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Titlebook: Nucleosides and Nucleotides as Antitumor and Antiviral Agents; Chung K. Chu,David C. Baker Book 1993 Springer Science+Business Media New Y

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书目名称Nucleosides and Nucleotides as Antitumor and Antiviral Agents
编辑Chung K. Chu,David C. Baker
视频video
图书封面Titlebook: Nucleosides and Nucleotides as Antitumor and Antiviral Agents;  Chung K. Chu,David C. Baker Book 1993 Springer Science+Business Media New Y
描述Due to the worldwide epidemic of acquired immunodeficiency syndrome (AIDS), the past ten years have witnessed a flurry of activity in the chemotherapy of viral diseases. Unprecedented scientific efforts have been made by scientists and clinicians to combat infections of human immunodeficiency virus (HIY), the causative agent. Looking back over the past ten years, we have made remarkable progress toward the treatment of the viral disease: isolation of HIV only two years after the identification of the disease, plus major strides in the areas of the molecular biology and virology of the retrovirus, etc. More remarkably, the discovery of the chemotherapeutic agent AZT (Retrovir) was made within two years after the isolation and identification of the virus, followed by unprecedented drug development efforts to culminate in the FDA approval of AZT in twenty-three months, which was a record-breaking time for approval of any drug for a major disease. The last six to seven years have particularly been an exciting and productive period for nucleoside chemists. Since the activity of AZI‘ was established in 1985, nucleoside chemists have had golden opportunities to discover additional anti-HI
出版日期Book 1993
关键词AIDS; HIV; biology; cancer; chemistry; chemotherapy; development; diseases; drug; drug development; molecular
版次1
doihttps://doi.org/10.1007/978-1-4615-2824-1
isbn_softcover978-1-4613-6221-0
isbn_ebook978-1-4615-2824-1
copyrightSpringer Science+Business Media New York 1993
The information of publication is updating

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Lithiation Chemistry of Uridine Derivatives: Access to a New Anti-HIV-1 Lead,erstanding of the reaction mechanism.. Since a number of functional groups have been recognized to have ortho-directing ability,. and since lithiated species usually react with a wide range of electrophiles under mild conditions, lithiation strategy has become an efficient alternative to classical electrophilic aromatic substitution.
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emotherapy of viral diseases. Unprecedented scientific efforts have been made by scientists and clinicians to combat infections of human immunodeficiency virus (HIY), the causative agent. Looking back over the past ten years, we have made remarkable progress toward the treatment of the viral disease
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,Allenols Derived from Nucleic Acid Bases — A New Class of Anti-HIV Agents: Chemistry and Biologicalles of two structurally different classes of nucleoside analogues. Acyclovir (1a) belongs to a series of open-chain compounds derived by cleavage of at least one C-C bond or deletion of one or more carbon atoms of the sugar ring, whereas AZT (3b) comprises an intact furanose moiety.
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,Adenosine-Derived 5′-α-Halo Thioether, Sulfoxide, Sulfone, and (5′-Halo)Methylene Analogues. Inhibidation/elimination processes.. It had been demonstrated that 4′,5′-didehydro-5′-deoxyadenosine [9-(5-deoxy-ß-D-erythro-pent-4-enofuranosyl)adenine, 6] was accepted as an alternative substrate by AdoHcy hydrolase and converted into Ado and AdoHcy.. Therefore, we also targeted 5′-halo analogues of 6 a
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