Ls Ukrainian Gentle Angels Sets 126 150 Zip [NEW]
公開日:2022/07/02 / 最終更新日:2022/07/02
Ls Ukrainian Gentle Angels Sets 126 150 Zip [NEW]
Ls Ukrainian Gentle Angels Sets 126 150 Zip
Under Ls Ukrainian (Gentle) Angels Sets 126 150 Description. Comments. 636
Ls Ukrainian (Gentle) Angels Sets 126 150 Zip
Synthetic, anti-HIV nucleoside-sparing therapy.
This review focuses on the most recent developments in AIDS research in the fields of anti-HIV nucleoside analogues (NRTI) and non-NRTI anti-HIV agents. A summary of new, patented nucleoside analogue classes is presented, including anti-HIV nucleosides, inhibitors of hepatitis C replication, and nucleosides as genetic targets. New, non-NRTI agents also have demonstrated anti-HIV activities. Of particular interest are the quinolone-derived diaryltetrahydrofurans (DHAs) and diaryltriazinones (DTAs) that have been found to have potent anti-HIV activity in vitro. Another interesting class of compounds is 5′-alkynyl-2′,3′-dideoxyadenosine (S-DABS), which is a nucleoside metabolite that inhibits HIV-1 replication. Finally, details are presented on the mode of action of each compound class and how the data can be interpreted in the context of anti-HIV therapy. In a recent survey of approximately 200 companies that are interested in anti-HIV research, more than 75% were interested in inducers of the 5′-nucleotidase enzyme that is responsible for the metabolism of nucleoside compounds, while more than 70% of these companies are interested in compounds that function by indirect action, including those that inhibit virus assembly or membrane fusion. Thus, the newly emerging compounds in the categories of ‘indirect’ nucleoside analogue activities, including NRTI and ‘nucleic acid’ based activities, should be highlighted in the development of combination drug therapies. In this regard, dideoxy-cytidine (ddC) is, to date, the most successful agent used in the treatment of AIDS, and the structure of this compound is thought to be critical in its anti-HIV activity. The newly developed NRTI and ‘nucleic acid’ agents described here may, however, have similar or greater potency and/or anti-HIV activity. The purpose of the review is to describe the current status of anti-HIV research to provide the new agent-based developments in an easily accessed format.The present invention pertains to
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