| Weight | 147.198 g/mol |
|---|---|
| Formula | C6H15N2O2+ |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Carbamylcholine (462-58-8, 74-97-5)
Carbachol · Doryl · Miostat
Score:
#458 in Neuroscience
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#770 in Biochemistry
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#2108 in Biology
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#2588 in Chemistry
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- Nicotine and Carbamylcholine Binding to Nicotinic Acetylcholine Receptors as Studied in Achbp Crystal Structures (Neuron, 2004)
- Mechanism of chloride secretion induced by carbachol in a colonic epithelial cell line. (Journal of Clinical Investigation, 1986)
- U73122 inhibits Ca2+ oscillations in response to cholecystokinin and carbachol but not to JMV-180 in rat pancreatic acinar cells. (Journal of Biological Chemistry, 1992)
- A model of gamma-frequency network oscillations induced in the rat CA3 region by carbachol in vitro (European Journal of Neuroscience, 2000)
- In vitro responsiveness of human asthmatic bronchus to carbachol, histamine, betaadrenoceptor agonists and theophylline. (British Journal of Clinical Pharmacology, 1986)
- Mechanisms of action of noradrenaline and carbachol on smooth muscle of guinea-pig anterior mesenteric artery. (The Journal of Physiology, 1984)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Carbachol
- Doryl
- Miostat
- Isopto Carbachol
- Carbamoylcholine
- Carboptic
- Carbastat
- Carbamann
- Carbocholine
- Jestryl
- Carbacholine
-
SMILESC[N+](C)(C)CCOC(=O)N
-
InChIKeyVPJXQGSRWJZDOB-UHFFFAOYSA-O
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