| Weight | 510.828 g/mol |
|---|---|
| Formula | C30H60N3O3+3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 21 |
UNII-VYJ027LZ05 (7006-17-9)
Gallamine · Flaxedil · Gallamine Triethiodide
Score:
#531 in Neuroscience
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#2437 in Biology
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- Modification of the binding properties of muscarinic receptors by gallamine. (Molecular Pharmacology, 1983)
- The inhibitory effect of gallamine on muscarinic receptors. (British Journal of Pharmacology, 1976)
- Pain responses to perineuromal injection of normal saline, gallamine, and lidocaine in humans. (Pain, 1989)
- The pharmacology of Flaxedil, with observations on certain analogs. (Annals of the New York Academy of Sciences, 1951)
- Antimuscarinic action of methoctramine, a new cardioselective M-2 muscarinic receptor antagonist alone and in combination with atropine and gallamine (European Journal of Pharmacology, 1987)
- Role of acidic amino acids in the allosteric modulation by gallamine of antagonist binding at the m2 muscarinic acetylcholine receptor. (Molecular Pharmacology, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Gallamine
- Flaxedil
- Gallamine Triethiodide
- Gallamine Triethyl Iodide
- Gallamine Triethochloride
- Gallamonium Iodide
-
SMILESCC[N+](CC)(CC)CCOC1=C(C(=CC=C1)OCC[N+](CC)(CC)CC)OCC[N+](CC)(CC)CC
-
InChIKeyOZLPUNFFCJDMJD-UHFFFAOYSA-N
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AC1N0J2C
(Williamson ether)
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