SKF 83566 hydrobromide

Pricing Availability   Qty
说明: Potent and selective D1-like antagonist; also inhibits adenylyl cyclase 2
化学名: 8-Bromo-2,3,4,5-tetrahydro-3-methyl-5-phenyl-1H-3-benzazepin-7-ol hydrobromide
纯度: ≥98% (HPLC)
说明书
引用文献 (10)
评论
文献 (4)

生物活性 for SKF 83566 hydrobromide

SKF 83566 hydrobromide is a potent and selective D1-like dopamine receptor antagonist (Ki~ 0.56 nM for D1; KB = 2 μM for D2). Also antagonist at the vascular 5-HT2 receptor (Ki = 11 nM). Displays selective inhibition of adenylyl cyclase 2 (AC2); inactive against AC1 or AC5. Centrally active following systemic administration in vivo.

化合物库 for SKF 83566 hydrobromide

SKF 83566 hydrobromide 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 SKF 83566 hydrobromide

分子量 413.15
公式 C17H18BrNO.HBr
储存 Desiccate at RT
纯度 ≥98% (HPLC)
CAS Number 108179-91-5
PubChem ID 23581817
InChI Key SDQJYYGODYRPBR-UHFFFAOYSA-N
Smiles Br.CN1CCC2=CC(Br)=C(O)C=C2C(C1)C1=CC=CC=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 SKF 83566 hydrobromide

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
water 2.07 5 温和加热
DMSO 41.31 100

制备储备液 for SKF 83566 hydrobromide

以下数据基于产品分子量 413.15。 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 2.42 mL 12.1 mL 24.2 mL
5 mM 0.48 mL 2.42 mL 4.84 mL
10 mM 0.24 mL 1.21 mL 2.42 mL
50 mM 0.05 mL 0.24 mL 0.48 mL

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产品说明书 for SKF 83566 hydrobromide

分析证书/产品说明书
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参考文献 for SKF 83566 hydrobromide

参考文献是支持产品生物活性的出版物。

Fritts et al (1998) Locomotor stereotypy produced by dexbenzetimide and scopol. is reduced by SKF 83566, not sulpiride. Pharmacol.Biochem.Behav. 60 639 PMID: 9678647

Meyer et al (1993) Effects of DA D1 antagonists SCH23390 and SK&F83566 on locomotor activities in rats. Pharmacol.Biochem.Behav. 44 429 PMID: 8446676

Ohlstein and Berkowitz (1985) SCH 23390 and SK&F 83566 are antagonists at vascular DA and serotonin receptors. Eur.J.Pharmacol. 108 205 PMID: 3884345

Conley et al (2013) Development of a high-throughput screening paradigm for the discovery of small-molecule modulators of adenylyl cyclase: identification of an adenylyl cyclase 2 inhibitor. J.Pharmacol.Exp.Ther. 347 276 PMID: 24008337


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查看全部 D1 and D5 Receptor Antagonists

关键词: SKF 83566 hydrobromide, SKF 83566 hydrobromide supplier, Potent, selective, D1-like, antagonists, Dopamine, Receptors, D5, dopaminergic, SKF83566, hydrobromide, D1, and, Adenylyl, Cyclase, 1586, Tocris Bioscience

10 篇 SKF 83566 hydrobromide 的引用文献

引用文献是使用了 Tocris 产品的出版物。 SKF 83566 hydrobromide 的部分引用包括:

Huang et al (2014) D1/D5 receptors and histone deacetylation mediate the Gateway Effect of LTP in hippocampal dentate gyrus. Learn Mem 21 153 PMID: 24549570

Stramiello (2008) D1/5 receptor-mediated enhancement of LTP requires PKA, Src family kinases, and NR2B-containing NMDARs. Neuropharmacology 55 871 PMID: 18644393

Liu et al (2008) Increased DA level enhances male-male courtship in Drosophila. World J Gastroenterol 28 5539 PMID: 18495888

Belinsky et al (2013) DA receptors in human embryonic stem cell neurodifferentiation. Stem Cells Dev 22 1522 PMID: 23286225


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