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Three-step synthetic procedure to prepare dolutegravir, cabotegravir, and bictegravir
Published in Green Chemistry Letters and Reviews, 2022
Xianheng Wang, Song Chen, Hanqi Cui, Yuqi He, Changkuo Zhao
AIDS remains a serious global public health threat to humans even in modern society. With the development of science and technology, it has been found that integrase plays an important role in the replication of HIV-1 virus, and this enzyme has become an attractive drug target over the past few years (1). So far, a lot of integrase inhibitors including raltegravir, elvitegravir, dolutegravir, cabotegravir, and bictegravir have been launched globally or approved to enter into phase III clinic trials (Figure 1) (2–4).