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Merck
CN

M3386

1-甲基组胺 二盐酸盐

别名:

1-甲基-4-(β-氨基乙基)咪唑 二盐酸盐

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关于此项目

经验公式(希尔记法):
C6H11N3 · 2HCl
化学文摘社编号:
分子量:
198.09
UNSPSC Code:
12352204
PubChem Substance ID:
MDL number:
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storage temp.

2-8°C

SMILES string

Cl[H].Cl[H].Cn1cnc(CCN)c1

InChI

1S/C6H11N3.2ClH/c1-9-4-6(2-3-7)8-5-9;;/h4-5H,2-3,7H2,1H3;2*1H

InChI key

AGXVEALMQHTMSW-UHFFFAOYSA-N

Biochem/physiol Actions

通过组胺N-甲基转移酶产生的组胺的主要代谢产物。

Other Notes

Similar to M 4910, but prepared for Sigma.

存储类别

11 - Combustible Solids

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Alcoholics show altered histaminergic neurotransmission in several cortical areas--preliminary report.
K Alakärppä et al.
Inflammation research : official journal of the European Histamine Research Society ... [et al.], 52 Suppl 1, S37-S38 (2003-05-21)
A Burban et al.
The Journal of pharmacology and experimental therapeutics, 332(3), 912-921 (2009-12-17)
Histamine potentiates activation of native and recombinant N-methyl-d-aspartate receptors (NMDARs), but its mechanisms of action and physiological functions in the brain remain controversial. Using four different models, we have further investigated the histamine-induced potentiation of various NMDAR-mediated responses. In single
F Gbahou et al.
The Journal of pharmacology and experimental therapeutics, 334(3), 945-954 (2010-06-10)
We previously suggested that therapeutic effects of betahistine in vestibular disorders result from its antagonist properties at histamine H(3) receptors (H(3)Rs). However, H(3)Rs exhibit constitutive activity, and most H(3)R antagonists act as inverse agonists. Here, we have investigated the effects
X Ligneau et al.
The Journal of pharmacology and experimental therapeutics, 320(1), 365-375 (2006-09-29)
Histamine H3 receptor inverse agonists are known to enhance the activity of histaminergic neurons in brain and thereby promote vigilance and cognition. 1-{3-[3-(4-Chlorophenyl)propoxy]propyl}piperidine, hydrochloride (BF2.649) is a novel, potent, and selective nonimidazole inverse agonist at the recombinant human H3 receptor.
M Motawaj et al.
The Journal of pharmacology and experimental therapeutics, 336(2), 479-487 (2010-11-09)
We previously reported that some N-methyl-D-aspartate (NMDA)-receptor antagonists enhanced histamine neuron activity in rodents. Here, we have investigated the effects of memantine, an NMDA-receptor antagonist used for the treatment of Alzheimer's disease, on histaminergic neurotransmission. In vitro, memantine antagonized native

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