Weight | 328.434 g/mol |
---|---|
Formula | C15H24N2O4S |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 8 |
tiapride (51012-32-9)
Tiapride Hydrochloride · Tiaprizal · Tiapride Monohydrochloride
Score:
#201 in Neurology
,
#904 in Neuroscience
,
#3970 in Biology
,
#4998 in Chemistry
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- Tiapride in the prevention of relapse in recently detoxified alcoholics. (British Journal of Psychiatry, 1994)
- Actions of sulpiride and tiapride in a simple model of anxiety in mice (Neuropharmacology, 1987)
- Clinical and neurobiological findings in children suffering from tic disease following treatment with tiapride (European Archives of Psychiatry and Clinical Neuroscience, 1988)
- Tiapride. A review of its pharmacology and therapeutic potential in the management of alcohol dependence syndrome. (Drugs, 1994)
- Tiapride in the long-term management of alcoholics of anxious or depressive temperament. (British Journal of Psychiatry, 1987)
- Double blind study of tiapride versus haloperidol and placebo in agitation and aggressiveness in elderly patients with cognitive impairment (Psychopharmacology, 2000)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Tiapride Hydrochloride
- Tiaprizal
- Tiapride Monohydrochloride
- FLO 1347
- FLO1347
- FLO-1347
- Tiapridex
- Equilium
- Tiapridal
-
SMILESCCN(CC)CCNC(=O)C1=C(C=CC(=C1)S(=O)(=O)C)OC
-
InChIKeyJTVPZMFULRWINT-UHFFFAOYSA-N
- Pubchem - tiapride
- Wikipedia - tiapride
Tiapride is a drug that selectively blocks D2 and D3 dopamine receptors in the brain. It is used to treat a variety of neurological and psychiatric disorders including dyskinesia, alcohol withdrawal syndrome, negative symptoms of psychosis, and agitation and aggression in the elderly. A derivative of benzamide, tiapride is chemically and functionally similar to other benzamide antipsychotics such as sulpiride and amisulpride known for their dopamine antagonist effects.
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