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首页> 外文期刊>Inorganic Chemistry Communications >Syntheses, characterization and biological activity of diorganotin(IV) derivatives of 2-amino-6-hydroxypurine (guanine)
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Syntheses, characterization and biological activity of diorganotin(IV) derivatives of 2-amino-6-hydroxypurine (guanine)

机译:2-氨基-6-羟基嘌呤(鸟嘌呤)的二有机锡(IV)衍生物的合成,表征和生物学活性

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摘要

Novel organotin(IV) derivatives of guanine of the general formula, R2Sn(HGu)2 (where, R = Me (1), n-Bu (2) and Ph (3)) have been synthesized by the reaction of R2SnCl2 with sodium salt of guanine (H2Gu or 2-amino-6-hydroxypurine). The 1R spectral studies suggest that guanine acts as a monobasic ligand coordinating through N(9) after its deprotonation. The weak bonding through C(6)=O may also be evidenced, whereas ~(119)Sn Mossbauer data suggest that the coordination number of tin is superior than four. The polyhedron around tin in R2Sn(HGu)2 is distorted trigonal-bipyramidal or pseudo-tetrahedral involving very weak interaction from C=O group of neighboring molecule leading to polymerized structure. All the compounds exhibited potent anti-inflammatory activity with no appreciable side effects on blood pressure as evidenced by their very mild cardiovascular activity.
机译:通式R2Sn(HGu)2(其中R = Me(1),n-Bu(2)和Ph(3))的鸟嘌呤的新型有机锡(IV)衍生物已经通过R2SnCl2与钠的反应合成鸟嘌呤的盐(H2Gu或2-氨基-6-羟基嘌呤)。 1R光谱研究表明,鸟嘌呤在去质子化后可作为一元配体通过N(9)进行配位。通过C(6)= O的弱键合也可能得到证明,而〜(119)Sn Mossbauer数据表明锡的配位数大于4。 R2Sn(HGu)2中锡周围的多面体是扭曲的三角-双锥体或伪四面体,涉及与邻近分子的C = O基团的相互作用非常弱,从而导致聚合结构。所有化合物均显示出有效的抗炎活性,并且对血压没有明显的副作用,如其非常温和的心血管活性所证明的那样。

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