SULFAZAMET

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C16H16N4O2S
Molecular Weight	328.389
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of SULFAZAMET

Structure Search

SMILES

CC1=NN(C(NS(=O)(=O)C2=CC=C(N)C=C2)=C1)C3=CC=CC=C3

InChI

InChIKey=MTERSQYMYBGZTP-UHFFFAOYSA-N

InChI=1S/C16H16N4O2S/c1-12-11-16(20(18-12)14-5-3-2-4-6-14)19-23(21,22)15-9-7-13(17)8-10-15/h2-11,19H,17H2,1H3

HIDE SMILES / InChI

Molecular Formula	C16H16N4O2S
Molecular Weight	328.389
Charge	0
Count

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

Description
Sources: https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=19600921&CC=GB&NR=848627A&KC=A

Sulfazamet is a sulfanilamide derivative that exhibits antibacterial activity against Streptococci sepsis

Originator

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:10:16 GMT 2023` Edited by `admin` on `Fri Dec 15 15:10:16 GMT 2023`
Record UNII	K980HZ9QO4
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

SULFAZAMET

Official Name

English

BENZENESULFONAMIDE, 4-AMINO-N-(3-METHYL-1-PHENYL-1H-PYRAZOL-5-YL)-

Systematic Name

English

sulfapyrazole [INN]

Common Name

English

SULFAPYRAZOLE

Official Name

English

SULFAZAMET [MI]

Common Name

English

SULFAZAMET [USAN]

Common Name

English

Classification Tree Code System Code

WHO-VATC

QJ01EQ01

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

NCI_THESAURUS

C29739

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

Code System Code Type Description

ECHA (EC/EINECS)

212-707-3

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

CAS

852-19-7

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

INN

2343

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

NCI_THESAURUS

C152460

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

SMS_ID

100000083296

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

FDA UNII

K980HZ9QO4

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

EPA CompTox

DTXSID30234391

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

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MERCK INDEX

m10346

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

Merck Index

PUBCHEM

13326

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

ChEMBL

CHEMBL2104908

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

EVMPD

SUB10723MIG

Created by admin on Fri Dec 15 15:10:16 GMT 2023 , Edited by admin on Fri Dec 15 15:10:16 GMT 2023

PRIMARY

Related Record Type Details


					NR381B8DF1

SULFAPYRAZOLE POTASSIUM

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					J49RL8EDMT

SULFAPYRAZOLE SODIUM

SALT/SOLVATE -> PARENT

Related Record Type Details


					K980HZ9QO4

ACTIVE MOIETY