Future considerations in HTS: the acute effect of chronic dilemmas

被引:12
作者
Sills, MA [1 ]
机构
[1] Novartis Pharmaceut Corp, Summit, NJ 07901 USA
关键词
D O I
10.1016/S1359-6446(98)01202-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Today, in the area of Biomolecular Screening, it would seem that 'something better' in terms of instrumentation or assay technology, is emerging almost every week. From the standpoint of planning, this presents significant challenges to decide whether to integrate the 'latest and greatest' advance, whether to wait just a few months for the next advance, which may make the current advance obsolete, or perhaps to maintain the status quo. This decision would be considerably simpler if there was a clear, optimal strategy for identifying and selecting lead compound This article attempts to look at this issue from the perspective of discussing the pros and cons to several approaches to lead discovery.
引用
收藏
页码:304 / 312
页数:9
相关论文
共 4 条
  • [1] Scintillation proximity assay: A versatile high-throughput screening technology
    Cook, ND
    [J]. DRUG DISCOVERY TODAY, 1996, 1 (07) : 287 - 294
  • [2] Time-resolved fluorometry: an overview of the labels and core technologies for drug screening applications
    Hemmila, I
    Webb, S
    [J]. DRUG DISCOVERY TODAY, 1997, 2 (09) : 373 - 381
  • [3] Kolb J.M., 1996, J BIOMOL NMR, V1, P203
  • [4] Assay miniaturization for ultra-high throughput screening of combinatorial and discrete compound libraries: A 9600-well (0.2 microliter) assay system
    Oldenburg, KR
    Zhang, JH
    Chen, TM
    Maffia, A
    Blom, KF
    Combs, AP
    Chung, TDY
    [J]. JOURNAL OF BIOMOLECULAR SCREENING, 1998, 3 (01) : 55 - 62