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Merck
CN
  • Discovery of biaryl anthranilides as full agonists for the high affinity niacin receptor.

Discovery of biaryl anthranilides as full agonists for the high affinity niacin receptor.

Journal of medicinal chemistry (2007-11-13)
Hong C Shen, Fa-Xiang Ding, Silvi Luell, Michael J Forrest, Ester Carballo-Jane, Kenneth K Wu, Tsuei-Ju Wu, Kang Cheng, Larissa C Wilsie, Mihajlo L Krsmanovic, Andrew K Taggart, Ning Ren, Tian-Quan Cai, Qiaolin Deng, Qing Chen, Junying Wang, Michael S Wolff, Xinchun Tong, Tom G Holt, M Gerard Waters, Milton L Hammond, James R Tata, Steven L Colletti
摘要

Biaryl anthranilides are reported as potent and selective full agonists for the high affinity niacin receptor GPR109A. The SAR presented outlines approaches to reduce serum shift and both CYPCYP2C8 and CYP2C9 liabilities, while improving PK and maintaining excellent receptor activity. Compound 2i exhibited good in vivo antilipolytic efficacy while providing a significantly improved therapeutic index over vasodilation (flushing) with respect to niacin in the mouse model.

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Sigma-Aldrich
烟酸, ≥99.5% (HPLC)
Sigma-Aldrich
烟酸, ≥98%
Supelco
烟酸, analytical standard
Sigma-Aldrich
烟酸, BioReagent, suitable for cell culture, suitable for insect cell culture, suitable for plant cell culture, ≥98%
Sigma-Aldrich
烟酸, meets USP testing specifications