Department of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz University, P.O. Box 80260, Jeddah 21589, Saudi Arabia.
Department of Pharmacognosy, Faculty of Pharmacy, Ain-Shams University, Abbasia, Cairo 11566, Egypt.
Molecules. 2022 Apr 27;27(9):2797. doi: 10.3390/molecules27092797.
L. is an annual herbaceous plant that belongs to the family Cannabinaceae. In this study, the potential use of forty-five cannabinoids, previously identified from to alleviate COVID-19 infection via prohibition of crucial SARS-CoV-2 proteins using molecular docking, was examined. In silico studies were performed on three vital enzymes that serve as principle therapeutic targets to prevent SARS-CoV-2 replication. These enzymes are the main protease SARS-CoV-2 M, papain-like protease SARS-CoV-2 PL and angiotensin-converting enzyme 2 (ACE2). Regarding SARS-CoV-2 M, cannabichromanon () showed the best fitting within its active centers, followed by cannabinolic acid () and cannabinol (), displaying ∆G of -33.63, -23.24, and -21.60 kcal/mol, respectively. Concerning SARS-CoV-2 PL, cannabichromanon () followed by cannabinolic acid () and cannabicyclolic acid () revealed the best binding within its active pockets owing to multiple bond formation with ∆G values of -28.36, -22.81, and -19.89 kcal/mol. Furthermore, cannabichromanon (), cannabinolic acid (), and cannabinol () showed considerable fitting within the active sites of angiotensin-converting enzyme 2 (ACE2) evidenced by their significant ∆G values that were estimated as -41.77, -31.34, and -30.36 kcal/mol, respectively. ADME/TOPKAT (absorption, distribution, metabolism, excretion, and toxicity) evaluation was performed on the tested cannabinoids to further explore their pharmacokinetics, pharmacodynamics, and toxicity properties. The results indicated the considerable pharmacokinetic, pharmacodynamic, and toxicity properties of cannabinol (), cannabinolic acid (), cannabichromanon (), and cannabicyclolic acid () that showed best fitting scores within the active sites of the tested enzymes. Multivariate data analysis revealed that cannabichromanon and cannabinolic acid showed a discriminant nature and hence can be incorporated in pharmaceutical dosage forms to alleviate COVID-19 infection.
大麻花(L.)是一种一年生草本植物,属于大麻科。在这项研究中,通过分子对接抑制关键的 SARS-CoV-2 蛋白,研究了之前从大麻中鉴定出的四十五种大麻素在缓解 COVID-19 感染方面的潜在用途。对三种作为预防 SARS-CoV-2 复制的主要治疗靶点的重要酶进行了计算机模拟研究。这些酶是 SARS-CoV-2 的主要蛋白酶(M)、木瓜蛋白酶样蛋白酶(PL)和血管紧张素转换酶 2(ACE2)。关于 SARS-CoV-2 M,大麻色胺()在其活性中心内表现出最佳拟合,其次是大麻酸()和大麻醇(),其 ∆G 值分别为-33.63、-23.24 和-21.60 kcal/mol。关于 SARS-CoV-2 PL,大麻色胺()其次是大麻酸()和大麻环酸(),由于与 ∆G 值为-28.36、-22.81 和 -19.89 kcal/mol 的多个键形成,在其活性口袋中表现出最佳结合。此外,大麻色胺()、大麻酸()和大麻醇()在血管紧张素转换酶 2(ACE2)的活性部位表现出相当大的拟合,这表明它们的 ∆G 值分别估计为-41.77、-31.34 和-30.36 kcal/mol。对测试大麻素进行了 ADME/TOPKAT(吸收、分布、代谢、排泄和毒性)评估,以进一步探索它们的药代动力学、药效学和毒性特性。结果表明,大麻醇()、大麻酸()、大麻色胺()和大麻环酸()具有相当的药代动力学、药效学和毒性特性,它们在测试酶的活性部位表现出最佳的拟合分数。多元数据分析表明,大麻色胺和大麻酸具有判别性质,因此可以被纳入药物剂型以缓解 COVID-19 感染。