CP 93129 dihydrochloride

Pricing Availability   Qty
说明: 5-HT1B agonist
化学名: 1,4-Dihydro-3-(1,2,3,6-tetrahydro-4-pyridinyl)-5H-pyrrol[3,2-b]pyridin-5-one dihydrochloride
说明书
引用文献 (9)
评论 (3)
文献 (2)

生物活性 for CP 93129 dihydrochloride

CP 93129 dihydrochloride is a potent and highly selective 5-HT1B agonist (Ki values are 8.1, 1100, 1500, 2900 and 7200 nM for 5-HT1B, 5-HT1D, 5-HT1A, 5-HT1c and 5-HT2, respectively). Reduces food intake and decreases body weight in rats.

许可信息

Sold for research purposes under agreement from Pfizer Inc.

技术数据 for CP 93129 dihydrochloride

分子量 288.18
公式 C12H13N3O.2HCl
储存 Desiccate at RT
CAS Number 879089-64-2
PubChem ID 46927988
InChI Key FLVJHUZZKVJQNH-UHFFFAOYSA-N
Smiles Cl.Cl.O=C1NC2=C(NC=C2C2=CCNCC2)C=C1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for CP 93129 dihydrochloride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 28.82 100
water 28.82 100

制备储备液 for CP 93129 dihydrochloride

以下数据基于产品分子量 288.18。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 3.47 mL 17.35 mL 34.7 mL
5 mM 0.69 mL 3.47 mL 6.94 mL
10 mM 0.35 mL 1.74 mL 3.47 mL
50 mM 0.07 mL 0.35 mL 0.69 mL

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产品说明书 for CP 93129 dihydrochloride

分析证书/产品说明书
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参考文献 for CP 93129 dihydrochloride

参考文献是支持产品生物活性的出版物。

Lee et al (1998) Infusion of the serotonin1B (5-HT1B) agonist CP-93,129 into the parabrachial nucleus potently and selectively reduces food intake in rats. Psychopharmacology 136 304 PMID: 9566817

Koe et al (1992) Biochemical and behavioral studies of the 5-HT1B receptor agonist, CP-94,253. Drug Development Research 26 241

Hamid et al (2014) Modulation of neurotransmission by GPCRs is dependent upon the microarchitecture of the primed vesicle complex. J Neurosci. 34 260 PMID: 24381287


If you know of a relevant reference for CP 93129 dihydrochloride, please let us know.

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关键词: CP 93129 dihydrochloride, CP 93129 dihydrochloride supplier, 5-HT1B, agonist, Serotonin, Receptors, CP93129, dihydrochloride, Pfizer, 1032, Tocris Bioscience

9 篇 CP 93129 dihydrochloride 的引用文献

引用文献是使用了 Tocris 产品的出版物。 CP 93129 dihydrochloride 的部分引用包括:

Medrihan et al (2017) Initiation of Behavioral Response to Antidepressants by Cholecystokinin Neurons of the Dentate Gyrus. Neuron 95 564 PMID: 28735749

Watakabe et al (2009) Enriched expression of serotonin 1B and 2A receptor genes in macaque visual cortex and their bidirectional modulatory effects on neuronal responses. Neuron 19 1915 PMID: 19056862

Zhou et al (2019) Modulation of Kalirin-7 Expression by Hippocampal CA1 5-HT1B Receptors in Spatial Memory Consolidation. Behav Brain Res 356 148 PMID: 29949735

Hirono (2017) Monoaminergic modulation of GABAergic transmission onto cerebellar globular cells. Neuropharmacology 118 79 PMID: 28300552


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Modulation of spontaneous interneuronal signalling.
By Sergiy Sylantyev on 12/10/2023
分析类型: In Vitro
种属: Mouse
细胞系/组织: Arcuate nucleus

CP 93129 was used to modulate spontaneous generation of action potentials in neurons of arcuate nucleus. Illustration: application of 100 nM CP 93129 (grey bar) decreases frequency of AP generation in living neuron.

PMID: 37827445
review image

5-HT has a potential for relaxant.
By Anonymous on 02/18/2020
分析类型: In Vivo
种属: Rat

CP93129 (5-HT1B)10nM

PMID: 25692021
review image

Antidepressantsby Cholecystokinin Neurons of the Dentate Gyrus.
By Anonymous on 02/03/2020
分析类型: In Vivo
种属: Mouse

CP (10mM)

PMID: 28735749
review image

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*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。


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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.

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Parkinson's disease (PD) causes chronic disability and is the second most common neurodegenerative condition. This poster outlines the neurobiology of the disease, as well as highlighting current therapeutic treatments for symptomatic PD, and emerging therapeutic strategies to delay PD onset and progression.