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DOI 10.1021/acs.jmedchem.4c01055

Медицинская библиотека · Journal of medicinal chemistry · 2024

Design, Synthesis, and Biological Activity of Novel Quinone Derivatives as Potent STAT3 Inhibitors for Psoriasis Treatment.

Chen Ling, Wang Liuliu, Gao Jinlei, Xie Yuanzhu, Deng Xu, Tian Guang, Li Mingjian, Sui Zhongtai, Luo Cailin, Liu Li, Huang Xinyu, Zhu Xinyu, Zhu Shuaiwen, Luo Zhiyong, Ma Dayou, Liu Suyou

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Psoriasis, which severely affects the sufferer's life quality, is a chronic skin disease still lacking satisfactory medication. Recently, signal transducer and activator of transcription 3 (STAT3) was revealed playing an important role in the progression of psoriasis. In this paper, a total of 59 quinone derivatives with various scaffolds were designed, synthesized, and evaluated for antipsoriatic potential as STAT3 inhibitors. Among them, 15e was identified as the most potent antipsoriatic agent and could bind to STAT3; reduce both total and phosphorylated STAT3 levels, inhibit the nuclear translocation of STAT3; and, therefore, inhibit the transcription and expression of the propsoriatic factor IL-17A. In vivo experiments on mice showed that the topical application of 15e was effective in alleviating IMQ-induced psoriasis without noticeable side effects. In all, this research rendered 15e as a promising drug candidate for psoriasis.

Для цитирования: Chen Ling, Wang Liuliu, Gao Jinlei, Xie Yuanzhu, Deng Xu, Tian Guang, Li Mingjian, Sui Zhongtai, Luo Cailin, Liu Li, Huang Xinyu, Zhu Xinyu, Zhu Shuaiwen, Luo Zhiyong, Ma Dayou, Liu Suyou. Design, Synthesis, and Biological Activity of Novel Quinone Derivatives as Potent STAT3 Inhibitors for Psoriasis Treatment.. Journal of medicinal chemistry. 2024. DOI: 10.1021/acs.jmedchem.4c01055.

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