Weight | 737.816 g/mol |
---|---|
Formula | C44H50Cl2N4O2 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 6 |
Alloferin (15180-03-7)
Alcuronium · Alcuronium Chloride · N,N'-Diallylnortoxiferinium Dichloride
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- Mechanisms of steric and cooperative actions of alcuronium on cardiac muscarinic acetylcholine receptors (Molecular Pharmacology, 1994)
- RELATIVE POTENCY OF ORG NC 45, PANCURONIUM, ALCURONIUM AND TUBOCURARINE IN ANAESTHETIZED MAN (BJA: British Journal of Anaesthesia, 1980)
- Subtype selectivity of the positive allosteric action of alcuronium at cloned M1-M5 muscarinic acetylcholine receptors. (Journal of Pharmacology and Experimental Therapeutics, 1995)
- Positive cooperativity in the binding of alcuronium and N-methylscopolamine to muscarinic acetylcholine receptors (Molecular Pharmacology, 1990)
- The immediate cardiovascular effects of pancuronium, alcuronium and tubocurarine in man (Anaesthesia, 1972)
- Detection of serum IgE antibodies that react with alcuronium and tubocurarine after life-threatening reactions to muscle-relaxant drugs. (Anaesthesia and Intensive Care, 1983)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Alcuronium
- Alcuronium Chloride
- N,N'-Diallylnortoxiferinium Dichloride
- Diallylnortoxiferine
- Alcuronium Dichloride
- Allnortoxiferine
- Dialferine
-
SMILESC=CC[N+]12CCC34C1CC(C(=CCO)C2)C5=CN6C7C(=CN(C53)C8=CC=CC=C48)C9CC1C7(CC[N+]1(CC9=CCO)CC=C)C1=CC=CC=C16.[Cl-].[Cl-]
-
InChIKeyCPYGBGOXCJJJGC-UHFFFAOYSA-L
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