S174
SDZ-205,557 hydrochloride
solid
别名:
4-Amino-5-chloro-2-methoxybenzoic acid 2-(diethylamino)ethyl ester hydrochloride
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关于此项目
经验公式(希尔记法):
C14H21ClN2O3 · HCl
化学文摘社编号:
分子量:
337.24
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
表单
solid
颜色
off-white
溶解性
DMSO: 100 mg/mL
H2O: 65 mg/mL
ethanol: insoluble
创始人
Sandoz
SMILES字符串
Cl[H].CCN(CC)CCOC(=O)c1cc(Cl)c(N)cc1OC
InChI
1S/C14H21ClN2O3.ClH/c1-4-17(5-2)6-7-20-14(18)10-8-11(15)12(16)9-13(10)19-3;/h8-9H,4-7,16H2,1-3H3;1H
InChI key
JOWUQCJWCRNVMQ-UHFFFAOYSA-N
基因信息
human ... HTR4(3360)
生化/生理作用
Potent, selective 5-HT4 serotonin receptor antagonist.
特点和优势
This compound was developed by Sandoz. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
N Amemiya et al.
European journal of pharmacology, 318(2-3), 403-409 (1996-12-30)
This study examined effects of 5-methoxytryptamine (5-MOT), an agonist at 5-HT4 and 5-HT2B receptors, on the contractile response and acetylcholine release in rat stomach fundus strips. 5-MOT (10(-9)-10(-5) M) produced a concentration-dependent increase in the contraction, while it evoked acetylcholine
G E Torres et al.
The Journal of pharmacology and experimental therapeutics, 271(1), 255-261 (1994-10-01)
The study of serotonin-4 (5-HT4) receptors in the central nervous system has been hindered by the lack of effective, selective antagonists. However, recently, several novel compounds have been synthesized and shown to act as antagonists at 5-HT4 receptors in smooth
J Lorrain et al.
European journal of pharmacology, 229(1), 105-108 (1992-12-08)
Putative 5-HT4 receptors were investigated in isolated piglet left atria and papillary muscles. In atrial tissues, 5-hydroxytryptamine (5-HT) was a potent positive inotropic agent with a pD2 of 6.7. Its effects were antagonised in a selective and competitive manner by
C M Franks et al.
The Journal of pharmacy and pharmacology, 47(3), 213-218 (1995-03-01)
The involvement of the recently characterized 5-HT4 receptor in the actions of 5-hydroxytryptamine (5-HT) on jejunal, ileal and colonic electrogenic ion secretion was investigated in the rat in-vivo. 5-HT and the 5-HT1-, 5-HT2- and 5-HT4-receptor agonist 5-methoxytryptamine (5-MeOT), induced a
J Coleman et al.
Naunyn-Schmiedeberg's archives of pharmacology, 352(1), 74-78 (1995-07-01)
A putative 5-HT4 receptor-mediated depolarization of the rat isolated vagus nerve has been studied using a grease-gap extracellular recording technique. Ondansetron (1 microM) was used to block the predominant 5-HT3 receptor mediated depolarization in this preparation and the effects of
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