| Weight | 624.778 g/mol |
|---|---|
| Formula | C38H44N2O6+2 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 2 |
Curarine (22260-42-0)
curarine dichloride, (1beta)-isomer · curarine dichloride, (1beta)-(+-)-isomer · curarine diiodide, (1beta)-isomer
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - curarine dichloride, (1beta)-isomer
- curarine dichloride, (1beta)-(+-)-isomer
- curarine diiodide, (1beta)-isomer
- curarine, (1'alpha)-isomer
- curarine chloride iodide
- 7',12'-dihydroxy-6,6'-dimethoxy-2,2,2',2'-tetramethyltubocuraranium
- curarine diiodide
- curarine diiodide, (1'alpha)-isomer
- curarine dichloride, (1'alpha)-isomer
- curarine, (1beta)-isomer
- curarine dihydroxide
- curarine diiodide, (1beta)-(+-)-isomer
- curarine dichloride
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SMILESC[N+]1(CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)O)O3)[N+](CCC6=CC(=C5O)OC)(C)C)OC)C
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InChIKeyPXXYOLIWFSWZNP-UHFFFAOYSA-P
- Pubchem - Curarine
- Wikipedia - curarine
Curare or is a common name for various plant extract alkaloid arrow poisons originating from Central and South America. These poisons function by competitively and reversibly inhibiting the nicotinic acetylcholine receptor (nAChR), which is a subtype of acetylcholine receptor found at the neuromuscular junction. This causes weakness of the skeletal muscles and, when administered in a sufficient dose, eventual death by asphyxiation due to paralysis of the diaphragm.
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