Submit a Review & Earn an Amazon Gift Card
You can now submit reviews for your favorite Tocris products. Your review will help other researchers decide on the best products for their research. Why not submit a review today?!
Submit Review(+)-Muscarine iodide
Description: Muscarinic receptor agonist
Chemical Name: 2,5-Anhydro-1,4,6-trideoxy-6-(trimethylammonio)-D-ribo-hexitol iodide
Biological Activity for (+)-Muscarine iodide
(+)-Muscarine iodide is a muscarinic acetylcholine receptor agonist; mimics the activity of acetylcholine.
Technical Data for (+)-Muscarine iodide
| M. Wt | 301.17 |
| Formula | C9H20INO2 |
| Storage | Store at -20°C |
| CAS Number | 24570-49-8 |
| PubChem ID | 102226 |
| InChI Key | PMFYONXEPDMBPE-CTERPIQNSA-M |
| Smiles | O[C@@H]1C[C@@H](C[N+](C)(C)C)O[C@H]1C.[I-] |
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.
Solubility Data for (+)-Muscarine iodide
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| water | 30.12 | 100 |
Preparing Stock Solutions for (+)-Muscarine iodide
The following data is based on the product molecular weight 301.17. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 3.32 mL | 16.6 mL | 33.2 mL |
| 5 mM | 0.66 mL | 3.32 mL | 6.64 mL |
| 10 mM | 0.33 mL | 1.66 mL | 3.32 mL |
| 50 mM | 0.07 mL | 0.33 mL | 0.66 mL |
Molarity Calculator
Molarity Calculator
Calculate the mass, volume, or concentration required for a solution.
Reconstitution Calculator
Reconstitution Calculator
Dilution Calculator
Dilution Calculator
Calculate the dilution required to prepare a stock solution.
Product Datasheets for (+)-Muscarine iodide
References for (+)-Muscarine iodide
References are publications that support the biological activity of the product.
Jin (2003) Muscarine, imidazole, oxazole and thiazole alkaloids. Nat.Prod.Rep. 20 584 PMID: 14700201
Boukouvalas et al (2007) A concise asymmetric synthesis of (+)-muscarine from (S)-γ-hydroxymethyl-γ-butyrolactone. Tetrahedron Lett. 48 2971
If you know of a relevant reference for (+)-Muscarine iodide, please let us know.
View Related Products by Target
View Related Products by Product Action
Keywords: (+)-Muscarine iodide, (+)-Muscarine iodide supplier, (+)-Muscarine, iodide, muscarinics, acetylcholine, ach, receptors, machrs, agonists, mimetic, Non-selective, Muscarinics, 3074, Tocris Bioscience
2 Citations for (+)-Muscarine iodide
Citations are publications that use Tocris products. Selected citations for (+)-Muscarine iodide include:
Liu et al (2016) Clemastine Enhances Myelination in the Prefrontal Cortex and Rescues Behavioral Changes in Socially Isolated Mice. J Neurosci 36 957 PMID: 26791223
Dumalska et al (2008) Excitatory effects of the puberty-initiating peptide kisspeptin and group I metabotropic glutamate receptor agonists differentiate two distinct subpopulations of gonadotropin-releasing hormone neurons. J Neurosci 28 8003 PMID: 18685025
Do you know of a great paper that uses (+)-Muscarine iodide from Tocris? Please let us know.
Reviews for (+)-Muscarine iodide
There are currently no reviews for this product. Be the first to review (+)-Muscarine iodide and earn rewards!
Have you used (+)-Muscarine iodide?
Submit a review and receive an Amazon gift card.
$50/€35/£30/$50CAN/¥300 Yuan/¥5000 Yen for first to review with an image
$25/€18/£15/$25CAN/¥75 Yuan/¥1250 Yen for a review with an image
$10/€7/£6/$10 CAD/¥70 Yuan/¥1110 Yen for a review without an image
Literature in this Area
Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*Please note that Tocris will only send literature to established scientific business / institute addresses.
GPCR Product Listing
A collection of over 450 products for G protein-coupled receptors, the listing includes research tools for the study of:
- Rhodopsin-like Receptors
- Glutamate Receptors
- Frizzled Receptors
- GPCR Signaling
Alzheimer's Poster
Alzheimer's disease (AD) is a degenerative brain disease and the most common cause of dementia, affecting approximately 47 million people worldwide. Updated in 2015, this poster summarizes the structural and functional changes observed in the progression of this neurodegenerative disease, as well as classic AD drug targets.
Cardiovascular Poster
Cardiovascular disease remains one of the major causes of morbidity and mortality in the Western world and therefore this therapeutic area continues to be of great interest to researchers. This poster highlights the key GPCRs regulating vascular reactivity.
Learning & Memory Poster
Recognition memory enables us to make judgements about whether or not we have encountered a particular stimulus before. This poster outlines the cellular mechanisms underlying recognition memory and its links to long-term depression, as well as the use of pharmacological intervention to assess the role of neurotransmitters in recognition memory.
Schizophrenia Poster
Schizophrenia is a debilitating psychiatric disorder that affects 1% of the worldwide population. This poster describes the neurobiology of Schizophrenia, as well as highlighting the genetic and environmental factors that play a fundamental role in the etiology of the disease. The current and emerging drug targets are also discussed.