GSK 626616
Chemical Name: (5Z)-2-[(2,6-Dichlorophenyl)amino]-5-(6-quinoxalinylmethylene)-4(5H)-thiazolone
Purity: ≥95%
Biological Activity
GSK 626616 is a potent and selective DYRK inhibitor (IC50 = 0.7 nM for DYRK3, similar potency for DYRK1 and 2). Exhibits ~20-fold selectivity over casein kinase 2 and negligible activity against a panel of 451 kinases screened. Enhances number of CFU-E stimulated by Epo from human marrow. Increases hemoglobin levels in anemic mice. Orally bioavailable.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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GSK626616: A DYRK3 inhibitor as a potential new therapy for the treatment of anemia.
Erickson-Miller et al.
Blood, 2007;110:510 -
Dual specificity kinase DYRK3 couples stress granule condensation/dissolution to mTORC1 signaling.
Wippich et al.
Cell, 2013;152:791 -
Kinase-controlled phase transition of membraneless organelles in mitosis.
Rai et al.
Nature, 2018;559:211
Product Datasheets
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Citation for GSK 626616
The citations listed below are publications that use Tocris products. Selected citations for GSK 626616 include:
1 Citation: Showing 1 - 1
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Mammalian cell growth dynamics in mitosis.
Authors: Scott R Et al.
Elife 2019;8
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