29048-34-8

5-(2-Nitrophenyl)-2-furoic acid Chemical Structure
29048-34-8

Chemical Structure

5-(2-Nitrophenyl)-2-furoic acid

Synonym(s): O-Nitrophenylfuroic acid

  • CAS No.: 29048-34-8
  • Formula:C11H7NO5
  • Molecular Weight:233.18

IUPAC Name: 5-(2-nitrophenyl)furan-2-carboxylic acid

InChIKey: XUFDYUSOQQYQRL-UHFFFAOYSA-N

SMILES: O=C(C1=CC=C(C2=CC=CC=C2[N+]([O-])=O)O1)O

Biological Activity: 5-(2-Nitrophenyl)-2-furoic acid (O-Nitrophenylfuroic acid) is a Mn2+-form Escherichia coli methionine aminopeptidase (EcMetAP) inhibitor with an IC50 of 1.08 μM against Escherichia coli. 5-(2-Nitrophenyl)-2-furoic acid selectively inhibits the Mn2+-form over the Co2+-, Ni2+-, and Fe2+-forms of EcMetAP, with its carboxyl group preferentially coordinating with Mn2+ ions as the major determinant for this metalloform selectivity. 5-(2-Nitrophenyl)-2-furoic acid can be used for the research of bacterial infection[1].

Cat. No. Product Name Purity Description Pricing
HY-128073
5-(2-Nitrophenyl)-2-furoic acid 5-(2-Nitrophenyl)-2-furoic acid (O-Nitrophenylfuroic acid) is a Mn2+-form Escherichia coli methionine aminopeptidase (EcMetAP) inhibitor with an IC50 of 1.08 μM against Escherichia coli. 5-(2-Nitrophenyl)-2-furoic acid selectively inhibits the Mn2+-form over the Co2+-, Ni2+-, and Fe2+-forms of EcMetAP, with its carboxyl group preferentially coordinating with Mn2+ ions as the major determinant for this metalloform selectivity. 5-(2-Nitrophenyl)-2-furoic acid can be used for the research of bacterial infection.
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