Synthesis, structural studies, molecular docking and DNA binding studies of 4N-substituted hydrazinecarbothioamides
作者:P. Murali Krishna、N.B. Gopal Reddy、B.G. Harish、Yogesh P. Patil、Munirathnam Nethaji
DOI:10.1016/j.molstruc.2018.07.053
日期:2019.1
calf-thymus-Deoxyribo Nucleic Acid (CT-DNA) were investigated by spectrophotometric method and the results indicated that ligands bound to Deoxyribo Nucleic Acid (DNA) by groove binding mode. The docking studies of ligands with glucosamine-6-phosphate synthase revealed that the ligands are potent as a drug for target enzyme. (C) 2018 Elsevier B.V. All rights reserved.
缩合反应合成了三种通式 H5C2(Ph)-CH=N-NH-C(S)-NHR R = H (L-1), CH3 (L-2), C2H5 (L-3)] 的缩氨基硫脲] 4-乙基苯甲醛和 N-4-取代-氨基硫脲 2HN-NH-C(S)-NHR] 之间的关系,并使用 X 射线单晶衍射、元素分析、红外、NMR 光谱分析进行表征。单晶数据表明配体L-1和L-3在空间群为P2(1/c)的单斜晶系中结晶,晶体L-2在空间群为P-1的三斜晶系中结晶 配体与小牛胸腺的相互作用通过分光光度法研究-脱氧核糖核酸(CT-DNA),结果表明配体通过凹槽结合模式与脱氧核糖核酸(DNA)结合。配体与葡萄糖胺-6-磷酸合酶的对接研究表明,这些配体作为靶酶的药物是有效的。(C) 2018 Elsevier BV 版权所有。