Structure-based Design of Indole Propionic Acids as Novel PPARag CO-Agonists
收藏Protein Data Bank Japan2024-04-03 更新2026-03-21 收录
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https://pdbj.org/mine/summary/2gtk
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Structure-based Design of Indole Propionic Acids as Novel PPARag CO-Agonists Descriptor: (2S)-3-(1-{[2-(2-CHLOROPHENYL)-5-METHYL-1,3-OXAZOL-4-YL]METHYL}-1H-INDOL-5-YL)-2-ETHOXYPROPANOIC ACID, Decamer from Nuclear receptor coactivator 1, Peroxisome proliferator-activated receptor gamma Authors: Kuhn, B, Hilpert, H, Benz, J, Binggeli, A, Grether, U, Humm, R, Maerki, H.-P, Meyer, M, Mohr, P. Deposit date: 2006-04-28 Release date: 2006-09-26 Last modified: 2024-04-03 Method: X-RAY DIFFRACTION (2.1 Å) Cite: Structure-based design of indole propionic acids as novel PPARalpha/gamma co-agonists Bioorg.Med.Chem.Lett., 16, 2006
创建时间：
2006-04-28
