Labeling of human Ether-a-go-go-Related Gene(hERG)potassium channel with fluorescent probe has been becoming an essential tool in hERG-associated studies.[1,2] In this research,three small-molecule fl
The B-cell lymphoma(Bcl-2)family proteins are potential targets for cancer treatment.In our studies,a series of pyrrolidine derivatives were developed as potent myeloid cell leukemia sequence 1(Mcl-1)
Histone deacetylase(HDAC)has emerged as an attractive target for the development of antitumor agents during the past decade.[1] In our previous study,we designed and synthesized a novel series of N-hy
The long-term usage of HIV-1 non-nucleoside reverse transcriptase inhibitors(NNRTIs)usually leads to rapid emergence of mutant stains and severe side effects.
A series of novel 6-substituted diarylpyridine derivatives targeting the entrance channel of the NNRTI binding pocket(NNIBP)of HIV-1 RT was designed through a molecular hybridization strategy.
Forty-two compounds(series 8,9 and 10)incorporated with diacylated piperazine have been synthesized and evaluated as novel Bcr-Abl inhibitors based on six-atom linker.