Journal article
Two new irreversible inhibitors of dihydrodipicolinate synthase: Diethyl (E,E)-4-oxo-2,5-heptadienedioate and diethyl (E)-4-oxo-2-heptenedioate
JJ Turner, JP Healy, RCJ Dobson, JA Gerrard, CA Hutton
Bioorganic and Medicinal Chemistry Letters | Published : 2005
Abstract
Dihydrodipicolinate synthase (DHDPS) is a key enzyme in lysine biosynthesis and an important antibiotic target. The enzyme catalyses the condensation of (S)-aspartate semialdehyde (ASA) and pyruvate to form dihydrodipicolinate. Two new irreversible inhibitors of dihydrodipicolinate synthase are reported, designed to mimic the acyclic enzyme-bound condensation product of ASA and pyruvate. These compounds represent an important new lead in the design of potent inhibitors for this enzyme. © 2004 Elsevier Ltd. All rights reserved.
Grants
Awarded by Australian Research Council