Human African trypanosomiasis (HAT) is a neglected tropical disease caused by infection with either of two subspecies of the parasite . Due to a lack of economic incentive to develop new drugs, current treatments have severe limitations in terms of safety, efficacy, and ease of administration. In an effort to develop new HAT therapeutics, we report the structure-activity relationships around for a series of benzoxazepinoindazoles previously identified through a high-throughput screen of human kinase inhibitors, and the subsequent experiments for HAT.
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