亲电有机硒化合物和sars-cov-2:促氧化活性作为更有希望的药物作用途径

C. Santi, L. Sancineto, Francesca Mangiavacchi, Cecilia Scimmi, Sougat Misra
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引用次数: 0

摘要

Ebselent最近被报道为Sars-Cov-2主蛋白酶(Mpro)最有效的抑制剂,其亲电共价促氧化活性半胱氨酸145。根据文献中类似的证据,我们可以提出一个普遍的机制,以探索温和的有机硒为中心的亲电试剂在药物化学中的新应用。本文将讨论在Mpro共价和非共价抑制以及新型有机硒化合物抗病毒SARS-Cov2活性领域的新见解
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ELECTROPHILIC ORGANOSELENIUM COMPOUNDS AND SARS-COV-2: PRO-OXIDANT ACTIVITY AS A MORE PROMISING WAY TOWARDS THE DRUGGABILITY
Ebselent has been recently reported as the most efficient hinibitors of Sars-Cov-2 main protease (Mpro) thought the electrophilic covalent pro-oxidation of the reactive Cysteine 145. According to similar evidences in literature we can propose a general mechanism to explore a novel and promising application of mild organoselenium centered electrophiles in medicinal chemistry. New insights in the field of covalent and non-covalent inhibition of Mpro as well as the antiviral SARS-Cov2 activity of novel organoselenium compounds will be here discussed
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ELECTROPHILIC ORGANOSELENIUM COMPOUNDS AND SARS-COV-2: PRO-OXIDANT ACTIVITY AS A MORE PROMISING WAY TOWARDS THE DRUGGABILITY DIRECT SCAVENGING ACTIVITY OF 4,7-DIHYDROXYCOUMARIN DERIVATIVE TOWARDS SERIES OF CHLOROMETHYLPEROXY RADICALS PLATINUM(IV) COMPLEX AND ITS CORRESPONDING LIGAND SUPPRESS CELL MOTILITY AND PROMOTE EXPRESSION OF FRIZZLED-7 RECEPTOR IN COLORECTAL CANCER CELLS A META-HEURISTIC MULTI-OBJECTIVE APPROACH TO THE MODEL SELECTION OF CONVOLUTION NEURAL NETWORKS FOR URINARY BLADDER CANCER DIAGNOSIS NOVEL LIGANDS OF HUMAN CYP7 ENZYMES – POSSIBLE MODULATORS OF CHOLESTEROL BLOOD LEVEL: COMPUTER SIMULATION STUDIES
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