PI 3-kinase inhibitor, more potent than LY 294002 (Cat. No. 1130)
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Key Product Details
Description: | PI 3-kinase inhibitor, more potent than LY 294002 (Cat. No. 1130) |
Chemical Name: | 2-(4-Morpholinyl)-8-(4-aminopheny)l-4H-1-benzopyran-4-one |
Purity: | ≥98% (HPLC) |
Molecular Weight: | 322.36 |
Citations for PI 828 (5)
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Citations are publications that use Bio-Techne products. Selected citations for PI 828 include:
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Liddell et al.
(2016)
Pyrrolidine dithiocarbamate activates the Nrf2 pathway in astrocytes.
J Neuroinflammation.
13:49
PMID: 26920699 -
Rogers and Gahring
(2015)
Upregulation of Nicotinic Acetylcholine Receptor α4+β2 through a Ligand-Independent PI3Kβ Mechanism That Is Enhanced by TNFα and the Jak2/p38Mapk Pathways.
J Neurosci.
10:e0143319
PMID: 26619345 -
Moser et al.
(2014)
Functional kinomics identifies candidate therapeutic targets in head and neck cancer.
Clin Cancer Res.
20:4274
PMID: 25125259 -
Grassin-Delyle et al.
(2013)
The expression and relaxant effect of bitter taste receptors in human bronchi.
Respir Res.
14:134
PMID: 24266887 -
Li et al.
(2011)
TRPV4-mediated calcium influx into human bronchial epithelia upon exposure to diesel exhaust particles.
Environ Health Perspect.
119:784
PMID: 21245013
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Customer Reviews for PI 828 (1)
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Species: HumanAssay Type: In VitroCell Line/Tissue: 293The HEK293 (293) cell line stably co-transfected with rat nAChR subunits alpha 4 and beta 2 are well characterized, and they were maintained as described previously. This cell line also expresses TNFR1 (only weak expression of TNFR2 is detected) and no additional human nAChR subunits or acetylcholine synthetic enzymes are detected. As before PI 828 (20 nM) treatments were conducted 48 hours after cell plating
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