Molecular structure of N,N,N-Trimethyl-1-(4-trans-stilbenoxy)-2-propylammonium iodide
N,N,N-Trimethyl-1-(4-trans-stilbenoxy)-2-propylammonium iodide
Alternate Names:
F3
Molecular Weight:
423.33
Molecular Formula:
C20H26INO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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It is an antagonist of nicotinic acetylcholine receptors.
N,N,N-Trimethyl-1-(4-trans-stilbenoxy)-2-propylammonium iodide References
- Antagonism of nicotinic receptors of rat chromaffin cells by N,N, N-trimethyl-1-(4-trans-stilbenoxy)-2-propylammonium iodide: a patch clamp and ligand binding study. | Di Angelantonio, S., et al. 2000. Br J Pharmacol. 129: 1771-9. PMID: 10780985
- Rapid relief of block by mecamylamine of neuronal nicotinic acetylcholine receptors of rat chromaffin cells in vitro: an electrophysiological and modeling study. | Giniatullin, RA., et al. 2000. Mol Pharmacol. 58: 778-87. PMID: 10999948
- Nitrogen substitution modifies the activity of cytisine on neuronal nicotinic receptor subtypes. | Carbonnelle, E., et al. 2003. Eur J Pharmacol. 471: 85-96. PMID: 12818695
- Modulation of neuronal nicotinic receptor function by the neuropeptides CGRP and substance P on autonomic nerve cells. | Di Angelantonio, S., et al. 2003. Br J Pharmacol. 139: 1061-73. PMID: 12871824
- Changes in cationic selectivity of the nicotinic channel at the rat ganglionic synapse: a role for chloride ions? | Sacchi, O., et al. 2011. PLoS One. 6: e17318. PMID: 21364885
- 4-Oxystilbene compounds are selective ligands for neuronal nicotinic alphaBungarotoxin receptors. | Gotti, C., et al. 1998. Br J Pharmacol. 124: 1197-206. PMID: 9720791
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
N,N,N-Trimethyl-1-(4-trans-stilbenoxy)-2-propylammonium iodide, 25 mg | sc-301439 | 25 mg | $750.00 |