首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >Organometallic complexes with biological molecules - XVII. Triorganotin(IV) complexes with amoxicillin and ampicillin
【24h】

Organometallic complexes with biological molecules - XVII. Triorganotin(IV) complexes with amoxicillin and ampicillin

机译:具有生物分子的有机金属配合物-XVII。三有机锡(IV)与阿莫西林和氨苄西林的复合物

获取原文
获取原文并翻译 | 示例
           

摘要

Novel triorganotin(IV) complexes of two beta-lactamic antibiotics; 6-[D-(-)-beta-amino-p-hydroxyphenyl-acetamido]penicillin (=amoxicillin) and 6-[D-(-)-alpha-aminobenzyl]penicillin (=ampicillin), have been synthesized and investigated both in solid and solution states. The complexes corresponded to the general formula R3Sn(IV)antib.H2O (R=Me, nLBu, Ph; antib=amox=amoxicillinate or amp=ampicillinate). Structural investigations about configuration in the solid state have been carried out by interpreting experimental IR and Sn-119 Mossbauer data. In particular, IR results suggested polymeric structures both for R3Sn(IV)amox-H2O and R3Sn(IV)amp.H2O. Moreover, both antibiotics appear to behave as monoanionic bidentate ligands coordinating the tin(IV) atom through ester-type carboxylate, as well as through the beta-lactamic carbonyl. Evidence that in none of these compounds water molecules were involved in coordination, was provided by thermogravimetric investigations. On the basis of Sn-119 Mossbauer spectroscopy it can be inferred that tin(IV) was pentacoordinate in all of the complexes in the solid state, showing an equatorial R3Sn(IV) trigonal bipyramidal (tbp) configuration. The nature of the complexes in solution state was investigated by using H-1 and C-13 nuclear magnetic resonance (NMR) spectroscopy, while an Sn-119 spectrum was obtained for n-Bu3Sn(IV)amp.H2O. Although H-1- and C-13-NMR measurements suggested that in dimethyl sulfoxide (DMSO)-d(6) solution the polymeric structure collapsed, due to a solvolysis process of the beta-lactamic carbonyl bonding to the organometallic moiety, the complexes have been shown to maintain the same trigonal bipyramidal configuration at tin(IV) atom by the coordination of a DMSO molecule. Cytotoxic activity of these novel semisynthetic antibiotic derivatives has been tested towards spermatocyte chromosomes of the mussel Brachidontes pharaonis (Mollusca: Bivalvia) using two different chromosome-staining techniques such as Giemsa and CMA(3). The occurrence of typical colchicinized-like (c-like) mitoses on slides obtained from animals exposed to organotin compounds, directly confirmed the high mitotic spindle-inhibiting potency of these chemicals. In addition, by comparative analysis of spermatocyte chromosomes from untreated specimens (negative controls) and specimens treated with the triorganotin(IV) complexes, structural damages such as 'achromatic lesions' and 'chromosome breakages' have been identified.
机译:两种β-乳杆菌抗生素的新型三有机锡(IV)复合物;合成并研究了6- [D-(-)-β-氨基-对羟基苯基-乙酰胺基]青霉素(=阿莫西林)和6- [D-(-)-α-氨基苄基]青霉素(=氨苄西林)处于固态和溶液状态。所述络合物对应于通式R 3 Sn(IV)antib.H 2 O(R = Me,nLBu,Ph; antib = amox = amoxicillinate或amp = ampicillinate)。通过解释实验IR和Sn-119 Mossbauer数据进行了有关固态构型的结构研究。特别是,IR结果表明R3Sn(IV)amox-H2O和R3Sn(IV)amp.H2O均具有聚合物结构。此外,两种抗生素似乎都表现为通过酯型羧酸盐以及通过β-内酰胺基羰基配位锡(IV)原子的单阴离子二齿配体。通过热重研究提供了在这些化合物中没有水分子参与配位的证据。根据Sn-119 Mossbauer光谱学,可以推断出,锡(IV)在所有固态络合物中都是五配位的,显示出赤道的R3Sn(IV)三角双锥体(tbp)构型。通过使用H-1和C-13核磁共振(NMR)光谱研究了溶液状态下的配合物的性质,同时获得了n-Bu3Sn(IV)amp.H2O的Sn-119光谱。尽管H-1-和C-13-NMR测量表明,在二甲基亚砜(DMSO)-d(6)溶液中,由于β-内酰胺基羰基与有机金属部分的键合溶剂化过程,聚合物结构发生了塌陷已经显示通过DMSO分子的配位在锡(IV)原子上保持相同的三角双锥体构型。这些新的半合成抗生素衍生物的细胞毒性活性已经通过使用Giemsa和CMA(3)等两种不同的染色体染色技术对贻贝Brachidontes pharaonis(Mollusca:Bivalvia)的精母细胞染色体进行了测试。从暴露于有机锡化合物的动物获得的载玻片上典型的趋化蛋白样(c样)有丝分裂的出现,直接证实了这些化学物质对丝分裂纺锤体的抑制力很高。此外,通过对未处理标本(阴性对照)和经三有机锡(IV)复合物处理过的标本中精细胞染色体的比较分析,已鉴定出结构损伤,如“无色病变”和“染色体断裂”。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号