ML 10302 hydrochloride

Discontinued Product

3499 has been discontinued.

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说明: Potent and selective 5-HT4 partial agonist
化学名: 4-Amino-5-chloro-2-methoxybenzoic acid 2-(1-piperidinyl)ethyl ester hydrochloride
纯度: ≥99% (HPLC)
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生物活性 for ML 10302 hydrochloride

ML 10302 hydrochloride is a potent 5-HT4 partial agonist (EC50 = 4 nM) that displays > 680-fold selectivity over 5-HT3 receptors (Ki values are 1.07 and 730 nM respectively). Increases sAPPα levels in the cortex in an animal model of Alzheimer's disease and exhibits progastrokinetic effects in vivo.

技术数据 for ML 10302 hydrochloride

分子量 349.25
公式 C15H21ClN2O3.HCl
储存 Desiccate at RT
纯度 ≥99% (HPLC)
CAS Number 186826-17-5
PubChem ID 56972230
InChI Key HBLRTSYSGOFQCK-UHFFFAOYSA-N
Smiles ClC1=CC(C(OCCN2CCCCC2)=O)=C(OC)C=C1N.Cl

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参考文献 for ML 10302 hydrochloride

参考文献是支持产品生物活性的出版物。

Yang et al (1997) New esters of 4-amino-5-chloro-2-methoxybenzoic acid as potent agonists and antagonists for 5-HT4 receptors. J.Med.Chem. 40 608 PMID: 9046352

Cachard-Chastel et al (2007) 5-HT4 receptor agonists increase sAPPα levels in the cortex and hippocampus of male C57BL/6j mice. Br.J.Pharmacol. 150 883 PMID: 17325649

Ponti et al (2001) Intestinal motor stimulation by the 5-HT4 receptor agonist ML10302: differential involvement of tachykininergic pathways in the canine small bowel and colon. Neurogastroenterol.Mot. 13 543

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关键词: ML 10302 hydrochloride, ML 10302 hydrochloride supplier, Potent, selective, 5-HT4, partial, agonists, Serotonin, Receptors, 5-Hydroxytryptamine, ML10302, hydrochloride, 3499, Tocris Bioscience

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5-HT Receptors Scientific Review

5-HT Receptors Scientific Review

Written by Nicholas M. Barnes and John F. Neumaier, this review summarizes the various serotonin receptor subtypes and their importance in mediating the role of serotonin in numerous physiological and pharmacological processes. Compounds available from Tocris are listed.

Depression Poster

Depression Poster

Major depressive disorder is characterized by depressed mood and a loss of interest and/or pleasure. Updated in 2015 this poster highlights presynaptic and postsynaptic targets for the potential treatment of major depressive disorder, as well as outlining the pharmacology of currently approved antidepressant drugs.