In vitro mutagenicity of anti-inflammatory parsalmide analogues PA7, PA10, and PA31 triggered by biotransformation into hydroxy derivatives-Reference-Cited by-同舟云学术

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In vitro mutagenicity of anti-inflammatory parsalmide analogues PA7, PA10, and PA31 triggered by biotransformation into hydroxy derivatives

Published:2006-03 Issue:3 Volume:41 Page:408-416
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Cardoso H.S.,Bicalho B.,Genari P.,Santagada V.,Caliendo G.,Perissutti E.,Donato J.L.,De Nucci G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference30 articles.

1. The non-steroidal anti-inflammatory agent parsalmide prevents aspirin-induced H+ back diffusion from the gastric lumen of the rat

2. Synthesis of substituted benzamides as anti-inflammatory agents that inhibit preferentially cyclooxygenase 1 but do not cause gastric damage

3. The Role of Cytochrome P450 in Cytotoxic Bioactivation: Future Therapeutic Directions

4. Idiosyncratic toxicity: the role of toxicophores and bioactivation

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2. The Brazilian medicinal chemistry from 1998 to 2008 in the Journal of Medicinal Chemistry, Bioorganic and Medicinal Chemistry, Bioorganic and Medicinal Chemistry Letters and European Journal of Medicinal Chemistry;Revista Virtual de Química;2009

3. Pharmacokinetic Profile of Atenolol Aspirinate;Archiv der Pharmazie;2007-09

4. Facile synthesis of non-steroidal anti-inflammatory active bisbenzamide-containing compounds;Bioorganic & Medicinal Chemistry;2006-12

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