化学
钌
异构化
配体(生物化学)
光解
吡啶
药物化学
光化学
联吡啶
一氧化氮
立体化学
结晶学
催化作用
晶体结构
有机化学
生物化学
受体
作者
Alexia Marques Silva,Laísa Bonafim Negri,Juliana C. Biazzotto,Sérgio de Paula Machado,Jeimison Duarte Santos,Jorge Fernandes Nasser Batista,Pedro Ivo da Silva Maia,Victor M. Deflon,Lusiane Maria Bendhack,Michael R. Hamblin,Roberto S. da Silva
标识
DOI:10.1016/j.jinorgbio.2023.112166
摘要
We have synthesized cis-[Ru(bpy)2(NO2-κN)Ln-](n-1) and cis-[Ru(bpy)2(NO2-κO)L n-](n-1) (bpy = 2,2'-bipyridine; k = indication of the coordinated center to Ruthenium; L = pyridine type ligand) by reacting cis-[Ru(bpy)2(H2O)Ln-](n-2) with sodium nitrite or conducting basic cis-[Ru(bpy)2NO(Ln-)](n-3) hydrolysis. Photolysis at the metal-ligand charge transfer band (MLCT) of the isomers yielded nitric oxide (NO) as determined by NO measurement. The NO photorelease rates obtained upon 447 nm laser irradiation of the ruthenium complexes showed that cis-[Ru(bpy)2(NO2-κO)Ln-](n-1) released NO three times faster than cis-[Ru(bpy)2(NO2-κN)Ln-](n-1). We investigated endothelium-dependent vasodilation induced by cis-[Ru(bpy)2(4-pic)(NO2-κN)]+ and cis-[Ru(bpy)2(4-pic)(NO2-κO)]+ (4-pic = 4-picoline) in isolated 3 mm aortic rings precontracted with L-phenylephrine. Maximum vasodilation was achieved under 447 nm laser irradiation of 0.5 μMol.L-1 ruthenium complexes for 100 s.
科研通智能强力驱动
Strongly Powered by AbleSci AI