| Weight | 318.393 g/mol |
|---|---|
| Formula | C18H24NO4+ |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
N-Methylscopolamine (13265-10-6)
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- Allosteric Site on Muscarinic Acetylcholine Receptors: Identification of Two Amino Acids in the Muscarinic M2 Receptor That Account Entirely for the M2/M5 Subtype Selectivities of Some Structurally Diverse Allosteric Ligands in N-Methylscopolamine-Occupied Receptors (Molecular Pharmacology, 2003)
- Distinct kinetic binding propeties of N-[3H]-methylscopolamine afford differential labeling and localization of M1, M2, and M3 muscarinic receptor subtypes in primate brain (Synapse, 1993)
- Kinetic studies of [3H]-N-methylscopolamine binding to muscarinic receptors in the rat central nervous system: evidence for the existence of three classes of binding sites. (Molecular Pharmacology, 1986)
- Positive cooperativity in the binding of alcuronium and N-methylscopolamine to muscarinic acetylcholine receptors (Molecular Pharmacology, 1990)
- Quantitative analysis of binding parameters of [3H]N-methylscopolamine in central nervous system of muscarinic acetylcholine receptor knockout mice. (Molecular Brain Research, 2005)
- Multiple binding affinities of N-methylscopolamine to brain muscarinic acetylcholine receptors: differentiation from M1 and M2 receptor subtypes. (Journal of Pharmacology and Experimental Therapeutics, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC[N+]1(C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4)C
-
InChIKeyLZCOQTDXKCNBEE-UHFFFAOYSA-N
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