PYRAZINAMIDE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C5H5N3O
Molecular Weight	123.1127
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of PYRAZINAMIDE

Structure Search

SMILES

NC(=O)C1=CN=CC=N1

InChI

InChIKey=IPEHBUMCGVEMRF-UHFFFAOYSA-N

InChI=1S/C5H5N3O/c6-5(9)4-3-7-1-2-8-4/h1-3H,(H2,6,9)

HIDE SMILES / InChI

Molecular Formula	C5H5N3O
Molecular Weight	123.1127
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:22:42 UTC 2023` Edited by `admin` on `Fri Dec 15 15:22:42 UTC 2023`
Record UNII	2KNI5N06TI
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

PYRAZINAMIDE

Official Name

English

PYRAZINAMIDE [USP-RS]

Common Name

English

D-50

Code

English

PYRAZIDE

Common Name

English

PYRAZINAMIDE [MART.]

Common Name

English

PYRAZINAMIDE COMPONENT OF RIFATER

Common Name

English

PYRAZINAMIDE [HSDB]

Common Name

English

PYRAZINAMIDE [USP MONOGRAPH]

Common Name

English

PYRAFAT

Common Name

English

PYRAMIZADE

Common Name

English

PIRAZINAMID

Common Name

English

PYRAZINAMIDE [MI]

Common Name

English

RIFATER COMPONENT PYRAZINAMIDE

Common Name

English

Pyrazinecarboxamide

Systematic Name

English

PYRAZINAMIDE [JAN]

Common Name

English

ZINAMIDE

Common Name

English

ALDINAMID

Common Name

English

NOVAMID

Common Name

English

PYRAZINAMIDE [VANDF]

Common Name

English

ALDINAMIDE

Common Name

English

PYRAZINAMIDE [USP IMPURITY]

Common Name

English

FARMIZINA

Common Name

English

NSC-14911

Code

English

pyrazinamide [INN]

Common Name

English

PYRAZINAMIDE [ORANGE BOOK]

Common Name

English

UNIPYRANAMIDE

Common Name

English

PIRAZIMIDA

Common Name

English

PYRAZINAMIDUM [WHO-IP LATIN]

Common Name

English

PYRAZINAMIDE [EP MONOGRAPH]

Common Name

English

MK-56

Code

English

PYRAZINE CARBOXYLAMIDE

Common Name

English

.ALPHA.-PYRAZINAMIDE

Common Name

English

ISOPAS

Common Name

English

PYRAZINAMIDE [WHO-IP]

Common Name

English

ROZIDE

Common Name

English

TEBRAZID

Common Name

English

Pyrazinamide [WHO-DD]

Common Name

English

EPRAZIN

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C280

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-VATC

QJ04AM05

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-ESSENTIAL MEDICINES LIST

6.2.4 (ISO/PYR/RIF)

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-ATC

J04AM06

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-ATC

J04AK01

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-ATC

J04AM05

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-ESSENTIAL MEDICINES LIST

6.2.4 (ETH/ISO/PYR/RIF)

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-ESSENTIAL MEDICINES LIST

6.2.4

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-VATC

QJ04AM06

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

LIVERTOX

NBK547856

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

NDF-RT

N0000175483

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

WHO-VATC

QJ04AK01

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

FDA ORPHAN DRUG

6585

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

Code System Code Type Description

EPA CompTox

DTXSID9021215

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

ChEMBL

CHEMBL614

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

DRUG CENTRAL

2328

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

LACTMED

Pyrazinamide

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

WIKIPEDIA

PYRAZINAMIDE

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

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WHO INTERNATIONAL PHARMACOPEIA

PYRAZINAMIDE

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

Description: A white or almost white, crystalline powder; odourless. Solubility: Sparingly soluble in water; slightly soluble in ethanol (~750 g/l) TS. Category: Antituberculosis drug. Storage: Pyrazinamide should be kept in a well-closed container. Definition: Pyrazinamide contains not less than 98.5% and not more than 101.0% of C5H5N3O, calculated with reference to the anhydrous substance.

ECHA (EC/EINECS)

202-717-6

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

PUBCHEM

1046

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

EVMPD

SUB10163MIG

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

INN

786

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

IUPHAR

7287

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

MESH

D011718

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

HSDB

3576

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

DAILYMED

2KNI5N06TI

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

NSC

14911

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

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CHEBI

45285

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

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SMS_ID

100000080846

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

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DRUG BANK

DB00339

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

CAS

98-96-4

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

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RXCUI

8987

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

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RxNorm

MERCK INDEX

m9337

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

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Merck Index

RS_ITEM_NUM

1585006

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

FDA UNII

2KNI5N06TI

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

NCI_THESAURUS

C29395

Created by admin on Fri Dec 15 15:22:42 UTC 2023 , Edited by admin on Fri Dec 15 15:22:42 UTC 2023

PRIMARY

Related Record Type Details


					6TC6NN0876

STEVIA REBAUDIUNA LEAF

PARENT -> CONSTITUENT ALWAYS PRESENT

Comments:

MIC value of the in vitro growth of Mycobacterium Tuberculosis (H37RV strain) of the new anti-tuberculosis terpenoid derived agent tested was 20 ug/ml.

Related Record Type Details


					2WB23298SP

PYRAZINOIC ACID

METABOLITE -> PARENT


					M2V0DP3ENP

5-HYDROXYPYRAZINOIC ACID

METABOLITE -> PARENT

Related Record Type Details


					90NZ6P9NG2

METHYL PYRAZINOATE

IMPURITY -> PARENT

Amount:


					74CP756B49

2-CYANOPYRAZINE

IMPURITY -> PARENT

Amount:

Related Record Type Details


					2KNI5N06TI

ACTIVE MOIETY

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Biological Half-life	PHARMACOKINETIC				Elimination PHARMACOKINETIC