YK 3-237

Discontinued Product

5667 has been discontinued.

View all Class III HDACs (Sirtuins) products.
Description: SIRT1 activator
Chemical Name: B-[2-Methoxy-5-[(1E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propen-1-yl]phenyl]boronic acid
Purity: ≥98% (HPLC)
Datasheet
Citations
Reviews
Literature (1)

Biological Activity for YK 3-237

YK 3-237 is a SIRT1 activator. Inhibits proliferation of breast cancer cell lines expressing mutant p53. Induces G2/M cell cycle arrest and apoptosis in triple negative breast cancer cells (TNBCs) in vitro.

Technical Data for YK 3-237

M. Wt 372.18
Formula C19H21BO7
Storage Store at -20°C
Purity ≥98% (HPLC)
CAS Number 1215281-19-8
PubChem ID 24881094
InChI Key AKNGHUAJAODDJA-FNORWQNLSA-N
Smiles O=C(/C=C/C1=CC=C(OC)C(B(O)O)=C1)C2=CC(OC)=C(OC)C(OC)=C2

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.

References for YK 3-237

References are publications that support the biological activity of the product.

Yi et al (2013) Targeting mutant p53 by a SIRT1 activator YK-3-237 inhibits the proliferation of triple-negative breast cancer cells. Oncotarget 4 984 PMID: 23846322

Ponnusamy et al (2015) Activation of sirtuin-1 promotes renal fibroblast activation and aggravates renal fibrogenesis. J.Pharmacol.Exp.Ther 354 142 PMID: 26022003

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Keywords: YK 3-237, YK 3-237 supplier, YK3-237, SIRT1, sirtuins, activators, activates, deacetylases, antiproliferative, Class, III, HDACs, (Sirtuins), 5667, Tocris Bioscience

Citations for YK 3-237

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Currently there are no citations for YK 3-237.

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Literature in this Area

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Rheumatoid Arthritis Poster

Rheumatoid Arthritis Poster

Rheumatoid arthritis (RA) is a chronic destructive inflammatory autoimmune disease that results from a breakdown in immune tolerance, for reasons that are as yet unknown. This poster summarizes the pathology of RA and the inflammatory processes involved, as well as describing some of the epigenetic modifications associated with the disease and the potential for targeting these changes in the discovery of new treatments.