Responsive image

Common name


Isoniazid

IUPAC name


pyridine-4-carbohydrazide

SMILES


NNC(=O)C1=CC=NC=C1

Compound class


Antitubercular Agents; Fatty Acid Synthesis Inhibitors; Antimycobacterials; Antiinfectives for Systemic Use; Drugs for Treatment of Tuberculosis; Hydrazides; Cytochrome P-450 CYP1A2 Inhibitors; Cytochrome P-450 CYP2C9 Inhibitors; Cytochrome P-450 CYP1A2 Inducers; Cytochrome P-450 CYP2C8 Inhibitors; Cytochrome P-450 CYP2C9 Inducers; Cytochrome P-450 CYP2C19 Inducers; Cytochrome P-450 CYP2C8 Inducers; CYP2A6 Inhibitors; CYP2A6 Inhibitors (strong); CYP2A6 Inhibitors (moderate); CYP2A6 Inducers; CYP2A6 Inducers (strong); CYP2D6 Inducers; CYP2D6 Inducers (strong); CYP2E1 Inhibitors; CYP2E1 Inducers; CYP2E1 Inducers (strong); CYP3A4 Inhibitors;

Therapeutic area


For the treatment of all forms of tuberculosis in which organisms are susceptible.

Common name


Isoniazid

IUPAC name


pyridine-4-carbohydrazide

SMILES


NNC(=O)C1=CC=NC=C1

INCHI


InChI=1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)

FORMULA


C6H7N3O

Responsive image

Common name


Isoniazid

IUPAC name


pyridine-4-carbohydrazide

Molecular weight


137.139

clogP


-0.273

clogS


-1.031

HBond Acceptor


2

HBond Donor


3

Total Polar
Surface Area


68.01

Number of Rings


1

Rotatable Bond


1

Drug ID Common name Structure CAS SMILE Frequency
FDBF00014 pyridine Responsive image c1cccnc1 0.0333
FDBF02157 formohydrazide Responsive image O=CNN 0.0010
2 , 1