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
相关论文
共 85 条
[1]  
ALBERICIO F, 1987, INT J PEPT PROT RES, V30, P206
[2]  
ALBERICIO F, 1991, INT J PEPT PROT RES, V37, P402
[3]   Residue-based control of helix shape in beta-peptide oligomers [J].
Appella, DH ;
Christianson, LA ;
Klein, DA ;
Powell, DR ;
Huang, XL ;
Barchi, JJ ;
Gellman, SH .
NATURE, 1997, 387 (6631) :381-384
[4]   STRUCTURAL STUDIES OF A FAMILY OF HIGH-AFFINITY LIGANDS FOR GPIIB/IIIA [J].
BACH, AC ;
EYERMANN, CJ ;
GROSS, JD ;
BOWER, MJ ;
HARLOW, RL ;
WEBER, PC ;
DEGRADO, WF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (08) :3207-3219
[5]   CYCLIC RGD PEPTIDE ANALOGS AS ANTIPLATELET ANTITHROMBOTICS [J].
BARKER, PL ;
BULLENS, S ;
BUNTING, S ;
BURDICK, DJ ;
CHAN, KS ;
DEISHER, T ;
EIGENBROT, C ;
GADEK, TR ;
GANTZOS, R ;
LIPARI, MT ;
MUIR, CD ;
NAPIER, MA ;
PITTI, RM ;
PADUA, A ;
QUAN, C ;
STANLEY, M ;
STRUBLE, M ;
TOM, JYK ;
BURNIER, JP .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (11) :2040-2048
[6]   1H-PYRAZOLE-1-CARBOXAMIDINE HYDROCHLORIDE - AN ATTRACTIVE REAGENT FOR GUANYLATION OF AMINES AND ITS APPLICATION TO PEPTIDE-SYNTHESIS [J].
BERNATOWICZ, MS ;
WU, YL ;
MATSUEDA, GR .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (08) :2497-2502
[7]   A MASS-SPECTROMETRIC SOLUTION TO THE ADDRESS PROBLEM OF COMBINATORIAL LIBRARIES [J].
BRUMMEL, CL ;
LEE, INW ;
ZHOU, Y ;
BENKOVIC, SJ ;
WINOGRAD, N .
SCIENCE, 1994, 264 (5157) :399-402
[8]   Solid phase syntheses of oligoureas [J].
Burgess, K ;
Ibarzo, J ;
Linthicum, DS ;
Russell, DH ;
Shin, H ;
Shitangkoon, A ;
Totani, R ;
Zhang, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (07) :1556-1564
[9]   BIASED COMBINATORIAL LIBRARIES - NOVEL LIGANDS FOR THE SH3 DOMAIN OF PHOSPHATIDYLINOSITOL 3-KINASE [J].
CHEN, JK ;
LANE, WS ;
BRAUER, AW ;
TANAKA, A ;
SCHREIBER, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (26) :12591-12592
[10]   DESIGN AND SYNTHESIS OF NOVEL CYCLIC RGD-CONTAINING PEPTIDES AS HIGHLY POTENT AND SELECTIVE INTEGRIN ALPHA(IIB)BETA(3) ANTAGONISTS [J].
CHENG, S ;
CRAIG, WS ;
MULLEN, D ;
TSCHOPP, JF ;
DIXON, D ;
PIERSCHBACHER, MD .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (01) :1-8