19-Hydroxyeicosatetraenoic acid analogs: Antagonism of 20-hydroxyeicosatetraenoic acid-induced vascular sensitization and hypertension

[Display omitted] 19-Hydroxyeicosatetraenoic acid (19-HETE, 1), a metabolically and chemically labile cytochrome P450 eicosanoid, has diverse biological activities including antagonism of the vasoconstrictor 20-hydroxyeicosatetraenoic acid (20-HETE, 2). A SAR study was conducted to develop robust an...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2019-10, Vol.29 (19), p.126616-126616, Article 126616
Hauptverfasser: Dakarapu, Rambabu, Errabelli, Ramu, Manthati, Vijaya L., Michael Adebesin, Adeniyi, Barma, Deb K., Barma, Deepan, Garcia, Victor, Zhang, Fan, Laniado Schwartzman, Michal, Falck, John R.
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Sprache:eng
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Zusammenfassung:[Display omitted] 19-Hydroxyeicosatetraenoic acid (19-HETE, 1), a metabolically and chemically labile cytochrome P450 eicosanoid, has diverse biological activities including antagonism of the vasoconstrictor 20-hydroxyeicosatetraenoic acid (20-HETE, 2). A SAR study was conducted to develop robust analogs of 1 with improved in vitro and in vivo efficacy. Analogs were screened in vitro for inhibition of 20-HETE-induced sensitization of rat renal preglomerular microvessels toward phenylephrine and demonstrated to normalize the blood pressure of male Cyp4a14(-/-) mice that display androgen-driven, 20-HETE-dependent hypertension.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2019.08.020