Perturbing pro-survival proteins using quinoxaline derivatives: A structure–activity relationship study

Perturbing pro-survival proteins using quinoxaline derivatives: A structure–activity relationship study Synthesis and biological activities of polyquinoline derivatives: New Bcl-2 family protein modulators Quinazoline Sulfonamides as Dual Binders of the Proteins B-Cell Lymphoma 2 and B-Cell Lymphoma Extra Long with Potent Proapoptotic Cell-Based Activity Pyrogallol-Based Molecules as Potent Inhibitors of the Antiapoptotic Bcl-2 Proteins Synthesis and biological evaluation of novel 6-chloro-quinazolin derivatives as potential antitumor agents Discovery of Potent and Selective Benzothiazole Hydrazone Inhibitors of Bcl-X_L Dual inhibitors of the pro-survival proteins Bcl-2 and Mcl-1 derived from natural compound meiogynin A Design of Bcl-2 and Bcl-xL Inhibitors with Subnanomolar Binding Affinities Based upon a New Scaffold Synthesis and anticancer activity of new 1-[(5 or 6-substituted 2-alkoxyquinoxalin-3-yl)aminocarbonyl]-4-(hetero)arylpiperazine derivatives New synthetic phenylquinazoline derivatives induce apoptosis by targeting the pro-survival members of the BCL-2 family