Discovery And Sar Study Of Furan-2-Carbohydrazides As Orally Active Glucagon Receptor Antagonists

Futoshi Hasegawa, Akihito Fujii, Kazumi Niidome,Daisuke Tanaka, Chiaki Migihashi,Yasunao Inoue,Shigeo Ueda, Tomoki Omodani,Makoto Murata, Tomoyuki Hirata,Kaori Kato,Takafumi Matsumoto

Bioorganic & Medicinal Chemistry Letters(2013)

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摘要
Furan-2-carbohydrazides were found as orally active glucagon receptor antagonists. Starting from the hit compound 5, we successfully determined the structure activity relationships of a series of derivatives obtained by modifying the acidity of the phenol. We identified the ortho-nitrophenol as a good scaffold for glucagon receptor inhibitory activity. Our efforts have led to the discovery of compound 7l as a potent glucagon receptor antagonist with good bioavailability and satisfactory long half-life.
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关键词
Glucagon,Type 2 diabetes,Furan-2-carbohydrazide,Glucagon receptor antagonist,Hyperglucagonemia
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