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大麻二酚环化类似物作为潜在抗癌剂的发现:合成与生物学评价

Discovery of Ring-Annulated Analogues of Cannabidiol as Potential Anticancer Agents: Synthesis and Biological Evaluation.

作者信息

Cham Pankaj Singh, Singh Ajeet, Jamwal Ashiya, Singh Rattandeep, Anand Radhika, Manhas Diksha, Sharma Sucheta, Singh Varun Pratap, Nandi Utpal, Singh Shashank K, Singh Parvinder Pal

机构信息

Natural Product & Medicinal Chemistry Division, CSIR-Indian Institute of Integrative Medicine (CSIR-IIIM), Canal Road, Jammu 180001, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.

出版信息

ACS Med Chem Lett. 2024 Oct 17;15(11):1832-1842. doi: 10.1021/acsmedchemlett.4c00233. eCollection 2024 Nov 14.

Abstract

Cannabidiol (CBD) is a nonpsychoactive cannabinoid derived from and its potential therapeutic effects extend beyond its well-known antiepileptic properties. Exploring CBD and its analogues as anticancer agents has gained significant attention in recent years. In this study, a series of novel ring-annulated analogues of CBD with oxazinyl moiety were synthesized and evaluated for their antiproliferative effect. The analogues and demonstrate promising activity against breast and colorectal cancer. Furthermore, mechanistic insights revealed that the identified candidates arrest the G1 phase of the cell cycle and induce apoptosis via the mitochondrial pathway in breast cancer cell lines. Notably, CBD ring-annulated analogues or exhibit enhanced solubility, better metabolic stability, and lowered cytochrome P450 (CYP) inhibition liability compared to CBD. These multifaceted attributes highlight the potential of cannabinoid-based candidates for further preclinical development.

摘要

大麻二酚(CBD)是一种从[来源未提及]中提取的非精神活性大麻素,其潜在治疗作用超出了其广为人知的抗癫痫特性。近年来,探索CBD及其类似物作为抗癌药物受到了广泛关注。在本研究中,合成了一系列具有恶嗪基部分的新型CBD环化类似物,并评估了它们的抗增殖作用。类似物[具体编号未提及]对乳腺癌和结直肠癌显示出有前景的活性。此外,机制研究表明,所鉴定的候选物使乳腺癌细胞系的细胞周期停滞于G1期,并通过线粒体途径诱导凋亡。值得注意的是,与CBD相比,CBD环化类似物[具体编号未提及]具有更高的溶解度、更好的代谢稳定性以及更低的细胞色素P450(CYP)抑制倾向。这些多方面的特性突出了基于大麻素的候选物进一步临床前开发的潜力。

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