Sereprid

Sereprid Uses, Dosage, Side Effects, Food Interaction and all others data.

Sereprid is a selective D2 and D3 dopamine receptor blocker in the brain.

Sereprid has a high degree of regional selectivity for limbic areas. One study found that tiapride shows over three times as much affinity for limbic areas than striatal areas as opposed to the near equal selectivity for limbic and striatal regions shown by haloperidol.Another study in rats found tiapride's affinity for the septum, a limbic region, to be over thirty times as high as for the striatum.Efficacy at the D2 receptor is moderate, with 80 percent of receptors occupied even in the presence of excess tiapride concentrations.

Trade Name Sereprid
Generic Tiapride
Tiapride Other Names Thiapride, Tiaprida, Tiapride, Tiapridum
Type
Formula C15H24N2O4S
Weight Average: 328.427
Monoisotopic: 328.145677956
Protein binding

Negligible

Groups Investigational
Therapeutic Class
Manufacturer
Available Country Chile
Last Updated: September 19, 2023 at 7:00 am
Sereprid
Sereprid

Uses

Sereprid is a dopamine D2 and D3 receptor antagonist indicated in the treatment of chorea in Huntington's disease, as well as agitation and anxiety in the elderly or with acute or chronic alcoholism.

Sereprid is indicated for the treatment of a variety of neurological and psychiatric disorders including dyskinesia, alcohol withdrawal syndrome, negative symptoms of psychosis, and agitation and aggression in the elderly.

Sereprid is also used to associated treatment for these conditions: Behavioural Disorders, Chorea

How Sereprid works

Sereprid is a selective dopamine D2 and D3 receptor antagonist, offering an advantage over other neuroleptic drugs, such as haloperidol and risperidone, which bind a range of targets including four of the five known dopamine receptor subtypes (D1-4), serotonin (5-HT2A, 2C), α1- and α2-adrenergic, and histamine H1 receptors. Compared to these drugs, tiapride has a relatively moderate affinity for its target receptors, displacing 50 percent of 3H-raclopride binding at a concentration of 320 nM at D2 receptors and a concentration of 180 nM at D3 receptors.

Volume of Distribution

Sereprid distributes rapidly and exhibits virtually no binding to plasma proteins, giving it a relatively high volume of distribution

Elimination Route

The bioavailability of tiapride is approximately 75 percent. It has a Tmax is 0.4-1.5 hours and Tss is 24-48 hours with 3 time daily dosing. Benzamide and its derivatives are highly water-soluble but known to cross the blood-brain barrier, necessitating carrier-mediated transport.

Half Life

2.9–3.6 hours

Clearance

16.6 l/h.

Elimination Route

Urine (70% as unchanged tiapride)

Innovators Monograph

You find simplified version here Sereprid

*** Taking medicines without doctor's advice can cause long-term problems.
Share