Endomorphin-2

Discontinued Product

1056 has been discontinued.

说明: Potent and selective μ agonist
纯度: ≥95% (HPLC)
说明书
引用文献 (1)
评论
文献 (2)

生物活性 for Endomorphin-2

Endomorphin-2 is a endogenous peptide with extremely high affinity and selectivity for μ-opioid receptors (with Ki values of 0.69, 9233 and 5240 nM for μ, δ and κ respectively).

技术数据 for Endomorphin-2

分子量 571.65
公式 C32H37N5O5
序列 YPFF

(Modifications: Phe-3 = C-terminal amide)

储存 Store at -20°C
纯度 ≥95% (HPLC)
CAS Number 141801-26-5
PubChem ID 5311081
InChI Key XIJHWXXXIMEHKW-LJWNLINESA-N
Smiles [H]N[C@@H](CC1=CC=C(O)C=C1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC1=CC=CC=C1)C(N)=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.

产品说明书 for Endomorphin-2

分析证书/产品说明书
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参考文献 for Endomorphin-2

参考文献是支持产品生物活性的出版物。

Chapman et al (1997) Distinct inhibitory effects of spinal endomorphin-1 and endomorphin-2 on evoked dorsal horn neuronal responses in the rat. Br.J.Pharmacol. 122 1537 PMID: 9422796

Goldberg et al (1998) Pharmacological characterization of endomorphin-1 and endomorphin-2 in mouse brain. J.Pharmacol.Exp.Ther. 286 1007 PMID: 9694962

Harrison et al (1998) Differential effects of endomorphin-1, endomorphin-2, and tyr-W-MIF-1 on activation of G-proteins in SH-SY5Y human neuroblastoma membranes. Peptides 19 749 PMID: 9622031

Zadina et al (1997) A potent and selective endogenous agonist for the μ-opiate receptor. Nature 386 499 PMID: 9087409

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关键词: Endomorphin-2, Endomorphin-2 supplier, Potent, selective, μ-opioid, mu-opioid, agonists, MOP, Receptors, OP3, Mu, Opioid, 1056, Tocris Bioscience

1 篇 Endomorphin-2 的引用文献

引用文献是使用了 Tocris 产品的出版物。 Endomorphin-2 的部分引用包括:

Garzón et al (2004) RGSZ1 and GAIP regulate mu- but not delta-opioid receptors in mouse CNS: role in tachyphylaxis and acute tolerance. Neuropsychopharmacology 29 1091 PMID: 14997173


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