Nifene
Systematic (IUPAC) name | |
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3-[(2S)-2,5-Dihydro-1H-pyrrol-2-ylmethoxy]-2-18F-fluoropyridine
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Clinical data | |
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ATC code | none |
PubChem | CID: 6917075 |
ChemSpider | 5292349 |
Chemical data | |
Formula | C10H11FN2O |
Molecular mass | 193.208078 g/mol |
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Nifene is a high affinity, selective nicotinic α4β2 receptor agonist used in medical research for nicotinic acetylcholine receptors, usually in the form of nifene (18F)[1][2] as a positron emission tomography (PET) radiotracer.[3][4]
Nifene has been used to assess the efficacy of acetylcholinesterase inhibitors in animal models, because the neurotransmitter acetylcholine competes with the binding of nifene at the nicotinic receptor site.[5][6] Learning and behavior studies in animal models using nifene have suggested a potential role of the nicotinic receptors located in distinct white matter tracts.[7] Nifene studies in animal models of lung cancer have suggested an upregulation of the nicotinic receptor in the lung tumors.[8][9] Novel PET and SPECT imaging agents as potential receptor antagonists have been developed based on the structure of nifene; niodene for SPECT,[10] nifrolene for PET [11] and niofene for PET/SPECT.[12] These new derivatives take advantage of the unique in vivo imaging properties of nifene.[13]
References
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External links
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- Radiopharmaceuticals
- Fluoroarenes
- Pyridines
- Pyrrolines