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Submit ReviewPotent and selective σ-ligand (Ki against [3H]-(+)-3-PPP = 0.34 nM).
分子量 | 463.08 |
公式 | C15H22Cl2N2.2HBr |
储存 | Store at -20°C |
CAS Number | 138356-09-9 |
PubChem ID | 45073417 |
InChI Key | YTBUMHOSKIAYCZ-UHFFFAOYSA-N |
Smiles | Br.Br.CN(CCN1CCCC1)CCC1=CC=C(Cl)C(Cl)=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.
参考文献是支持产品生物活性的出版物。
De Costa et al (1992) Synthesis, characterization, and biological evaluation of a novel class of N-(arylethyl)-N-alkyl-2-(1-pyrrolidinyl)ethylamines - structural requirements and binding affinity at the σ receptor. J.Med.Chem. 35 38 PMID: 1310114
Monnet et al (1996) Differentiation of σ ligand-activated receptor subtypes that modulate NMDA-evoked [3H]-noradrenaline release in rat hippocampal slices. Br.J.Pharmacol. 119 65 PMID: 8872358
Whittemore et al (1997) Antagonism of N-MthD.-aspartate receptors by σ site ligands: potency, subtype-selectivity and mechanisms of inhibition. J.Pharmacol.Exp.Ther. 282 326 PMID: 9223571
关键词: BD 1008 dihydrobromide, BD 1008 dihydrobromide supplier, Potent, selective, σ, sigma, ligand, General, Receptors, BD1008, dihydrobromide, Sigma-Related, 0511, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 BD 1008 dihydrobromide 的部分引用包括:
Hiranita et al (2011) Decreases in cocaine self-administration with dual inhibition of the DA transporter and σ receptors. J Pharmacol Exp Ther 339 662 PMID: 21859929
Hiranita et al (2013) Stimulants as specific inducers of DA-independentσ agonist self-administration in rats. Neurochem Int 347 42633 PMID: 23908387
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