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Home > Encyclopedia > Tiapride hydrochloride

Tiapride hydrochloride

pharmaceutical raw materials
Tiapride hydrochloride structure

Tiapride hydrochloride 

structure
  • CAS No:

    51012-33-0

  • Formula:

    C15H24N2O4S.ClH

  • Chemical Name:

    Tiapride hydrochloride

  • Synonyms:

    Benzamide,N-[2-(diethylamino)ethyl]-2-methoxy-5-(methylsulfonyl)-,hydrochloride (1:1);Benzamide,N-[2-(diethylamino)ethyl]-2-methoxy-5-(methylsulfonyl)-,monohydrochloride;Tiapride hydrochloride;Luxoben;Tiapridal;Italprid;Gramalil;Tiapridex;Sereprile

  • Categories:

    Active Pharmaceutical Ingredients  >  Nervous System Drugs

Description

Tiapride hydrochloride 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.

Tiapride hydrochloride Basic Attributes

364.89

364.12200

256-908-4

2924299090

Characteristics

84.1

3.62790

1.15 g/cm3

approximate 200℃ (dec.)

498.1ºC at 760 mmHg

255.1ºC

52.5 [ug/mL]

2-8°C

Safety Information

NONH for all modes of transport

2

CV4203800

P201, P202, P261, P264, P271, P280, P281, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

Tiapride hydrochloride Use and Manufacturing

Dopamine antagonist;Antidyskinetic

Computed Properties

Molecular Weight:364.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:364.1223562
Monoisotopic Mass:364.1223562
Topological Polar Surface Area:85.3
Heavy Atom Count:23
Complexity:443
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Drug Function and Efficacy

This product belongs to the benzamide antipsychotic drug, which has an inhibitory effect on the hyperfunction of dopaminergic nerves in the midbrain limbic system and an antagonistic effect on dopaminergic nerve movement disorders in the striatum, thereby producing a calming and sedative effect. It is characterized by its good effect on sensory and motor neurological diseases and psychomotor behavioral disorders. Animal experiments have confirmed that this product can block the conduction of pain impulses through the spinal thalamic tract to the reticular formation. The analgesic effect of this drug may be related to the integration of pain impulses by the thalamus. In addition, it has an antiemetic effect.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • ICROM S.P.A.

    Italy Italy
    Active
  • 株式会社パーマケム・アジア

    Japan Japan
    Active
  • Daito Pharmaceutical Co.,Ltd.

    Japan Japan
    Active

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