[Met5]-Enkephalin, amide TFA
CAS No. ——
[Met5]-Enkephalin, amide TFA( 5-Methionine-enkephalin amide (TFA) )
Catalog No. M22518 CAS No. ——
[Met5]-Enkephalin, amide TFA is a δ opioid receptors agonist as well as putative ζ (zeta) opioid receptors.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 124 | In Stock |
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| 50MG | 190 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name[Met5]-Enkephalin, amide TFA
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NoteResearch use only, not for human use.
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Brief Description[Met5]-Enkephalin, amide TFA is a δ opioid receptors agonist as well as putative ζ (zeta) opioid receptors.
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Description[Met5]-Enkephalin, amide TFA is a δ opioid receptors agonist as well as putative ζ (zeta) opioid receptors.[Met5]-Enkephalin at 0.1 nM, 10 nM, and 1 μM significantly reduces the total number of glial cells in culture. [Met5]-Enkephalin, amide acts via δ-opioid receptor to inhibit pelvic nerve-evoked contractions of cat distal colon. [Met5]-enkephalin causes concentration-dependent, reversible inhibition of pelvic nerve-evoked contractions, with an IC50 value of 2.2 nM. [Met5]enkephalin at a concentration (3 nM) which produces a large inhibition of neurogenic contractions, has no effect on contractions to exogenous acetylcholine.
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In Vitro——
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In Vivo——
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Synonyms5-Methionine-enkephalin amide (TFA)
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PathwayEndocrinology/Hormones
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TargetOpioid Receptor
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Recptorδ and ζ opioid receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number——
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Formula Weight686.7
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Molecular FormulaC29H37F3N6O8S
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Purity>98% (HPLC)
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SolubilityH2O:soluble
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SMILESOc2ccc(C[C@H](N)C(=O)NCC(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCSC)C(N)=O)cc2.FC(F)(F)C(=O)O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Stiene-Martin A, et al. Glial growth is regulated by agonists selective for multiple opioid receptor types in vitro. J Neurosci Res. 1991 Aug;29(4):538-48.
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