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机译:旧药物新诀窍:氯己胺作为潜在的崩解抑制剂,朝向Pak1
Department of Surgical Oncology and General Surgery First Affiliated Hospital of China Medical;
Key Laboratory of Structure-Based Drug Design and Discovery of Ministry of Education Shenyang;
Key Laboratory of Structure-Based Drug Design and Discovery of Ministry of Education Shenyang;
Key Laboratory of Structure-Based Drug Design and Discovery of Ministry of Education Shenyang;
Department of Pharmaceutical Engineering Shenyang University of Chemical Technology;
Department of Surgical Oncology and General Surgery First Affiliated Hospital of China Medical;
Key Laboratory of Structure-Based Drug Design and Discovery of Ministry of Education Shenyang;
Department of Surgical Oncology and General Surgery First Affiliated Hospital of China Medical;
Chlorhexidine; PAK1; Allosteric inhibitor; Virtual screening;
机译:旧药物新诀窍:氯己胺作为潜在的崩解抑制剂,朝向Pak1
机译:计算机辅助药物设计,合成和鉴定二硫键化合物作为新型和潜在的变构PAK1抑制剂
机译:旧药的新窍门:DNA修复抑制剂的抗癌潜力。
机译:基于片段的药物设计,发现二肽基肽酶-4(DPP-4)的新型抑制剂作为2型糖尿病治疗的潜在药物
机译:鉴定新型α-淀粉酶抑制剂作为潜在抗糖尿病药物的分子建模方法
机译:最有效的二苯并二氮杂卓的优化和选择性变构PAK1抑制剂
机译:计算机辅助药物设计,合成及二硫化物化合物的鉴定为新颖的和潜在的颠振PAK1抑制剂