Page last updated: 2024-08-23

staurosporine and sar 020106

staurosporine has been researched along with sar 020106 in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Addison, G; Aherne, GW; Box, G; Boxall, K; Burns, S; Cherry, M; Cheung, KM; Collins, I; de Haven Brandon, A; Eccles, SA; Ellard, J; Eve, P; Fisher, M; Garrett, MD; Hayes, A; Klair, S; Matthews, TP; Piton, N; Proisy, N; Raynaud, FI; Reader, JC; Scanlon, J; Taylor, S; Valenti, M; van Montfort, RL; Walton, MI; Westwood, IM; Williams, DH	1

Other Studies

1 other study(ies) available for staurosporine and sar 020106

Article	Year
Structure-guided evolution of potent and selective CHK1 inhibitors through scaffold morphing. Journal of medicinal chemistry, 2011, Dec-22, Volume: 54, Issue:24 Topics: Adenosine Triphosphate; Animals; Antineoplastic Agents; Binding Sites; Biological Availability; Cell Line, Tumor; Checkpoint Kinase 1; Crystallography, X-Ray; Drug Screening Assays, Antitumor; Humans; Isoquinolines; Mice; Mice, Nude; Molecular Conformation; Neoplasm Transplantation; Protein Kinase Inhibitors; Protein Kinases; Pyrazines; Pyridines; Stereoisomerism; Structure-Activity Relationship; Transplantation, Heterologous	2011

Article

Year

Structure-guided evolution of potent and selective CHK1 inhibitors through scaffold morphing.

Journal of medicinal chemistry, 2011, Dec-22, Volume: 54, Issue:24

Topics: Adenosine Triphosphate; Animals; Antineoplastic Agents; Binding Sites; Biological Availability; Cell Line, Tumor; Checkpoint Kinase 1; Crystallography, X-Ray; Drug Screening Assays, Antitumor; Humans; Isoquinolines; Mice; Mice, Nude; Molecular Conformation; Neoplasm Transplantation; Protein Kinase Inhibitors; Protein Kinases; Pyrazines; Pyridines; Stereoisomerism; Structure-Activity Relationship; Transplantation, Heterologous

2011