Naikoo Rayees Ahmad, Painuli Ritu, Akhter Zaheen, Singh Parvinder Pal
Natural Product & Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu 180001, India.
Natural Product & Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu 180001, India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
Bioorg Chem. 2024 Dec;153:107775. doi: 10.1016/j.bioorg.2024.107775. Epub 2024 Sep 2.
Cannabinoid receptors CB1 and CB2 play critical roles in regulating numerous central and peripheral physiological activities. While efforts have been made to develop ligands for both CB1 and CB2 receptors, CB1 receptor ligands often have restricted use due to undesirable psychotropic side effects. Consequently, recent cannabis research has increasingly focused on CB2-specific ligands. Pharmacological agonists of CB2 receptors have shown potential in managing pain, inflammation, arthritis, neuroprotection, cancer, and other disorders. Despite several CB2 receptor ligands entering clinical trials, none have achieved market approval except natural cannabinoids and their derivatives, primarily due to insufficient CB2/CB1 receptor selectivity. However, new-generation ligands developed in recent years have demonstrated improved selectivity. This review covers patent literature on CB2 modulators from 2016 to 2024, highlighting the major advances in the field. During this period, the majority of research has concentrated on using CB2 modulators to alleviate inflammation and pain. Additionally, patents have explored CB2 modulators for a range of specific diseases, including: psychiatric and neuropsychiatric disorders, schizophrenia, multiple myeloma and osteoporosis, ocular inflammation and neuropathic Pain, cancer anorexia and weight loss, antioxidant and anti-aging agents, lymphocytopenia, hearing loss, Alzheimer's disease, cancer and non-malignant tumors. Notably, recent years have seen increased interest in CB2 antagonists/inverse agonists, with few candidates advancing to clinical studies. Significant progress has been made in the synthesis and modulation of selective CB2 agonists and antagonists, paving the way for future developments in CB2 modulators. This review provides insights and prospects for the continued evolution of CB2-targeted therapies.
大麻素受体CB1和CB2在调节众多中枢和外周生理活动中发挥着关键作用。虽然人们已努力开发CB1和CB2受体的配体,但CB1受体配体由于不良的精神副作用,其使用往往受到限制。因此,最近对大麻的研究越来越集中在CB2特异性配体上。CB2受体的药理激动剂在治疗疼痛、炎症、关节炎、神经保护、癌症和其他疾病方面已显示出潜力。尽管有几种CB2受体配体进入了临床试验,但除了天然大麻素及其衍生物外,没有一种获得市场批准,主要原因是CB2/CB1受体选择性不足。然而,近年来开发的新一代配体已显示出更好的选择性。本综述涵盖了2016年至2024年关于CB2调节剂的专利文献,突出了该领域的主要进展。在此期间,大多数研究集中在使用CB2调节剂来减轻炎症和疼痛。此外,专利还探索了用于一系列特定疾病的CB2调节剂,包括:精神和神经精神疾病、精神分裂症、多发性骨髓瘤和骨质疏松症、眼部炎症和神经性疼痛、癌症厌食和体重减轻、抗氧化剂和抗衰老剂、淋巴细胞减少症、听力损失、阿尔茨海默病、癌症和非恶性肿瘤。值得注意的是,近年来对CB2拮抗剂/反向激动剂的兴趣有所增加,但很少有候选药物进入临床研究。在选择性CB2激动剂和拮抗剂的合成和调节方面取得了重大进展,为CB2调节剂的未来发展铺平了道路。本综述为以CB2为靶点的治疗方法的持续发展提供了见解和前景。