Read e-book online Antiviral Drugs: From Basic Discovery Through Clinical PDF

By Wieslaw M. Kazmierski

ISBN-10: 0470455632

ISBN-13: 9780470455630

This booklet makes a speciality of new small molecule techniques to wrestle viral infections. The chapters describe the invention and improvement from bench throughout the hospital of fairly recently-approved antiviral medicines and compounds in complicated medical improvement. equipped through an epidemic (such as HIV, HCV, RSV, influenza, HBV and CMV) and written through best educational and business gurus within the box, the booklet offers a different chance to check, comprehend and observe discovery and improvement ideas and studying with out the necessity for somebody to analyze, examine and synthesize all tremendous sourcing references.  subject matters show off demanding situations and strategies of concerns encountered, offering tremendous event amassed over a long time of analysis that might be quite precious to easy and bench scientists in addition to clinicians as they proceed learning and constructing new medicinal drugs and remedies.

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Extra info for Antiviral Drugs: From Basic Discovery Through Clinical Trials

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In the absence of any adverse effects on mating, fertility, or reproductive performance or microscopic changes in the ovaries and female reproductive tract in toxicity studies, the perturbation of estrous cyclicity in female rats was considered to be of limited toxicological significance. 5 (F) times the human exposure with 300 mg/day atazanavir with ritonavir. 9 times the human exposure with 300 mg/day atazanavir with ritonavir, or 400 mg/day atazanavir dose, respectively. In the embryo–fetal development studies, atazanavir produced no adverse embryonic or fetal effects at maternally toxic doses (up to 1920 mg/kg per day in rats and 60 mg/kg per day in rabbits).

Mulder, J. ; Beijnen, J. ; Huitema, A. D. R. Identification and profiling of circulating metabolites of atazanavir, a HIV protease inhibitor. Drug Metab. Dispos. 2009, 37, 1826–1840. [11] Williams, G. ; Whysner, J. Epigenetic carcinogens: evaluation and risk assessment. Exp. Toxicol. Pathol. 1996, 48, 189–195. [12] Williams, G. ; Iatropoulos, M. ; Weisburger, J. H. Chemical carcinogen mechanisms of action and implications for testing methodology. Exp. Toxicol. Pathol. 1996, 48, 101–111. [13] Lima, B.

Atazanavir is currently approved unboosted for antiretroviral-naive patients who cannot tolerate ritonavir and boosted with ritonavir for both antiretroviral-naive and antiretroviral-experienced patients. Atazanavir is being evaluated in new treatment paradigms as antiretroviral therapy, and patients’ medical needs continue to evolve. ; Lang, M. Novel pseudosymmetric inhibitors of HIV-1 protease. Bioorg. Med. Chem. Lett. 1993, 3, 2837–2842. 15 [2] Sham, H. ; Marsh, K. ; Betebenner, D. ; et al. Potent inhibitors of the HIV-1 protease with good oral bioavailabilities.

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Antiviral Drugs: From Basic Discovery Through Clinical Trials by Wieslaw M. Kazmierski


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