Exploring biologically active hybrid pharmacophore N-substituted hydrazine-carbothioamides for urease inhibition: In vitro and in silico approach-论文-万方医学网

Exploring biologically active hybrid pharmacophore N-substituted hydrazine-carbothioamides for urease inhibition: In vitro and in silico approach

导出原文传递

翻译打印收藏纠错

作者： Saira Naseem ^[1] ; Muhammad Ashraf ^[2] ; Samra Khan ^[3] ; Muhammad Rafiq ^[4] ; Muhammad Kashif ^[5] ; Jameel Rahman ^[6] ; Muhammad Khawar Rauf ^[7] ; Sobia Ahsan Halim ; Jalal Uddin ; Ajmal Khan ; Ahmed Al-Harrasi ; Zahid Shafiq

作者单位： Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800, Pakistan ^[1] Institute of Chemistry, The Islamia University Bahawalpur, Bahawalpur 63100, Pakistan ^[2] School of Chemistry and Chemical Engineering, South China University of Technology, Guanzhou 510640, China ^[3] Department of Chemistry, Emerson University Multan, Bosan Road, Multan, Pakistan ^[4] Department of Chemistry, Govt. Post-Graduate Gordon College Rawalpindi, Pakistan ^[5] Natural and Medical Sciences Research Center, University of Nizwa, PO Box 33, 616 Birkat Al Mauz, Nizwa, Oman ^[6] Department of Pharmaceutical Chemistry, College of Pharmacy, King Khalid University, Abha 62529, Saudi Arabia ^[7]

关键词 Hydrazine-carbothioamides Urease inhibition Molecular docking studies SAR studies

发布时间 2022-11-15

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除