NU 9056
Chemical Name: 5-(1,2-Thiazol-5-yldisulfanyl)-1,2-thiazole
Biological Activity
NU 9056 is a selective KAT5 (Tip60) histone acetyltransferase inhibitor (IC50 values are < 2, 60, 36, and >100 μM for KAT5, p300, pCAF and GCN5, respectively). Inhibits protein acetylation in prostate cancer cell lines and blocks DNA damage response. Decreases proliferation of LNCaP cells; induces apoptosis via caspase activation.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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Characterisation of a Tip60 specific inhibitor, NU9056, in prostate cancer.
Coffey et al.
PLoS One, 2012;7:e45539
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Citations for NU 9056
The citations listed below are publications that use Tocris products. Selected citations for NU 9056 include:
6 Citations: Showing 1 - 6
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PRMT5-mediated regulation of developmental myelination.
Authors: Scaglione Et al.
Nat Commun 2018;9:2840
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Blocking H2A.Z Incorporation via Tip60 Inhibition Promotes Systems Consolidation of Fear Memory in Mice.
Authors: Narkaj Et al.
Eneuro 2018;5
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Expression of DHA-Metabolizing Enzyme Alox15 is Regulated by Selective Histone Acetylation in Neuroblastoma Cells.
Authors: Ho Et al.
Neurochem Res 2018;43:540
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Novel complex of HAT protein TIP60 and nuclear receptor PXR promotes cell migration and adhesion.
Authors: Bakshi Et al.
Sci Rep 2017;7:3635
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Novel detection of post-translational modifications in human monocyte-derived dendritic cells after chronic alcohol exposure: Role of inflammation regulator H4K12ac.
Authors: Parira Et al.
Sci Rep 2017;7:11236
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Lysine acetyltransferase NuA4 and acetyl-CoA regulate glucose-deprived stress granule formation in Saccharomyces cerevisiae.
Authors: Rollins Et al.
PLoS Genet 2017;13:e1006626
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