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Like all of the other inhibitors of HDAC, belinostat PXD101 is also an efficient kinase inhibitor of HDACs. It is relatively newer inhibitor and there is still a lot of space in experiments concentrating on the elucidation of it's mechanism of action as a result of HTS together with computational approaches. Also, there is a lot of room in the development of its analogs just by virtual screening technology. Being successful in aiming and preventing ovarian cancer, bladder cancer whilst others, belinostat is no doubt a useful addition to compound libraries for HTS.

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