[Nphe1]Nociceptin(1-13)NH2

Discontinued Product

1308 has been discontinued.

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说明: Selective, competitive nociceptin antagonist
说明书
引用文献 (3)
评论
文献 (1)

生物活性 for [Nphe1]Nociceptin(1-13)NH2

[Nphe1]Nociceptin(1-13)NH2 is a selective and competitive nociceptin receptor antagonist, devoid of any agonist activity. Binds selectively to recombinant nociceptin receptors (pKi = 8.4), and competitively antagonizes the actions of nociceptin in vitro and in vivo.

技术数据 for [Nphe1]Nociceptin(1-13)NH2

分子量 1381.6
公式 C61H100N22O15
序列 GGGFTGARKSARK

(Modifications: Gly-1 = N-Bn-Gly, Lys-13 = C-terminal amide)

储存 Desiccate at -20°C
CAS Number 267234-08-2
PubChem ID 10654047
InChI Key NMBZIPCESQREMT-UVDGFCMYSA-N
Smiles [H]N(CC(=O)NCC(=O)NCC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(N)=O)CC1=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.

产品说明书 for [Nphe1]Nociceptin(1-13)NH2

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参考文献 for [Nphe1]Nociceptin(1-13)NH2

参考文献是支持产品生物活性的出版物。

Calo et al (2000) Characterization of [Nphe1]nociceptin(1-13)NH2, a new selective nociceptin receptor antagonist. Br.J.Pharmacol. 129 1183 PMID: 10725267

Hashimoto et al (2000) Antagonistic effects of [Nphe1]nociceptin(1-13)NH2 on nociceptin receptor mediated inhibition of cAMP formation in Chinese hamster ovary cells stably expressing the recombinant human nociceptin receptor. Neurosci.Lett. 278 109 PMID: 10643813

Pheng et al (2000) [Nphe1]nociceptin-(1-13)NH2 selectively antagonizes nociceptin effects in the rabbit isolated ileum. Eur.J.Pharmacol. 397 383 PMID: 10844138

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关键词: [NPhe1]Nociceptin(1-13)NH2, [NPhe1]Nociceptin(1-13)NH2 supplier, Selective, competitive, nociceptin, antagonists, Receptors, ORL1, OP4, NOP, Opioid, 1308, Tocris Bioscience

3 篇 [Nphe1]Nociceptin(1-13)NH2 的引用文献

引用文献是使用了 Tocris 产品的出版物。 [Nphe1]Nociceptin(1-13)NH2 的部分引用包括:

Schmid et al (2017) Bias Factor and Therapeutic Window Correlate to Predict Safer Opioid Analgesics. Cell 171 1165 PMID: 29149605

Kallupi et al (2014) Nociceptin/orphanin FQ decreases glutamate transmission and blocks ethanol-induced effects in the central amygdala of naive and ethanol-dependent rats. Neuropsychopharmacology 39 1081 PMID: 24169802

Wu & Liu (2018) ORL1 activation mediates a novel ORL1 receptor agonist SCH221510 analgesia in neuropathic pain in rats. J Mol Neurosci 66 10 PMID: 30074175


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