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机译:苯并[d]恶唑-2(3h) - 衍生物作为染色体蛋白质CDYL的第一种有效和选择性小分子抑制剂的鉴定和表征
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Key Lab Carcinogenesis &
Translat Res Dept Biochem &
Mol Biol Sch Basic Med Sci;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
Peking Univ Sch Pharmaceut Sci State Key Lab Nat &
Biomimet Drugs Beijing 100191 Peoples R China;
CDYL; Benzodoxazol-2(3H)-ones; Small-molecule inhibitors; Computer-aided drug design; SAR study; Dendritic morphogenesis;
机译:苯并[d]恶唑-2(3h) - 衍生物作为染色体蛋白质CDYL的第一种有效和选择性小分子抑制剂的鉴定和表征
机译:鉴定2-取代的乙磺酸酯衍生物是新型,有效和选择性的蛋白酪氨酸磷酸酶1B抑制剂
机译:靶向蛋白酪氨酸磷酸酶1B(PTP1b)的有效和选择性抑制剂的鉴定与表征
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:有力和选择性的成纤维细胞活化蛋白(FAP)抑制剂。
机译:含苯氧杂环和磺酰胺部分的二氢吡唑衍生物选择性并有效抑制COX-2:设计合成和抗结肠癌活性评估
机译:可卡因拮抗剂6-乙酰基-3-(4-(4-(4-(4-氟苯基)哌嗪-1-基)丁基)苯并[d]恶唑-2(3H)-one(SN79)的合成及药理评价在啮齿动物中