DPDPE TFA

CAS No. 172888-59-4

DPDPE TFA( —— )

Catalog No. M22974 CAS No. 172888-59-4

DPDPE TFA is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 245 In Stock
10MG 372 In Stock
25MG 608 In Stock
50MG 849 In Stock
100MG 1143 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    DPDPE TFA
  • Note
    Research use only, not for human use.
  • Brief Description
    DPDPE TFA is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo.
  • Description
    DPDPE TFA is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Endocrinology/Hormones
  • Target
    Opioid Receptor
  • Recptor
    δ-opioid receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    172888-59-4
  • Formula Weight
    645.79
  • Molecular Formula
    C30H39N5O7S2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 50 mg/mL (65.81 mM)
  • SMILES
    O=C(O)C(F)(F)F.O=C([C@H](NC([C@H](CC1=CC=CC=C1)NC(CN2)=O)=O)C(C)(C)SSC(C)(C)[C@@H](NC([C@@H](N)CC3=CC=C(O)C=C3)=O)C2=O)O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Chandrakumar et al (1992) Analogs of the δ opioid receptor selective cyclic peptide [2-D-penicillamine,5-D-penicillamine]-enkephalin: 2',6'-dimethyltyrosine and Gly3-Phe4 amide bond isostere substitutions. J.Med.Chem.
molnova catalog
related products
  • Deltorphin I(TFA)

    Deltorphin I(TFA) is an agonist of δ-opioid receptor.

  • (-)-U-50488 hydrochl...

    The more active enantiomer of (±)-U-50488, a potent, selective kappa-opioid receptor agonist with no μ-opioid antagonist effects.

  • CTAP

    Potent and selective μ opioid receptor antagonist (IC50 = 3.5 nM). Displays > 1200-fold selectivity over δ opioid and somatostatin receptors. Brain penetrant and active in vivo.