Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education; Yunnan Provincial Center for Research & Development of Natural Products; School of Chemical Science and Technology, Yunnan University, Kunming 650091, P. R. China.
Inorg Chem. 2022 Jul 18;61(28):10774-10780. doi: 10.1021/acs.inorgchem.2c00975. Epub 2022 Jul 7.
HIV-1 reverse transcriptase (RT) inhibitors are fundamental to the discovery and development of anti-HIV drugs. Their main target is RT, and only a tiny number of them can bind to viral RNA. In this paper, five new Zn(II) porphyrin compounds were developed with different characters. has both the appearance and the functions of a scorpion with a rigid tail and stinger to selectively hunt HIV-1 TAR RNA based on the molecular recognition of hydrogen bonds, a fierce chelicera to bite RNA by metal coordination, mighty pedipalps to grasp the bound RNA by supramolecular inclusion, and a broad body maintaining the configuration of each functional area so that they can cooperate with each other and providing accommodation space for the bound RNA. This tetrafunctional Zn(II) porphyrin is relatively nontoxic to normal cells and can produce sensitive responses for RNA. Moreover, this work offers practical construction methodologies for medication of AIDS and other diseases closely related to RT like EBOV and SARS-CoV-2.
HIV-1 逆转录酶(RT)抑制剂是发现和开发抗 HIV 药物的基础。它们的主要靶标是 RT,而且只有极少数能够与病毒 RNA 结合。在本文中,我们开发了五种具有不同性质的新型 Zn(II)卟啉化合物。基于氢键的分子识别, 具有刚性尾巴和毒刺的蝎子外观和功能,以选择性地猎取 HIV-1 TAR RNA,凶猛的螯肢通过金属配位来咬 RNA,强大的触须通过超分子包合来抓住结合的 RNA,宽阔的身体保持每个功能区域的构型,以便它们能够相互配合,并为结合的 RNA 提供容纳空间。这种四功能 Zn(II)卟啉对正常细胞相对无毒,并且可以对 RNA 产生敏感反应。此外,这项工作为治疗艾滋病和其他与 RT 密切相关的疾病(如 EBOV 和 SARS-CoV-2)提供了实用的药物构建方法。