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Merck
CN

D3775

Sigma-Aldrich

多西拉敏 琥珀酸盐

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关于此项目

经验公式(希尔记法):
C17H22N2O · C4H6O4
CAS Number:
分子量:
388.46
EC 号:
MDL编号:
UNSPSC代码:
12352116
PubChem化学物质编号:
NACRES:
NA.77
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表单

powder

质量水平

创始人

Sanofi Aventis

SMILES字符串

OC(=O)CCC(O)=O.CN(C)CCOC(C)(c1ccccc1)c2ccccn2

InChI

1S/C17H22N2O.C4H6O4/c1-17(20-14-13-19(2)3,15-9-5-4-6-10-15)16-11-7-8-12-18-16;5-3(6)1-2-4(7)8/h4-12H,13-14H2,1-3H3;1-2H2,(H,5,6)(H,7,8)

InChI key

KBAUFVUYFNWQFM-UHFFFAOYSA-N

基因信息

human ... HRH1(3269)

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一般描述

多西拉敏属于乙醇胺类抗组胺药,经肝脏代谢为 N -去甲基多西拉敏和 N , N -二去甲基多西拉敏。 它通常是一种非处方药 (OTC),用于治疗过敏和感冒症状。

应用

琥珀酸多西拉敏已被用于研究在CS培养基低视黄酸浓度的情况下,非致畸性暴露(non-teratogenic exposures )对人胚胎干细胞聚集体(HESCA)-CSR的形态和基因表达的影响。
琥珀酸多西拉敏盐已被用作检查发育毒性的治疗药物。

生化/生理作用

H 1 组胺受体拮抗剂;催眠药。
多西拉敏抑制组胺 H1 受体。它与失眠的短期管理和普通感冒症状的暂时缓解有关。另一方面,多西拉敏中毒与横纹肌溶解和继发性急性肾功能衰竭有关。
对小鼠的研究显示,多西拉敏诱导肝微粒体细胞色素 P450 和其它与甲状腺素 (T4) 代谢有关的酶。本药与盐酸吡哆醇合用,可治疗晨吐。

特点和优势

该化合物是由赛诺菲安万特开发的。想要浏览其他由制药公司开发的化合物以及已批准药物/候选药物清单, 请单击此处

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 2

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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