2. GPCR/G Protein Neuronal Signaling
  3. Opioid Receptor
  4. Mitragynine pseudoindoxyl

Mitragynine pseudoindoxyl 是一种有效的 MOR 激动剂。Mitragynine pseudoindoxyl 表现为减少运动过度，抑制GI 转运和增强特性。

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Mitragynine pseudoindoxyl Chemical Structure

Mitragynine pseudoindoxyl Chemical Structure

CAS No. : 2035457-43-1

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Mitragynine pseudoindoxyl 相关抗体

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查看 Opioid Receptor 亚型特异性产品:

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μ Opioid Receptor/MOR κ Opioid Receptor/KOR δ Opioid Receptor/DOR NOP Receptor/ORL1

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Mitragynine pseudoindoxyl is a potent MOR agonist. Mitragynine pseudoindoxyl displays reduced hyperlocomotion, inhibition of GI transit and reinforcing properties[1].

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
CHO EC50
1.7 nM
Compound: 3; Mitragynine Pseudoindoxyl
Agonist activity at mouse mu opioid receptor-1 expressed in CHO cell membranes assessed as [35S]GTPgammaS binding incubated for 60 mins by scintillation spectroscopic analysis
Agonist activity at mouse mu opioid receptor-1 expressed in CHO cell membranes assessed as [35S]GTPgammaS binding incubated for 60 mins by scintillation spectroscopic analysis
[PMID: 27556704]
CHO IC50
31 nM
Compound: 3; Mitragynine Pseudoindoxyl
Antagonist activity at mouse kappa opioid receptor-1 expressed in CHO cell membranes assessed as inhibition of U50,488H-induced [35S]GTPgammaS binding incubated for 60 mins by scintillation spectroscopic analysis
Antagonist activity at mouse kappa opioid receptor-1 expressed in CHO cell membranes assessed as inhibition of U50,488H-induced [35S]GTPgammaS binding incubated for 60 mins by scintillation spectroscopic analysis
[PMID: 27556704]
CHO IC50
34 nM
Compound: 3; Mitragynine Pseudoindoxyl
Inhibition of DAMGO-induced beta-arrestin-2 recruitment at mu opioid receptor-1 (unknown origin) expressed in CHO cells preincubated for 30 mins followed by DAMGO addition measured after 90 mins by beta-galactosidase complementation assay
Inhibition of DAMGO-induced beta-arrestin-2 recruitment at mu opioid receptor-1 (unknown origin) expressed in CHO cells preincubated for 30 mins followed by DAMGO addition measured after 90 mins by beta-galactosidase complementation assay
[PMID: 27556704]
CHO IC50
61 nM
Compound: 3; Mitragynine Pseudoindoxyl
Antagonist activity at mouse delta opioid receptor-1 expressed in CHO cell membranes assessed as inhibition of DPDPE-induced [35S]GTPgammaS binding incubated for 60 mins by scintillation spectroscopic analysis
Antagonist activity at mouse delta opioid receptor-1 expressed in CHO cell membranes assessed as inhibition of DPDPE-induced [35S]GTPgammaS binding incubated for 60 mins by scintillation spectroscopic analysis
[PMID: 27556704]
分子量

414.49

Formula

C23H30N2O5
CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献

Mitragynine pseudoindoxyl 相关分类

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Mitragynine pseudoindoxyl2035457-43-1Opioid ReceptorhYperlocomotionGI transitOxidative MetabolismInhibitorinhibitorinhibit

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