[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2

Discontinued Product

1092 has been discontinued.

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说明: Selective nociceptin receptor agonist
说明书
引用文献 (1)
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文献 (1)

生物活性

[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 is a potent agonist of the nociceptin (ORL1) receptor, demonstrated both in vitro and in vivo. Selective, competitive antagonism at the nociceptin receptor has also been reported (pA2 = 7.02 and 6.75 in the guinea pig ileum and mouse vas deferens respectively).

技术数据

分子量 1367.6
公式 C61H102N22O14
序列 FGGFTGARKSARK

(Modifications: Phe-1 - Gly-2 peptide bond replace with Psi-(CH2-NH), Lys-13 = C-terminal amide)

储存 Desiccate at -20°C
CAS Number 213130-17-7
PubChem ID 6324602
InChI Key ZHKMSRDIVOXQKP-YILJZHMHSA-N
Smiles [H]N[C@H](CNCC(=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.

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关键词: [Phe1Psi(CH2-NH)Gly2]Nociceptin(1-13)NH2, [Phe1Psi(CH2-NH)Gly2]Nociceptin(1-13)NH2 supplier, Selective, nociceptin, agonists, Receptors, ORL1, OP4, NOP, Opioid, [Phe1Psi(CH2-NH)Gly2]Nociceptin(1-13)NH2, 1092, Tocris Bioscience

1 篇 [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 的引用文献

引用文献是使用了 Tocris 产品的出版物。 [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 的部分引用包括:

McLeod et al (2001) Nociceptin inhibits cough in the guinea-pig by activation of ORL(1) receptors. J Biol Chem 132 1175 PMID: 11250866


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