| Weight | 174.264 g/mol |
|---|---|
| Formula | C9H20NO2+ |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
MUSCARINE (300-54-9)
Score:
#1201 in Neuroscience
,
#2724 in Biochemistry
,
#5164 in Biology
,
#6741 in Chemistry
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- Loss of M2 muscarine receptors in the cerebral cortex in Alzheimer's disease and experimental cholinergic denervation (Science, 1985)
- THE ACTION OF CERTAIN ESTERS AND ETHERS OF CHOLINE, AND THEIR RELATION TO MUSCARINE (Journal of Pharmacology and Experimental Therapeutics, 1914)
- Binding profile of a novel cardioselective muscarine receptor antagonist, AF-DX 116, to membranes of peripheral tissues and brain in the rat (Life Sciences, 1986)
- Autoradiographic localization of M1 and M2 muscarine receptors in the rat brain. (Neuroscience, 1986)
- A comparison of affinity constants for muscarine-sensitive acetylcholine receptors in guinea-pig atrial pacemaker cells at 29 degrees C and in ileum at 29 degrees C and 37 degrees C. (British Journal of Pharmacology, 1976)
- Cardioselective profile of AF-DX 116, a muscarine M2 receptor antagonist. (Life Sciences, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1C(CC(O1)C[N+](C)(C)C)O
-
InChIKeyUQOFGTXDASPNLL-UHFFFAOYSA-N
- Pubchem - MUSCARINE
- Wikipedia - muscarine
Muscarine, L-(+)-muscarine, or muscarin is a natural product found in certain mushrooms, particularly in Inocybe and Clitocybe species, such as the deadly C.dealbata. Mushrooms in the genera Entoloma and Mycena have also been found to contain levels of muscarine which can be dangerous if ingested. Muscarine has been found in harmless trace amounts in Boletus, Hygrocybe, Lactarius and Russula.
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