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Merck
CN

N3529

Sigma-Aldrich

NAN-190 hydrobromide

别名:

1-(2-Methoxyphenyl)-4-[4-(2-phthalimido)butyl]piperazine hydrobromide

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关于此项目

经验公式(希尔记法):
C23H27N3O3 · HBr
化学文摘社编号:
分子量:
474.39
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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SMILES字符串

Br.COc1ccccc1N2CCN(CCCCN3C(=O)c4ccccc4C3=O)CC2

InChI

1S/C23H27N3O3.BrH/c1-29-21-11-5-4-10-20(21)25-16-14-24(15-17-25)12-6-7-13-26-22(27)18-8-2-3-9-19(18)23(26)28;/h2-5,8-11H,6-7,12-17H2,1H3;1H

InChI key

AXRUEPFPTQYHQD-UHFFFAOYSA-N

基因信息

human ... HTR1A(3350)

生化/生理作用

Potent 5-HT1A serotonin receptor antagonist active in the nM range.

象形图

Exclamation markEnvironment

警示用语:

Warning

危险分类

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

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

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jordan D Chambers et al.
PloS one, 6(5), e19597-e19597 (2011-05-17)
After a meal, the gastrointestinal tract exhibits a set of behaviours known as the fed state. A major feature of the fed state is a little understood motor pattern known as segmentation, which is essential for digestion and nutrient absorption.
R Sterniczuk et al.
Neuroscience, 153(3), 571-580 (2008-04-15)
Chronic desynchronization between the mammalian circadian pacemaker and its external environment, such as that observed from shift work or jet lag, can lead to various long-term health consequences. The circadian clock can be reset by exposure to light, although the
Pei-Lu Yi et al.
Journal of biomedical science, 14(6), 829-840 (2007-07-28)
Sedative-hypnotic medications, including benzodiazepines and non-benzodiazepines, are usually prescribed for the insomniac patients; however, the addiction, dependence and adverse effects of those medications have drawn much attention. In contrast, suanzaorentang, a traditional Chinese herb remedy, has been efficiently used for
Mohammad Charkhpour et al.
Anesthesia and analgesia, 111(5), 1316-1321 (2010-08-26)
Previously, we found that activation of serotonin 1A (5-HT1A) receptors in the dorsal raphe nucleus (DRN) decreased the development of tolerance to the analgesic effect of morphine. It has been indicated that tolerance to the analgesic effect of morphine is
M H Paluchowska et al.
Journal of medicinal chemistry, 42(24), 4952-4960 (1999-12-10)
Structural modifications of 1, a postsynaptic 5-HT(1A) receptor antagonist, provided its flexible (8, 12) and rigid (7, 9, 11, 13) analogues. Compounds 7, 8, 9, and 11 showed high 5-HT(1A) receptor affinity (K(i) = 4-72 nM). They acted as 5-HT(1A)

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