GSK2606414

  Cat. No.:  DC7142   Featured
Chemical Structure
1337531-36-8
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Field of application
GSK2606414 is an orally available, potent, and selective PERK inhibitor with an IC50 of 0.4 nM.
Cas No.: 1337531-36-8
Chemical Name: 7Methyl-5-(1-{[3-(trifluoroMethyl)phenyl]acetyl}-2,3-dihydro1Hindol-5-yl)7Hpyrrolo[2,3d]pyrimidin-4-amine
Synonyms: GSK2606414,GSK-2606414,GSK 2606414
SMILES: C1=CC(C2C3C(N)=NC=NC=3N(C)C=2)=CC2CCN(C(=O)CC3=CC=CC(C(F)(F)F)=C3)C1=2
Formula: C24H20F3N5O
M.Wt: 451.44
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: GSK2606414 is a cell-permeable and orally available PERK inhibitor with an IC50 of 0.4 nM.
In Vivo: GSK2606414 (50 and 150 mg/kg, p.o.) inhibits the growth of a human tumor xenograft in mice[1].
In Vitro: GSK2606414 inhibits PERK activation in cells[1].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC7431 ISRIB ISRIB (trans-isomer), the trans-isomer of ISRIB, is a potent and selective PERK inhibitor with IC50 of 5 nM.
DC7142 GSK2606414 GSK2606414 is an orally available, potent, and selective PERK inhibitor with an IC50 of 0.4 nM.
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