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Details

Stereochemistry ACHIRAL
Molecular Formula C12H12N2O3
Molecular Weight 232.2353
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NALIDIXIC ACID

SMILES

CCN1C=C(C(O)=O)C(=O)C2=C1N=C(C)C=C2

InChI

InChIKey=MHWLWQUZZRMNGJ-UHFFFAOYSA-N
InChI=1S/C12H12N2O3/c1-3-14-6-9(12(16)17)10(15)8-5-4-7(2)13-11(8)14/h4-6H,3H2,1-2H3,(H,16,17)

HIDE SMILES / InChI
Molecular Formula C12H12N2O3
Molecular Weight 232.2353
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 16:23:22 UTC 2023
Edited
by admin
on Sat Dec 16 16:23:22 UTC 2023
Record UNII
3B91HWA56M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NALIDIXIC ACID
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
WIN-18320
Code English
1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID, 1-ETHYL-1,4-DIHYDRO-7-METHYL-4-OXO-
Common Name English
NALIDIXIC ACID [VANDF]
Common Name English
NALIDIXIC ACID [MI]
Common Name English
NSC-82174
Code English
NALIDIXIC ACID [JAN]
Common Name English
NALIDIXIC ACID [HSDB]
Common Name English
NALIDIXIC ACID [ORANGE BOOK]
Common Name English
NALIDIXIC ACID [EP IMPURITY]
Common Name English
WIN 18,320
Code English
1-Ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid
Systematic Name English
NALIDIXATE
Common Name English
nalidixic acid [INN]
Common Name English
NALIDIXIC ACID [MART.]
Common Name English
NEGGRAM
Brand Name English
NALIDIXIC ACID [USAN]
Common Name English
Nalidixic acid [WHO-DD]
Common Name English
NALIDIXIC ACID [USP IMPURITY]
Common Name English
Classification Tree Code System Code
LIVERTOX 663
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
WHO-ATC J01MB02
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
NCI_THESAURUS C795
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
WHO-VATC QJ01MB02
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
NCI_THESAURUS C255
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
Code System Code Type Description
RXCUI
7240
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
SMS_ID
100000092361
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
INN
1450
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
MERCK INDEX
m7714
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY Merck Index
FDA UNII
3B91HWA56M
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
PUBCHEM
4421
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
ECHA (EC/EINECS)
206-864-7
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
CHEBI
100147
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
RXCUI
618425
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
ALTERNATIVE
ChEMBL
CHEMBL5
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
CHEBI
62070
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
MESH
D009268
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
NSC
82174
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
NCI_THESAURUS
C47630
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
HSDB
3241
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
EPA CompTox
DTXSID3020912
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
DRUG CENTRAL
1875
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
LACTMED
Nalidixic Acid
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
WIKIPEDIA
NALIDIXIC ACID
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
CAS
389-08-2
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
EVMPD
SUB09138MIG
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
DRUG BANK
DB00779
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
DAILYMED
3B91HWA56M
Created by admin on Sat Dec 16 16:23:23 UTC 2023 , Edited by admin on Sat Dec 16 16:23:23 UTC 2023
PRIMARY
Related Record Type Details
Structure of NALIDIXATE SODIUM
SALT/SOLVATE -> PARENT
Structure of MEGLUMINE NALIDIXIC ACID
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of 1-ETHYL-1,4-DIHYDRO-7-HYDROXYMETHYL-4-OXO-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID
METABOLITE -> PARENT
Metabolite to parent drug ratio in non-uraemic human plasma.
METABOLITE TO PARENT DRUG RATIO
PLASMA; URINE
Related Record Type Details
Structure of NALIDIXIC ACID
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