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Tiapride

HCID 5467
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
51012-32-9
표준 SMILES
CCN(CC)CCNC(=O)c1cc(S(C)(=O)=O)ccc1OC
InChIKey
JTVPZMFULRWINT-UHFFFAOYSA-N
분자식
C15H24N2O4S
평균 분자량
328.4 g/mol
단동위원소 질량
328.14567825

개요

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

이름 및 식별자

우선 이름
Tiapride
IUPAC
N-[2-(diethylamino)ethyl]-2-methoxy-5-methylsulfonylbenzamide
영어명
Tiapride
분자식
C15H24N2O4S
분자량
328.43

이름 및 동의어

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
이름 더 보기
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]

데이터베이스 식별자

CAS
51012-32-9
PubChem CID
5467
DTXSID
DTXSID0023664
ChEMBL

물성

구조 계산 물성

XLogP
0.9
극성 표면적
84.1 Ų
수소 결합 공여자 수
1
수소 결합 수용자 수
5
회전 가능 결합 수
8
무거운 원자 수
22
형식 전하
0
복잡도
443

실험 및 물리화학적 성질

Drugs · 3건

Pharmaceuticals

Pharmaceuticals -> Listed in ZINC15

Pharmaceuticals -> Antipsychotics

LogP0.90
Melting Point124 °C
Physical DescriptionSolid

물리화학적 성질

녹는점
123 · 123-125°
증기압
0 Pa · 0Pa at 25℃
저장 조건
2 · 2-8°C
산도 계수 (pKa)
9.14 · 9.14[at 20 ℃]
수용성
349 mg/L · 349mg/L at 25℃
LogP
0.9 · 0.9

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

GHS 분류

GHS Classification · 3건

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.

유해성 정보

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

독성 정보

Drug Induced Liver Injury · 4건

Drug-Induced Liver Injury Severity and Toxicity (DILIst)

Tiapride

DILI Positive

DOI:10.1016/j.drudis.2019.09.022

안전 데이터

wgk
2
rtecs
CV4203800

화학 및 산업

약리 정보

ATC Code · 3건

N05AL03

N - Nervous system

QN - Nervous system

Protein BindingNegligible
Pharmacodynamics · 1건

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 · 1건

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 · 2건

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.

관련 반응

2건
반응 기록 만들기
HRID 982575 반응식
HRID 982575반응물로uspto-grants-2005_03
HRID 1283488 반응식
HRID 1283488생성물로uspto-grants-1976_08

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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 · 4건

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.

용도 및 제조

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

응용 분야

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

상·하류 제품 정보

상류 원료

클로로탄산 이소부틸에스테르2-메톡시-5-(메틸술포닐)벤조산디에틸에틸렌디아민1.4-다이옥세인

공급사52 곳

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