(RS)-(±)-Sulpiride

Pricing Availability   Qty
说明: Standard selective D2-like antagonist
化学名: (RS)-(±)-5-Aminosulfonyl-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide
纯度: ≥98% (HPLC)
说明书
引用文献 (7)
评论 (2)
文献 (2)

生物活性 for (RS)-(±)-Sulpiride

(RS)-(±)-Sulpiride is a standard D2-like dopamine receptor antagonist.

S-enantiomer also available.

化合物库 for (RS)-(±)-Sulpiride

(RS)-(±)-Sulpiride is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for (RS)-(±)-Sulpiride

分子量 341.42
公式 C15H23N3O4S
储存 Store at RT
纯度 ≥98% (HPLC)
CAS Number 15676-16-1
PubChem ID 5355
InChI Key BGRJTUBHPOOWDU-UHFFFAOYSA-N
Smiles CCN1CCCC1CNC(=O)C1=C(OC)C=CC(=C1)S(N)(=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 (RS)-(±)-Sulpiride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 34.14 100

制备储备液 for (RS)-(±)-Sulpiride

以下数据基于产品分子量 341.42。 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 2.93 mL 14.64 mL 29.29 mL
5 mM 0.59 mL 2.93 mL 5.86 mL
10 mM 0.29 mL 1.46 mL 2.93 mL
50 mM 0.06 mL 0.29 mL 0.59 mL

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产品说明书 for (RS)-(±)-Sulpiride

分析证书/产品说明书
选择另一批次:

参考文献 for (RS)-(±)-Sulpiride

参考文献是支持产品生物活性的出版物。

Seeman and Van Tol (1993) DA D4 receptors bind inactive (+)-aporphines, suggesting neuroleptic role. Sulpiride not stereoselective. Eur.J.Pharmacol. 233 173 PMID: 8097160

Seeman and Van Tol (1994) DA receptor pharmacology. TiPS 15 264 PMID: 7940991

Merck Index 12 9163


If you know of a relevant reference for (RS)-(±)-Sulpiride, please let us know.

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关键词: (RS)-(±)-Sulpiride, (RS)-(±)-Sulpiride supplier, selective, D2-like, antagonists, Dopamine, Non-Selective, Receptors, dopaminergic, Non-selective, 0894, Tocris Bioscience

7 篇 (RS)-(±)-Sulpiride 的引用文献

引用文献是使用了 Tocris 产品的出版物。 (RS)-(±)-Sulpiride 的部分引用包括:

Shin et al (2011) Exposure to extremely low frequency magnetic fields induces fos-related antigen-immunoreactivity via activation of DArgic d1 receptor. Neuropsychopharmacology 20 130 PMID: 22110371

Leyrer-Jackson (2017) Subtype-specific effects of DArgic D2 receptor activation on synaptic trains in layer V pyramidal neurons in the mouse prefrontal cortex. Physiol Rep 5 e13499 PMID: 29150590

Huang (2018) DA D1 Receptors Contribute Critically to the Apomorphine-Induced Inhibition of Form-Deprivation Myopia in Mice. Invest Ophthalmol Vis Sci 59 2623 PMID: 29847669

Zhang et al (2018) DA Receptor Subtypes Mediate Opposing Effects on Form Deprivation Myopia in Pigmented Guinea Pigs. Invest Ophthalmol Vis Sci 59 4441 PMID: 30193315


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(RS)-(±)-Sulpiride 的评论

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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

sulpiride (1 μM)

PMID: 29949769
review image

Sulpiride reverses quinpirole effects on dopamine release.
By Anonymous on 03/28/2018
分析类型: Ex Vivo
种属: Mouse

In voltammetry experiments measuring evoked dopamine release, quinpirole was used to activate D2 receptors to inhibit dopamine release. Sulpiride (600 nM) was applied afterward to reverse quinpirole effects.

We mix sulpiride at 2mM in ethanol. It goes into solution well.

review image

该领域的文献

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。


Dopamine Receptors Scientific Review

Dopamine Receptors Scientific Review

Written by Phillip Strange and revised by Kim Neve in 2013, this review summarizes the history of the dopamine receptors and provides an overview of individual receptor subtype properties, their distribution and identifies ligands which act at each receptor subtype. Compounds available from Tocris are listed.

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