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J Med Chem ; 67(17): 15438-15455, 2024 Sep 12.
Article in English | MEDLINE | ID: mdl-39151117

ABSTRACT

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.


Subject(s)
Drug Design , Psoriasis , STAT3 Transcription Factor , Psoriasis/drug therapy , STAT3 Transcription Factor/antagonists & inhibitors , STAT3 Transcription Factor/metabolism , Animals , Humans , Mice , Interleukin-17/metabolism , Interleukin-17/antagonists & inhibitors , Quinones/pharmacology , Quinones/chemical synthesis , Quinones/therapeutic use , Quinones/chemistry , Structure-Activity Relationship , Mice, Inbred BALB C
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