CHEBI:189548 - 3,5-dinitrosalicylic acid hydrazide

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ChEBI Name 3,5-dinitrosalicylic acid hydrazide
ChEBI ID CHEBI:189548
Definition A carbohydrazide resulting from the formal condensation of the carboxy group of 3,5-dinitrosalicylic acid with one of the amino groups of hydrazine. It is a metabolite of nifursol found in foodstuffs of animal origin.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C7H6N4O6
Net Charge 0
Average Mass 242.147
Monoisotopic Mass 242.02873
InChI InChI=1S/C7H6N4O6/c8-9-7(13)4-1-3(10(14)15)2-5(6(4)12)11(16)17/h1-2,12H,8H2,(H,9,13)
InChIKey HWTXGJCHJRRKNS-UHFFFAOYSA-N
SMILES NNC(=O)C1=C(O)C(=CC(=C1)[N+]([O-])=O)[N+]([O-])=O
Roles Classification
Biological Role(s): drug metabolite

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ChEBI Ontology
Outgoing 3,5-dinitrosalicylic acid hydrazide (CHEBI:189548) has functional parent 3,5-dinitrosalicylic acid (CHEBI:53648)
3,5-dinitrosalicylic acid hydrazide (CHEBI:189548) has role drug metabolite (CHEBI:49103)
3,5-dinitrosalicylic acid hydrazide (CHEBI:189548) is a carbohydrazide (CHEBI:35363)
3,5-dinitrosalicylic acid hydrazide (CHEBI:189548) is a dinitrophenol (CHEBI:39352)
IUPAC Name
2-hydroxy-3,5-dinitrobenzohydrazide
Synonyms Sources
2-hydroxy-3,5-dinitro-benzoic acid hydrazide ChEBI
2-hydroxy-3,5-dinitrobenzoic acid hydrazide ChEBI
3,5-dinitrosalicylhydrazide ChEBI
3,5-dinitrosalicylohydrazide ChemIDplus
benzoic acid, 2-hydroxy-3,5-dinitro-, hydrazide ChemIDplus
DNSAH
Note: (2022-01-24) Used as an abbreviation in journal articles.
 ChEBI
DNSH
Note: (2022-01-24) Used as an abbreviation in journal articles.
 ChEBI
DSH
Note: (2022-01-24) Used as an abbreviation in journal articles.
 ChEBI
Manual Xref Database
2896464 ChemSpider
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Registry Number Type Source
955-07-7 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
15824001 PubMed citation Europe PMC
15852149 PubMed citation Europe PMC
22486660 PubMed citation Europe PMC
27935246 PubMed citation Europe PMC
32032421 PubMed citation Europe PMC
33268173 PubMed citation Europe PMC
Last Modified
24 January 2022