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发现基于 3-苯基吲唑的新型趋化因子样受体 1 拮抗剂,用于治疗银屑病。

Discovery of 3-Phenyl Indazole-Based Novel Chemokine-like Receptor 1 Antagonists for the Treatment of Psoriasis.

机构信息

School of Life Sciences, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Republic of Korea.

Innovo Therapeutics Inc., Daeduck Biz Center C-313, 17 Techno 4-ro, Yuseong-gu, Daejeon 34013, Republic of Korea.

出版信息

J Med Chem. 2023 Nov 9;66(21):14564-14582. doi: 10.1021/acs.jmedchem.3c01011. Epub 2023 Oct 26.

Abstract

Chemokine-like receptor 1 (CMKLR1)─a G protein-coupled receptor─has functional roles in the immune system and related diseases, including psoriasis and metabolic diseases. Psoriasis is a chronic inflammatory disease characterized by skin redness, scaliness, and itching. In this study, we sought to develop novel CMKLR1 antagonists by screening our in-house GPCR-targeting compound library. Moreover, we optimized a phenylindazole-based hit compound with antagonistic activities and evaluated its oral pharmacokinetic properties in a murine model. A structure-based design on the human CMKLR1 homology model identified - as an optimized compound that serves as a potent and orally available antagonist with a pIC value of 7.44 in CMKLR1-transfected CHO cells. Furthermore, in the imiquimod-induced psoriasis-like mouse model, oral administration of - for 1 week significantly alleviated modified psoriasis area and severity index scores (severity of erythema, scaliness, skin thickness) compared with the control group.

摘要

趋化因子样受体 1(CMKLR1)是一种 G 蛋白偶联受体,在免疫系统和相关疾病中具有功能作用,包括银屑病和代谢疾病。银屑病是一种慢性炎症性疾病,其特征是皮肤发红、鳞屑和瘙痒。在这项研究中,我们通过筛选我们内部的 GPCR 靶向化合物库,旨在开发新型 CMKLR1 拮抗剂。此外,我们优化了一种具有拮抗活性的基于苯基吲唑的先导化合物,并在小鼠模型中评估了其口服药代动力学特性。基于人 CMKLR1 同源模型的结构设计确定了 - 作为一种优化的化合物,作为一种有效的口服可用拮抗剂,在 CMKLR1 转染的 CHO 细胞中 pIC 值为 7.44。此外,在咪喹莫特诱导的银屑病样小鼠模型中,与对照组相比,- 口服给药 1 周可显著缓解改良银屑病面积和严重度指数评分(红斑严重程度、鳞屑、皮肤厚度)。

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