Use of Markush structure analysis techniques for descriptor generation and clustering of large combinatorial libraries

被引:41
作者
Barnard, JM
Downs, GM
von Scholley-Pfab, A
Brown, RD
机构
[1] Barnard Chem Informat Ltd, Sheffield S6 6BX, S Yorkshire, England
[2] Mol Simulat Inc, San Diego, CA USA
关键词
clustering; combinatorial library; descriptor generation; fingerprint; Markush structure;
D O I
10.1016/S1093-3263(00)80091-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This article outlines a system in which a Markush structure representation is used for analysis of a combinatorial library, giving savings in terms of storage and processing requirements when compared with an enumerated library. The Markush representation used is described, along with the way in which it can be built from a reaction- and precursor-based description of a library. The process used to generate SMILES, and structure fingerprint and calculated property descriptors for each specific molecule in the library is discussed. Comparative performance figures are given for the Markush approach and various standard fingerprint generation programs based on the enumerated members of the library; the former shows time savings of a couple of orders of magnitude. The use of these rapidly generated fingerprints for clustering of large combinatorial libraries is described. (C) 2000 by Elsevier Science Inc.
引用
收藏
页码:452 / 463
页数:12
相关论文
共 28 条
  • [1] SYBYL line notation (SLN): A versatile language for chemical structure representation
    Ash, S
    Cline, MA
    Homer, RW
    Hurst, T
    Smith, GB
    [J]. JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1997, 37 (01): : 71 - 79
  • [2] APPLICATIONS OF GRAPH-THEORY IN CHEMISTRY
    BALABAN, AT
    [J]. JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1985, 25 (03): : 334 - 343
  • [3] Chemical fragment generation and clustering software
    Barnard, JM
    Downs, GM
    [J]. JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1997, 37 (01): : 141 - 142
  • [4] COMPUTER-STORAGE AND RETRIEVAL OF GENERIC STRUCTURES IN CHEMICAL PATENTS .4. AN EXTENDED CONNECTION TABLE REPRESENTATION FOR GENERIC STRUCTURES
    BARNARD, JM
    LYNCH, MF
    WELFORD, SM
    [J]. JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1982, 22 (03): : 160 - 164
  • [5] A COMPARISON OF DIFFERENT APPROACHES TO MARKUSH STRUCTURE HANDLING
    BARNARD, JM
    [J]. JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1991, 31 (01): : 64 - 68
  • [6] Barnard JM, 1997, PERSPECT DRUG DISCOV, V7-8, P13
  • [7] BARNARD JM, 1997, DDAYL CHEM INF SYST
  • [8] BARNARD JM, 1999, DAYL CHEM INF SYST I
  • [9] BAYADA DM, 1995, 210 ACS NAT M CHIC I
  • [10] Use of structure Activity data to compare structure-based clustering methods and descriptors for use in compound selection
    Brown, RD
    Martin, YC
    [J]. JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1996, 36 (03): : 572 - 584