Term Name: aspirin-based probe AP
Synonyms: 2-(1,3-benzothiazol-2-yl)-4-fluorophenyl 2-(acetyloxy)benzoate, 2-(1,3-benzothiazol-2-yl)-4-fluorophenyl 2-acetoxybenzoate, 2-(1,3-benzothiazol-2-yl)-4-fluorophenyl salicylate, probe AP
Definition: A benzoate ester resulting from the formal condensation of the carboxy group of acetylsalicylic acid with the phenolic hydroxy group of 2-(1,3-benzothiazol-2-yl)-4-fluorophenol. The latter is a fluorophore which is to the aspirin moiety via an H2O2-responsive bond. It can be used as probe for imaging H2O2 (overproduction of H2O2 causes oxidative stress and is characteristic of vascular diseases). In contrast to arylboronat-based probes, it shows high specificity for H2O2 over peroxynitrite (which is much more reactive than H2O2, but exists at much lower abundance).
Ontology: ChEBI [CHEBI:141699]  ( EBI )

Relationships
is a type of: benzoate ester benzothiazoles monofluorobenzenes salicylates
has_functional_parent: 2-(1,3-benzothiazol-2-yl)-4-fluorophenol acetylsalicylic acid
has_role: pharmaceutical