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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO3
Molecular Weight 153.1354
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MESALAMINE

SMILES

NC1=CC(C(O)=O)=C(O)C=C1

InChI

InChIKey=KBOPZPXVLCULAV-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,8H2,(H,10,11)

HIDE SMILES / InChI
Molecular Formula C7H7NO3
Molecular Weight 153.1354
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 17:31:32 UTC 2023
Edited
by admin
on Sat Dec 16 17:31:32 UTC 2023
Record UNII
4Q81I59GXC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MESALAMINE
HSDB   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF  
USAN  
Official Name English
MESALAMINE [VANDF]
Common Name English
MESALAMINE [HSDB]
Common Name English
MESALAZINE [EP MONOGRAPH]
Common Name English
mesalazine [INN]
Common Name English
MESALAMINE [USP MONOGRAPH]
Common Name English
FISALAMINE
Common Name English
ASACOL
Brand Name English
MESALAZINE [JAN]
Common Name English
ROWASA
Brand Name English
MESALAMINE [MI]
Common Name English
Mesalazine [WHO-DD]
Common Name English
5-Aminosalicylic acid
Systematic Name English
APRISO
Brand Name English
NSC-38877
Code English
5-AMINO-2-HYDROXYBENZOIC ACID
Systematic Name English
BENZOIC ACID, 5-AMINO-2-HYDROXY-
Common Name English
MESALAZINE [EP IMPURITY]
Common Name English
PENTASA
Brand Name English
MESALAZINE [MART.]
Common Name English
SFROWASA
Brand Name English
MESALAMINE [USAN]
Common Name English
LIALDA
Brand Name English
MAX-002
Code English
MESALAZINE
EP   INN   JAN   MART.   WHO-DD  
INN  
Official Name English
MESALAMINE [ORANGE BOOK]
Common Name English
MESALAMINE [USP-RS]
Common Name English
CANASA
Brand Name English
IIALDA
Brand Name English
M-AMINOSALICYLIC ACID
Systematic Name English
Classification Tree Code System Code
WHO-VATC QA07EC02
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
NDF-RT N0000005760
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
LIVERTOX NBK547995
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
NDF-RT N0000005760
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
FDA ORPHAN DRUG 275909
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
FDA ORPHAN DRUG 298109
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
NDF-RT N0000005760
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
NDF-RT N0000005760
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
NDF-RT N0000175781
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
NCI_THESAURUS C257
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
WHO-ATC A07EC02
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
FDA ORPHAN DRUG 253607
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C29249
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
LACTMED
Mesalamine
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
MESH
D019804
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
CAS
89-57-6
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-919-1
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
RS_ITEM_NUM
1392705
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
USAN
X-60
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
DRUG CENTRAL
1710
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
SMS_ID
100000091953
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
FDA UNII
4Q81I59GXC
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
NSC
38877
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
HSDB
7512
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
PUBCHEM
4075
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
EVMPD
SUB08782MIG
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
EPA CompTox
DTXSID5024506
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
IUPHAR
2700
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
RXCUI
52582
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY RxNorm
CHEBI
6775
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
WIKIPEDIA
MESALAZINE
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
DRUG BANK
DB00244
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
DAILYMED
4Q81I59GXC
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
ChEMBL
CHEMBL704
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
INN
5444
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY
MERCK INDEX
m7244
Created by admin on Sat Dec 16 17:31:37 UTC 2023 , Edited by admin on Sat Dec 16 17:31:37 UTC 2023
PRIMARY Merck Index
Related Record Type Details
Structure of MESALAMINE HYDROCHLORIDE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of Methylsulfasalazine
PARENT -> METABOLITE ACTIVE
Structure of DERSALAZINE
PRODRUG -> METABOLITE ACTIVE
Structure of OLSALAZINE
PRODRUG -> METABOLITE ACTIVE
Structure of SULFASALAZINE
PARENT -> METABOLITE ACTIVE
Inhibite the Hb-catalyzed peroxidative reaction
Structure of IPSALAZIDE
PRODRUG -> METABOLITE ACTIVE
Structure of BALSALAZIDE
PRODRUG -> METABOLITE ACTIVE
Related Record Type Details
Structure of 5-NITROSALICYLIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 5-AMINO-2-HYDROXYISOPHTHALIC ACID
IMPURITY -> PARENT
Structure of 2-CHLORO-3-NITROBENZOIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of SULFANILIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of m-AMINOBENZOIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of O-AMINOPHENOL
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (GC)
USP
Structure of 3-NITROSALICYLIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 1.3
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 2-HYDROXY-5-((2-CARBOXY-4-AMINOPHENYL)AMINO)BENZOIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of P-AMINOPHENOL
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (GC)
USP
Structure of 3,5-DIAMINO-2-HYDROXYBENZOIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 2.0
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of M-AMINOPHENOL
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of ANILINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (GC)
USP
Structure of Salicylic acid
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 1.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of AMINOSALICYLIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 1.3
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 2-CHLORO-5-NITROBENZOIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 1.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 3-AMINOSALICYLIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of O-CHLOROBENZOIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 4.5
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 5-(2-FORMYL-5-(HYDROXYMETHYL)-1H-PYRROL-1-YL)-2-HYDROXYBENZOIC ACID
IMPURITY -> PARENT
Structure of ANILINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of PHENYLAZOSALICYLIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of GENTISIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 1.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 5-AMINO-2-HYDROXY-3-(4-SULFOPHENYL)BENZOIC ACID
IMPURITY -> PARENT
Correction factors: for the calculation of contents, multiply the peak areas by 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of MESALAMINE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC Elimination
PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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