2-Phenylmelatonin
Chemical Name: N-[2-(5-Methoxy-2-phenylindol-3-yl)ethyl]acetamide
Purity: ≥98%
Biological Activity
2-Phenylmelatonin is a highly potent melatonin agonist; displays higher affinity and greater potency than melatonin itself. The EC50 values for G protein activation in MT1 and MT2-transfected cells are 65 and 58 pM respectively.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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High-throughput genotoxicity assay identifies antioxidants as inducers of DNA damage response and cell death.
Fox JT, Sakamuru S, Huang R
Proc. Natl. Acad. Sci. U.S.A., 2012;109(14):5423-8. -
2-Substituted 5-methoxy-N-acetyltryptamines: synthesis, binding affinity for the melatonin receptor, and evaluation of the biological activity.
Spadoni et al.
J.Med.Chem., 1993;36:4069 -
Pharmacological characterization of the human melatonin Mel1a receptor following stable transfection into NIH3T3 cells.
Nonno et al.
Br.J.Pharmacol., 1998;124:485 -
Ligand efficacy and potency at recombinant human MT2 melatonin receptors: evidence for agonist activity of some mt1-antagonists.
Nonno et al.
Br.J.Pharmacol., 1999;127:1288
Product Datasheets
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Citations for 2-Phenylmelatonin
The citations listed below are publications that use Tocris products. Selected citations for 2-Phenylmelatonin include:
3 Citations: Showing 1 - 3
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A Differential Hypofunctionality of Gαi Proteins Occurs in Adolescent Idiopathic Scoliosis and Correlates with the Risk of Disease Progression.
Authors: Akoume Et al.
Sci Rep 2019;9:10074
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XFEL structures of the human MT2 melatonin receptor reveal the basis of subtype selectivity.
Authors: Johansson Et al.
Nature 2019;569:289
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Structural basis of ligand recognition at the human MT1 melatonin receptor
Authors: Stauch Et al.
Nature 2019;569:284
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