| Literature DB >> 23268609 |
Pravin S Shirude1, Prashanti Madhavapeddi, Julie A Tucker, Kannan Murugan, Vikas Patil, Halesha Basavarajappa, Anandkumar V Raichurkar, Vaishali Humnabadkar, Syeed Hussein, Sreevalli Sharma, V K Ramya, Chandan B Narayan, Tanjore S Balganesh, Vasan K Sambandamurthy.
Abstract
Aminopyrazinamides originated from a high throughput screen targeting the Mycobacterium smegmatis (Msm) GyrB ATPase. This series displays chemical tractability, robust structure-activity relationship, and potent antitubercular activity. The crystal structure of Msm GyrB in complex with one of the aminopyrazinamides revealed promising attributes of specificity against other broad spectrum pathogens and selectivity against eukaryotic kinases due to novel interactions at hydrophobic pocket, unlike other known GyrB inhibitors. The aminopyrazinamides display excellent mycobacterial kill under in vitro, intracellular, and hypoxic conditions.Entities:
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Year: 2012 PMID: 23268609 DOI: 10.1021/cb300510w
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100