Adrenorphin(3TFA)
CAS No. 88377-68-8
Adrenorphin(3TFA)( Metorphamide )
Catalog No. M21026 CAS No. 88377-68-8
Adrenorphin(3TFA) is an agonist of μ-opioid receptor(Ki :12 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 230 | Get Quote |
|
| 10MG | 346 | Get Quote |
|
| 25MG | 622 | Get Quote |
|
| 50MG | 933 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameAdrenorphin(3TFA)
-
NoteResearch use only, not for human use.
-
Brief DescriptionAdrenorphin(3TFA) is an agonist of μ-opioid receptor(Ki :12 nM).
-
DescriptionAdrenorphin(3TFA) is an agonist of μ-opioid receptor(Ki :12 nM).
-
In VitroAdrenorphin (Metorphamide) is a opioid octapeptide from bovine brain, acts as a potent agonist of μ-opioid receptor, with Ki of 12 nM. The binding ratios of Ki for μ-opioid receptor/Ki for δ-opioid receptor of 0.04 and of Ki for μ-opioid receptor/Ki for κ-opioid receptor of 0.46. Adrenorphin potently inhibits catecholamine secretion evoked by 10 μM nicotine in cultured human pheochromocytoma 6 cells, with an IC50 of 1.1 μM.
-
In Vivo——
-
SynonymsMetorphamide
-
PathwayEndocrinology/Hormones
-
TargetOpioid Receptor
-
Recptorμ-opioid receptor
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number88377-68-8
-
Formula Weight984.18
-
Molecular FormulaC44H69N15O9S
-
Purity>98% (HPLC)
-
SolubilityDMSO:50 mg/mL (50.80 mM)
-
SMILESCSCCC(NC(=O)C(Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)C(N)Cc1ccc(O)cc1)C(=O)NC(CCCNC(=N)N)C(=O)NC(CCCNC(=N)N)C(=O)NC(C(N)=O)C(C)C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Miyata A Mizuno K Minamino N et al. Regional distribution of adrenorphin in rat brain: Comparative study with PH-8P[J]. Biochemical and Biophysical Research Communications 1984 120(3):1030-1036.
molnova catalog
related products
-
Nociceptin (1-13) am...
Nociceptin (1-13), amide is a potent agonist Opioid receptor-like1 (ORL1) receptor with a pEC50 of 7.9 for mouse vas deferens and a Ki of 0.75 nM for binding to rat forebrain membranes.
-
PF-CBP1 hydrochlorid...
PF-CBP1 is a highly selective inhibitor of the bromodomain of CREB-binding protein(CREBBP).It inhibits CREBBP and p300 bromodomains with IC50 of 125 and 363 nM respectively.
-
Orphanin FQ (1-11)
Peptide fragment containing amino acids 1-11 of Nociceptin. Potent agonist of the ORL1/KOR-3 receptor (Ki = 55 nM); displays no affinity for opioid receptors, including μ, δ, κ1 and κ3 receptors (Ki >1000 nM). Displays analgesic properties in CD-1 mice.
Cart
sales@molnova.com