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FMK
SKU
HY-52101A-10 mg
Category Reference compound
Tags Cancer, MAPK/ERK Pathway, Ribosomal S6 Kinase (RSK)
$132 – $768
Products Details
Product Description
– FMK is a an irreversible RSK2 kinase inhibitor, that covalently modifies the C-terminal kinase domain of RSK.
Web ID
– HY-52101A
Storage Temperature
– 4°C (Powder, stored under nitrogen)
Shipping
– Room Temperature
Applications
– Cancer-Kinase/protease
Molecular Formula
– C18H19FN4O2
References
– [1]Bain J, et al.
The selectivity of protein kinase inhibitors: a further update.
Biochem J. 2007 Dec 15;408(3):297-315.|[2]Kang S, et al. FGFR3 activates RSK2 to mediate hematopoietic transformation through tyrosine phosphorylation of RSK2 and activation of the MEK/ERK pathway. Cancer Cell. 2007 Sep;12(3):187-9.|[3]Cuello F, et al.
Evidence for direct regulation of myocardial Na+/H+ exchanger isoform 1 phosphorylation and activity by 90-kDa ribosomal S6 kinase (RSK): effects of the novel and specific RSK inhibitor fmk on responses to alpha1-adrenergic stimulation.
CAS Number
– 821794-92-7
Molecular Weight
– 342.37
Compound Purity
– 99.45
SMILES
– FCC(C1=C(C2=C(N=CN=C2N1CCCO)N)C3=CC=C(C=C3)C)=O
Clinical Information
– No Development Reported
Research Area
– Cancer
Solubility
– DMSO : 50 mg/mL (ultrasonic)
Target
– Ribosomal S6 Kinase (RSK)
Isoform
– RSK2
Pathway
– MAPK/ERK Pathway
Product type
– Reference compound
Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.