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pro vyhledávání: '"Bingliu Lu"'
Publikováno v:
Bioorganicmedicinal chemistry letters. 27(21)
A series of hydroxamic acid-based HDACIs with 4-aminoquinazolinyl moieties as capping groups was profiled. Most compounds showed more potent HDACs inhibition activity than clinically used drug SAHA. Among them, compounds 5f and 5h selectively inhibit
Publikováno v:
Bioorganicmedicinal chemistry letters. 27(14)
The synthesis and biological evaluation of a variety of 4-piperazinyl-containing Chidamide derivatives is described. Some of these compounds were shown to inhibit HDAC1 with IC50 values below micromolar range, and inhibited proliferation of several h