3R01

The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors

3R01 の概要

• エントリーDOI: 10.2210/pdb3r01/pdb
• 関連するPDBエントリー: 3R00 3R02 3R04
• 分子名称: Proto-oncogene serine/threonine-protein kinase pim-1, IMIDAZOLE, 5-bromo-7-methoxy-1-benzofuran-2-carboxylic acid, ... (4 entities in total)
• 機能のキーワード: kinase, pim1, inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor
• 由来する生物種: Homo sapiens (human)
• 細胞内の位置: Isoform 2: Cytoplasm. Isoform 1: Cell membrane: P11309
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34890.33

構造登録者

Liu, J. (登録日: 2011-03-07, 公開日: 2011-05-11, 最終更新日: 2024-02-21)

主引用文献

Xiang, Y.,Hirth, B.,Asmussen, G.,Biemann, H.P.,Bishop, K.A.,Good, A.,Fitzgerald, M.,Gladysheva, T.,Jain, A.,Jancsics, K.,Liu, J.,Metz, M.,Papoulis, A.,Skerlj, R.,Stepp, J.D.,Wei, R.R.
The discovery of novel benzofuran-2-carboxylic acids as potent Pim-1 inhibitors.
Bioorg.Med.Chem.Lett., 21:3050-3056, 2011

PubMed Abstract: Novel benzofuran-2-carboxylic acids, exemplified by 29, 38 and 39, have been discovered as potent Pim-1 inhibitors using fragment based screening followed by X-ray structure guided medicinal chemistry optimization. The compounds demonstrate potent inhibition against Pim-1 and Pim-2 in enzyme assays. Compound 29 has been tested in the Ambit 442 kinase panel and demonstrates good selectivity for the Pim kinase family. X-ray structures of the inhibitor/Pim-1 binding complex reveal important salt-bridge and hydrogen bond interactions mediated by the compound's carboxylic acid and amino groups.

PubMed: 21507633
DOI: 10.1016/j.bmcl.2011.03.030

実験手法

X-RAY DIFFRACTION (2.6 Å)