FK 866
Tocris Bioscience | Catalog # 8072
Key Product Details
Description
Product Description
FK 866 is a non-competitive and high-affinity inhibitor of NAMPT (nicotinamide phosphoribosyltransferase, PBEF1) (Ki = 0.3 nM); inhibits NAD biosynthesis. Induces delayed cell death by apoptosis in HepG2 human liver carcinoma cells (IC50 ~1 nM). Induces apoptosis in four different neuroblastoma cell lines; also induces autophagy in SH-SY5Y cells. Potentiates the cytotoxic effects induced by Etoposide (Cat. No. 1226) and Cisplatin (Cat. No. 2251).
Product Specifications for FK 866
Molecular Weight
Formula
Storage
Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 39.15 | 100 | |
| Ethanol | 39.15 | 100 |
Preparing Stock Solutions for FK 866
The following data is based on the product molecular weight 391.51.
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.55 mL | 12.77 mL | 25.54 mL |
| 5 mM | 0.51 mL | 2.55 mL | 5.11 mL |
| 10 mM | 0.26 mL | 1.28 mL | 2.55 mL |
| 50 mM | 0.05 mL | 0.26 mL | 0.51 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 16 publications citing the usage of this product.
- Travelli Reciprocal potentiation of the antitumoral activities of FK866, an inhibitor of nicotinamide phosphoribosyltransferase, and etop. or cisp. in neuroblastoma cells. J.Pharmacol.Exp.Ther. 2011 PMID: 21685314
- Galli Synthesis and biological evaluation of isosteric analogues of FK866, an inhibitor of NAD salvage. Chem.Med.Chem. 2008 PMID: 18247435
- Hasmann FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis. Cancer Res. 2003 PMID: 14612543
Product Documents for FK 866
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for FK 866
For research use only
Related Research Areas
Citations for FK 866
Customer Reviews for FK 866 (1)
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Species: HumanAssay Type: In VitroCell Line/Tissue: RBE and HepG2Verified Customer | Posted 12/19/2023Treat this drug for 72 hours for best results.I used FK 866 in 10–50 nM concentrations for 24-72 hours and noted significant differences in cellular NAD level and cell growth.
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