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Details

Stereochemistry ACHIRAL
Molecular Formula C11H11N3O2S
Molecular Weight 249.289
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFAPYRIDINE

SMILES

NC1=CC=C(C=C1)S(=O)(=O)NC2=CC=CC=N2

InChI

InChIKey=GECHUMIMRBOMGK-UHFFFAOYSA-N
InChI=1S/C11H11N3O2S/c12-9-4-6-10(7-5-9)17(15,16)14-11-3-1-2-8-13-11/h1-8H,12H2,(H,13,14)

HIDE SMILES / InChI
Molecular Formula C11H11N3O2S
Molecular Weight 249.289
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:50:21 UTC 2023
Edited
by admin
on Sat Dec 16 17:50:21 UTC 2023
Record UNII
Y5V2N1KE8U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFAPYRIDINE
INN   MART.   MI   ORANGE BOOK   USP   VANDF   WHO-DD  
INN  
Official Name English
NSC-41791
Code English
SULFAPYRIDINE [USP-RS]
Common Name English
SULFAPYRIDINE [USP MONOGRAPH]
Common Name English
SULFASALAZINE IMPURITY J [EP IMPURITY]
Common Name English
N(SUP 1)-2-PYRIDYLSULFANILAMIDE
Systematic Name English
SULFAPYRIDINE [USP IMPURITY]
Common Name English
BENZENESULFONAMIDE, 4-AMINO-N-2-PYRIDINYL-
Systematic Name English
NSC-4753
Code English
Sulfapyridine [WHO-DD]
Common Name English
sulfapyridine [INN]
Common Name English
SULPHAPYRIDINE
Common Name English
SULFAPYRIDINE MELTING POINT STANDARD
USP-RS  
Common Name English
SULFAPYRIDINE [MART.]
Common Name English
SULFAPYRIDINE [MI]
Common Name English
SULFAPYRIDINE [ORANGE BOOK]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ01EQ04
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
NCI_THESAURUS C29739
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
FDA ORPHAN DRUG 51090
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
WHO-ATC J01EB04
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
Code System Code Type Description
EVMPD
SUB10724MIG
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
WIKIPEDIA
Sulfapyridine
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
ECHA (EC/EINECS)
205-642-7
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
SMS_ID
100000083277
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
DRUG CENTRAL
2524
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
ChEMBL
CHEMBL700
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
NSC
41791
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
DRUG BANK
DB00891
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
CHEBI
132842
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
FDA UNII
Y5V2N1KE8U
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
RS_ITEM_NUM
1634000
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
EPA CompTox
DTXSID3026067
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
NCI_THESAURUS
C66570
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
RXCUI
10188
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY RxNorm
PUBCHEM
5336
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
INN
4165
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
CAS
144-83-2
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
MESH
D013427
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
MERCK INDEX
m10339
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY Merck Index
NSC
4753
Created by admin on Sat Dec 16 17:50:22 UTC 2023 , Edited by admin on Sat Dec 16 17:50:22 UTC 2023
PRIMARY
Related Record Type Details
Structure of SULFAPYRIDINE CALCIUM
SALT/SOLVATE -> PARENT
Structure of SULFAPYRIDINE SODIUM
SALT/SOLVATE -> PARENT
Structure of SULFAPYRIDINE SODIUM MONOHYDRATE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of SULFASALAZINE
PARENT -> METABOLITE INACTIVE
Not inhibite the Hb-catalyzed peroxidative reaction
Related Record Type Details
Structure of SULFASALAZINE
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of SULFAPYRIDINE
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