Compounds > erlotinib
Page last updated: 2024-09-05

erlotinib and gw8510

erlotinib has been researched along with gw8510 in 2 studies

Compound Research Comparison

Studies
(erlotinib)		Trials
(erlotinib)		Recent Studies (post-2010)
(erlotinib)		Studies
(gw8510)		Trials
(gw8510)		Recent Studies (post-2010) (gw8510)
221018025016

Protein Interaction Comparison

ProteinTaxonomyerlotinib (IC50)gw8510 (IC50)
Cyclin-T1Homo sapiens (human)0.54
High affinity nerve growth factor receptorHomo sapiens (human)0.009
Cyclin-dependent kinase 1Homo sapiens (human)0.0745
Cyclin-dependent kinase 4Homo sapiens (human)0.139
G2/mitotic-specific cyclin-B1Homo sapiens (human)0.049
Cyclin-A2Homo sapiens (human)0.0065
G1/S-specific cyclin-D1Homo sapiens (human)0.139
G1/S-specific cyclin-E1Homo sapiens (human)0.003
Cyclin-dependent kinase 2Homo sapiens (human)0.0079
Cyclin-dependent kinase 7Homo sapiens (human)0.317
Cyclin-dependent kinase 9Homo sapiens (human)0.54
Cyclin-HHomo sapiens (human)0.317
CDK-activating kinase assembly factor MAT1Homo sapiens (human)0.317
Cyclin-A1Homo sapiens (human)0.01
Cyclin-dependent-like kinase 5 Homo sapiens (human)0.007
Cyclin-dependent kinase 5 activator 1Homo sapiens (human)0.007
Serine/threonine-protein kinase TBK1Homo sapiens (human)0.17

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
Hajduk, PJ; Johnson, EF; Kifle, L; Merta, PJ; Metz, JT; Soni, NB1
Balke-Want, H; Basu, D; Engel, J; Ercanoglu, MS; Rauh, D; Richters, A; Tesch, R; Thomas, RK1

Other Studies

2 other study(ies) available for erlotinib and gw8510

ArticleYear
Navigating the kinome.
    Nature chemical biology, 2011, Volume: 7, Issue:4

    Topics: Drug Design; Pharmacogenetics; Protein Kinases; Proteome; Systems Biology

2011
Identification and further development of potent TBK1 inhibitors.
    ACS chemical biology, 2015, Jan-16, Volume: 10, Issue:1

    Topics: Animals; Cell Line; Drug Design; Humans; Macrophages; Mice; Molecular Docking Simulation; Molecular Structure; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Small Molecule Libraries; Structure-Activity Relationship

2015