Discovery of 6-({4-[2-(4-tert-Butylphenyl)-1H-benzimidazol-4-yl]piperazin-1-yl}methyl)quinoxaline (WAY-207024): An Orally Active Antagonist of the Gonadotropin Releasing Hormone Receptor (GnRH-R)

A potent, highly insoluble, GnRH antagonist with a 2-phenyl-4-piperazinylbenzimidazole template and a quinoxaline-2,3-dione pharmacophore was modified to maintain GnRH antagonist activity and improve in vitro pharmaceutical properties. Structural changes to the quinoxaline-2,3-dione portion of the m...

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Veröffentlicht in:Journal of medicinal chemistry 2009-04, Vol.52 (7), p.2148-2152
Hauptverfasser: Pelletier, Jeffrey C, Chengalvala, Murty V, Cottom, Joshua E, Feingold, Irene B, Green, Daniel M, Hauze, Diane B, Huselton, Christine A, Jetter, James W, Kopf, Gregory S, Lundquist, Joseph T, Magolda, Ronald L, Mann, Charles W, Mehlmann, John F, Rogers, John F, Shanno, Linda K, Adams, William R, Tio, Cesario O, Wrobel, Jay E
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Sprache:eng
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Zusammenfassung:A potent, highly insoluble, GnRH antagonist with a 2-phenyl-4-piperazinylbenzimidazole template and a quinoxaline-2,3-dione pharmacophore was modified to maintain GnRH antagonist activity and improve in vitro pharmaceutical properties. Structural changes to the quinoxaline-2,3-dione portion of the molecule resulted in several structures with improved properties and culminated in the discovery of 6-({4-[2-(4-tert-butylphenyl)-1H-benzimidazol-4-yl]piperazin-1-yl}methyl)quinoxaline (WAY-207024). The compound was shown to have excellent pharmacokinetic parameters and lowered rat plasma LH levels after oral administration.
ISSN:0022-2623
1520-4804
DOI:10.1021/jm801572m