Parallel solid-phase synthesis of vitronectin receptor (αvβ3) inhibitors
A combinatorial approach for rapid optimization of a vitronectin receptor (αvβ3) inhibitor lead was accomplished by solid-phase synthesis. Orthogonally bis protected 2,3-diaminopropionic acid was used to immobilize the C-terminus of the molecule. Selective deprotection and functionalization of the α-amino group followed by acyl resorcinol scaffold attachment and N-terminus diversification was used to explore structure-activity relationship (SAR). (C) 2000 Elsevier Science Ltd. All rights reserved.
Gopalsamy, Ariamala,Yang, Hui,Ellingboe, John W.,Kees, Kenneth L.,Yoon, Jeanne,Murrills, Richard
p. 1715 - 1718
(2007/10/03)
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