JAK抑制剂的药物化学视角:合成、生物学特性、选择性及构效关系

Medicinal chemistry perspective of JAK inhibitors: synthesis, biological profile, selectivity, and structure activity relationship.

作者信息

Maji Lalmohan, Sengupta Sindhuja, Purawarga Matada Gurubasavaraja Swamy, Teli Ghanshyam, Biswas Gourab, Das Pronoy Kanti, Panduranga Mudgal Manjunatha

机构信息

Integrated Drug Discovery Centre, Department of Pharmaceutical Chemistry, Acharya & BM Reddy College of Pharmacy, Bengaluru, Karnataka, India.

School of Pharmacy, Sangam University, Atoon, Bhilwara, 311001, Rajasthan, India.

出版信息

Mol Divers. 2024 Dec;28(6):4467-4513. doi: 10.1007/s11030-023-10794-5. Epub 2024 Jan 18.

Abstract

JAK-STAT signalling pathway was discovered more than quarter century ago. The JAK-STAT pathway protein is considered as one of the crucial hubs for cytokine secretion which mediates activation of different inflammatory, cellular responses and hence involved in different etiological factors. The various etiological factors involved are haematopoiesis, immune fitness, tissue repair, inflammation, apoptosis, and adipogenesis. The presence of the active mutation V617K plays a significant role in the progression of the JAK-STAT pathway-related disease. Consequently, targeting the JAK-STAT pathway could be a promising therapeutic approach for addressing a range of causative factors. In this current review, we provided a comprehensive discussion for the in-detail study of anatomy and physiology of the JAK-STAT pathway which contributes structural domain rearrangement, activation, and negative regulation associated with the downstream signaling pathway, relationship between different cytokines and diseases. This review also discussed the recent development of clinical trial entities. Additionally, this review also provides updates on FDA-approved drugs. In the current investigation, we have classified recently developed small molecule inhibitors of JAK-STAT pathway according to different chemical classes and we emphasized their synthetic routes, biological evaluation, selectivity, and structure-activity relationship.

摘要

JAK-STAT信号通路在25多年前就被发现了。JAK-STAT通路蛋白被认为是细胞因子分泌的关键枢纽之一,它介导不同的炎症和细胞反应的激活,因此涉及不同的病因。所涉及的各种病因包括造血、免疫适应性、组织修复、炎症、细胞凋亡和脂肪生成。活性突变V617K的存在在JAK-STAT通路相关疾病的进展中起重要作用。因此,靶向JAK-STAT通路可能是解决一系列致病因素的一种有前景的治疗方法。在本综述中,我们对JAK-STAT通路的解剖学和生理学进行了详细研究,全面讨论了其结构域重排、激活以及与下游信号通路相关的负调控、不同细胞因子与疾病之间的关系。本综述还讨论了临床试验实体的最新进展。此外,本综述还提供了美国食品药品监督管理局(FDA)批准药物的最新信息。在当前的研究中,我们根据不同的化学类别对最近开发的JAK-STAT通路小分子抑制剂进行了分类,并强调了它们的合成路线、生物学评价、选择性以及构效关系。

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