Synthesis and biological evaluation of new conformationally biased integrin ligands based on a tetrahydroazoninone scaffold
摘要:
The synthesis of new conformationally biased cyclic pentapeptides, incorporating the RGD sequence, and built around a tetrahydroazoninone scaffold, is reported. They exhibit interesting activity towards integrin 043 and a remarkable selectivity in comparison with integrin alpha(v)beta(5). (c) 2006 Elsevier Ltd. All rights reserved.