Design, synthesis, and biological activities of novel hexahydropyrazino[1,2-a]indole derivatives as potent inhibitors of apoptosis (IAP) proteins antagonists with improved membrane permeability across MDR1 expressing cells
Keywords: ایزو; HATU; O-(7-azabenzotriazol-1-yl)-N,N,Nâ²,Nâ²-tetramethyluronium hexafluorophosphate; DIPEA; N-ethyldiisopropylamine; Ac; acetyl; CDCl3; deuteratedchloroform; DMF; N,N-dimethylformamide; DMSO; dimethyl sulfoxide; DMT-MM; 4-(4,6-dimethoxy-1,3,5-triazin-2-