2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)-

2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)- Suppliers list
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
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2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)- Basic information
Product Name:2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)-
Synonyms:2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)-
CAS:2727965-45-7
MF:C24H30ClN3O2
MW:427.97
EINECS:
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Mol File:2727965-45-7.mol
2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)- Structure
2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)- Chemical Properties
solubility Soluble to 5 mM in water with gentle warming and to 100 mM in DMSO
Safety Information
MSDS Information
2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)- Usage And Synthesis
Biological ActivityFK 866 hydrochloride is a non-competitive and potent 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 and cisplatin .
storageStore at -20°C
2-Propenamide, N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-, hydrochloride (1:1), (2E)- Preparation Products And Raw materials
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