Page last updated: 2024-09-03

4-(3-chloroanilino)quinazoline and N-[3-(trifluoromethyl)phenyl]-4-quinazolinamine

4-(3-chloroanilino)quinazoline has been researched along with N-[3-(trifluoromethyl)phenyl]-4-quinazolinamine in 3 studies

Compound Research Comparison

Studies
(4-(3-chloroanilino)quinazoline)
Trials
(4-(3-chloroanilino)quinazoline)
Recent Studies (post-2010)
(4-(3-chloroanilino)quinazoline)
Studies
(N-[3-(trifluoromethyl)phenyl]-4-quinazolinamine)
Trials
(N-[3-(trifluoromethyl)phenyl]-4-quinazolinamine)
Recent Studies (post-2010) (N-[3-(trifluoromethyl)phenyl]-4-quinazolinamine)
802703

Protein Interaction Comparison

ProteinTaxonomy4-(3-chloroanilino)quinazoline (IC50)N-[3-(trifluoromethyl)phenyl]-4-quinazolinamine (IC50)
Epidermal growth factor receptorHomo sapiens (human)0.5794
Broad substrate specificity ATP-binding cassette transporter ABCG2Homo sapiens (human)1.245

Research

Studies (3)

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

Authors

AuthorsStudies
Bridges, AJ; Cody, DR; Denny, WA; Fry, DW; McMichael, A; Rewcastle, GW; Zhou, H1
Bridges, AJ; Cody, DR; Denny, WA; Fry, DW; Kraker, AJ; McMichael, A; Rewcastle, GW; Showalter, HD; Zhou, H1
Caflisch, A; Dey, F; Huang, D; Kolb, P1

Other Studies

3 other study(ies) available for 4-(3-chloroanilino)quinazoline and N-[3-(trifluoromethyl)phenyl]-4-quinazolinamine

ArticleYear
Tyrosine kinase inhibitors. 5. Synthesis and structure-activity relationships for 4-[(phenylmethyl)amino]- and 4-(phenylamino)quinazolines as potent adenosine 5'-triphosphate binding site inhibitors of the tyrosine kinase domain of the epidermal growth fa
    Journal of medicinal chemistry, 1995, Sep-01, Volume: 38, Issue:18

    Topics: Adenosine Triphosphate; Amino Acid Sequence; ErbB Receptors; Humans; Molecular Sequence Data; Protein-Tyrosine Kinases; Quinazolines; Structure-Activity Relationship; Tumor Cells, Cultured; Type C Phospholipases

1995
Tyrosine kinase inhibitors. 8. An unusually steep structure-activity relationship for analogues of 4-(3-bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a potent inhibitor of the epidermal growth factor receptor.
    Journal of medicinal chemistry, 1996, Jan-05, Volume: 39, Issue:1

    Topics: Aniline Compounds; Binding Sites; Blotting, Western; Enzyme Inhibitors; Epidermal Growth Factor; ErbB Receptors; Humans; Kinetics; Molecular Conformation; Molecular Structure; Phosphorylation; Protein Binding; Quinazolines; Structure-Activity Relationship; Tumor Cells, Cultured

1996
Discovery of kinase inhibitors by high-throughput docking and scoring based on a transferable linear interaction energy model.
    Journal of medicinal chemistry, 2008, Mar-13, Volume: 51, Issue:5

    Topics: Humans; Models, Molecular; Protein Binding; Protein Kinase Inhibitors; Protein Kinases; Quantitative Structure-Activity Relationship; Static Electricity; Thermodynamics

2008