"CLICK CHEMISTRY" ASSEMBLY OF HIV PROTEASE INHIBITORS

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 HIV蛋白酶靶标的性质和重要性是众所周知的。 抗药性演变的问题现在被认为是有效的长期治疗的主要障碍。 由计算对接指导的新型合成方法有望产生更有效的HIV蛋白酶抑制剂，这些抑制剂在面对耐药性时是稳健的。在蛋白酶突变体的背景下，利用“点击化学”原位合成抑制剂的可能性，指出了一个新的灵活的方法来解决这个问题。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The nature and importance of the HIV protease target is well known. The problem of the evolution of drug resistance is now recognized as a major impediment to effective long-term therapeutic treatment. Novel synthetic approaches, guided by computational docking hold the promise of generating more effective HIV protease inhibitors, that are robust in the face of resistance. The possibilities of in situ synthesis of inhibitors utilizing "click chemistry" in the context of protease mutants points to a new flexible approach to this problem.