Synthesis and screening of linear and cyclic oligocarbamate libraries. Discovery of high affinity ligands for GPIIb/IIIa

被引:50
作者
Cho, CY
Youngquist, RS
Paikoff, SJ
Beresini, MH
Hebert, AR
Berleau, LT
Liu, CW
Wemmer, DE
Keough, T
Schultz, PG [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[3] Procter & Gamble Co, Miami Valley Labs, Cincinnati, OH 45253 USA
[4] Genentech Inc, Dept Bioanalyt Technol, S San Francisco, CA USA
[5] Genentech Inc, Dept Metab & Pharmacokinet, S San Francisco, CA USA
[6] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Berkeley, CA 94720 USA
关键词
D O I
10.1021/ja9734399
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Synthetic methodology has been developed for the generation of large, diverse libraries of "unnatural" carbamate oligomers using the "one bead, one peptide" method. Using a pool of 27 structurally and functionally diverse monomers, one acyclic and two cyclic libraries were synthesized and screened for binding to the integrin GPIIb/IIIa. Several classes of oligocarbamate ligands for GPIlb/IIIa were discovered, and two cyclic ligands have activities that are within a factor of 3 of kistrin, a snake venom protein that effectively inhibits platelet aggregation. Preliminary pharmacokinetic characterization was performed on a-linear oligocarbamate ligand, which was cleared from plasma with a half-life of 3.6 min.
引用
收藏
页码:7706 / 7718
页数:13
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