CHEBI:55341 - 1-((4-hydroxy-3-nitrophenyl)acetoxy)pyrrolidine-2,5-dione

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ChEBI Name 1-((4-hydroxy-3-nitrophenyl)acetoxy)pyrrolidine-2,5-dione
ChEBI ID CHEBI:55341
Definition The ester formed between N-hydroxysuccinimide and (4-hydroxy-3-nitrophenyl)acetic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C12H10N2O7
Net Charge 0
Average Mass 294.21700
Monoisotopic Mass 294.04880
InChI InChI=1S/C12H10N2O7/c15-9-2-1-7(5-8(9)14(19)20)6-12(18)21-13-10(16)3-4-11(13)17/h1-2,5,15H,3-4,6H2
InChIKey WXEZCVSZMLAVNV-UHFFFAOYSA-N
SMILES Oc1ccc(CC(=O)ON2C(=O)CCC2=O)cc1[N+]([O-])=O
Roles Classification
Biological Role(s): hapten
Any substance capable of eliciting an immune response only when attached to a large carrier such as a protein. Examples include dinitrophenols; oligosaccharides; peptides; and heavy metals.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 1-((4-hydroxy-3-nitrophenyl)acetoxy)pyrrolidine-2,5-dione (CHEBI:55341) has functional parent (4-hydroxy-3-nitrophenyl)acetic acid (CHEBI:546274)
1-((4-hydroxy-3-nitrophenyl)acetoxy)pyrrolidine-2,5-dione (CHEBI:55341) has part (4-hydroxy-3-nitrophenyl)acetyl group (CHEBI:53793)
1-((4-hydroxy-3-nitrophenyl)acetoxy)pyrrolidine-2,5-dione (CHEBI:55341) has role hapten (CHEBI:59174)
1-((4-hydroxy-3-nitrophenyl)acetoxy)pyrrolidine-2,5-dione (CHEBI:55341) is a 2-nitrophenols (CHEBI:86421)
1-((4-hydroxy-3-nitrophenyl)acetoxy)pyrrolidine-2,5-dione (CHEBI:55341) is a N-hydroxysuccinimide ester (CHEBI:53165)
IUPAC Name
1-[2-(4-hydroxy-3-nitrophenyl)acetoxy]pyrrolidine-2,5-dione
Synonyms Sources
1-((4-hydroxy-3-nitrophenyl)acetoxy)-2,5-pyrrolidinedione ChEBI
1-[[(4-hydroxy-3-nitrophenyl)acetyl]oxy]-2,5-pyrrolidinedione ChEBI
4-hydroxy-3-nitrobenzeneacetic acid 2,5-dioxo-1-pyrrolidinyl ester ChEBI
4-hydroxy-3-nitrobenzeneacetic acid, 2,5-dioxo-1-pyrrolidinyl ester ChEBI
4-hydroxy-3-nitrophenylacetyl-O-succinimide ester ChEBI
NP-O-Su ChEBI
NP-O-succinimide ChEBI
NP-O-succinimide ester ChEBI
Registry Numbers Types Sources
15492433 Reaxys Registry Number Reaxys
75679-31-1 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
18432796 PubMed citation Europe PMC
6183362 PubMed citation Europe PMC
6967910 PubMed citation Europe PMC
6969772 PubMed citation Europe PMC
6972973 PubMed citation Europe PMC
Last Modified
21 October 2015