2ONC
Crystal structure of human DPP-4
2ONC の概要
エントリーDOI | 10.2210/pdb2onc/pdb |
分子名称 | Dipeptidyl peptidase 4, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total) |
機能のキーワード | dpp4 protein-inhibitor complex, hydrolase |
由来する生物種 | Homo sapiens (human) |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 346989.81 |
構造登録者 | Feng, J.,Zhang, Z.,Wallace, M.B.,Stafford, J.A.,Kaldor, S.W.,Kassel, D.B.,Navre, M.,Shi, L.,Skene, R.J.,Asakawa, T.,Takeuchi, K.,Xu, R.,Webb, D.R.,Gwaltney, S.L. (登録日: 2007-01-23, 公開日: 2008-03-04, 最終更新日: 2023-12-27) |
主引用文献 | Feng, J.,Zhang, Z.,Wallace, M.B.,Stafford, J.A.,Kaldor, S.W.,Kassel, D.B.,Navre, M.,Shi, L.,Skene, R.J.,Asakawa, T.,Takeuchi, K.,Xu, R.,Webb, D.R.,Gwaltney, S.L. Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV. J.Med.Chem., 50:2297-2300, 2007 Cited by PubMed Abstract: Alogliptin is a potent, selective inhibitor of the serine protease dipeptidyl peptidase IV (DPP-4). Herein, we describe the structure-based design and optimization of alogliptin and related quinazolinone-based DPP-4 inhibitors. Following an oral dose, these noncovalent inhibitors provide sustained reduction of plasma DPP-4 activity and a lowering of blood glucose in animal models of diabetes. Alogliptin is currently undergoing phase III trials in patients with type 2 diabetes. PubMed: 17441705DOI: 10.1021/jm070104l 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.55 Å) |
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