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N-terminally acetylated Leu-enkephalin(Ac-L-Tyr-Gly-Gly-L-Phe-D-Leu-COOH)
本产品不向个人销售，仅用作科学研究，不用于任何人体实验及非科研性质的动物实验。
N-terminally acetylated Leu-enkephalin(Ac-L-Tyr-Gly-Gly-L-Phe-D-Leu-COOH)图片
规格:98%
分子量:597.66
包装与价格：
包装价格(元)
1mg电议
5mg电议
10mg电议
25mg电议

产品介绍
N-terminallyacetylatedLeu-enkephalin是N-末端乙酰化的Leu-enkephalin。Leu-enkephalin是一种五氨基酸的内源性肽，作为阿片受体的激动剂。
货号:ajcx13500
CAS:N/A
分子式:C30H39N5O8
分子量：597.66
溶解度:Soluble in H2O
纯度：98%
存储：Store at -20°C
库存：现货

Background:

N-terminally acetylated Leu-enkephalin is the N-terminally acetylated form of Leu-enkephalin. Leu-enkephalin is a five amino acid endogenous peptide that acts as an agonist at opioid receptors.

Enkephalins (met- , leu-enkephalin, and enkephalin 8) and dynorphins are two classes of opioid peptides found in the spinal dorsal horn. Mu, delta, and kappa are three major subtypes of opioid receptors. Enkephalins are putative endogenous ligands for delta opioid receptors, and dynorphins are endogenous ligands for the kappa opioid receptors. Three receptor types resembling the vertebrate δ- and κ-type opioid receptors have been characterized pharmacologically in nervous tissues (e.g. Ki=18.9 nM for Leu-enkephalin) and localized by autoradiography at CHH terminals in the SG of C. maenas[1].


[1]. Leu-enkephalin is a five amino acid endogenous peptide that acts as an agonist at opioid receptors.