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Cyclobutanone Inhibitors of Diaminopimelate Desuccinylase (DapE) as Potential New Antibiotics.

Thahani S Habeeb MohammadEmma H KelleyCory T ReidlKatherine KonczakMegan BeulkeJanielle JavierKenneth W OlsenDaniel P Becker
Published in: International journal of molecular sciences (2024)
Based on our previous success in using cyclobutanone derivatives as enzyme inhibitors, we have designed and prepared a 37-member library of α-aminocyclobutanone amides and sulfonamides, screened for inhibition of the bacterial enzyme diaminopimelate desuccinylase (DapE), which is a promising antibiotic target, and identified several inhibitors with micromolar inhibitory potency. Molecular docking suggests binding of the deprotonated hydrate of the strained cyclobutanone, and thermal shift analysis with the most potent inhibitor ( 3y , IC 50 = 23.1 µM) enabled determination of a K i value of 10.2 +/- 0.26 µM and observed two separate T m values for H. influenzae DapE ( Hi DapE).
Keyphrases
  • molecular docking
  • molecular dynamics simulations
  • climate change
  • dna binding