药效团
化学
背景(考古学)
计算生物学
功能(生物学)
酶
体外
高通量筛选
生物化学
组合化学
细胞生物学
生物
古生物学
作者
Séverine Ravez,Cyril Corbet,Quentin Spillier,Alice Dutu,Anita D. Robin,Edouard Mullarky,Lewis C. Cantley,Olivier Féron,Raphaël Frédérick
标识
DOI:10.1021/acs.jmedchem.6b01166
摘要
Given the putative role of PHGDH in cancer, development of inhibitors is required to explore its function. In this context, we established and validated a straightforward enzymatic assay suitable for high-throughput screening and we identified inhibitors with similar chemical scaffolds. Through a convergent pharmacophore approach, we synthesized α-ketothioamides that exhibit interesting in vitro PHGDH inhibition and encouraging cellular results. These novel probes may be used to understand the emerging biology of this metabolic target.
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