Raju Subramanian, Matthew R Lee, John G Allen, Matthew P Bourbeau, Christopher Fotsch, Fang-Tsao Hong, Seifu Tadesse, Guomin Yao, Chester C Yuan, Sekhar Surapaneni, Gary L Skiles, Xianghong Wang, G Erich Wohlhieter, Qingping Zeng, Yihong Zhou, Xiaochun Zhu, Chun Li
Index: Chem. Res. Toxicol. 23(3) , 653-63, (2010)
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A 2-aminothiazole derivative 1 was developed as a potential inhibitor of the oncology target AKT, a serine/threonine kinase. When incubated in rat and human liver microsomes in the presence of NADPH, 1 underwent significant metabolic activation on its 2-aminothiazole ring, leading to substantial covalent protein binding. Upon addition of glutathione, covalent binding was reduced significantly, and multiple glutathione adducts were detected. Novel metabolites from the in vitro incubates were characterized by LC-MS and NMR to discern the mechanism of bioactivation. An in silico model was developed based on the proposed mechanism and was employed to predict bioactivation in 23 structural analogues. The predictions were confirmed empirically for the bioactivation liability, in vitro, by LC-MS methods screening for glutathione incorporation. New compounds were identified with a low propensity for bioactivation.
Structure | Name/CAS No. | Molecular Formula | Articles |
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2-Aminothiazole
CAS:96-50-4 |
C3H4N2S |
Quantitative structure-activity relationship and complex net...
2008-11-13 [J. Med. Chem. 51 , 6740-51, (2008)] |
Design, synthesis, and evaluation of potential inhibitors of...
2008-06-01 [Bioorg. Med. Chem. 16 , 6193-206, (2008)] |
Effects of L-arginine, mirabegron, and oxybutynin on the pri...
2015-04-01 [Neurourol. Urodyn. 34(4) , 368-74, (2015)] |
Multicomponent assembly of proposed DNA precursors in water.
2012-08-22 [J. Am. Chem. Soc. 134(33) , 13889-95, (2012)] |
A combination strategy to inhibit Pim-1: synergism between n...
2013-03-01 [ChemMedChem 8(3) , 484-96, (2013)] |
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