Dermorphin

CAS No. 77614-16-5

Dermorphin( —— )

Catalog No. M20802 CAS No. 77614-16-5

Dermorphin is agonist of μ-opioid receptor (MOR) agonist.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 46 In Stock
5MG 93 In Stock
10MG 158 In Stock
25MG 316 In Stock
50MG 536 In Stock
100MG 791 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Dermorphin
  • Note
    Research use only, not for human use.
  • Brief Description
    Dermorphin is agonist of μ-opioid receptor (MOR) agonist.
  • Description
    Dermorphin is agonist of μ-opioid receptor (MOR) agonist.
  • In Vitro
    Dermorphin, a peptide isolated from the skin of Phyllomedusa frogs and the peptide receptor (NOP) component by the endogenous agonist nociceptin/orphanin FQ (N/OFQ). In displacement binding studies at CHOhMu, Dermorphin and DeNo displac the binding of [3H]-DPN in a concentration dependent and saturable manner. Dermorphin displays an affinity of 7.17, while N/OFQ fails to displace [3H]-DPN at the Delta receptor. Dermorphin and DeNo stimulate the binding of GTPγ[35S] in a concentration dependent and saturable manner at the Mu receptor.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    μ-opioid receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    77614-16-5
  • Formula Weight
    802.87
  • Molecular Formula
    C40H50N8O10
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 120 mg/mL (149.46 mM)
  • SMILES
    CC(NC(=O)C(N)Cc1ccc(O)cc1)C(=O)NC(Cc1ccccc1)C(=O)NCC(=O)NC(Cc1ccc(O)cc1)C(=O)N1CCCC1C(=O)NC(CO)C(N)=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Robinson M A Guan F Mcdonnell S et al. Pharmacokinetics and pharmacodynamics of dermorphin in the horse[J]. Journal of Veterinary Pharmacology and Therapeutics 2015 38(4):321-329.
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