Salvinorin B

Pricing Availability   Qty
说明: Activator of κ-opioid DREADD (KORD)
化学名: (2S,4aR,6aR,7R,9S,10aS,10bR)-2-(3-Furanyl)dodecahydro-9-hydroxy-6a,10b-dimethyl-4,10-dioxo-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester
纯度: ≥98% (HPLC)
说明书
引用文献 (4)
评论 (1)
文献 (3)

生物活性 for Salvinorin B

Salvinorin B is a potent and selective κ-opioid DREADD (KORD) activator (EC50 = 11.8 nM). Selective for KORD over endogenous κ opioid receptor and a range of other related targets. Exhibits no analgesic or ataxic effects in wild type mice. Induces neuronal hyperpolarization, and modifies locomotor activity and feeding behavior in KORD-expressing mouse models. Brain penetrant. Metabolite of salvinorin A.

技术数据 for Salvinorin B

分子量 390.43
公式 C21H26O7
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 92545-30-7
PubChem ID 11440685
InChI Key BLTMVAIOAAGYAR-CEFSSPBYSA-N
Smiles O=C3[C@]2([H])CC[C@@]([C@]([H])1[C@](C)2C[C@@H]([C@]4=COC=C4)O3)(C)[C@H]([C@@](OC)=O)C[C@H](O)C1=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 Salvinorin B

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 7.81 20

制备储备液 for Salvinorin B

以下数据基于产品分子量 390.43。 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
0.2 mM 12.81 mL 64.03 mL 128.06 mL
1 mM 2.56 mL 12.81 mL 25.61 mL
2 mM 1.28 mL 6.4 mL 12.81 mL
10 mM 0.26 mL 1.28 mL 2.56 mL

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产品说明书 for Salvinorin B

分析证书/产品说明书
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参考文献 for Salvinorin B

参考文献是支持产品生物活性的出版物。

Vardy et al (2015) A new DREADD facilitates the multiplexed chemogenetic interrogation of behavior. Neuron 86 936 PMID: 25937170

Ansonoff et al (2006) Antinociceptive and hypothermic effects of Salvinorin A are abolished in a novel strain of κ-opioid receptor-1 knockout mice. J.Pharmacol.Exp.Ther. 318 641 PMID: 16672569


If you know of a relevant reference for Salvinorin B, please let us know.

关键词: Salvinorin B, Salvinorin B supplier, Activates, κ-opioid, designer, receptors, drugs, KORD, DREADDs, salvinorin, A, agonists, agonism, chemogenetics, Kappa, Opioid, Receptors, 5611, Tocris Bioscience

4 篇 Salvinorin B 的引用文献

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

Yun Ha et al (2020) Dopaminergic Regulation of Nucleus Accumbens Cholinergic Interneurons Demarcates Susceptibility to Cocaine Addiction. Biol Psychiatry 88 746-757 PMID: 32622465

Smith et al (2016) DREADDS: Use and application in behavioral neuroscience. Behav Neurosci 130 137 PMID: 26913540

Pina et al (2020) The kappa opioid receptor modulates GABA neuron excitability and synaptic transmission in midbrain-projections from the insular cortex. Neuropharmacology 165 107831 PMID: 31870854

Xiong et al (2021) Human Stem Cell-Derived Neurons Repair Circuits and Restore Neural Function Cell Stem Cell 28 112 PMID: 32966778


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Salvinorin B 的评论

平均评分: 5 (Based on 1 Review.)

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Great version that works reliably.
By Melanie Pina on 12/22/2019
分析类型: Ex Vivo
种属: Human
细胞系/组织: neuron

Great version that is easily dissolved in DMSO. Worked well in slice electrophysiology and produced reliable hyperpolarization in neurons expressing KOR DREADD at 100 nM.

参考文献
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。


Chemogenetics Research Bulletin

Chemogenetics Research Bulletin

Produced by Tocris, the chemogenetics research bulletin provides an introduction to chemogenetic methods to manipulate neuronal activity. It outlines the development of RASSLs, DREADDs and PSAMs, and the use of chemogenetic compounds. DREADD ligands and PSEMs available from Tocris are highlighted.

Allosteric GPCR Pharmacology Poster

Allosteric GPCR Pharmacology Poster

G protein-coupled receptors (GPCRs) are intrinsically allosteric proteins. This poster provides insights into allosteric mechanisms of GPCR biology, highlighting key facets of GPCR allostery and therapeutic applications of allosteric modulators.

GPCR Efficacy and Biased Agonism Poster

GPCR Efficacy and Biased Agonism Poster

GPCRs can interact with multiple distinct transducers or regulatory proteins and these can be preferentially engaged in an agonist-specific manner giving rise to biased agonism. This poster discusses cutting edge GPCR signaling pharmacology and highlights therapeutic applications of biased agonism.