Weight | 314.257 g/mol |
---|---|
Formula | C14H10N4O5 |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
dantrolene (7261-97-4)
Dantrolene Sodium · Dantrium
Score:
#80 in Neurology
,
#403 in Neuroscience
,
#1842 in Biology
,
#2206 in Chemistry
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- Dantrolene A review of its pharmacology, therapeutic use and new developments (Anaesthesia, 2004)
- Studies on the mechanism of action of dantrolene sodium. A skeletal muscle relaxant. (Naunyn-schmiedebergs Archives of Pharmacology, 1972)
- Dantrolene Prevents Glutamate Cytotoxicity and Ca2+ Release from Intracellular Stores in Cultured Cerebral Cortical Neurons (Journal of Neurochemistry, 1991)
- Calcium release from skeletal muscle sarcoplasmic reticulum: site of action of dantrolene sodium (Science, 1976)
- In vitro antioxidant properties of dantrolene sodium. (Pharmacological Research, 2001)
- Dantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia (Embo Molecular Medicine, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Dantrolene Sodium
- Dantrium
-
SMILESC1C(=O)NC(=O)N1N=CC2=CC=C(O2)C3=CC=C(C=C3)[N+](=O)[O-]
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InChIKeyOZOMQRBLCMDCEG-UHFFFAOYSA-N
- Pubchem - dantrolene
- Wikipedia - dantrolene
Dantrolene sodium is a postsynaptic muscle relaxant that lessens excitation-contraction coupling in muscle cells. It achieves this by inhibiting Ca2+ ions release from sarcoplasmic reticulum stores by antagonizing ryanodine receptors. It is the primary drug used for the treatment and prevention of malignant hyperthermia, a rare, life-threatening disorder triggered by general anesthesia.
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Synthesis
Reactant
+
4-Chloronitrobenzene
(Suzuki)
Reactant
+
4-Chloronitrobenzene
(Decarboxylative coupling)
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