Feasible Synthesis of Antagonist of GPR40 by Constructing 2-Thiouracil Ring viaAcid Mediated Cyclization.

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Pharmacology and physiology of gastrointestinal enteroendocrine cells Activation of GPR40 as a therapeutic target for the treatment of type 2 diabetes.

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Feasible Synthesis of Antagonist of GPR40 by Constructing 2-Thiouracil Ring viaAcid Mediated Cyclization.

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2011 nî lūn-bûn

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2011年論文

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Feasible Synthesis of Antagoni ...... viaAcid Mediated Cyclization.

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Feasible Synthesis of Antagoni ...... viaAcid Mediated Cyclization.

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Feasible Synthesis of Antagoni ...... viaAcid Mediated Cyclization.

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Feasible Synthesis of Antagoni ...... viaAcid Mediated Cyclization.

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Feasible Synthesis of Antagoni ...... viaAcid Mediated Cyclization.

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Feasible Synthesis of Antagoni ...... viaAcid Mediated Cyclization.

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P1476

Feasible Synthesis of Antagoni ...... viaAcid Mediated Cyclization.

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P2093

Jiayu Liao

http://www.w3.org/2001/XMLSchema#string

Xiulin Shen

http://www.w3.org/2001/XMLSchema#string

Yang Song

http://www.w3.org/2001/XMLSchema#string

Yongfeng Zhao

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P2860

Free fatty acids regulate insulin secretion from pancreatic beta cells through GPR40.

Synthesis and evaluation of a new series of substituted acyl(thio)urea and thiadiazolo [2,3-a] pyrimidine derivatives as potent inhibitors of influenza virus neuraminidase.

Pharmacological regulation of insulin secretion in MIN6 cells through the fatty acid receptor GPR40: identification of agonist and antagonist small molecules.

Total synthesis of pinnamine and anatoxin-a via a common intermediate. A caveat on the anatoxin-a endgame.

The FFA receptor GPR40 links hyperinsulinemia, hepatic steatosis, and impaired glucose homeostasis in mouse.

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1145-1151

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scholarly article

P356

10.3987/COM-11-12175

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2011-05-01T00:00:00Z

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51508710

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21776181

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3137925

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Feasible Synthesis of Antagonist of GPR40 by Constructing 2-Thiouracil Ring viaAcid Mediated Cyclization.

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P2860

P2860

Feasible Synthesis of Antagonist of GPR40 by Constructing 2-Thiouracil Ring viaAcid Mediated Cyclization.

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