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非天然氨基酸及其它砌块合成
(Tyr0,Trp2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor;Tyr-W-MIF I
名称
(Tyr0,Trp2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor;Tyr-W-MIF I
分子结构式
CAS号
144450-13-5
分子式
C27H32N6O5
分子量
520.58
作用靶点
Opioid Receptor
序列号
Tyr-Pro-Trp-Gly-NH2
短序列号
YPWG-NH2
国际标识符代码
HWGSOAJXZHSMGE-PMVMPFDFSA-N
纯度
≥95%
引用文献
[1]. Yang YR, et L. Opioid and antiopioid actions of Tyr-MIF-1, Tyr-W-MIF-1 and hemorphin-4 on rat locus coeruleus neurons: intracellular recording in vitro. Chin J Physiol. 1997 Sep 30;40(3):131-5. [2]. Gergen KA, et al. Expression of the FOS proto-oncogene protein in brain after ICV administration of Tyr-W-MIF-1 (Tyr-Pro-Trp-Gly-NH2). Peptides. 1994;15(8):1505-11. [3]. Gergen KA, et al. Intrathecal Tyr-W-MIF-1 produces potent, naloxone-reversible analgesia modulated by alpha 2-adrenoceptors. Eur J Pharmacol. 1996 Mar 18;298(3):235-9. [4]. Harrison LM, et al. Tyr-W-MIF-1 attenuates down-regulation of opiate receptors in SH-SY5Y human neuroblastoma cells. J Pharmacol Exp Ther. 1998 Feb;284(2):611-7. [5]. Erchegyi J, et al. Isolation of a novel tetrapeptide with opiate and antiopiate activity from human brain cortex: Tyr-Pro-Trp-Gly-NH2 (Tyr-W-MIF-1). Peptides. 1992 Jul-Aug;13(4):623-31.
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Tyr-W-MIF-I, a member of the Tyr-MIF-I family, was isolated from the frontal cortex of human brain tissue as well as from bovine hypothalami. It can act as an opiate agonist as well as an antagonist. As an opiate agonist, it was more potent than the other structurally similar peptides, including Tyr-MIF-I.