WAY 100635 maleate

Pricing Availability   Qty
说明: Potent 5-HT1A antagonist; also D4 agonist
化学名: N-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-N-2-pyridinylcyclohexanecarboxamide maleate
纯度: ≥99% (HPLC)
说明书
引用文献 (13)
评论 (1)
文献 (3)

生物活性 for WAY 100635 maleate

WAY 100635 maleate is a potent, silent antagonist of 5-HT1A receptors (IC50 = 2.2 nM; Ki = 0.84 nM for rat 5-HT1A receptors). Displays 100-fold selectivity for 5-HT1A over other 5-HT subtypes. Also exhibits agonist activity at dopamine D4 receptors.

技术数据 for WAY 100635 maleate

分子量 538.64
公式 C25H34N4O2.C4H4O4
储存 Desiccate at RT
纯度 ≥99% (HPLC)
CAS Number 1092679-51-0
PubChem ID 11957721
InChI Key XIGAHNVCEFUYOV-BTJKTKAUSA-N
Smiles O=C(C4CCCCC4)N(C3=NC=CC=C3)CCN(CC2)CCN2C1=C(OC)C=CC=C1.O=C(\C=C/C(O)=O)O

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 WAY 100635 maleate

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
water 13.47 25

制备储备液 for WAY 100635 maleate

以下数据基于产品分子量 538.64。 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
0.25 mM 7.43 mL 37.13 mL 74.26 mL
1.25 mM 1.49 mL 7.43 mL 14.85 mL
2.5 mM 0.74 mL 3.71 mL 7.43 mL
12.5 mM 0.15 mL 0.74 mL 1.49 mL

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产品说明书 for WAY 100635 maleate

分析证书/产品说明书
选择另一批次:

参考文献 for WAY 100635 maleate

参考文献是支持产品生物活性的出版物。

Mensonides-Harsema et al (2000) Synthesis and in vitro and in vivo functional studies of ortho-substituted phenylpiperazine and N-substituted 4-N-(o-methoxyphenyl)aminopiperidine analogues of WAY100635. J.Med.Chem. 43 432 PMID: 10669570

Zhuang et al (1994) Synthesis and evaluation of 4-(2'-methoxyphenyl)-1-[2'-[N-(2''-pyridinyl)-p-iodobenzamido]ethyl]piperazine (p-MPPI): a new iodinated 5-HT1A ligand. J.Med.Chem. 37 1406 PMID: 8182697

Forster et al (1995) A pharmacological profile of the selective silent 5-HT1A receptor antagonist, WAY-100635. Eur.J.Pharmacol. 281 81 PMID: 8566121

Chemel et al (2006) WAY-100635 is a potent DA D4 receptor agonist. Psychopharmacology (Berl). 188 244 PMID: 16915381


If you know of a relevant reference for WAY 100635 maleate, please let us know.

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关键词: WAY 100635 maleate, WAY 100635 maleate supplier, WAY100635, maleate, 5-ht1a, serotonin, serotonergics, selective, antagonists, dopamine, D4, dopaminergics, 634908-75-1, 5-HT1A, Receptors, 4380, Tocris Bioscience

13 篇 WAY 100635 maleate 的引用文献

引用文献是使用了 Tocris 产品的出版物。 WAY 100635 maleate 的部分引用包括:

Khaled et al (2020) Delta glutamate receptor conductance drives excitation of mouse dorsal raphe neurons. Elife 9 PMID: 32234214

Anna et al (2020) Discovery of Novel pERK1/2- or β-Arrestin-Preferring 5-HT1A Receptor-Biased Agonists: Diversified Therapeutic-like versus Side Effect Profile. J Med Chem 63 10946-10971 PMID: 32883072

Rodríguez-Muñoz et al (2018) Cannabidiol enhances MOR antinociception, diminishes NMDA-mediated seizures and reduces stroke damage via the sigma 1 receptor. Mol Brain 11 51 PMID: 30223868

Walory et al (2018) Oncotoxic Properties of Serotonin Transporter Inhibitors and 5-HT1A Receptor Ligands. Int J Mol Sci 19 PMID: 30347827

Greene et al (2009) Vascular endothelial growth factor signaling is required for the behavioral actions of antidepressant treatment: pharmacological and cellular characterization. Neuropsychopharmacology 34 2459 PMID: 19553916

Yin et al (2017) Selective Modulation of Axonal Sodium Channel Subtypes by 5-HT1A Receptor in Cortical Pyramidal Neuron. Cereb Cortex 27 509 PMID: 26494800

Shimizu et al (2017) Brain serotoninergic nervous system is involved in bombesin-induced frequent urination through brain 5-HT7 receptors in rats. Br J Pharmacol 174 3072 PMID: 28675470

Wierońska et al (2015) The antipsychotic-like effects in rodents of the positive allosteric modulator Lu AF21934 involve 5-HT1A receptor signaling: mechanistic studies. Sci Transl Med 232 259 PMID: 25012236

Nguyen et al (2019) Potentiation of the glycine response by serotonin on the substantia gelatinosa neurons of the trigeminal subnucleus caudalis in mice. Korean J Physiol Pharmacol 23 271 PMID: 31297011

Zhou et al (2019) A neural circuit for comorbid depressive symptoms in chronic pain. Nat Neurosci 22 1649 PMID: 31451801

Sonal et al (2019) Serotonin receptor oligomerization regulates cAMP-based signaling. J Cell Sci 132 PMID: 31371490

Andrew et al (2019) A Discrete Dorsal Raphe to Basal Amygdala 5-HT Circuit Calibrates Aversive Memory. Neuron 103 489-505.e7 PMID: 31204082

Rawls et al (2010) 5-HT(1A)-like receptor activation inhibits abstinence-induced metha. withdrawal in planarians. Neurosci Lett 484 113 PMID: 20709144


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Easy to use, goes into solution well.
By Corinne Kiessling on 01/04/2018
分析类型: In Vivo
种属: Rat

Used this for validation of a molecular target during behavioral testing in rats. This was used to selectively block central 5-HT1A receptors. Dissolved in water at a dose of 0.5 mg/ ml and 1.0 mg/ml and injected subcutaneously in rats. Injections were followed by behavioral testing.


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