Page last updated: 2024-09-04

birb 796 and bi 2536

birb 796 has been researched along with bi 2536 in 2 studies

Compound Research Comparison

Studies
(birb 796)
Trials
(birb 796)
Recent Studies (post-2010)
(birb 796)
Studies
(bi 2536)
Trials
(bi 2536)
Recent Studies (post-2010) (bi 2536)
13758019313169

Protein Interaction Comparison

ProteinTaxonomybirb 796 (IC50)bi 2536 (IC50)
Bromodomain-containing protein 4Homo sapiens (human)0.1211
Cytochrome P450 3A4Homo sapiens (human)0.0593
Transcription initiation factor TFIID subunit 1Homo sapiens (human)0.16
Serine/threonine-protein kinase PLK1Homo sapiens (human)0.0549
Bromodomain testis-specific proteinHomo sapiens (human)0.83
Serine/threonine-protein kinase PLK3Homo sapiens (human)0.0148
Serine/threonine-protein kinase PLK2Homo sapiens (human)0.0123
ALK tyrosine kinase receptorHomo sapiens (human)0.408

Research

Studies (2)

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 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ciceri, P; Davis, MI; Herrgard, S; Hocker, M; Hunt, JP; Pallares, G; Treiber, DK; Wodicka, LM; Zarrinkar, PP1
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ1

Other Studies

2 other study(ies) available for birb 796 and bi 2536

ArticleYear
Comprehensive analysis of kinase inhibitor selectivity.
    Nature biotechnology, 2011, Oct-30, Volume: 29, Issue:11

    Topics: Catalysis; Drug Design; Enzyme Stability; High-Throughput Screening Assays; Humans; Protein Binding; Protein Kinase Inhibitors; Protein Kinases; Proteomics; Signal Transduction; Substrate Specificity

2011
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