β-Funaltrexamine hydrochloride

Discontinued Product

0926 has been discontinued.

说明: Irreversible and selective μ antagonist
别名: β-FNA
化学名: (E)-4-[[5α,6β)-17-Cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxymorphinan-6-yl]amino]-4-oxo-2-butenoicacid methyl ester hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献 (7)
评论
文献 (2)

生物活性 for β-Funaltrexamine hydrochloride

β-Funaltrexamine hydrochloride is a selective μ opioid receptor antagonist.

许可信息

Sold with the permission of the University of Minnesota

技术数据 for β-Funaltrexamine hydrochloride

分子量 490.99
公式 C25H30N2O6.HCl
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 72786-10-8
PubChem ID 44522395
InChI Key BIPHUOBUKMPSQR-NQGXHZAGSA-N
Smiles Cl.[H][C@@]12OC3=C4C(C[C@@]5([H])N(CC6CC6)CC[C@@]14[C@@]5(O)CC[C@H]2NC(=O)\C=C\C(=O)OC)=CC=C3O

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.

产品说明书 for β-Funaltrexamine hydrochloride

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参考文献 for β-Funaltrexamine hydrochloride

参考文献是支持产品生物活性的出版物。

Jiang et al (1990) μ Antagonist and κ agonist properties of β-funaltrexamine (β-FNA) in vivo: long lasting spinal analgesia in mice. J.Pharmacol.Exp.Ther. 252 1006 PMID: 2156986

Takemorei et al (1981) The irreversible narcotic antagonist and reversible agonist properties of the fumarate methyl ester derivative of naltr. Eur.J.Pharmacol. 70 445 PMID: 6263637

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关键词: beta-Funaltrexamine hydrochloride, beta-Funaltrexamine hydrochloride supplier, Irreversible, μ-opioid, mu-opioid, selective, antagonists, MOP, Receptors, OP3, β-Funaltrexamine, beta-Funaltrexamine, hydrochloride, β-FNA, beta-FNA, b-FNA, Mu, Opioid, 0926, Tocris Bioscience

7 篇 β-Funaltrexamine hydrochloride 的引用文献

引用文献是使用了 Tocris 产品的出版物。 β-Funaltrexamine hydrochloride 的部分引用包括:

Crowley et al (2020) Synthetic Studies of Neoclerodane Diterpenes from Salvia divinorum: Design, Synthesis, and Evaluation of Analogues with Improved Potency and G-protein Activation Bias at the μ Opioid Receptor. ACS Chem Neurosci 11 1781 PMID: 32383854

Phillips et al (2012) Pain-facilitating medullary neurons contribute to opioid-induced respiratory depression. J Neurophysiol 108 2393 PMID: 22956800

Largent-Milnes et al (2010) Spinal or systemic TY005, a peptidic opioid agonist/neurokinin 1 antagonist, attenuates pain with reduced tolerance. Br J Pharmacol 161 986 PMID: 20977451

Chen et al (2015) Berberine Improves Intestinal Motility and Visceral Pain in the Mouse Models Mimicking Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D) Symptoms in an Opioid-Receptor Dependent Manner. Neuropsychopharmacology 10 e0145556 PMID: 26700862

Tzeng et al (2011) Myricetin Ameliorates Defective Post-Receptor Ins Signaling via β-Endorphin Signaling in the Skeletal Muscles of Fructose-Fed Rats. Evid Based Complement Alternat Med 2011 150752 PMID: 21785619

Cecchi et al (2008) Differential responses to morphine-induced analgesia in the tail-flick test. Behav Brain Res 194 146 PMID: 18656501

Romero-Picó et al (2013) Hypothalamic κ-opioid receptor modulates the orexigenic effect of ghrelin. Circulation 38 1296 PMID: 23348063


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