Spirohypertones A and B as potent antipsoriatics: Tumor necrosis factor- α inhibitors with unprecedented chemical architectures

螺环高分子 A 和 B 作为强效抗银屑病药物:具有前所未有的化学结构的肿瘤坏死因子-α 抑制剂

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作者:Yulin Duan, Weiguang Sun, Yongqi Li, Zhengyi Shi, Lanqin Li, Yeting Zhang, Kun Huang, Zhiping Zhang, Changxing Qi, Yonghui Zhang

Abstract

Tumor necrosis factor-α (TNF-α) is a promising target for inflammatory and autoimmune diseases. Spirohypertones A (1) and B (2), two unprecedented polycyclic polyprenylated acylphloroglucinols with highly rearranged skeletons, were isolated from Hypericum patulum. The structures of 1 and 2 were confirmed through comprehensive spectroscopic analysis, single-crystal X-ray diffraction and electronic circular dichroism calculations. Importantly, 2 showed remarkable TNF-α inhibitory activity, which could protect L929 cells from death induced by co-incubation with TNF-α and actinomycin D. It also demonstrated the ability to suppress the inflammatory response in HaCaT cells stimulated with TNF-α. Notably, in an imiquimod-induced psoriasis murine model, 2 restrained symptoms of epidermal hyperplasia associated with psoriasis, presenting anti-inflammatory and antiproliferative effects. This discovery positions 2 as a potent TNF-α inhibitor, providing a promising lead compound for developing an antipsoriatic agent.

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