Antiviral Nucleosides-Flu Viruses-Quinolines-COVID-19

Krishnasarma Pathy
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Abstract

Hydroquinone as a volatile aromatic hydrocarbon; There is a huge confusion in the public, as well as among politicians and even some scientists, about those two molecules. That confusion ultimately led to people accidently overdosing. Both molecules can be classified as 4-aminoquinolines, and both have anti-plasmodial activities, but they remain two different molecules with some different metabolites. Chloroquine has been widely used since the 1950s for prophylactic and curative treatments of malaria. Its extensive use has led to the emergence of chloroquine-resistant strains of Plasmodium falciparum, the parasite responsible for the severest form of malaria. Such strains are also resistant to the structurally related hydroxychloroquine. This article describes how Guanosine andHydroxychloroquineiscommercially prepared. Also, we have recently prepared several processes leading to known antiviral agents starting with guanosine. The processes developed by using enzymatic transglycosylation for stavudine (d4T), chemical transpurination for acyclovir and ganciclovir, and novel alkylation for penciclovir and famciclovir.
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抗病毒核苷类-流感病毒-喹啉类- covid -19
对苯二酚是一种挥发性芳烃;公众、政治家甚至一些科学家对这两种分子存在着巨大的困惑。这种混乱最终导致人们意外过量服用。这两种分子都可以归类为4-氨基喹啉类,都具有抗疟原虫活性,但它们仍然是两种不同的分子,有一些不同的代谢产物。自20世纪50年代以来,氯喹已被广泛用于疟疾的预防和治疗。它的广泛使用导致了氯喹耐药恶性疟原虫菌株的出现,恶性疟原虫是导致最严重形式疟疾的寄生虫。这些菌株也对结构上相关的羟氯喹具有耐药性。本文介绍了鸟苷和羟氯喹的商业制备方法。此外,我们最近准备了几个过程,导致从鸟苷开始的已知抗病毒药物。采用酶转糖基化法合成司他夫定(d4T),化学转尿法合成阿昔洛韦和更昔洛韦,烷基化法合成喷昔洛韦和泛昔洛韦。
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