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Titlebook: Deoxynucleoside Analogs in Cancer Therapy; Godefridus J. Peters (Professor of Medical Oncolog Book 2006 Humana Press 2006 HIV.cancer.cance

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发表于 2025-3-21 17:34:01 | 显示全部楼层 |阅读模式
书目名称Deoxynucleoside Analogs in Cancer Therapy
编辑Godefridus J. Peters (Professor of Medical Oncolog
视频video
概述Includes supplementary material:
丛书名称Cancer Drug Discovery and Development
图书封面Titlebook: Deoxynucleoside Analogs in Cancer Therapy;  Godefridus J. Peters (Professor of Medical Oncolog Book 2006 Humana Press 2006 HIV.cancer.cance
描述Successful cancer chemotherapy relies heavily on the application of various deoxynucleoside analogs. Since the very beginning of modern cancer chemotherapy, a number of antimetabolites have been introduced into the clinic and subsequently applied widely for the treatment of many malignancies, both solid tumors and hematological disorders. In the latter diseases, cytarabine has been the mainstay of treatment of acute myeloid leukemia. Although many novel compounds were synthesized in the 1980s and 1990s, no real improvement was made. However, novel technology is now capable of elucidating the molecular basis of several inborn errors as well as some specific malignancies. This has enabled the synthesis of several deoxynucleoside analogs that could be applied for specific malignancies, such as pentostatin and subsequently chlorodeoxyadenosine (cladribine) for the treatment of hairy cell leukemia. Already in the early stage of deoxynucleoside analog development, it was recognized that several of these compounds were very effective in the treatment of various viral infections, such as for the treatment of herpes infections. This formed the basis initially for the design of azidothymidin
出版日期Book 2006
关键词HIV; cancer; cancer therapy; cell; chemotherapy; drug; drug discovery; gene therapy; kinetics; leukemia; metab
版次1
doihttps://doi.org/10.1007/978-1-59745-148-2
isbn_softcover978-1-61737-497-5
isbn_ebook978-1-59745-148-2Series ISSN 2196-9906 Series E-ISSN 2196-9914
issn_series 2196-9906
copyrightHumana Press 2006
The information of publication is updating

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Wolfgang Beitz,Karl-Heinz KüttnerGX Pharmaceuticals, Inc.) is the first nucleoside analog with anticancer activity that has an unnatural stereochemical configuration. Its broad preclinical antineoplastic spectrum led to its clinical development. Summaries of the preclinical data and of the initial phase I and II clinical trials are presented.
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Hydrostatik (Statik der Flüssigkeiten)ionales to be evaluated with minimal likelihood of untoward toxicity. Exploration of additional schedules and combinations along with availability of an oral formulation strongly indicate promising possibilities with this agent.
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Clofarabine,ionales to be evaluated with minimal likelihood of untoward toxicity. Exploration of additional schedules and combinations along with availability of an oral formulation strongly indicate promising possibilities with this agent.
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Kurven und Flächen, Vektoranalysisand FLT. Consequently, FLT labeled with .F is a PET tracer of TK1 activity, and as such an indirect marker of DNA synthesizing activity and cell proliferation. Potential applications of FLT are in detecting and staging tumors.
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Ergänzungen zur Mathematik für Ingenieurenation chemotherapy based on its multiple mechanisms of action and relatively mild toxicity profile. This chapter summarizes the current preclinical and clinical knowledge of gemcitabine as a single agent and in combinations in non-small cell lung cancer, and pancreatic, bladder, breast, ovarian, gastric, and esophageal cancer.
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