Weight | 491.626 g/mol |
---|---|
Formula | C30H35F2N3O |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 3 |
Rotatable Bonds | 9 |
LIDOFLAZINE (3416-26-0)
Ordiflazine · Clinium
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- Cerebral Ischemia and Reperfusion: Prevention of Brain Mitochondrial Injury by Lidoflazine (Journal of Cerebral Blood Flow and Metabolism, 1987)
- A randomized clinical study of a calcium-entry blocker (lidoflazine) in the treatment of comatose survivors of cardiac arrest (Journal of Emergency Medicine, 1991)
- Amelioration of brain damage by lidoflazine after prolonged ventricular fibrillation cardiac arrest in dogs (Critical Care Medicine, 1984)
- Comparative protective effects of nicardipine, flunarizine, lidoflazine and nimodipine against ischaemic injury in the hippocampus of the Mongolian gerbil (British Journal of Pharmacology, 1988)
- Early amelioration of neurologic deficit by lidoflazine after fifteen minutes of cardiopulmonary arrest in dogs (Annals of Emergency Medicine, 1983)
- Cardioprotective effects of lidoflazine during 1-hour normothermic global ischemia. (Circulation, 1981)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ordiflazine
- Clinium
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SMILESCC1=C(C(=CC=C1)C)NC(=O)CN2CCN(CC2)CCCC(C3=CC=C(C=C3)F)C4=CC=C(C=C4)F
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InChIKeyZBIAKUMOEKILTF-UHFFFAOYSA-N
- Pubchem - LIDOFLAZINE
- Wikipedia - lidoflazine
Lidoflazine is a piperazine calcium channel blocker. It is a coronary vasodilator with some antiarrhythmic action. Lidoflazine was discovered at Janssen Pharmaceutica in 1964.
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