化学
洛比那韦
效力
对接(动物)
部分
生物利用度
药理学
蛋白酶
人类免疫缺陷病毒(HIV)
铅化合物
生物化学
丝氨酸蛋白酶
药品
结构-活动关系
小分子
HIV-1蛋白酶
酶抑制剂
抑制性突触后电位
酶
结合位点
蛋白酶抑制剂(药理学)
立体化学
组合化学
药代动力学
作者
Danwen Qiu,Komal Hayat,Yuanyuan Wang,Konstantinos Douroudis,Md Imtaiyaz Hassan,Faez Iqbal Khan,Magdalini Matziari
摘要
Human immunodeficiency virus (HIV) remains a significant health issue with no vaccine available. Targeting the HIV‐1 protease (HIV‐1 PR) is essential in treatment, with inhibitors like lopinavir being historically an important component. However, lopinavir alone has low bioavailability and causes side effects when combined with ritonavir, leading to efforts to develop improved analogs. In this study, we designed and synthesized a phosphinic analog of lopinavir, PL1, by replacing its hydroxyethylene moiety with a phosphinic group. The inhibitory evaluation demonstrated a promising inhibition potency of PL1 against HIV‐1 PR, supported by molecular dynamics simulations predicting its favorable interactions. Integrating AI‐based docking tools confirmed PL1’s strong potential, with an IC 50 /EC 50 of 1.32 × 10 −8 mol/L and a binding affinity of 6.142, surpassing lopinavir’s 5.928. PL1’s binding efficacy index of 0.0119, comparable to lopinavir’s 0.0132, indicates efficient inhibition. Importantly, PL1 is less toxic than lopinavir, making it a promising lead molecule for HIV‐1 PR targeting.
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