Department of Chemistry and Biochemistry, UCLA, 607 Charles E Young Dr E, Los Angeles, California 90095, United States.
Department of Molecular Cell and Developmental Biology, UCLA, 610 Charles E Young Dr E, Los Angeles, California 90095, United States.
J Med Chem. 2021 Feb 25;64(4):2046-2063. doi: 10.1021/acs.jmedchem.0c01570. Epub 2021 Feb 3.
Herein, we report the synthesis and evaluation of novel analogues of UK-5099 both and for the development of mitochondrial pyruvate carrier (MPC) inhibitors to treat hair loss. A comprehensive understanding of the structure-activity relationship was obtained by varying four positions of the hit compound, namely, the alkyl group on the N1 position, substituents on the indole core, various aromatic and heteroaromatic core structures, and various Michael acceptors. The major discovery was that the inhibitors with a 3,5-bis(trifluoromethyl)benzyl group at the N1 position were shown to have much better activity than (UK-5099) to increase cellular lactate production. Additionally, analogue , possessing a 7-azaindole heterocycle, was also shown to have significant MPC inhibition activity, which further increases the chemical space for drug design. Finally, more than 10 analogues were tested on shaved mice by topical treatment and promoted obvious hair growth on mice.
在此,我们报告了新型 UK-5099 类似物[和]的合成和评估,用于开发治疗脱发的线粒体丙酮酸载体 (MPC) 抑制剂。通过改变命中化合物的四个位置,即 N1 位置上的烷基、吲哚核心上的取代基、各种芳基和杂芳基核心结构以及各种迈克尔受体,我们全面了解了结构-活性关系。主要发现是,具有 N1 位置上的 3,5-双(三氟甲基)苄基的抑制剂在增加细胞内乳酸产量方面显示出比[(UK-5099)]更好的活性。此外,具有 7-氮杂吲哚杂环的类似物[也]表现出显著的 MPC 抑制活性,这进一步增加了药物设计的化学空间。最后,通过局部治疗在剃毛小鼠上测试了 10 多种类似物,促进了小鼠明显的毛发生长。