Names | |
---|---|
Preferred IUPAC name 4--1,1-dimethylpiperidin-1-ium iodide | |
Other names 4-(2,2-Diphenylacetoxy)-1,1-dimethylpiperidin-1-ium iodide | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChemSpider | |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | C21H26INO2 |
Molar mass | 451.348 g·mol |
Appearance | White to beige powder |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references |
4-DAMP (1,1-dimethyl-4-diphenylacetoxypiperidinium iodide) is a selective muscarinic acetylcholine receptor (mAChR) M3 antagonist. It is also able to antagonize M1 receptors but has preferential activity at the M3 receptor. It competitively binds to the acetylcholine binding site on mAChRs, causing right-ward shift in the dose response curves for mAChR agonists.
References
- "4-DAMP". Sigma-Aldrich.
- Zhu, MH; Sung, IK; Zheng, H; Sung, TS; Britton, FC; O'Driscoll, K; Koh, SD; Sanders, KM (2011). "Muscarinic activation of Ca2+-activated Cl- current in interstitial cells of Cajal". J Physiol. 589 (Pt18): 4565–4582. doi:10.1113/jphysiol.2011.211094. PMC 3208225. PMID 21768263.
- Teixeira-Neto, FJ; McDonell, WN; Black, WD; Harris, W and; Grovum, L (2012). "Effects of muscarinic receptor antagonists on acetylcholine-induced contractions of jejunal smooth muscle in horses". Journal of Veterinary Pharmacology and Therapeutics. 35 (4): 313–318. doi:10.1111/j.1365-2885.2011.01330.x. PMID 21859432.
- Greenwood, JM and; Dragunow, M (2010). "M3 muscarinic receptors promote cell survival through activation of the extracellular regulated kinase (ERK1/2) pathway". Eur J Pharmacol. 640 (1–3): 38–45. doi:10.1016/j.ejphar.2010.05.013. PMID 20519144.
This article about an organic compound is a stub. You can help Misplaced Pages by expanding it. |