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机译:新型噻虫[3,2-D]嘧啶衍生物作为有效的FAK抑制剂的设计,合成,生物学评价和分子对接研究
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
Shenyang Pharmaceut Univ Sch Pharmaceut Engn Minist Educ Key Lab Struct Based Drug Design &
FAK inhibitor; Thieno3.2-dpyrimidine; Structure-activity relationship; Apoptosis; Migration;
机译:新型噻虫[3,2-D]嘧啶衍生物作为有效的FAK抑制剂的设计,合成,生物学评价和分子对接研究
机译:铬嘧啶衍生物作为有效抗癌剂的合理设计,合成,生物学评价和分子对接研究
机译:具有二芳基半脲酮骨架作为有效抗肿瘤剂的新型噻吩并[3,2-d]嘧啶衍生物的设计,合成和生物学评价
机译:洛叶葡萄球菌毒素衍生物的分子对接分析蛋白酶激酶有效抑制剂
机译:噻吩并[3,2-d]-和吡咯并[3,2-d]嘧啶及其C-核苷的合成及生物学评价
机译:四氢喹啉酮衍生物作为有效的P-糖蛋白抑制剂:设计合成生物学评估和分子对接分析
机译:四氢喹啉酮衍生物作为有效的p-糖蛋白抑制剂:设计,合成,生物学评估和分子对接分析