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Tiaprid

Tiapride

HCID 5467
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Grundinformationen

CAS
51012-32-9
Standard-SMILES
CCN(CC)CCNC(=O)c1cc(S(C)(=O)=O)ccc1OC
InChIKey
JTVPZMFULRWINT-UHFFFAOYSA-N
Summenformel
C15H24N2O4S
Durchschnittliche Molmasse
328,4 g/mol
Monoisotopische Masse
328,14567825

Überblick

N-[2-(diethylamino)ethyl]-2-methoxy-5-methylsulfonylbenzamide is a member of benzamides.

Namen und Bezeichner

Bevorzugter Name
Tiapride
IUPAC
N-[2-(diethylamino)ethyl]-2-methoxy-5-methylsulfonylbenzamide
Lokaler Name
Tiaprid
Englischer Name
Tiapride
Summenformel
C15H24N2O4S
Molmasse
328.43

Namen und Synonyme

tiapride51012-32-9ThiaprideTiapridaTiapridumLAH70H9JPHNSC-758225DTXSID0023664N-(2-(diethylamino)ethyl)-5-methanesulfonyl-2-methoxybenzene-1-carboximidic acidN-[2-(diethylamino)ethyl]-5-methanesulfonyl-2-methoxybenzene-1-carboximidic acidRefChem:898104DTXCID903664
Weitere Namen anzeigen
Tiapride hclflo1347Cyclovirobune DTiapride USP/EP/BPTiapride ImpurityLABOTEST-BB LT00772311N-[2-(Diethylamino)ethyl]-5-mesyl-2-methoxybenzamideN-[2-Diethylamino ethyl]-5-[methylsufonyl]-o-anisamide
N05AL03256-907-9N-(2-(Diethylamino)ethyl)-2-methoxy-5-(methylsulfonyl)benzamideThiapride; TiaprideN-[2-(diethylamino)ethyl]-2-methoxy-5-methylsulfonylbenzamideTiapride (INN)N-(2-(Diethylamino)ethyl)-5-(methylsulfonyl)-o-anisamideTIAPRIDE [INN]

Datenbank-Bezeichner

CAS
51012-32-9

Eigenschaften

Berechnete Struktureigenschaften

XLogP
0,9
Polarare Oberfläche (TPSA)
84,1 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
5
Frei drehbare Bindungen
8
Schwere Atome
22
Formalladung
0
Komplexität
443

Experimentelle und physikochemische Eigenschaften

Drugs · 3 Einträge

Pharmaceuticals

Pharmaceuticals -> Listed in ZINC15

Pharmaceuticals -> Antipsychotics

LogP0.90
Melting Point124 °C
Physical DescriptionSolid

Physikochemische Eigenschaften

Schmelzpunkt
123 · 123-125°
Dampfdruck
0 Pa · 0Pa at 25℃
storage temp.
2 · 2-8°C
pka
9.14 · 9.14[at 20 ℃]
Wasserlöslichkeit
349 mg/L · 349mg/L at 25℃
LogP
0.9 · 0.9
CAS Datenbank
51012 · 51012-32-9(CAS DataBase Reference)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 3 Einträge

This chemical does not meet GHS hazard criteria for 100% (5 of 5) of all reports.

Not Classified

Aggregated GHS information provided per 5 reports by companies from 1 notifications to the ECHA C&L Inventory.

Gefahrenhinweise

Regulatory InformationStatus: Active Update: 10-07-2018 https://echa.europa.eu/registration-dossier/-/registered-dossier/23340
Hazard Classes and CategoriesNot Classified

Toxikologische Informationen

Drug Induced Liver Injury · 4 Einträge

Drug-Induced Liver Injury Severity and Toxicity (DILIst)

Tiapride

DILI Positive

DOI:10.1016/j.drudis.2019.09.022

Sicherheitsdaten

wgk
2
RTECS-Nr.
CV4203800

Chemie und Industrie

Pharmakologische Informationen

ATC Code · 3 Einträge

N05AL03

N - Nervous system

QN - Nervous system

Protein BindingNegligible
Pharmacodynamics · 1 Eintrag

Tiapride 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.

Mechanism of Action · 1 Eintrag

Tiapride 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.

Biological Half-Life2.9–3.6 hours
Metabolism/MetabolitesTiapride is minimally metabolized in humans, 70 % of the drug is eliminated in unchanged form in the urine within 24 hours. Only low concentration of N-desethyl tiapride and tiapride N-oxide and no phase II metabolites were detected.
MeSH Pharmacological Classification · 2 Einträge

Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus.

Zugehörige Reaktionen

2
Reaktionsaufzeichnung erstellen
Reaktionsgleichung von HRID 982575
HRID 982575als Eduktuspto-grants-2005_03
Reaktionsgleichung von HRID 1283488
HRID 1283488als Produktuspto-grants-1976_08

Notizen zur Verbindung

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Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
PubChem CID
5467
DTXSID
DTXSID0023664
ChEMBL
CHEMBL84158
ChEBI
CHEBI:94666
UNII
LAH70H9JPH
EC Number
256-907-9
Nikkaji
J11.205D

Drugs that bind to but do not activate DOPAMINE RECEPTORS, thereby blocking the actions of dopamine or exogenous agonists. Many drugs used in the treatment of psychotic disorders (ANTIPSYCHOTIC AGENTS) are dopamine antagonists, although their therapeutic effects may be due to long-term adjustments of the brain rather than to the acute effects of blocking dopamine receptors. Dopamine antagonists have been used for several other clinical purposes including as ANTIEMETICS, in the treatment of Tourette syndrome, and for hiccup. Dopamine receptor blockade is associated with NEUROLEPTIC MALIGNANT SYNDROME.

Absorption, Distribution and Excretion · 4 Einträge

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.

Urine (70% as unchanged tiapride)

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

16.6 l/h.

Verwendung und Herstellung

UsesUse (kg) in Switzerland (2009): >50

Anwendungen

VerwendenTiapride hydrochloride is a D2DR and D3DR inhibitor; Anti-psychotic agent and alternative treatment for Tourette’s syndrome.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

Isobutylchlorformiat5-Mesyl-o-anissure2-Aminoethyldiethylamin1,4-Dioxan

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