pd 173074 and chir 258

pd 173074 has been researched along with chir 258 in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ1
Cheng, W; Tian, X; Wang, M; Zhang, X1
Dubiel, K; Dzwonek, K; Hucz-Kalitowska, J; Lamparska-Przybysz, M; Lipner, J; Magdycz, M; Olejkowska, P; Pieczykolan, J; Piórkowska, N; Popiel, D; Stańczak, A; Stańczak, PS; Wieczorek, M; Yamani, A; Zdżalik-Bielecka, D1

Reviews

2 review(s) available for pd 173074 and chir 258

ArticleYear
An overview of the binding models of FGFR tyrosine kinases in complex with small molecule inhibitors.
    European journal of medicinal chemistry, 2017, Jan-27, Volume: 126

    Topics: Humans; Protein Binding; Protein Kinase Inhibitors; Receptor Protein-Tyrosine Kinases; Small Molecule Libraries

2017
Discovery and optimization of novel pyrazole-benzimidazole CPL304110, as a potent and selective inhibitor of fibroblast growth factor receptors FGFR (1-3).
    European journal of medicinal chemistry, 2021, Jan-15, Volume: 210

    Topics: Antineoplastic Agents; Benzimidazoles; Cell Proliferation; Drug Discovery; Humans; Protein Kinase Inhibitors; Pyrazoles; Receptor, Fibroblast Growth Factor, Type 1; Receptor, Fibroblast Growth Factor, Type 2; Receptor, Fibroblast Growth Factor, Type 3

2021

Other Studies

1 other study(ies) available for pd 173074 and chir 258

ArticleYear
Identification of potent Yes1 kinase inhibitors using a library screening approach.
    Bioorganic & medicinal chemistry letters, 2013, Aug-01, Volume: 23, Issue:15

    Topics: Binding Sites; Cell Line; Cell Survival; Drug Design; Humans; Hydrogen Bonding; Molecular Docking Simulation; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-yes; Small Molecule Libraries; Structure-Activity Relationship

2013
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