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Details

Stereochemistry ACHIRAL
Molecular Formula C18H14N4O5S
Molecular Weight 398.393
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of SULFASALAZINE

SMILES

OC(=O)C1=C(O)C=CC(=C1)\N=N\C2=CC=C(C=C2)S(=O)(=O)NC3=CC=CC=N3

InChI

InChIKey=NCEXYHBECQHGNR-QZQOTICOSA-N
InChI=1S/C18H14N4O5S/c23-16-9-6-13(11-15(16)18(24)25)21-20-12-4-7-14(8-5-12)28(26,27)22-17-3-1-2-10-19-17/h1-11,23H,(H,19,22)(H,24,25)/b21-20+

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
SULFASALAZINE
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
USAN   INN  
Official Name English
SULFASALAZINE [USAN]
Common Name English
sulfasalazine [INN]
Common Name English
SULFASALAZINE [ORANGE BOOK]
Common Name English
SALAZOSULFAPYRIDINE [JAN]
Common Name English
SALAZOPYRIN
Brand Name English
SULFASALAZINE [EP MONOGRAPH]
Common Name English
SULFASALAZINE [MART.]
Common Name English
SULFASALAZINE [MI]
Common Name English
SULFASALAZINE [USP-RS]
Common Name English
SULFASALAZINE [VANDF]
Common Name English
SULFASALAZINUM [WHO-IP LATIN]
Common Name English
AZULFIDINE
Brand Name English
SALICYLAZOSULFAPYRIDINE
Common Name English
NSC-203730
Code English
NSC-667219
Code English
Sulfasalazine [WHO-DD]
Common Name English
SULFASALAZINE [USP MONOGRAPH]
Common Name English
BENZOSULFA
Common Name English
SULFASALAZINE [IARC]
Common Name English
SULFASALAZOPYRIDINE
Common Name English
SULFASALAZINE [WHO-IP]
Common Name English
2-HYDROXY-5-((4-((2-PYRIDINYLAMINO)SULFONYL)PHENYL)AZO)BENZOIC ACID [WHO-IP]
Common Name English
BENZOIC ACID, 2-HYDROXY-5-(2-(4-((2-PYRIDINYLAMINO)SULFONYL)PHENYL)DIAZENYL)-
Systematic Name English
SULFASALAZINE [HSDB]
Common Name English
SULPHASALAZINE
Common Name English
Classification Tree Code System Code
NDF-RT N0000005760
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
NDF-RT N0000005760
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
WHO-VATC QA07EC01
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
NCI_THESAURUS C257
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
LIVERTOX NBK548792
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
NDF-RT N0000005760
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
NDF-RT N0000175781
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 2.4
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
WHO-ATC A07EC01
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
WHO-ESSENTIAL MEDICINES LIST 17.3
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
NDF-RT N0000005760
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
Code System Code Type Description
MESH
D012460
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
EPA CompTox
DTXSID0021256
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
FDA UNII
3XC8GUZ6CB
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
NCI_THESAURUS
C29469
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
INN
2210
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
CAS
599-79-1
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
DRUG CENTRAL
2525
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
DAILYMED
3XC8GUZ6CB
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
NSC
203730
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
RS_ITEM_NUM
1636005
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
EVMPD
SUB20720
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
RXCUI
9524
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY RxNorm
NSC
667219
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
EVMPD
SUB10727MIG
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
SMS_ID
100000091572
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
SULFASALAZINE
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY Description: A bright yellow to brownish yellow powder; odourless. Solubility: Practically insoluble in water and ether R; very slightly soluble in ethanol (~750 g/l) TS; soluble in alkali hydroxides. Category: Antibacterial drug. Storage: Sulfasalazine should be kept in a tightly closed container, protected from light. Additional information: Sulfasalazine melts at about 255?C with decomposition. Definition: Sulfasalazine contains not less than 93.0% and not more than 103.0% of C18H14N4O5S, calculated with reference to the dried substance.
DRUG BANK
DB00795
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
HSDB
3395
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
ECHA (EC/EINECS)
209-974-3
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
MERCK INDEX
m10343
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL421
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
IUPHAR
4840
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
WIKIPEDIA
Sulfasalazine
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
CHEBI
9334
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
LACTMED
Sulfasalazine
Created by admin on Fri Dec 15 15:46:48 UTC 2023 , Edited by admin on Fri Dec 15 15:46:48 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of SULFASALAZINE
METABOLITE (PARENT)
Structure of ACETYLSULFAPYRIDINE
METABOLITE ACTIVE (PARENT)
Structure of MESALAMINE
METABOLITE INACTIVE (PARENT)
Structure of SULFAPYRIDINE
METABOLITE LESS ACTIVE (PARENT)
Structure of N-ACETYL-5-AMINOSALICYLIC ACID
NIH
NCATS
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