Synthesis and pharmacological characterization of potent, selective, and orally bioavailable isoindoline class dipeptidyl peptidase IV inhibitors.

Noriyasu Kato, Mitsuru Oka, Takayo Murase, Masahiro Yoshida, Masao Sakairi, Mirensha Yakufu, Satoko Yamashita, Yoshika Yasuda, Aya Yoshikawa, Yuji Hayashi, Masahiro Shirai, Yukie Mizuno, Mitsuaki Takeuchi, Mitsuhiro Makino, Motohiro Takeda, Takuji Kakigami
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引用次数: 20

Abstract

Focused structure-activity relationships of isoindoline class DPP-IV inhibitors have led to the discovery of 4b as a highly selective, potent inhibitor of DPP-IV. In vivo studies in Wistar/ST rats showed that 4b was converted into the strongly active metabolite 4l in high yield, resulting in good in vivo efficacy for antihyperglycemic activity.

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强效、选择性和口服生物可利用的异吲哚啉类二肽基肽酶IV抑制剂的合成和药理学表征。
关注异吲哚啉类DPP-IV抑制剂的结构-活性关系导致发现4b是DPP-IV的高选择性有效抑制剂。Wistar/ST大鼠体内实验表明,4b能高产地转化为活性强的代谢产物4l,具有良好的体内降糖活性。
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