High throughput screening for new drug discovery

被引:0
|
作者
Lin, BB [1 ]
机构
[1] PANLABA TAIWAN LTD,TAIPEI 112,TAIWAN
关键词
high throughput screening (HTS); drug discovery; laboratory information management systems (LIMS); natural products discovery; secondary microbial metabolites; combinatorial chemistry; peptide combinatorial libraries; combinatorial organic synthesis;
D O I
暂无
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The world pharmaceutical market, which was valued at $247.9 billion in 1994, is forecasted to grow to $342 billion by 1999. High throughput screening(HTS) is attracting attention as a novel methodology for new drug discovery, HTS is expected to expand the scale from one thousand to one hundred thousand times the current level by utilizing robots, laboratory information management systems(LIMS), various sources to screen natural products(plant extracts, secondary microbial metabolites), peptide combinatorial libraries and combinatorial organic synthesis(COS) for new therapeutics, Instrumentation, target selection, source material, sample preparation, primary and secondary assays, isolation, purification and structure elucidation are all important for HTS.
引用
收藏
页码:233 / 241
页数:9
相关论文
共 50 条
  • [41] High throughput gene expression screening: Its emerging role in drug discovery
    Freeman, T
    MEDICINAL RESEARCH REVIEWS, 2000, 20 (03) : 197 - 202
  • [42] High Throughput Screening of Physicochemical Properties and In Vitro ADME Profiling in Drug Discovery
    Wan, Hong
    Holmen, Anders G.
    COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2009, 12 (03) : 315 - 329
  • [43] Application of high-throughput ADME screening to the drug discovery process.
    Polzer, RJ
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2001, 221 : U64 - U64
  • [44] Fluorescence lifetime techniques in high-throughput screening for drug discovery.
    French, T
    Owicki, JC
    Modlin, DN
    Crawford, K
    BIOPHYSICAL JOURNAL, 1998, 74 (02) : A37 - A37
  • [45] Cloud computing platform for high-throughput virtual screening and drug discovery
    Wein, Samuel
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 244
  • [46] In vivo quantitative high-throughput screening for drug discovery and comparative toxicology
    Dranchak, Patricia K.
    Oliphant, Erin
    Queme, Bryan
    Lamy, Laurence
    Wang, Yuhong
    Huang, Ruili
    Xia, Menghang
    Tao, Dingyin
    Inglese, James
    DISEASE MODELS & MECHANISMS, 2023, 16 (03)
  • [47] In vitro high throughput screening of compounds for favorable metabolic properties in drug discovery
    Masimirembwa, CM
    Thompson, R
    Andersson, TB
    COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2001, 4 (03) : 245 - 263
  • [48] Advances in high-throughput screening for drug discovery - Results of a worldwide study
    Fox, SJ
    Wang, HSL
    CHIMICA OGGI-CHEMISTRY TODAY, 2000, 18 (1-2) : 20 - 22
  • [49] Integration of organoids in peptide drug discovery: Rise of the high-throughput screening
    Zhang, Siqi
    Shen, Jieting
    Wang, Xingkai
    Sun, Xiaona
    Wu, Yuxuan
    Zhang, Ming-Rong
    Wang, Rui
    Hu, Kuan
    VIEW, 2023, 4 (06)
  • [50] Flow cytometry for drug discovery, receptor pharmacology and high-throughput screening
    Sklar, Larry A.
    Carter, Mark B.
    Edwards, Bruce S.
    CURRENT OPINION IN PHARMACOLOGY, 2007, 7 (05) : 527 - 534