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Merck
CN

SML0033

Sigma-Aldrich

伊托必利 盐酸盐

≥98% (HPLC), dopamine D2-receptor antagonist, powder

别名:

N- [ [4- [2-(二甲氨基)乙氧基] 苯基] 甲基]-3,4-二甲氧基苯甲酰胺盐酸盐, N- [p- [2-(二甲氨基)乙氧基] 苄基] 维拉曲米盐酸盐

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关于此项目

经验公式(希尔记法):
C20H26N2O4 ·HCl
化学文摘社编号:
分子量:
394.89
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
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产品名称

伊托必利 盐酸盐, ≥98% (HPLC)

质量水平

方案

≥98% (HPLC)

表单

powder

储存条件

desiccated

颜色

white to tan

溶解性

H2O: ≥48 mg/mL

创始人

Abbott

储存温度

2-8°C

SMILES字符串

Cl.COc1ccc(cc1OC)C(=O)NCc2ccc(OCCN(C)C)cc2

InChI

1S/C20H26N2O4.ClH/c1-22(2)11-12-26-17-8-5-15(6-9-17)14-21-20(23)16-7-10-18(24-3)19(13-16)25-4;/h5-10,13H,11-12,14H2,1-4H3,(H,21,23);1H

InChI key

ZTOUXLLIPWWHSR-UHFFFAOYSA-N

一般描述

盐酸伊托必利是一种新型的促胃肠动力药。

生化/生理作用

伊托必利是乙酰胆碱酯酶 (AChE) 抑制剂和 D2 多巴胺受体拮抗剂。伊托必利是一种促胃动力药。
具有抗胆碱酯酶活性的多巴胺 D2 受体拮抗剂。
盐酸伊托必利通过阻断 D2 受体、突触后胆碱能神经上多巴胺的活性和诱导肌间神经丛中乙酰胆碱的释放,增强胃肠动力。它还能在乙酰胆碱酯酶的帮助下抑制释放的乙酰胆碱的水解。

特点和优势

该化合物由Abbott开发。要浏览其他药物开发化合物和批准的药物/候选药物列表,单击此处

象形图

Environment

警示用语:

Warning

危险声明

预防措施声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Sanjay Bansal et al.
Drug delivery, 23(2), 437-451 (2014-05-29)
The objectives of present studies were to develop the systematically optimized multiple-unit gastroretentive microballoons, i.e. hollow microspheres of itopride hydrochloride (ITH) employing quality by design (QbD)-based approach. Initially, the patient-centric QTPP and CQAs were earmarked, and preliminary studies were conducted
[Effect of HSR-803 on gastrointestinal motility].
H Iwanaga et al.
Nihon Heikatsukin Gakkai zasshi, 25(6), 313-315 (1989-12-01)
N Kishibayashi et al.
Japanese journal of pharmacology, 66(4), 397-403 (1994-12-01)
KW-5092 ([1-[2-[[[5-(piperidinomethyl)-2- furanyl]methyl]amino]ethyl]-2-imidazolidinylidene] propanedinitrile fumarate) is a novel gastroprokinetic agent with acetylcholinesterase (AChE) inhibitory activity and acetylcholine release facilitatory activity. The present study used guinea pig ileal homogenates to examine the inhibitory effects of KW-5092 on the activities of AChE
Y Iwanaga et al.
Japanese journal of pharmacology, 62(4), 395-401 (1993-08-01)
Stimulatory effects of HSR-803 on intestinal motor activity in vitro were studied in guinea pig ileum. HSR-803 (1 x 10(-6)-1 x 10(-4) M) increased the amplitude of longitudinal muscle contractions and increased the frequency of peristalsis in isolated segments of
Comparative evaluation of the efficacy and tolerability of itopride hydrochloride and domperidone in patients with non-ulcer dyspepsia.
Sawant P, et al.
The Journal of the Association of Physicians of India, 52, 626-628 (2004)

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