6-Methyl-3-nitro-2(5H)-pyridinone

Odors

Receptor Interaction

No receptors available

General Information

Common Name: 6-Methyl-3-nitro-2(5H)-pyridinone
IUPAC Name: (4R,5R)-2-hydroxy-3,4,5-trimethylcyclopent-2-en-1-one
Molecular Formula: C8H12O2
SMILES: C[C@@H]1[C@H](C(=O)C(=C1C)O)C
Inchi: 1S/C8H12O2/c1-4-5(2)7(9)8(10)6(4)3/h4-5,10H,1-3H3/t4-,5-/m1/s1
Inchi Key: RMXYMRMUZJILGN-RFZPGFLSSA-N
Cas No: 125476-23-5

Functional Group

Alcohols
Alkene
Ketones

Drug Likeness

Name Value
Lipinski Violations 0
Ghose Violations 2
Veber Violations 0
Egan Violations 0
Muegge Violations 1

Cross References

PubChem: 6431224
Zinc: ZINC32166563
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 140.18
Mass (g/mol) 140.084
Molar Refractivity 39.75
Net Charge
HBD 1
HBA 2
Rt Bonds 0
Rings 1
TPSA 37.30
Hetero Atoms 2
Heavy Atoms 10
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 249.61 
Vapor Pressure (mmHg@25.00 °C) 0.004
Vapor Density (Air =1)
Fraction Csp3 0.62
LogP 1.673
iLOGP 1.76
XLOGP3 1.21
WLOGP 1.67
MLOGP 0.65
ESOL Log S -1.47
ESOL Solubility (mg/ml) 4.73
ESOL Solubility (mol/l) 0.034
ESOL Class: esol_class Very soluble
Ali Log S -1.59
Ali Solubility (mg/ml) 3.6
Ali Solubility (mol/l) 0.03
Ali Class Very soluble
Silicos-IT LogSw -1.23
Silicos-IT Solubility (mg/ml) 8.33
Silicos-IT Solubility (mol/l) 0.06
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -6.30
Bioavailability Score 0.55
Caco2 0
Human Intestinal Absorption 1
Plasm Protein Binding 0.48
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.416
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