Page last updated: 2024-09-05

orantinib and su 5402

orantinib has been researched along with su 5402 in 2 studies

Compound Research Comparison

Studies
(orantinib)
Trials
(orantinib)
Recent Studies (post-2010)
(orantinib)
Studies
(su 5402)
Trials
(su 5402)
Recent Studies (post-2010) (su 5402)
1101936191077

Protein Interaction Comparison

ProteinTaxonomyorantinib (IC50)su 5402 (IC50)
Epidermal growth factor receptorHomo sapiens (human)0.1867
Platelet-derived growth factor receptor betaHomo sapiens (human)0.2675
Fibroblast growth factor receptor 1Homo sapiens (human)2.0262
Proto-oncogene tyrosine-protein kinase SrcHomo sapiens (human)0.1867
Fibroblast growth factor receptor 1Mus musculus (house mouse)10
Vascular endothelial growth factor receptor 2Homo sapiens (human)0.1136
Vascular endothelial growth factor receptor 1Mus musculus (house mouse)0.4
Mu-type opioid receptorCavia porcellus (domestic guinea pig)0.02

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Liang, C; McMahon, G; Rice, A; Schreck, R; Shawver, LK; Sun, L; Tang, C; Tang, F; Tran, N; Waltz, K1
Al-awar, R; Fladd, C; Jiang, C; Nguyen, L; Prakesch, M; Rotin, D; Trzcinska-Daneluti, AM; Uehling, D1

Other Studies

2 other study(ies) available for orantinib and su 5402

ArticleYear
Design, synthesis, and evaluations of substituted 3-[(3- or 4-carboxyethylpyrrol-2-yl)methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases.
    Journal of medicinal chemistry, 1999, Dec-16, Volume: 42, Issue:25

    Topics: Drug Design; Drug Evaluation, Preclinical; Endothelial Growth Factors; Enzyme Inhibitors; Fibroblast Growth Factors; Humans; Indoles; Lymphokines; Magnetic Resonance Spectroscopy; Mass Spectrometry; Molecular Structure; Platelet-Derived Growth Factor; Receptor Protein-Tyrosine Kinases; Vascular Endothelial Growth Factor A; Vascular Endothelial Growth Factors

1999
Use of kinase inhibitors to correct ΔF508-CFTR function.
    Molecular & cellular proteomics : MCP, 2012, Volume: 11, Issue:9

    Topics: Animals; Benzazepines; Cell Line; Cricetinae; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Dogs; Glycogen Synthase Kinase 3; Glycogen Synthase Kinase 3 beta; HEK293 Cells; Humans; Indoles; Ion Transport; Membrane Proteins; Oxindoles; Propionates; Protein Kinase Inhibitors; Protein Transport; Protein-Tyrosine Kinases; Pyrroles; Receptor, Fibroblast Growth Factor, Type 1; Receptors, Platelet-Derived Growth Factor; Receptors, Vascular Endothelial Growth Factor; RNA Interference; RNA, Small Interfering; Sequence Deletion; Signal Transduction; Zearalenone

2012