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Titlebook: Chemotherapy; Volume 8 Cancer Chem K. Hellmann,T. A. Connors Book 1976 Plenum Press, New York 1976 cancer.chemotherapy.kinetics.pharmacokin

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书目名称Chemotherapy
副标题Volume 8 Cancer Chem
编辑K. Hellmann,T. A. Connors
视频video
丛书名称Chemotherapy
图书封面Titlebook: Chemotherapy; Volume 8 Cancer Chem K. Hellmann,T. A. Connors Book 1976 Plenum Press, New York 1976 cancer.chemotherapy.kinetics.pharmacokin
描述The International Society of Chemotherapy meets every two years to review progress in chemotherapy of infections and of malignant disease. Each meeting gets larger to encompass the extension of chemotherapy into new areas. In some instances, exp~sion has been rapid, for example in cephalosporins, pen­ icillins and combination chemotherapy of cancer - in others slow, as in the field of parasitology. New problems of resistance and untoward effects arise; reduction of host toxicity without loss of antitumour activity by new substances occupies wide attention. The improved results with cancer chemotherapy, es­ pecially in leukaemias, are leading to a greater prevalence of severe infection in patients so treated, pharmacokinetics of drugs in normal and diseased subjects is rece1v1ng increasing attention along with related problems of bioavailability and interactions between drugs. Meanwhile the attack on some of the major bacterial infections, such as gonorrhoea and tubercu­ losis, which were among the first infections to feel the impact of chemotherapy, still continue to be major world problems and are now under attack with new agents and new methods. From this wide field and the 1,000
出版日期Book 1976
关键词cancer; chemotherapy; kinetics; pharmacokinetics; research; resistance; toxicity
版次1
doihttps://doi.org/10.1007/978-1-4613-4352-3
isbn_softcover978-1-4613-4354-7
isbn_ebook978-1-4613-4352-3
copyrightPlenum Press, New York 1976
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,Operational Mappings – Anwendungen,lear that FT-207 is a masked or transport form. Therefore although FT-207 itself shows a very week direct activity against tumor cells, after entering the body, FT-207 is activated to 5-FU and thus becomes a potent carcinostatic substance.
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978-1-4613-4354-7Plenum Press, New York 1976
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Chemotherapyhttp://image.papertrans.cn/c/image/224962.jpg
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https://doi.org/10.1007/978-3-642-00292-2Mimosine, β-N-(3-hydroxy-4-pyridone) α-aminopropionic acid, and its hydrochloride produced significant inhibition of subcutaneously transplanted murine B16 melanoma in BDF. female mice. In such mice during mimosine treatment differences developed in the reactivity of both surface membrane and cytoplasmic antigens as compared to untreated cells.
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Christian Flender,Kirsty Kitto,Peter BruzaIn a series of 4-Amino-7-Nitrobenzofuroxans, those with 4-piperazinyl substituents showed significant antitumour activity in mice.
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