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5G3M

Discovery of a novel secreted phospholipase A2 (sPLA2) inhibitor.

5G3M の概要
エントリーDOI10.2210/pdb5g3m/pdb
関連するPDBエントリー5G3N
分子名称GROUP 10 SECRETORY PHOSPHOLIPASE A2, CALCIUM ION, DIMETHYL SULFOXIDE, ... (6 entities in total)
機能のキーワードhydrolase, spla2, cardiovascular disease, inhibitor, fragment
由来する生物種HOMO SAPIENS (HUMAN)
細胞内の位置Secreted : O15496
タンパク質・核酸の鎖数2
化学式量合計29740.39
構造登録者
Sandmark, J.,Bodin, C.,Hallberg, K. (登録日: 2016-04-29, 公開日: 2016-09-14, 最終更新日: 2024-11-06)
主引用文献Giordanetto, F.,Pettersen, D.,Starke, I.,Nordberg, P.,Dahlstrom, M.,Knerr, L.,Selmi, N.,Rosengren, B.,Larsson, L.O.,Sandmark, J.,Castaldo, M.,Dekker, N.,Karlsson, U.,Hurt-Camejo, E.
Discovery of Azd2716: A Novel Secreted Phospholipase A2 (Spla2) Inhibitor for the Treatment of Coronary Artery Disease
Acs Med.Chem.Lett., 7:884-, 2016
Cited by
PubMed Abstract: Expedited structure-based optimization of the initial fragment hit led to the design of ()- (AZD2716) a novel, potent secreted phospholipase A (sPLA) inhibitor with excellent preclinical pharmacokinetic properties across species, clear efficacy, and minimized safety risk. Based on accumulated profiling data, ()- was selected as a clinical candidate for the treatment of coronary artery disease.
PubMed: 27774123
DOI: 10.1021/ACSMEDCHEMLETT.6B00188
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.85 Å)
構造検証レポート
Validation report summary of 5g3m
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-06に公開中

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