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Blanca G Baldanti F Paolucci S Skoblov AY Victorova L Hübscher U Gerna G Spadari S Maga G 《The Journal of biological chemistry》2003,278(18):15469-15472
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Cesarini S Spallarossa A Ranise A Fossa P La Colla P Sanna G Collu G Loddo R 《Bioorganic & medicinal chemistry》2008,16(7):4160-4172
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《Bioorganic & medicinal chemistry》2014,22(4):1459-1467
A series of novel N1-aryl-2-arylthioacetamido-benzimidazoles were synthesized and evaluated as inhibitors of human immunodeficiency virus type-1 (HIV-1). Some of them proved to be effective in inhibiting HIV-1 replication at submicromolar and nanomolar concentration acting as HIV-1 non-nucleoside RT inhibitors (NNRTIs), with low cytotoxicity. The preliminary structure–activity relationship (SAR) of these new derivatives was discussed and rationalized by docking studies. 相似文献
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