Weight | 681.657 g/mol |
---|---|
Formula | C37H42Cl2N2O6 |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 3 |
Aromatic Rings | 4 |
Rotatable Bonds | 2 |
Amelizol (57-94-3)
Tubocurarine · Tubocurarine Chloride · Tubocurare
Score:
#968 in Neuroscience
,
#2041 in Biochemistry
,
#4260 in Biology
,
#5372 in Chemistry
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- Simultaneous modeling of pharmacokinetics and pharmacodynamics: application to d-tubocurarine. (Clinical Pharmacology & Therapeutics, 1979)
- Determinants of Apamin and d-Tubocurarine Block in SK Potassium Channels (Journal of Biological Chemistry, 1997)
- d-Tubocurarine binding sites are located at alpha-gamma and alpha-delta subunit interfaces of the nicotinic acetylcholine receptor (Proceedings of the National Academy of Sciences of the United States of America, 1990)
- Significant entry of tubocurarine into the brain of rats by adsorption to polysorbate 80coated polybutylcyanoacrylate nanoparticles: An in situ brain perfusion study (Journal of Microencapsulation, 1998)
- Equilibrium binding of [3H]tubocurarine and [3H]acetylcholine by Torpedo postsynaptic membranes: stoichiometry and ligand interactions. (Biochemistry, 1979)
- THE EFFECT OF TUBOCURARINE ON INDIRECTLY ELICITED TRAIN-OF-FOUR MUSCLE RESPONSE AND RESPIRATORY MEASUREMENTS IN HUMANS (BJA: British Journal of Anaesthesia, 1975)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Tubocurarine
- Tubocurarine Chloride
- Tubocurare
- d-Tubocurare
- d-Tubocurarine
-
SMILESC[NH+]1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)O)O3)[N+](CCC6=CC(=C5O)OC)(C)C)OC.[Cl-].[Cl-]
-
InChIKeyGXFZCDMWGMFGFL-UHFFFAOYSA-N
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