyl-5-(2-methylbutyl)pyrazine

Odors

Receptor Interaction

No receptors available

General Information

Common Name: 2,3-Dimethyl-5-(2-methylbutyl)pyrazine
IUPAC Name: 2,3-dimethyl-5-(2-methylbutyl)pyrazine
Molecular Formula: C10H16N2
SMILES: CCC(C)CC1=CN=C(C(=N1)C)C
Inchi: 1S/C11H18N2/c1-5-8(2)6-11-7-12-9(3)10(4)13-11/h7-8H,5-6H2,1-4H3
Inchi Key: QJQUDEDFDDMKGC-UHFFFAOYSA-N
Cas No: 75492-01-2

Functional Group

Pyrazine

Drug Likeness

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

Cross References

PubChem: 528106
Zinc: ZINC32166231
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 164.25
Mass (g/mol) 178.147
Molar Refractivity 51.35
Net Charge
HBD
HBA 2
Rt Bonds 3
Rings 1
TPSA 25.78
Hetero Atoms 2
Heavy Atoms 12
Aromatic Heavy Atoms 6
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 244.00 to 245.00
Vapor Pressure (mmHg@25.00 °C) 0.046
Vapor Density (Air =1)
Fraction Csp3 0.60
LogP 2.682
iLOGP 2.41
XLOGP3 2.28
WLOGP 2.44
MLOGP 1.17
ESOL Log S -2.47
ESOL Solubility (mg/ml) 0.561
ESOL Solubility (mol/l) 0.003
ESOL Class: esol_class Soluble
Ali Log S -2.46
Ali Solubility (mg/ml) 0.57
Ali Solubility (mol/l) 0
Ali Class Soluble
Silicos-IT LogSw -4.02
Silicos-IT Solubility (mg/ml) 0.02
Silicos-IT Solubility (mol/l) 0
Silicos-IT Class Moderately soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -5.68
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.687
CYP1A2 Inhibitor 1
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 0.801
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