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(+)-Muscarine iodide , CAS No.24570-49-8
Muscarinic receptor agonist
Basic Description
Synonyms
(+-)-Muscarine iodide | (+)-Muscarine Iodide | Muscarine, iodide | HY-107654 | 2,5-Anhydro-1,4,6-trideoxy-6-(trimethylammonio)-D-ribohexitol Iodide | 2,5-anhydro-1,4,6-trideoxy-6-(trimethylammonio)-d-ribo-hexitol iodide | 1-((2S,4R,5S)-4-Hydroxy-5-methylt
Biochemical and Physiological Mechanisms
Muscarinic acetylcholine receptor agonist; mimics the activity of acetylcholine.
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Monosaccharides
Direct Parent
Pentoses
Alternative Parents
Tetrahydrofurans Tetraalkylammonium salts Secondary alcohols Oxacyclic compounds Dialkyl ethers Organopnictogen compounds Organic zwitterions Organic iodide salts Hydrocarbon derivatives Amines
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Pentose monosaccharide - Quaternary ammonium salt - Tetraalkylammonium salt - Tetrahydrofuran - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Organonitrogen compound - Organic zwitterion - Organic salt - Alcohol - Organic iodide salt - Aliphatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
[(2S,4R,5S)-4-hydroxy-5-methyloxolan-2-yl]methyl-trimethylazanium;iodide
INCHI
InChI=1S/C9H20NO2.HI/c1-7-9(11)5-8(12-7)6-10(2,3)4;/h7-9,11H,5-6H2,1-4H3;1H/q+1;/p-1/t7-,8-,9+;/m0./s1
InChIKey
PMFYONXEPDMBPE-CTERPIQNSA-M
Smiles
CC1C(CC(O1)C[N+](C)(C)C)O.[I-]
Isomeric SMILES
C[C@H]1[C@@H](C[C@H](O1)C[N+](C)(C)C)O.[I-]
PubChem CID
102226
Molecular Weight
301.17
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Solvent:water, Max Conc. mg/mL: 30.12, Max Conc. mM: 100
Molecular Weight
301.170 g/mol
XLogP3
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
2
Exact Mass
301.054 Da
Monoisotopic Mass
301.054 Da
Topological Polar Surface Area
29.500 Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
153.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
3
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
2
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