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FK-866

AG-CR1-0011-M001 1 mg $40.00
AG-CR1-0011-M005 5 mg $120.00
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Additional Information

Product Data
Synonyms K 22.175; FK866; APO866; WK175; N-[4-(1-Benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-2E-propenamide
Properties
Formula C24H29N3O2
MW 391.5
CAS 658084-64-1
Purity ≥98% (NMR)
Appearance White to yellow solid. (Tends to easily liquefy.)
Solubility Soluble in 100% ethanol, dimethylformamide (40 mg/ml) or DMSO (25 mg/ml); sparingly soluble in aqueous buffers.
InChi Key KPBNHDGDUADAGP-VAWYXSNFSA-N
Product Type Chemical
Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Hygroscopic. Keep under inert gas.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
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Product Description

  • Nampt/visfatin inhibitor [1].
  • Inhibitor of NAD+ biosynthesis [1].
  • Inhibits the enzyme/substrate complex and the free enzyme (Ki = 0.4 nM and Ki = 0.3 nM, respectively) [1].
  • Apoptosis inducer [1].
  • Autophagy inducer [2].
  • Causes premature senescence [3].
  • Angiogenesis inhibitor [4].

Product References

  1. FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis: M. Hasmann & I. Schemainda; Cancer Res. 63, 7436 (2003) 
  2. NAD depletion by FK866 induces autophagy: R.A. Billington, et al.; Autophagy 4, 385 (2008) 
  3. Extension of human cell lifespan by nicotinamide phosphoribosyltransferase: E. van der Veer, et al.; J. Biol. Chem. 282, 10841 (2007) 
  4. Antiangiogenic potency of FK866/K22.175, a new inhibitor of intracellular NAD biosynthesis, in murine renal cell carcinoma: J. Drevs, et al.; Anticancer Res. 23, 4853 (2003) 
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