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Discovery of a vorapaxar analog with increased aqueous solubility
Authors:Xia Yan  Chackalamannil Samuel  Greenlee William J  Wang Yuguang  Hu Zhiyong  Root Yuriko  Wong Jesse  Kong Jianshe  Ahn Ho-Sam  Boykow George  Hsieh Yunsheng  Kurowski Stan  Chintala Madhu
Affiliation:Merck Research Laboratories, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA. yan.xia@merck.com
Abstract:An analog of the thrombin receptor antagonist vorapaxar (SCH 530348) with increased aqueous solubility, compound 9c (SCH 602539), was discovered through incorporation of polar substituents on the pyridine ring of the himbacine-derived lead series. This analog retained the excellent potency, pharmacokinetic and safety properties of vorapaxar while increasing the aqueous solubility by 20-fold. Also presented are in vivo evaluations of this compound in a cynomolgus monkey platelet aggregation assay and in a Folts model of thrombosis in anesthetized monkeys.
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