Compounds > quinazolines

Page last updated: 2024-08-21

quinazolines and hesperadin

quinazolines has been researched along with hesperadin in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (50.00)	29.6817
2010's	3 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Doggrell, SA	1
Beckmann, R; Burke, T; Collins, E; Dempsey, J; Diaz, B; Toth, J; Yang, H; Ye, X	1
McLaughlin, ML; Talele, TT	1
Foley, EA; Kapoor, TM; Maldonado, M	1
Beullens, M; Bollen, M; Lesage, B; Qian, J	1
Ali, N; Bhattacharyya, A; Chhajer, R; Das, N; Didwania, N; Palit, P; Shadab, M; Vaidya, T	1

Reviews

1 review(s) available for quinazolines and hesperadin

Article	Year
Dawn of Aurora kinase inhibitors as anticancer drugs. Expert opinion on investigational drugs, 2004, Volume: 13, Issue:9 Topics: Animals; Antineoplastic Agents; Aurora Kinase A; Aurora Kinases; Benzamides; Enzyme Inhibitors; Humans; Indoles; Molecular Structure; Piperazines; Protein Serine-Threonine Kinases; Quinazolines; Sulfonamides	2004

Other Studies

5 other study(ies) available for quinazolines and hesperadin

Article	Year
Mitotic requirement for aurora A kinase is bypassed in the absence of aurora B kinase. FEBS letters, 2005, Jun-20, Volume: 579, Issue:16 Topics: Aurora Kinase B; Aurora Kinases; Benzamides; Cell Cycle Proteins; Cell Line, Tumor; Humans; Indoles; Mitosis; Polyploidy; Protein Kinase Inhibitors; Protein Kinases; Protein Serine-Threonine Kinases; Quinazolines; RNA Interference; Sulfonamides	2005
Molecular docking/dynamics studies of Aurora A kinase inhibitors. Journal of molecular graphics & modelling, 2008, Volume: 26, Issue:8 Topics: Aurora Kinases; Binding Sites; Computer Simulation; Hydrogen Bonding; Indoles; Inhibitory Concentration 50; Models, Molecular; Molecular Conformation; Molecular Structure; Protein Binding; Protein Conformation; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Pyrazoles; Pyrimidines; Quinazolines; Structure-Activity Relationship; Sulfonamides	2008
Formation of stable attachments between kinetochores and microtubules depends on the B56-PP2A phosphatase. Nature cell biology, 2011, Aug-28, Volume: 13, Issue:10 Topics: Aurora Kinase B; Aurora Kinases; Benzamides; Cell Cycle Proteins; Chromosome Segregation; HeLa Cells; Humans; Indoles; Kinetochores; Leupeptins; Microscopy, Fluorescence; Microtubules; Nocodazole; Phosphorylation; Polo-Like Kinase 1; Protein Kinase Inhibitors; Protein Phosphatase 2; Protein Serine-Threonine Kinases; Proto-Oncogene Proteins; Pteridines; Quinazolines; Recombinant Fusion Proteins; RNA Interference; Sulfonamides; Time Factors; Transfection; Tumor Suppressor Proteins	2011
Aurora B defines its own chromosomal targeting by opposing the recruitment of the phosphatase scaffold Repo-Man. Current biology : CB, 2013, Jun-17, Volume: 23, Issue:12 Topics: Amino Acid Sequence; Animals; Aurora Kinase B; Benzamides; Carrier Proteins; Cell Cycle Proteins; Cell Line, Tumor; Centromere; Chromosomes; Histones; Humans; Indoles; Intracellular Signaling Peptides and Proteins; Kinetochores; Lactams; Mice; Mitosis; Molecular Sequence Data; Nuclear Proteins; Phosphorylation; Proteasome Inhibitors; Protein Binding; Protein Serine-Threonine Kinases; Quinazolines; Spindle Apparatus; Sulfonamides	2013
Leishmania donovani Aurora kinase: A promising therapeutic target against visceral leishmaniasis. Biochimica et biophysica acta, 2016, Volume: 1860, Issue:9 Topics: Adenosine Triphosphate; Amino Acid Sequence; Animals; Aurora Kinases; Aza Compounds; Catalytic Domain; Cell Cycle; Cell Survival; Cytokinesis; Female; Indoles; Kinetics; Leishmania donovani; Leishmaniasis, Visceral; Mice; Mice, Inbred BALB C; Molecular Docking Simulation; Organophosphates; Protein Kinase Inhibitors; Quinazolines; Sulfonamides	2016