Co-crystal structure of Inhibitor compound in complex with human PPARdelta LBD
收藏Protein Data Bank Japan2023-11-22 更新2026-03-21 收录
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Co-crystal structure of Inhibitor compound in complex with human PPARdelta LBD Descriptor: (E)-6-[2-[[[4-(furan-2-yl)phenyl]carbonyl-methyl-amino]methyl]phenoxy]-4-methyl-hex-4-enoic acid, Peroxisome proliferator-activated receptor delta Authors: Lakshminarasimhan, A, Rani, S.T, Senaiar, R.S, Krishnamurthy, N. Deposit date: 2017-05-16 Release date: 2018-05-23 Last modified: 2023-11-22 Method: X-RAY DIFFRACTION (2 Å) Cite: Novel highly selective peroxisome proliferator-activated receptor delta (PPAR delta) modulators with pharmacokinetic properties suitable for once-daily oral dosing. Bioorg. Med. Chem. Lett., 27, 2017
创建时间：
2017-05-16
