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Adrenorphin 3TFA(88377-68-8(free base))
Adrenorphin 3TFA(88377-68-8(free base))
CAS No. ——
Adrenorphin 3TFA(88377-68-8(free base))( Metorphamide )
Catalog No. M22776 CAS No. ——
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 | 250 | In Stock |
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| 10MG | 417 | In Stock |
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| 25MG | 617 | In Stock |
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| 50MG | 944 | In Stock |
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| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameAdrenorphin 3TFA(88377-68-8(free base))
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NoteResearch use only, not for human use.
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Brief DescriptionAdrenorphin(3TFA) is an agonist of μ-opioid receptor(Ki :12 nM).
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DescriptionAdrenorphin(3TFA) is an agonist of μ-opioid receptor(Ki :12 nM).
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In Vitro——
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In Vivo——
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SynonymsMetorphamide
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PathwayEndocrinology/Hormones
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TargetOpioid Receptor
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Recptorμ-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 Weight984.18
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Molecular FormulaC44H69N15O9S
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Purity>98% (HPLC)
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Solubility——
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SMILESOC(=O)C(F)(F)F.CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(N)=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
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EST73502
EST73502 is an agonist of μ-opioid receptor(Ki = 64 nM) agonist and an antagonist of σ1 receptor (Ki = 118 nM). EST73502 displays antinociceptive activity.
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Hemorphin-7
Hemorphin-7 binds to the angiotensin IV receptor, triggering multiple effects including cellular proliferation and memory enhancement. Hemorphins are endogenous peptides belonging to the family of atypical opioid peptides released from hydrolyzed hemoglobin. Hemorphin-7 is investigated as a potential biomarker for breast cancer.
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[Nphe1]Nociceptin(1-...
Selective and competitive nociceptin receptor antagonist, devoid of any agonist activity. Binds selectively to recombinant nociceptin receptors (pKi = 8.4), and competitively antagonizes the actions of nociceptin in vitro and in vivo.
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