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机译:使用氟硫酸盐弹头的野生型HIV-1逆转录酶的共价抑制
Department of Chemistry Yale University;
Department of Chemistry Yale University;
Department of Pharmacology Yale University School of Medicine;
Department of Chemistry Yale University;
Department of Pharmacology Yale University School of Medicine;
Department of Pharmacology Yale University School of Medicine;
Department of Chemistry Yale University;
Department of Chemistry Yale University;
Department of Chemistry Yale University;
Department of Pharmacology Yale University School of Medicine;
Department of Chemistry Yale University;
anti-HIV agents; reverse transcriptase inhibitors; covalent inhibitors; fluorosulfates;
机译:噻唑烷苯磺酰胺衍生物抑制野生型和耐药性HIV-1逆转录酶的理论研究
机译:2,4,5-三取代噻唑衍生物作为HIV-1 NNRTI,对野生型和突变型HIV-1逆转录酶均有效:优化位置4和5的取代
机译:2,4,5-三取代的噻唑衍生物作为HIV-1 NNRTIS在野生型和突变体HIV-1逆转录酶的有效性:优化位置4和5的替代
机译:共价抑制蛋白质 - 蛋白质相互作用(1):基于N-酰基-N-烷基磺酰胺(NASA)弹头的共价抑制剂的发育
机译:第一部分:模拟AZT抑制K65R HIV-1逆转录酶突变体的环丁基核苷类似物的合成。第二部分:截短雷公藤甲素类似物的合成和评估,以抑制慢性炎症
机译:易位缺陷型逆转录酶抑制剂4-乙炔基-2-氟-2-脱氧腺苷三磷酸抑制HIV-1逆转录酶的机制
机译:易位缺陷型逆转录酶抑制剂4'-乙炔基-2-氟-2'-脱氧腺苷三磷酸抑制HIV-1逆转录酶的机制*
机译:酶联免疫分析(ELIsa),逆转录聚合酶链反应(RT-pCR)和流式细胞术评价人全血中细胞因子的合成