| Literature DB >> 24900541 |
Pravin S Shirude1, Beena Paul1, Nilanjana Roy Choudhury1, Chaitanya Kedari1, Balachandra Bandodkar1, Bheemarao G Ugarkar1.
Abstract
NDH-2 is an essential respiratory enzyme in Mycobacterium tuberculosis (Mtb), which plays an important role in the physiology of Mtb. Herein, we present a target-based effort to identify a new structural class of inhibitors for NDH-2. High-throughput screening of the AstraZeneca corporate collection resulted in the identification of quinolinyl pyrimidines as the most promising class of NDH-2 inhibitors. Structure-activity relationship studies showed improved enzyme inhibition (IC50) against the NDH-2 target, which in turn translated into cellular activity against Mtb. Thus, the compounds in this class show a good correlation between enzyme inhibition and cellular potency. Furthermore, early ADME profiling of the best compounds showed promising results and highlighted the quinolinyl pyrimidine class as a potential lead for further development.Entities:
Keywords: NDH-2; antituberculosis; quinolinyl pyrimidines; respiratory chain
Year: 2012 PMID: 24900541 PMCID: PMC4025736 DOI: 10.1021/ml300134b
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345