A multifaceted approach to identify non-specific enzyme inhibition: Application to Mycobacterium tuberculosis shikimate kinase

• Published in: Bioorganic & medicinal chemistry letters 2018-02, Vol.28 (4), p.802-808
• Main Authors: Alturki, Mansour S., Fuanta, Ngolui Rene, Jarrard, Madison A., Hobrath, Judith V., Goodwin, Douglas C., Rants'o, Thankhoe A., Calderón, Angela I.
• Format: Article
• Language: English
• Subjects: Aggregator; Antitubercular Agents - chemistry; Antitubercular Agents - pharmacology; Benzothiazoles - chemistry; Benzothiazoles - pharmacology; Enzyme Inhibitors - chemistry; Enzyme Inhibitors - pharmacology; LC-MS; MtSK; Mycobacterium tuberculosis - enzymology; NMR; Non-specific inhibition; Oxadiazoles - chemistry; Oxadiazoles - pharmacology; Particle Size; Phosphotransferases (Alcohol Group Acceptor) - antagonists & inhibitors; Riluzole - pharmacology; Solubility; Triton X-100
• ISSN: 0960-894X; 1464-3405
• DOI: 10.1016/j.bmcl.2017.12.002

[Display omitted] Single dose high-throughput screening (HTS) followed by dose-response evaluations is a common strategy for the identification of initial hits for further development. Early identification and exclusion of false positives is a cost-saving and essential step in early drug discovery. One of the mechanisms of false positive compounds is the formation of aggregates in assays. This study evaluates the mechanism(s) of inhibition of a set of 14 compounds identified previously as actives in Mycobacterium tuberculosis (Mt) cell culture screening and in vitro actives in Mt shikimate kinase (MtSK) assay. Aggregation of hit compounds was characterized using multiple experimental methods, LC-MS, 1HNMR, dynamic light scattering (DLS), transmission electron microscopy (TEM), and visual inspection after centrifugation for orthogonal confirmation. Our results suggest that the investigated compounds containing oxadiazole-amide and aminobenzothiazole moieties are false positive hits and non-specific inhibitors of MtSK through aggregate formation.