SIRT1 Inhibitor
Catalog No. S35-904F
| Catalog No. | Pack Size | Price (USD) | |
|---|---|---|---|
| S35-904F-5 | 5 mg | $75 | |
| S35-904F-25 | 25 mg | $165 | |
| S35-904F-BULK | BULK | Contact Us |
Overview:
Selective Sirt1 inhibitor (IC50=98 nM). Does not inhibit other HDACs or Sirt family members. Increases p53 acetylation following DNA damage1. Causes cell cycle arrest at G12. Inhibits differentiation and facilitates expansion of hematopoietic progenitor cells3. An extremely useful tool for determining the involvement of Sirt1 in cellular physiology4. Cell permeable.
References:
1. JM Solomon et al. Mol. Cell. Biol. 2006 26:28
2. B Peck et al. Mol. Cancer Ther. 2010 9:844
3. T Peled et al. Exp. Hematol. 2012 40:342
4. JL Andersen et al. Mol. Cell 2011 43:834
CAS Registry Number:
49843-98-3
Molecular Formula:
C13H13ClN2O
Appearance:
Light yellow powder
Molecular Weight:
248.7
Purity:
98% (TLC)
Solubilization:
May be dissolved in DMSO (18 mg/ml); or Ethanol (10 mg/ml).
Aliases:
6-Chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide (racemic)
Storage and Stability:
Store desiccated as supplied at 4oC for up to 2 years. Store solutions at -20oC for up to 2 months.
Molecular Structure:
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There are no related publications available for this product.
Cancer, Cell Cycle, Inflammation
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