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5M6U

HUMAN PI3KDELTA IN COMPLEX WITH LASW1579

5M6U の概要
エントリーDOI10.2210/pdb5m6u/pdb
分子名称Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform, Phosphatidylinositol 3-kinase regulatory subunit alpha, 4-azanyl-6-[[(1~{S})-1-(4-oxidanylidene-3-phenyl-pyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl]amino]pyrimidine-5-carbonitrile (3 entities in total)
機能のキーワードpi3kdelta kinase, proteros biostructures gmbh, transferase
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数2
化学式量合計199769.15
構造登録者
Segarra, V.,Hernandez, B.,Lozoya, E.,Blaesse, M.,Hoeppner, S.,Jestel, A. (登録日: 2016-10-26, 公開日: 2017-02-01, 最終更新日: 2024-01-17)
主引用文献Erra, M.,Taltavull, J.,Greco, A.,Bernal, F.J.,Caturla, J.F.,Gracia, J.,Dominguez, M.,Sabate, M.,Paris, S.,Soria, S.,Hernandez, B.,Armengol, C.,Cabedo, J.,Bravo, M.,Calama, E.,Miralpeix, M.,Lehner, M.D.
Discovery of a Potent, Selective, and Orally Available PI3K delta Inhibitor for the Treatment of Inflammatory Diseases.
ACS Med Chem Lett, 8:118-123, 2017
Cited by
PubMed Abstract: The delta isoform of the phosphatidylinositol 3-kinase (PI3Kδ) has been shown to have an essential role in specific immune cell functions and thus represents a potential therapeutic target for autoimmune and inflammatory diseases. Herein, the optimization of a series of pyrrolotriazinones as potent and selective PI3Kδ inhibitors is described. The main challenge of the optimization process was to identify an orally available compound with a good pharmacokinetic profile in preclinical species that predicted a suitable dosing regimen in humans. Structure-activity relationships and structure-property relationships are discussed. This medicinal chemistry exercise led to the identification of LAS191954 as a candidate for clinical development.
PubMed: 28105286
DOI: 10.1021/acsmedchemlett.6b00438
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.85 Å)
構造検証レポート
Validation report summary of 5m6u
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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