## Abstract Anandamide (Figure 1a) (arachidonyl ethanolamide, AEA), (5Z,8Z,11Z,14Z)โNโ(2โhydroxyethyl)โ5,8,11,14โEicosatetraenamide, is an endogenous cannabinoid ligand possessing important biological activity. The conformation of AEA in its native receptor binding environment is particularly of in
Synthesis of labeled acrylamide and N-methylolacrylamide (NMA): 15N-acrylamide, 13C-NMA, 15N-NMA, and 13C,15N-NMA
โ Scribed by N. R. Brown; C. E. Frazier
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- French
- Weight
- 115 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-2135
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โฆ Synopsis
Labeled derivatives of N-methylolacrylamide (NMA) including 15 N-NMA, 13 C-NMA, and 13 C, 15 N-NMA were synthesized and purified. A required chemical precursor, 15 N-acrylamide, was also prepared. Reported methods for synthesizing unlabeled analogs are noted, and modifications to these methods for achieving the labeled materials are specified. Monomers were examined via 1 H, 13 C, and 15 N nuclear magnetic resonance (NMR) spectroscopy. Peak assignments and coupling constants are reported for each compound. To our knowledge, this is the first reported publication on the preparation and characterization of 13 C-NMA, 15 N-NMA, 13 C, 15 N-NMA, and 15 N-acrylamide.
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