Strategies for rapid deconvolution of combinatorial libraries: Comparative evaluation using a model system

被引:21
作者
Konings, DAM
Wyatt, JR
Ecker, DJ
Freier, SM
机构
[1] ISIS Pharmaceut, Carlsbad, CA 92008 USA
[2] So Illinois Univ, Dept Microbiol, Carbondale, IL 62901 USA
关键词
D O I
10.1021/jm970503o
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Synthesis and testing of complex mixtures maximize the number of compounds that can be prepared and tested in a combinatorial library. When mixtures of compounds are screened, however, the identity of the compound(s) selected may depend on the deconvolution procedure employed. Previously, we developed a model system for evaluation of deconvolution procedures and used it to compare pooling strategies for iterative and noniterative deconvolution [Freier et al. J. Med. Chem. 1995, 38, 344-352]. We have now extended the model studies to include simulations of procedures with overlapping subsets such as subtractive pooling [Carell et al. Angew. Chem., Int. Ed. Engl. 1994, 33, 2061-2064], bogus coin pooling [Blake and Litzi-Davis. Bioconjugate Chem. 1992, 3, 510-513], and orthogonal pooling [D'Prez et al. J. Am. Chem. Sec. 1995, 117, 5405-5406]. These strategies required synthesis and testing of fewer subsets than did the more traditional nonoverlapping iterative strategies. The compounds identified using simulations of these strategies, however, were not the most active compounds in the library and were substantially less active than those identified by simulations of more traditional strategies.
引用
收藏
页码:4386 / 4395
页数:10
相关论文
共 74 条
[1]   Solution phase combinatorial chemistry .1. Synthesis of polyazacyclophane scaffolds and tertiary amine libraries [J].
An, HY ;
Cook, PD .
TETRAHEDRON LETTERS, 1996, 37 (40) :7233-7236
[2]   Solution phase combinatorial chemistry. Discovery of novel polyazapyridinophanes with potent antibacterial activity by a solution phase simultaneous addition of functionalities approach [J].
An, HY ;
Cummins, LL ;
Griffey, RH ;
Bharadwaj, R ;
Haly, BD ;
Fraser, AS ;
WilsonLingardo, L ;
Risen, LM ;
Wyatt, JR ;
Cook, PD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (16) :3696-3708
[3]  
Appel JR, 1996, PEPTIDE RES, V9, P174
[4]  
BAUER BE, 1996, P C MOL DIV COMB CHE, P233
[5]  
BEVINGTON PR, 1992, DATA REDUCTION ERROR, P75
[6]   EVALUATION OF PEPTIDE LIBRARIES - AN ITERATIVE STRATEGY TO ANALYZE THE REACTIVITY OF PEPTIDE MIXTURES WITH ANTIBODIES [J].
BLAKE, J ;
LITZIDAVIS, L .
BIOCONJUGATE CHEMISTRY, 1992, 3 (06) :510-513
[7]   Rapid identification of compounds with enhanced antimicrobial activity by using conformationally defined combinatorial libraries [J].
Blondelle, SE ;
Takahashi, E ;
Houghten, RA ;
PerezPaya, E .
BIOCHEMICAL JOURNAL, 1996, 313 :141-147
[8]  
BOUTIN JA, 1996, AM BIOTECHNOL LAB, V14, P36
[9]   DIRECT CLEAVAGE OF PEPTIDES FROM A SOLID SUPPORT INTO AQUEOUS BUFFER - APPLICATION IN SIMULTANEOUS MULTIPLE PEPTIDE-SYNTHESIS [J].
BRAY, AM ;
MAEJI, NJ ;
VALERIO, RM ;
CAMPBELL, RA ;
GEYSEN, HM .
JOURNAL OF ORGANIC CHEMISTRY, 1991, 56 (23) :6659-6666
[10]   POTENT AND SPECIFIC-INHIBITION OF HIV ENVELOPE-MEDIATED CELL-FUSION AND VIRUS BINDING BY G-QUARTET-FORMING OLIGONUCLEOTIDE (ISIS-5320) [J].
BUCKHEIT, RW ;
ROBERSON, JL ;
LACKMANSMITH, C ;
WYATT, JR ;
VICKERS, TA ;
ECKER, DJ .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1994, 10 (11) :1497-1506