L-745,870 trihydrochloride

Pricing Availability   Qty
说明: Highly selective D4 antagonist
化学名: 3-(4-[4-Chlorophenyl]piperazin-1-yl)-methyl-1H-pyrrolo[2,3-b]pyridine trihydrochloride
纯度: ≥99% (HPLC)
说明书
引用文献 (13)
评论 (1)
文献 (3)

生物活性 for L-745,870 trihydrochloride

L-745,870 trihydrochloride is a highly potent and selective D4 dopamine receptor antagonist; L-745,870 has Ki values of 0.51, 2300 and 960 nM for D4, D3 and D2 subtypes respectively and > 1000-fold selectivity over 5-HT2, D1 and D5 receptors.

许可信息

Sold with the permission of Merck Sharp and Dohme Ltd.

技术数据 for L-745,870 trihydrochloride

分子量 436.21
公式 C18H19N4Cl.3HCl
储存 Desiccate at +4°C
纯度 ≥99% (HPLC)
CAS Number 866021-03-6
PubChem ID 49759035
InChI Key KJSOYZLYCFYXFC-UHFFFAOYSA-N
Smiles Cl.Cl.Cl.ClC1=CC=C(C=C1)N1CCN(CC2=CNC3=NC=CC=C23)CC1

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 L-745,870 trihydrochloride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
water 43.62 100

制备储备液 for L-745,870 trihydrochloride

以下数据基于产品分子量 436.21。 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 2.29 mL 11.46 mL 22.92 mL
5 mM 0.46 mL 2.29 mL 4.58 mL
10 mM 0.23 mL 1.15 mL 2.29 mL
50 mM 0.05 mL 0.23 mL 0.46 mL

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产品说明书 for L-745,870 trihydrochloride

分析证书/产品说明书
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参考文献 for L-745,870 trihydrochloride

参考文献是支持产品生物活性的出版物。

Bristow et al (1997) Schizophrenia and L-745, 870 a novel DA D4 receptor antagonist. TiPS 18 186 PMID: 9226994

Kulagowski et al (1996) 3-[[4-(4-Chlorophenyl)piperazin-1-yl]methyl-1H-pyrrolo[2,3-b]pyridine: an antagonist with high affinity and selectivity for the human D4 receptor. J.Med.Chem. 39 1941 PMID: 8642550

Patel et al (1997) Biological profile of L-745,870, a selective antagonist with high affinity for the DA D4 receptor. J.Pharmacol.Exp.Ther. 283 636 PMID: 9353380

Pillai et al (1998) Human D2 and D4 DA receptors couple through βγ G-protein subunits to inwardly rectifying K+ channels (GIRK1) in a Xenopus oocyte expression system: selective antagonism by L-741,626 and L-745,870 respect Neuropharmacology 37 983 PMID: 9833627


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关键词: L-745,870 trihydrochloride, L-745,870 trihydrochloride supplier, selective, D4, antagonists, Dopamine, Receptors, dopaminergic, L745870, 1002, Tocris Bioscience

13 篇 L-745,870 trihydrochloride 的引用文献

引用文献是使用了 Tocris 产品的出版物。 L-745,870 trihydrochloride 的部分引用包括:

Sharma et al (2021) Epithelial phenotype restoring drugs suppress macular degeneration phenotypes in an iPSC model. Nat Commun 12 7293 PMID: 34911940

Huang (2017) Neurochemical arguments for the use of DA D4 receptor stimulation to improve cognitive impairment associated with schizophrenia. Pharmacol Biochem Behav 157 16 PMID: 28455127

Guo (2017) DA D4 receptor activation restores CA1 LTP in hippocampal slices from aged mice. Aging Cell 16 1323 PMID: 28975698

Herwerth et al (2012) D4 DA receptors modulate NR2B NMDA receptors and LTP in stratum oriens of hippocampal CA1. Cereb Cortex 22 1786 PMID: 21955919

Chen et al (2015) Activation of D4 DA receptor decreases angiotensin II type 1 receptor expression in rat renal proximal tubule cells. Autophagy 65 153 PMID: 25368031

Matsui and Alvarez (2018) Cocaine Inhibition of Synaptic Transmission in the Ventral Pallidum Is Pathway-Specific and Mediated by Serotonin. Cell Rep 23 3852 PMID: 29949769

Picton et al (2016) Mechanisms underlying the endogenous DArgic inhibition of spinal locomotor circuit function in Xenopus tadpoles. Scientific Reports 6 35749 PMID: 27760989

Jensen (2015) Effects of DA D2-Like Receptor Antagonists on Light Responses of Ganglion Cells in Wild-Type and P23H Rat Retinas. PLoS One 10 e0146154 PMID: 26717015

Suárez-Boomgaard et al (2014) DA D4 receptor counteracts morphine-induced changes in µ opioid receptor signaling in the striosomes of the rat caudate putamen. Int J Mol Sci 15 1481 PMID: 24451133

Steullet et al (2014) Fast oscillatory activity in the anterior cingulate cortex: DArgic modulation and effect of perineuronal net loss. Front Cell Neurosci 8 244 PMID: 25191228

Dai et al (2017) Is DA transporter-mediated DArgic signaling in the retina a noninvasive biomarker for attention-deficit/ hyperactivity disorder? A study in a novel DA transporter variant Val559 transgenic mouse model. J Neurodev Disord 9 38 PMID: 29281965

Okada et al (2005) A DA D4 receptor antagonist attenuates ischemia-induced neuronal cell damage via upregulation of neuronal apoptosis inhibitory protein. Hypertension 25 794 PMID: 15729293

Basso et al (2005) Antidepressant-like effect of D(2/3) receptor-, but not D(4) receptor-activation in the rat forced swim test. Neuropsychopharmacology 30 1257 PMID: 15688083


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Inhibition of Synaptic Transmission in the VP.
By Anonymous on 02/02/2020
分析类型: In Vivo
种属: Mouse

L-745870 (100 nM)

PMID: 29949769
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