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• W2079893326 abstract "Introduction: LTA4H is a bifunctional enzyme with hydrolase and aminopeptidase activities. The hydrolase function of this enzyme specifically catalyzes the rate-limiting step in the conversion of LTA4 to LTB4, one of the most potent chemoattractant and activator of neutrophils. The wealth of in vitro and in vivo data favors in support of LTA4H as an appealing target for the discovery and development of anti-inflammatory drugs. Areas covered: The authors provide an overview of the recent advances on LTA4H inhibitors since 2000. The review details the medicinal chemistry efforts leading to the generation of novel inhibitor chemotypes with desirable drug-like properties as well as the advantages and disadvantages of LTA4H as a desirable therapeutic target. Expert opinion: Most of the LTA4H inhibitors block pro-inflammatory LTB4 biosynthesis by concomitant inhibition of both the hydrolase and aminopeptidase activities of LTA4H. However, the degradation of another endogenous chemoattractant substrate (PGP) by aminopeptidase function of LTA4H was shown, introducing a new anti-inflammatory mission for this pro-inflammatory enzyme. LTA4H inhibitors were also shown to maintain anti-inflammatory lipoxin formation. Hence, the data on new LTA4H inhibitors should be cautiously interpreted with regard to potential repercussions of preventing PGP degradation as well as for the clinical benefits of concomitant lipoxin formation." @default.
• W2079893326 created "2016-06-24" @default.
• W2079893326 creator A5001160108 @default.
• W2079893326 creator A5089670488 @default.
• W2079893326 date "2012-10-25" @default.
• W2079893326 modified "2023-10-04" @default.
• W2079893326 title "Overview of recent drug discovery approaches for new generation leukotriene A₄hydrolase inhibitors" @default.
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• W2079893326 doi "https://doi.org/10.1517/17460441.2013.735228" @default.
• W2079893326 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23095029" @default.
• W2079893326 hasPublicationYear "2012" @default.
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