Page last updated: 2024-09-04

cyc 202 and whi p180

cyc 202 has been researched along with whi p180 in 2 studies

Compound Research Comparison

Studies (cyc 202)	Trials (cyc 202)	Recent Studies (post-2010) (cyc 202)	Studies (whi p180)	Trials (whi p180)	Recent Studies (post-2010) (whi p180)
979	7	393	15	0	8

Protein Interaction Comparison

Protein	Taxonomy	whi p180 (IC50)
Chain A, CYCLIN-DEPENDENT KINASE 2	Homo sapiens (human)	1
Chain A, P38 KINASE	Homo sapiens (human)	1
Proto-oncogene tyrosine-protein kinase receptor Ret	Homo sapiens (human)	0.1922
Fibroblast growth factor receptor 1	Homo sapiens (human)	0.125
Vascular endothelial growth factor receptor 1	Homo sapiens (human)	0.1625
Cyclin-dependent kinase 2	Homo sapiens (human)	1
Phosphatidylinositol 3-kinase regulatory subunit alpha	Homo sapiens (human)	0.002
Ephrin type-B receptor 2	Homo sapiens (human)	1.2
Kinesin-1 heavy chain	Homo sapiens (human)	0.38
Vascular endothelial growth factor receptor 2	Homo sapiens (human)	0.1787
Mu-type opioid receptor	Cavia porcellus (domestic guinea pig)	0.05

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	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bhattacharjee, AK; Ellis, W; Gerena, L; Geyer, JA; Kathcart, AK; Kyle, DE; Li, Z; Lopez-Sanchez, M; Nichols, DA; Prigge, ST; Terrell, J; Waters, NC; Woodard, CL	1
Bullock, AN; Fedorov, O; Knapp, S; Marsden, B; Müller, S; Pogacic, V; Rellos, P; Schwaller, J; Sundström, M	1

Other Studies

2 other study(ies) available for cyc 202 and whi p180

Article	Year
Oxindole-based compounds are selective inhibitors of Plasmodium falciparum cyclin dependent protein kinases. Journal of medicinal chemistry, 2003, Aug-28, Volume: 46, Issue:18 Topics: Amino Acid Sequence; Animals; Antimalarials; Cyclin-Dependent Kinase-Activating Kinase; Cyclin-Dependent Kinases; Enzyme Inhibitors; Humans; Indoles; Models, Molecular; Molecular Sequence Data; Plasmodium falciparum; Structure-Activity Relationship	2003
A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. Proceedings of the National Academy of Sciences of the United States of America, 2007, Dec-18, Volume: 104, Issue:51 Topics: Amino Acid Sequence; Binding Sites; Clinical Trials as Topic; Drug Evaluation, Preclinical; Enzyme Stability; Humans; Molecular Sequence Data; Phylogeny; Protein Array Analysis; Protein Conformation; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases	2007

Article

Year

Oxindole-based compounds are selective inhibitors of Plasmodium falciparum cyclin dependent protein kinases.

Journal of medicinal chemistry, 2003, Aug-28, Volume: 46, Issue:18

Topics: Amino Acid Sequence; Animals; Antimalarials; Cyclin-Dependent Kinase-Activating Kinase; Cyclin-Dependent Kinases; Enzyme Inhibitors; Humans; Indoles; Models, Molecular; Molecular Sequence Data; Plasmodium falciparum; Structure-Activity Relationship

2003

A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases.

Proceedings of the National Academy of Sciences of the United States of America, 2007, Dec-18, Volume: 104, Issue:51

Topics: Amino Acid Sequence; Binding Sites; Clinical Trials as Topic; Drug Evaluation, Preclinical; Enzyme Stability; Humans; Molecular Sequence Data; Phylogeny; Protein Array Analysis; Protein Conformation; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases

2007