Page last updated: 2024-09-02

fingolimod hydrochloride and mk 2206

fingolimod hydrochloride has been researched along with mk 2206 in 1 studies

Compound Research Comparison

Studies
(fingolimod hydrochloride)
Trials
(fingolimod hydrochloride)
Recent Studies (post-2010)
(fingolimod hydrochloride)
Studies
(mk 2206)
Trials
(mk 2206)
Recent Studies (post-2010) (mk 2206)
2,7711572,06235528347

Protein Interaction Comparison

ProteinTaxonomyfingolimod hydrochloride (IC50)mk 2206 (IC50)
RAC-alpha serine/threonine-protein kinaseHomo sapiens (human)0.008
RAC-beta serine/threonine-protein kinaseHomo sapiens (human)0.012
RAC-gamma serine/threonine-protein kinaseHomo sapiens (human)0.065

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, CS; de Necochea-Campion, R; Liu, X; Mirshahidi, S; Shouse, G1

Other Studies

1 other study(ies) available for fingolimod hydrochloride and mk 2206

ArticleYear
Novel B55α-PP2A mutations in AML promote AKT T308 phosphorylation and sensitivity to AKT inhibitor-induced growth arrest.
    Oncotarget, 2016, Sep-20, Volume: 7, Issue:38

    Topics: Cell Line, Tumor; Cell Proliferation; Cell Survival; Codon; Enzyme Inhibitors; Fingolimod Hydrochloride; Gene Expression Regulation, Leukemic; Heterocyclic Compounds, 3-Ring; Humans; Immunophenotyping; Leukemia, Myeloid, Acute; Mutation; Phosphorylation; Protein Phosphatase 2; Proto-Oncogene Proteins c-akt

2016