2-Ethenyl-3-ethyl-5-methylpyrazine

Odors

Receptor Interaction

No receptors available

General Information

Common Name: 2-Ethenyl-3-ethyl-5-methylpyrazine
IUPAC Name: 2-ethenyl-3-ethyl-5-methylpyrazine
Molecular Formula: C9H12N2
SMILES: CCC1=NC(=CN=C1C=C)C
Inchi: 1S/C9H12N2/c1-4-8-9(5-2)11-7(3)6-10-8/h4,6H,1,5H2,2-3H3
Inchi Key: YSQNQOKRWIKETP-UHFFFAOYSA-N
Cas No: 181589-32-2

Functional Group

Pyrazine

Drug Likeness

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

Cross References

PubChem: 6431144
Zinc: ZINC22058494
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 148.20
Mass (g/mol) 148.1
Molar Refractivity 46.86
Net Charge
HBD
HBA 2
Rt Bonds 2
Rings 1
TPSA 25.78
Hetero Atoms 2
Heavy Atoms 11
Aromatic Heavy Atoms 6
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 202.00 to 203.00
Vapor Pressure (mmHg@25.00 °C) 0.417
Vapor Density (Air =1)
Fraction Csp3 0.33
LogP 1.99
iLOGP 2.14
XLOGP3 1.93
WLOGP 1.88
MLOGP 0.78
ESOL Log S -2.25
ESOL Solubility (mg/ml) 0.84
ESOL Solubility (mol/l) 0.006
ESOL Class: esol_class Soluble
Ali Log S -2.10
Ali Solubility (mg/ml) 1.19
Ali Solubility (mol/l) 0.01
Ali Class Soluble
Silicos-IT LogSw -3.26
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) -5.83
Bioavailability Score 0.55
Caco2 0
Human Intestinal Absorption 1
Plasm Protein Binding 0.626
CYP1A2 Inhibitor 1
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 2.372
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