YK-3-237
CAS No. 1215281-19-8
YK-3-237( YK-3 237 )
Catalog No. M10805 CAS No. 1215281-19-8
A novel small molecule sirtuin-1 (SIRT1) activator that reduces acetylation of mutant 53 and exhibits anti-proliferative effects against TNBC cells carrying mutant p53.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 31 | Get Quote |
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| 5MG | 50 | Get Quote |
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| 10MG | 80 | Get Quote |
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| 25MG | 170 | Get Quote |
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| 50MG | 290 | Get Quote |
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| 100MG | 507 | Get Quote |
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| 200MG | 654 | Get Quote |
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| 500MG | 1017 | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameYK-3-237
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NoteResearch use only, not for human use.
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Brief DescriptionA novel small molecule sirtuin-1 (SIRT1) activator that reduces acetylation of mutant 53 and exhibits anti-proliferative effects against TNBC cells carrying mutant p53.
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DescriptionA novel small molecule sirtuin-1 (SIRT1) activator that reduces acetylation of mutant 53 and exhibits anti-proliferative effects against TNBC cells carrying mutant p53; demonstrates proliferation inhibition in breast cancer cell panel with EC50 of 0.1-5 uM, also induces PARP-dependent apoptotic cell death and arrests the cell cycle at G2/M phase; enhances expression of α-SMA and fibronectin in cultured rat renal interstitial fibroblasts (NRK-49F).
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In VitroYK-3-237 exhibits the anti-proliferative activities toward most of the breast cancer cell lines tested at submicromolar concentration. YK-3-237 preferentially inhibits the proliferation of breast cancer cell lines carrying mtp53.YK-3-237 inhibits the proliferation of triple-negative breast cancer (TNBC) HS578T, MDA-MB-453, SUM1315MO2, SUM149PT, BT549, MDA-MB-231, MDA-MB-436, MDA-MB-468, HCC1937 with IC50s of 0.160±0.043, 0.241±0.086, 0.253±0.028, 0.289±0.066, 0.353±0.017, 0.431±0.136, 0.501±0.062, 1.436±0.754, 5.031±2.010 μM, respectively.YK-3-237 inhibits the proliferation of Luminal T47D, MCF7, and ZR-75-1 with IC50s of 1.573±0.370, 2.402±0.256, 3.822±0.967 μM, respectively.YK-3-237 inhibits the proliferation of HER2 BT474 and SK-BR-3 with IC50s of 1.249±0.372 and 0.346±0.066 μM, respectively.YK-3-237 (0.01-10 μM; 24 hours) deacetylates mtp53 in TNBC cell lines.YK-3-237 is a potent activator of Sirt1, on the activation of renal interstitial fibroblasts using NRK-49F cells.Exposure of cells to YK-3-237 also significantly reduces expression of α-SMA and fibronectin in a dose-dependent manner, with the maximum inhibition occurring at 10 μM. Cell Viability Assay Cell Line:BT549, MDA-MB-468, HS578T, SUM149PT Concentration:0, 0.01, 0.03, 0.1, 0.3, 1, 3, 10 μM Incubation Time:24 hours Result:Reduced both the acetylation of K382 and the level of mtp53 in a dose-dependent manner in mtp53 TNBC cell lines.
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In Vivo——
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SynonymsYK-3 237
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PathwayChromatin/Epigenetic
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TargetSirtuin
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RecptorSirtuin
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Research Area——
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Indication——
Chemical Information
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CAS Number1215281-19-8
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Formula Weight372.18
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Molecular FormulaC19H21BO7
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (268.69 mM)
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SMILESB(C1=C(C=CC(=C1)C=CC(=O)C2=CC(=C(C(=C2)OC)OC)OC)OC)(O)O
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Chemical NameB-[2-methoxy-5-[(1E)-3-oxo-3-(3,4,5-trimethoxyphenyl)-1-propen-1-yl]phenyl]-boronic acid
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Yi YW, et al. Oncotarget. 2013 Jul;4(7):984-94.
2. Ponnusamy M, et al. J Pharmacol Exp Ther. 2015 Aug;354(2):142-51.
3. Kong Y, et al. Bioorg Med Chem. 2010 Jan 15;18(2):971-7.
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