Optimum utilization of a compound collection or chemical library for drug discovery

被引:24
作者
Young, SS
Sheffield, CF
Farmen, M
机构
[1] OHIO STATE UNIV, DEPT STAT, COLUMBUS, OH 43210 USA
[2] GLAXO WELLCOME INC, RES TRIANGLE PK, NC 27709 USA
来源
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES | 1997年 / 37卷 / 05期
关键词
D O I
10.1021/ci970224+
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pharmaceutical companies have a large inventory of compounds for screening projects. This inventory is valuable. The optimal use of inventory requires predictions of the largest potencies that will be observed in a large potential screening set. These predictions can be made using potency values observed on a large, but smaller set of compounds using statistical methods for analyzing extreme values, The break-even point between screening and synthetic modification of lead molecules is assessed and shown to depend critically on the cost of screening and synthetic modification. The validity of the extreme value theory approach is assessed using a large set of single point assay values.
引用
收藏
页码:892 / 899
页数:8
相关论文
共 24 条
  • [1] [Anonymous], FLOOD STUD REP
  • [2] Broach JR, 1996, NATURE, V384, P14
  • [3] A GENERAL AND EXPEDIENT METHOD FOR THE SOLID-PHASE SYNTHESIS OF 1,4-BENZODIAZEPINE DERIVATIVES
    BUNIN, BA
    ELLMAN, JA
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) : 10997 - 10998
  • [4] BURDEN FR, 1989, J CHEM INF COMP SCI, V29, P255
  • [5] CASTILLO E, 1993, EXPERT SYSTEMS ANAL
  • [6] CASTILLO E, 1994, J RES NATL I STAND T
  • [7] CASTILLO E, 1988, EXTREME VALUE THEORY, pCH4
  • [8] CASTILLO E, 1988, EXTREME VALUE THEORY, pCH5
  • [9] CHAIKEN IM, 1996, MOL DIVERSITY COMBIN
  • [10] DAVISON AC, 1990, J ROY STAT SOC B MET, V52, P393