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9Q4S

Structure of rat neuronal nitric oxide synthase R349A mutant heme domain bound with 6-((5-(2-(azetidin-1-yl)ethyl)-2,3-difluorophenxy)methyl)-4-methylpyridin-2-amine

これはPDB形式変換不可エントリーです。
9Q4S の概要
エントリーDOI10.2210/pdb9q4s/pdb
分子名称Nitric oxide synthase, brain, PROTOPORPHYRIN IX CONTAINING FE, 5,6,7,8-TETRAHYDROBIOPTERIN, ... (6 entities in total)
機能のキーワードnitric oxide synthase inhibitor binding, oxidoreductase-inhibitor complex, oxidoreductase, oxidoreductase/inhibitor
由来する生物種Rattus norvegicus (Norway rat)
タンパク質・核酸の鎖数1
化学式量合計49982.93
構造登録者
Li, H.,Poulos, T.L. (登録日: 2025-08-20, 公開日: 2025-09-10, 最終更新日: 2026-03-25)
主引用文献Ansari, A.,Chrzanowski, R.T.,Li, H.,Hardy, C.D.,Awasthi, A.,Poulos, T.L.,Silverman, R.B.
Potent, Selective, and Brain Penetrant Ether-Linked 2-Aminopyridine Inhibitors of Human Neuronal Nitric Oxide Synthase with Excellent Oral Bioavailability.
J.Med.Chem., 69:3506-3518, 2026
Cited by
PubMed Abstract: Neuronal nitric oxide synthase (nNOS) is a therapeutic target for the treatment of various neurological disorders and for melanoma. As part of our ongoing efforts to develop potent and selective nNOS inhibitors, we modified our previously reported compound to by introducing an ether linker, leading to a new series of ether-linked 2-aminopyridine-based compounds that exhibit high potency, isoform selectivity, and membrane permeability. Among them, lead compound inhibits human nNOS with a of 25 nM and exhibits 2300-fold selectivity over human endothelial NOS (eNOS) while also displaying high effective permeability in the parallel artificial membrane permeability assay for the blood-brain barrier (PAMPA-BBB) assay ( = 16.67 × 10 cm/s), indicating favorable blood-brain barrier penetration. Pharmacokinetic evaluation confirmed the brain penetrance of and demonstrated a high oral bioavailability (77%). Moreover, the X-ray crystal structures of representative compounds bound to three NOS isoforms (hnNOS, rnNOS, and heNOS) revealed key binding interactions that contribute to both potency and selectivity.
PubMed: 41630196
DOI: 10.1021/acs.jmedchem.5c03568
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.15 Å)
構造検証レポート
Validation report summary of 9q4s
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2026-04-22に公開中

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