Page last updated: 2024-09-05

N-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide and jnj-7706621

N-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide has been researched along with jnj-7706621 in 1 studies

Compound Research Comparison

Studies
(N-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide)
Trials
(N-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide)
Recent Studies (post-2010)
(N-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide)
Studies
(jnj-7706621)
Trials
(jnj-7706621)
Recent Studies (post-2010) (jnj-7706621)
90740032

Protein Interaction Comparison

ProteinTaxonomyN-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide (IC50)jnj-7706621 (IC50)
[tau protein] kinase Oryctolagus cuniculus (rabbit)0.0849
Vascular endothelial growth factor receptor 2Rattus norvegicus (Norway rat)0.0849
Aurora kinase AHomo sapiens (human)0.011
Tyrosine-protein kinase JAK2Homo sapiens (human)1.4805
G2/mitotic-specific cyclin-B2Homo sapiens (human)0.0062
cAMP-dependent protein kinase catalytic subunit alphaBos taurus (cattle)0.0849
Epidermal growth factor receptorHomo sapiens (human)0.0849
Insulin receptorHomo sapiens (human)0.0849
Cyclin-dependent kinase 1Homo sapiens (human)0.0537
Platelet-derived growth factor receptor betaHomo sapiens (human)0.0849
Calcium/calmodulin-dependent protein kinase type II subunit alphaRattus norvegicus (Norway rat)0.0849
Cyclin-dependent kinase 4Homo sapiens (human)0.11
G2/mitotic-specific cyclin-B1Homo sapiens (human)0.0652
Cyclin-A2Homo sapiens (human)0.0731
Fibroblast growth factor receptor 2Homo sapiens (human)0.1042
G1/S-specific cyclin-D1Homo sapiens (human)0.11
Cyclin-dependent kinase 2Homo sapiens (human)0.0575
G1/S-specific cyclin-D1Mus musculus (house mouse)0.0849
Cyclin-dependent kinase 4Mus musculus (house mouse)0.0849
Vascular endothelial growth factor receptor 2Homo sapiens (human)0.13
Glycogen synthase kinase-3 alphaHomo sapiens (human)0.041
Glycogen synthase kinase-3 betaHomo sapiens (human)0.041
Mitogen-activated protein kinase 1Rattus norvegicus (Norway rat)0.0849
Cyclin-A1Homo sapiens (human)0.002
Disintegrin and metalloproteinase domain-containing protein 17Homo sapiens (human)0.0062
Cyclin-dependent kinase 3Homo sapiens (human)0.058
Cyclin-dependent-like kinase 5 Homo sapiens (human)0.0126
Casein kinase I isoform deltaRattus norvegicus (Norway rat)0.0849
G2/mitotic-specific cyclin-B3Homo sapiens (human)0.0062
Aurora kinase BHomo sapiens (human)0.0095

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ1

Other Studies

1 other study(ies) available for N-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamide and jnj-7706621

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