机译:苯并噻嗪酮抑制剂抑制结核分枝杆菌DprE1的结构基础
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
lnstitut fur Biotechnologie I, Forschungszentrum Julich, D-52428 Julich, Germany;
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, United Kingdom;
mycobacterial cell wall; x-ray crystallography; multi drug resistance arabinan; decaprenylphosphoryl-d-arabinose;
机译:基于结构的药物设计和表征磺酰哌嗪苯并噻唑啉抑制剂从结核分枝杆菌中的DPRE1
机译:8-吡咯-苯并噻嗪酮是结核分枝杆菌DprE1的非共价抑制剂。
机译:硝基,亚硝基和羟氨基苯并噻嗪酮和苯并ac嗪酮与结核分枝杆菌DprE1反应的新颖见解
机译:基于质谱基于船只海绵代谢物ilimaquinnons的重组分枝杆菌性结核分枝杆菌的不可逆抑制研究
机译:铁依赖性调节剂和休眠存活调节剂在结核分枝杆菌中转录调节的结构基础。
机译:苯并噻嗪酮抑制剂抑制结核分枝杆菌DprE1的结构基础
机译:苯并噻嗪酮抑制剂抑制结核分枝杆菌DprE1的结构基础