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Bioorg Med Chem ; 78: 117109, 2023 01 15.
Article in English | MEDLINE | ID: mdl-36603397

ABSTRACT

3Z,5E-Octa-3,5-diene-1,3,4-tricarboxylic acid-3,4-anhydride (ODTAA, 1) was isolated from Paecilomyces sp. FKI-6801 for its selective IMP-1 MBL inhibitory activity. The first total synthesis of 1 from the commercially available compound was achieved in 9 steps with 28% overall yield. Introduction of catechol to the maleic anhydride of 1 improved the IC50 toward IMP-1 MBL and the inhibitory activity against IMP-1 MBL-producing P. aeruginosa. Treatment of the maleic anhydride scaffold with amine showed that the ß-carbonyl-α,ß-unsaturated carboxylic acid moiety is required as a pharmacophore for IMP-1 MBL inhibition.


Subject(s)
Pseudomonas Infections , Humans , Anhydrides , Maleic Anhydrides , Microbial Sensitivity Tests , Pseudomonas aeruginosa , beta-Lactamases , Anti-Bacterial Agents/pharmacology
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