go 6976 and axitinib

go 6976 has been researched along with axitinib in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Giranda, VL; Johnson, EF; Luo, Y; Stewart, KD; Woods, KW	1
Awrey, DE; Ban, F; Beletskaya, I; Edwards, L; Feher, M; Forrest, B; Green, E; Hodgson, R; Kiarash, R; Lang, Y; Laufer, R; Leung, G; Li, SW; Liu, Y; Luo, X; Mak, TW; Mao, G; Mason, JM; Pan, G; Pauls, HW; Plotnikova, O; Sampson, P; Wei, X; Yao, Y	1

Other Studies

2 other study(ies) available for go 6976 and axitinib

Article	Year
Pharmacological and functional comparison of the polo-like kinase family: insight into inhibitor and substrate specificity. Biochemistry, 2007, Aug-21, Volume: 46, Issue:33 Topics: Adenosine Triphosphate; Amino Acid Sequence; Androstadienes; Binding Sites; Cell Cycle Proteins; Humans; Models, Molecular; Molecular Sequence Data; Peptide Library; Polo-Like Kinase 1; Protein Conformation; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Proto-Oncogene Proteins; Pteridines; Substrate Specificity; Wortmannin	2007
The discovery of PLK4 inhibitors: (E)-3-((1H-Indazol-6-yl)methylene)indolin-2-ones as novel antiproliferative agents. Journal of medicinal chemistry, 2013, Aug-08, Volume: 56, Issue:15 Topics: Animals; Antineoplastic Agents; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; Female; Indazoles; Indoles; Mice; Mice, SCID; Models, Molecular; Protein Serine-Threonine Kinases; Stereoisomerism; Structure-Activity Relationship; Transplantation, Heterologous	2013

Article

Year

Pharmacological and functional comparison of the polo-like kinase family: insight into inhibitor and substrate specificity.

Biochemistry, 2007, Aug-21, Volume: 46, Issue:33

Topics: Adenosine Triphosphate; Amino Acid Sequence; Androstadienes; Binding Sites; Cell Cycle Proteins; Humans; Models, Molecular; Molecular Sequence Data; Peptide Library; Polo-Like Kinase 1; Protein Conformation; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Proto-Oncogene Proteins; Pteridines; Substrate Specificity; Wortmannin

2007

The discovery of PLK4 inhibitors: (E)-3-((1H-Indazol-6-yl)methylene)indolin-2-ones as novel antiproliferative agents.

Journal of medicinal chemistry, 2013, Aug-08, Volume: 56, Issue:15

Topics: Animals; Antineoplastic Agents; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; Female; Indazoles; Indoles; Mice; Mice, SCID; Models, Molecular; Protein Serine-Threonine Kinases; Stereoisomerism; Structure-Activity Relationship; Transplantation, Heterologous

2013