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Titlebook: Razoxane and Dexrazoxane - Two Multifunctional Agents; Experimental and Cli Kurt Hellmann,Walter Rhomberg Book 2011 Springer Science+Busine

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11#
發(fā)表于 2025-3-23 10:18:47 | 只看該作者
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發(fā)表于 2025-3-23 17:39:34 | 只看該作者
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發(fā)表于 2025-3-23 20:02:13 | 只看該作者
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發(fā)表于 2025-3-24 01:05:36 | 只看該作者
dexrazoxane are two novel drugs with some uniquely useful features. They block cell division at the G2/M border, but nowhere else, so that they have a low toxicity profile. They suppress tumor metastasis and haemorrhages through normalization of pathological blood vessels. Razoxane potentiates radi
15#
發(fā)表于 2025-3-24 02:26:20 | 只看該作者
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發(fā)表于 2025-3-24 08:21:58 | 只看該作者
Introduction,dexrazoxane (ICRF-187) which are the subject of this book. Their history dates back to 1965 and gradually revealed a variety of modes of action which are as unexpected as they are unique – at present. The influence of razoxane and dexrazoxane on the differentiation of a pathologic neovasculature of
17#
發(fā)表于 2025-3-24 13:25:21 | 只看該作者
Razoxane,mmarized, e.g. the block of the cell cycle in the G2/M phase, the antimetastatic and antiinvasive activity, the ability to normalize pathological tumor blood vessels, the inhibition of topoisomerase II α, and the metal chelating activity. These activites are associated with a marked radiosensitizati
18#
發(fā)表于 2025-3-24 14:52:48 | 只看該作者
Dexrazoxane,. Dexrazoxane has two potential pharmacological activities: it is a prodrug that is hydrolyzed to an iron chelating EDTA-type structure, and it is also a strong inhibitor of topoisomerase II. The anthracycline doxorubicin is able to be reductively activated to produce damaging reactive oxygen specie
19#
發(fā)表于 2025-3-24 20:58:25 | 只看該作者
Summary and Outlook,antiinvasive activity in preclinical experiments, and they are able to normalize pathological tumour blood vessels. In addition, the drugs inhibit topoisomerase II α (the full implications have yet to emerge) and they are powerful chelating agents which not only chelate iron, but also a variety of o
20#
發(fā)表于 2025-3-25 01:31:49 | 只看該作者
Introduction,s an impressive cytoprotective activity in mitigating accidental anthracycline extravasation. In retrospect, the history of the two drugs justifies random screening as a valid method for the discovery of novel and effective drugs.
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