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机译:基于结构的单喹诺酮系列的基于结构的设计,合成和生物学评价,纤维素1作为潜在抗转移剂的纤维素1的吡唑啉醇[4,3-C]吡啶抑制剂
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Cell Migrat Lab Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Cell Migrat Lab Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
CRUK Beatson Inst Drug Discovery Unit Glasgow G61 1BD Lanark Scotland;
Virtual screening; Fragments; Drug discovery; Medicinal chemistry; Cancer;
机译:基于结构的单喹诺酮系列的基于结构的设计,合成和生物学评价,纤维素1作为潜在抗转移剂的纤维素1的吡唑啉醇[4,3-C]吡啶抑制剂
机译:新型烷基酰胺官能化的三氟甲基取代的吡唑并[3,4-b]吡啶衍生物作为潜在的抗癌药的合成和生物评价
机译:新型吡咯并[1,5-a]吡啶-3-羧酰胺的设计,合成及生物学评价
机译:小肝素模拟物的设计,合成及生物学评价,作为复合HGF / SF-COME的潜在抑制剂
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机译:基于结构的设计合成和生物评价新型fascin 1的异喹诺酮和吡唑并43-c吡啶抑制剂作为潜在的抗转移剂
机译:基于1H-吡唑并[3,4-d]嘧啶支架的双芳基脲作为具有强效抗增殖活性的新型泛RaF抑制剂:基于结构的设计,合成,生物评价和分子模拟研究