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Hydrolysis Mechanism of the NAMI-A-type Antitumor Complex (HL)[trans-RuCl4L(dmso-S)] (L=1-methyl-1,2,4-triazole)
Lan-mei Chen,Jin-can Chen*,Si-yan Liao,Jiang-qin Liu,Hui Luo,Kang-cheng Zheng
Author NameAffiliationE-mail
Lan-mei Chen School of Pharmacy, Guangdong Medical College, Zhanjiang 524023, China  
Jin-can Chen* School of Pharmacy, Guangdong Medical College, Zhanjiang 524023, China jincanchen@126.com 
Si-yan Liao Department of Chemistry, Guangzhou Medical College, Guangzhou 510182, China  
Jiang-qin Liu School of Pharmacy, Guangdong Medical College, Zhanjiang 524023, China  
Hui Luo School of Pharmacy, Guangdong Medical College, Zhanjiang 524023, China  
Kang-cheng Zheng School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China  
Abstract:
The hydrolysis process of Ru(III) complex (HL)[trans-RuCl4L(dmso-S)] (L=1-methyl-1,2,4-triazole and dmso-S=S-dimethyl sulfoxide) (1), a potential antitumor complex similar to the well-known antitumor agent (Him)[trans-RuCl4L(dmso-S)(im)] (NAMI-A, im=imidazole), was investigated using density functional theory combined with the conductor-like polarizable continuum model approach. The structural characteristics and the detailed energy profiles for the hydrolysis processes of this complex were obtained. For the first hydrolysis step, complex 1 has slightly higher barrier energies than the reported anticancer drug NAMI-A, and the result is in accordance with the experimental evidence indicating larger half-life for complex 1. For the second hydrolysis step, the formation of cis-diaqua species is thermodynamic preferred to that of trans isomers. In addition, on the basis of the analysis of electronic characteristics of species in the hydrolysis process, the trend in nucleophilic attack abilities of hydrolysis products by pertinent biomolecules is revealed and predicted.
Key words:  NAMI-A-type complex, Anticancer activity, Hydrolysis, Density functional theory, Conductor-like polarizable continuum model
FundProject:
NAMI-A型钌配合物(HL)[trans-RuCl4L(dmso-S)] (L=1-methyl-1,2,4-triazole)水解机理的理论研究
陈兰美,陈锦灿*,廖思燕,刘江琴,罗辉,郑康成
摘要:
用量子化学密度泛函方法结合导体极化连续模型研究了具有潜在抗肿瘤活性的NAMI-A型钌配合物(HL)[trans-RuCl4L(dmso-S)](L=1-methyl-1,2,4-triazole,dmso-S=S-dimethyl sulfoxide) (1)的水解反应过程.计算得到该配合物水解反应过程中相应的结构特征和详细的反应势能面.对于第一步水解,液相中配合物1的活化能垒比已经报道的抗肿瘤药物(Him)[trans-RuCl4(
关键词:  NAMI-A型配合物,水解,密度泛函理论,导体极化连续模型
DOI:10.1088/1674-0068/24/04/383-390
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