Journal of Natural Products · 2010 · 63 citations · 34 references
MedicineMedicinal ChemistryPharmacologyDrug DiscoveryNeuropharmacologyStructure-activity RelationshipsCholinergic NeurochemistryCholinergic PharmacologyReceptor PharmacologyStructure-activity Relationship AnalysisAgonist ActivityCholinergic Receptor PharmacologyComputational Spectral SimulationMolecular Formula AssignmentNicotinic Acetylcholine Receptor AgonismNicotinic Receptor PharmacologySelectivitySpectral Simulation
The skin of the Ecuadorian poison frog Epipedobates anthonyi contains the potent nicotinic agonists epibatidine (1) and N-methylepibatidine (3). In addition, a condensed tetracyclic epibatidine congener has been identified with activity at nicotinic acetylcholine receptors, but different selectivity than epibatidine. This rigid tetracycle has been named phantasmidine (4). Phantasmidine has a molecular formula of C(11)H(11)N(2)OCl, shares a chloropyridine moiety with 1, and also contains furan, pyrrolidine, and cyclobutane rings. A combination of GC-MS and GC-FTIR analysis with on-column derivatization, 1D NMR spectroscopy with selective irradiation, and spectral simulation, along with 2D NMR, were used to elucidate the structure from a total sample of approximately 20 microg of HPLC-purified 4 and its corresponding acetamide (5). After synthesis, this novel rigid agonist may serve as a selective probe for beta4-containing nicotinic receptors and potentially lead to useful pharmaceuticals.
34
Douglas E. Jorenby · JAMA · 2006 · 1.7K citations
<i>High-resolution Nuclear Magnetic Resonance</i>
John A. Pople, W. G. Schneider, H. J. Bernstein et al. · Physics Today · 1960 · 1.6K citations
Natural Sciences, Physics, Radiology +10
High-Resolution Nuclear Magnetic Resonance
H. S. Gutowsky · Journal of the American Chemical Society · 1960 · 1.6K citations