[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 |
|
| 50MG | 190 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name[Met5]-Enkephalin, amide TFA
-
NoteResearch use only, not for human use.
-
Brief Description[Met5]-Enkephalin, amide TFA is a δ opioid receptors agonist as well as putative ζ (zeta) opioid receptors.
-
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.
-
In Vitro——
-
In Vivo——
-
Synonyms5-Methionine-enkephalin amide (TFA)
-
PathwayEndocrinology/Hormones
-
TargetOpioid Receptor
-
Recptorδ and ζ opioid receptor
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number——
-
Formula Weight686.7
-
Molecular FormulaC29H37F3N6O8S
-
Purity>98% (HPLC)
-
SolubilityH2O:soluble
-
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
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
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.
molnova catalog
related products
-
beta-Neoendorphin ac...
beta-Neoendorphin acetate is an agonist of κ-opioid receptor
-
Nalfurafine hydrochl...
Nalfurafine (TRK-820, TRK820) is potent, selective agonist of kappa-opioid receptor with Ki of 3.5 nM, 15-fold less potent for μOR and little affinity for δOR (Ki=53 and 1,200 nM, respectively).
-
BTRX-335140
BTRX-335140 is a potent and selective, orally active κ opioid receptor (KOR) antagonist, has antagonist activity for κOR, μOR and δOR with IC50 values of 0.8 nM, 110 nM, and 6500 nM, respectively.
Cart
sales@molnova.com