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Synthesis, crystal structures, and urease inhibition studies of two new Schiff-base copper complexes derived from n-butylamine

机译:两种新的正丁胺衍生的席夫碱铜配合物的合成,晶体结构和脲酶抑制研究

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Two Schiff-base copper(II) complexes, bis(N-n-butyl-5-chlorosalicylaldiminato) copper(II) (1) and bis(N-n-butyl-4-methoxysalicylaldiminato) copper(II) (2), were synthesized and their solid-state structures were determined by X-ray crystallography. Complex 1 displays a distorted square-planar geometry, while 2 possesses square-planar geometry. Copper(II) complexes 1 and 2 showed strong inhibitory activity against jack bean urease (IC50 = 2.7, 3.5 µmol L−1), compared with acetohydroxamic acid (IC50 = 63.00 µmol L−1). A molecular modeling study was carried out via the DOCK program to gain understanding of the potent inhibitory activity of these copper species against jack bean urease.View full textDownload full textKeywordsSchiff-base copper(II) complexes, Crystal structures, 5-Chlorosalicylaldehyde, 4-Methoxysalicylaldehyde, Urease inhibitorsRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/00958972.2011.637169
机译:合成了两种席夫碱铜(II)配合物双(Nn-丁基-5-氯水杨基铝杂二氨基)铜(II)(1)和双(Nn-丁基-4-甲氧基水杨基铝杂二氨基)铜(II)(2),并对其进行了合成通过X射线晶体学确定固态结构。复数1显示扭曲的正方形平面几何形状,而复合物2具有正方形的几何形状。铜(II)配合物1和2显示出强大的抑制活性,对抗波克豆脲酶(IC 50 ≥2.7、3.5 µmol·L -1 ),与乙酰氧肟酸(IC 50 == 63.00µmol·L -1”)比较。通过DOCK程序进行了分子建模研究,以了解这些铜物种对杰克豆脲酶的强抑制活性。查看全文下载全文关键词席夫碱铜(II)配合物,晶体结构,5-氯水杨醛,4-甲氧基水杨醛,脲酶抑制剂相关的变量add add_config = {ui_cobrand:“ Taylor&Francis Online”,services_compact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more”,pubid:“ ra-4dff56cd6bb1830b” };添加到候选列表链接永久链接http://dx.doi.org/10.1080/00958972.2011.637169

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