Pyridoxine hydrochloride

Odors

No information available

Receptor Interaction

No receptors available

General Information

Common Name: Pyridoxine hydrochloride
IUPAC Name: 4,5-bis(hydroxymethyl)-2-methylpyridin-3-ol;hydrochloride
Molecular Formula: C8H11NO3
SMILES: CC1=NC=C(C(=C1O)CO)CO.Cl
Inchi: 1S/C8H11NO3.ClH/c1-5-8(12)7(4-11)6(3-10)2-9-5;/h2,10-12H,3-4H2,1H3;1H
Inchi Key: ZUFQODAHGAHPFQ-UHFFFAOYSA-N
Cas No: 58-56-0

Functional Group

Drug Likeness

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

Cross References

PubChem: 6019
Zinc: ZINC49154
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 205.64
Mass (g/mol) 205.051
Molar Refractivity 50.45
Net Charge
HBD 3
HBA 4
Rt Bonds 2
Rings 1
TPSA 73.58
Hetero Atoms 4
Heavy Atoms 13
Aromatic Heavy Atoms 6
Melting Point (°C) 207
Boiling Point (°C@760.00mm Hg) 491.9
Vapor Pressure (mmHg@25.00 °C) 0
Vapor Density (Air =1)
Fraction Csp3 0.38
LogP 0.08
iLOGP 0.00
XLOGP3 0.03
WLOGP 0.58
MLOGP -0.59
ESOL Log S -1.34
ESOL Solubility (mg/ml) 9.33
ESOL Solubility (mol/l) 0.045
ESOL Class: esol_class Very soluble
Ali Log S -1.13
Ali Solubility (mg/ml) 15.3
Ali Solubility (mol/l) 0.07
Ali Class Very soluble
Silicos-IT LogSw -1.49
Silicos-IT Solubility (mg/ml) 6.64
Silicos-IT Solubility (mol/l) 0.03
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 0
PgP Substrate 0
Log Kp (cm/s) -7.53
Bioavailability Score 0.55
Caco2 0
Human Intestinal Absorption 1
Plasm Protein Binding 0.215
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 2.767
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