LIBRARIES FROM LIBRARIES - CHEMICAL TRANSFORMATION OF COMBINATORIAL LIBRARIES TO EXTEND THE RANGE AND REPERTOIRE OF CHEMICAL DIVERSITY

被引:192
|
作者
OSTRESH, JM
HUSAR, GM
BLONDELLE, SE
DORNER, B
WEBER, PA
HOUGHTEN, RA
机构
[1] TORREY PINES INST MOLEC STUDIES,SAN DIEGO,CA 92121
[2] HOUGHTEN PHARMACEUT,SAN DIEGO,CA 92121
关键词
TRANSFORMATION; PERALKYLATED COMBINATORIAL LIBRARIES; PERMETHYLATED PEPTIDES; PEPTIDE LIBRARY; ANTIMICROBIAL;
D O I
10.1073/pnas.91.23.11138
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The generation of diverse chemical libraries using a ''libraries from libraries'' concept is described. The central features of the approaches presented are the use of well-established solid-phase synthesis methods for the generation of combinatorial libraries, combined with the chemical transformation of such libraries while they remain attached to the solid support. The chemical libraries that are generated by this process have very different physical, chemical, and biological properties compared to the libraries from which they were derived. A wide range of chemical transformations are possible for peptide-based or other libraries, and an almost unlimited range of useful chemical diversities can be envisioned. In the example presented, the amide functionalities in an existing combinatorial library made up of peptides were permethylated while the library remained attached to the solid phase support used in its synthesis. After removal of the permethylated mixtures from their solid support, this library, now lacking the typical -CONH- amide bonds of peptides, can be tested in solution with virtually all existing assay systems to identify individual compounds having specific biological activities of interest. An illustration of the use of such Libraries is presented, in which the described permethylated library was used to identify individual permethylated compounds having potent antimicrobial activity against Gram-positive bacteria.
引用
收藏
页码:11138 / 11142
页数:5
相关论文
共 50 条
  • [21] Chemical libraries from a double click
    Topczewski, Joseph J.
    Liu, En-Chih
    [J]. NATURE, 2019, 576 (7787) : 396 - 396
  • [22] Chemical libraries from a double click
    Topczewski, Joseph J.
    Liu, En-Chih
    [J]. NATURE, 2019, 574 (7776) : 42 - 43
  • [23] Natural product-like combinatorial libraries based on privileged structures. 3. The "libraries from libraries" principle for diversity enhancement of benzopyran libraries
    Nicolaou, KC
    Pfefferkorn, JA
    Barluenga, S
    Mitchell, HJ
    Roecker, AJ
    Cao, GQ
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (41) : 9968 - 9976
  • [24] Consensus Diversity Plots: a global diversity analysis of chemical libraries
    Gonzalez-Medina, Mariana
    Prieto-Martinez, Fernando D.
    Owen, John R.
    Medina-Franco, Jose L.
    [J]. JOURNAL OF CHEMINFORMATICS, 2016, 8 : 1 - 11
  • [25] Consensus Diversity Plots: a global diversity analysis of chemical libraries
    Mariana González-Medina
    Fernando D. Prieto-Martínez
    John R. Owen
    José L. Medina-Franco
    [J]. Journal of Cheminformatics, 8
  • [27] USE OF LARGE COMBINATORIAL CHEMICAL LIBRARIES FOR ANTICANCER DRUG DISCOVERY
    SALMON, SE
    LAM, KS
    FELDER, S
    YEOMAN, H
    SCHLESSINGER, J
    ULLRICH, A
    KRCHNAK, V
    LEBL, M
    [J]. INTERNATIONAL JOURNAL OF PHARMACOGNOSY, 1995, 33 : 67 - 74
  • [28] Application of topological indices in rational design of combinatorial chemical libraries
    Tropsha, A
    Zheng, WF
    Cho, SJ
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1996, 211 : 68 - CINF
  • [29] Physico-chemical and biological analysis of true combinatorial libraries
    Boutin, JA
    Lambert, PH
    Bertin, S
    Volland, JP
    Fauchère, JL
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1999, 725 (01): : 17 - 37
  • [30] Diversity generation and chemical evolution in supramolecular libraries.
    Timmerman, P
    Reinhoudt, DN
    Calama, MC
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 220 : U110 - U110