Titlebook: Chemotherapy of Viral Infections; Paul E. Came,Lawrence A. Caliguiri Book 1982 Springer-Verlag Berlin Heidelberg 1982 Arzneitherapie.Infec

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Yi Deng,Akshay Rajhans,A. Agung Juliusiral activity with promising results. One of these compounds, arildone, was extensively studied and shown to be active against a wide variety of DNA and RNA viruses in vitro. In addition, arildone was shown to be effective against herpesvirus infections in vivo. Arildone and its metabolites were wel

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https://doi.org/10.1007/978-3-642-40916-5s such as rauwolfia alkaloids, opium, belladonna, and digitalis continue to be used in modern medicine. With the exception of antibiotics, the use of natural substances in the area of infectious disease has not met with the success apparent in other areas of human disease. Until Pasteur, Koch, Semme

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https://doi.org/10.1007/978-3-642-41002-4a an aliphatic ansa chain. Originally, a mixture of five compounds, designated rifamycins A–E, was isolated from the fermentation broth of . (. et al. 1959 a, b). It was subsequently found that one of the compounds, rifamycin B, was produced almost exclusively when sodium diethylbarbiturate was pres

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Handbook of Experimental Pharmacologyhttp://image.papertrans.cn/c/image/224976.jpg

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https://doi.org/10.1007/978-3-642-37688-7United States. However, despite the demonstrated efficacy of this compound in the prophylaxis (and more recently in the treatment) of influenza A virus infections, it has never been widely employed and its recommended use remains the subject of considerable controversy (. 1978).