trimethyl-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]azanium:iodide
- Product Name
- trimethyl-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]azanium:iodide
- CAS No.
- 3854-04-4
- Chemical Name
- trimethyl-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]azanium:iodide
- Synonyms
- CPD3509;Oxotremorine M (iodide);Oxotremorine M iodide, 10 mM in DMSO;trimethyl-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]azanium:iodide
- CBNumber
- CB63387012
- Molecular Formula
- C11H19IN2O
- Formula Weight
- 322.19
- MOL File
- 3854-04-4.mol
trimethyl-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]azanium:iodide Property
- storage temp.
- Desiccate at -20°C
- solubility
- DMSO : 125 mg/mL (387.97 mM; Need ultrasonic)
- form
- Powder
- color
- Light yellow to yellow
- Water Solubility
- Soluble to 100 mM in water
N-Bromosuccinimide Price
- Product number
- 20847
- Product name
- Oxotremorine M (iodide)
- Purity
- ≥98%
- Packaging
- 50mg
- Price
- $72
- Updated
- 2024/03/01
- Product number
- 20847
- Product name
- Oxotremorine M (iodide)
- Purity
- ≥98%
- Packaging
- 100mg
- Price
- $128
- Updated
- 2024/03/01
- Product number
- O870518
- Product name
- Oxotremorine M
- Packaging
- 25mg
- Price
- $140
- Updated
- 2021/12/16
- Product number
- 1713CA
- Product name
- (4-(2-Oxo-1-pyrrolidinyl)-2-butynyl)trimethylammoniumiodide
- Packaging
- 50mg
- Price
- $178
- Updated
- 2021/12/16
- Product number
- 1713CA
- Product name
- (4-(2-Oxo-1-pyrrolidinyl)-2-butynyl)trimethylammoniumiodide
- Packaging
- 100mg
- Price
- $240
- Updated
- 2021/12/16
trimethyl-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]azanium:iodide Chemical Properties,Usage,Production
Description
Oxotremorine M is a non-selective muscarinic (M) acetylcholine receptor agonist that induces phosphoinositide hydrolysis in mouse ileum isolated from wild-type, M2, M3, and M2/M3 knockout mice (EC50s = 0.36, 0.52, 1.62, and 1.48 μM, respectively). It also increases M4-induced inhibition of calcium currents in NG108-15 mouse neuroblastoma X rat glioma hybrid cells (EC50 = 0.14 μM). Oxotremorine M inhibits KCNQ2/3 potassium currents in Xenopus oocytes expressing M1 receptors and KCNQ2/3 potassium channels (IC50 = 1.1 μM). It also directly inhibits KCNQ2/3 potassium channels, decreasing KCNQ2/3 potassium currents in Xenopus oocytes lacking muscarinic receptors in a dose-dependent manner.
Uses
Oxotremorine M is a muscarinic receptor agonist.
in vivo
Oxotremorine M iodide (0.5 mg/kg; s.c.) increases Ddopamine (DA) release in the medial prefrontal cortex (mPFC) and has no effect in the nucleus accumbens (NAC) in male sprague-dawley albino rats weighing 250-350 g[4].
storage
Desiccate at -20°C
References
[1] JOHN A TRAN F J E Minoru Matsui. Differential coupling of muscarinic M1, M2, and M3 receptors to phosphoinositide hydrolysis in urinary bladder and longitudinal muscle of the ileum of the mouse.[J]. Journal of Pharmacology and Experimental Therapeutics, 2006, 318 2: 649-656. DOI: 10.1124/jpet.106.103093
[2] M.P. CAULFIELD D. A B. Pharmacology of the putative M4 muscarinic receptor mediating Ca-current inhibition in neuroblastoma × glioma hybrid (NG 108–15) cells[J]. British Journal of Pharmacology, 1991, 104 1: 39-44. DOI: 10.1111/j.1476-5381.1991.tb12381.x
[3] RUUD ZWART. A novel muscarinic receptor-independent mechanism of KCNQ2/3 potassium channel blockade by Oxotremorine-M[J]. European journal of pharmacology, 2016, 791: Pages 221-228. DOI: 10.1016/j.ejphar.2016.08.037
trimethyl-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]azanium:iodide Preparation Products And Raw materials
Raw materials
Preparation Products
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