BXT-51072 and the Prevention of Myocardial Ischemia-Reperfusion Injury
Authors: Asaf, Roy; Blum, Shany; Miller-Lotan, Rachel; Levy, Andrew P.
Source: Letters in Drug Design & Discovery, Volume 4, Number 2, March 2007 , pp. 160-162(3)
Publisher: Bentham Science Publishers
Abstract:
Oxidative stress is responsible for myocardial injury occurring after ischemia and reperfusion (IR) and has been shown to be modulated by the Haptoglobin (Hp) genotype. In this manuscript we demonstrate that the antioxidant BXT -51072, a glutathione peroxidase synthetic mimic, provides protection against IR injury in a Hp genotype dependent fashion.Keywords: Diabetes; Myocardial ischemia-reperfusion; Oxidative stress; BXT-51072
Document Type: Research article
DOI: http://dx.doi.org/10.2174/157018007779422479
Affiliations: 1: Technion Faculty of Medicine, Haifa, 31096, Israel.
Publication date: 2007-03-01
- Letters in Drug Design & Discovery publishes original letters on all areas of rational drug design and discovery including medicinal chemistry, in-silico drug design, combinatorial chemistry, high-throughput screening, drug targets, and structure-activity relationships. The emphasis will be on publishing quality papers very rapidly. Letters will be processed rapidly by taking full advantage of Internet technology for both the submission and review of manuscripts. The journal is essential reading to all pharmaceutical scientists involved in research in drug design and discovery.
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- By this: publisher
- In this Subject: Biotechnology , Pharmacology
- By this author: Asaf, Roy ; Blum, Shany ; Miller-Lotan, Rachel ; Levy, Andrew P.

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