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Opioid Receptor

Opioid receptor is a group of G protein-coupled receptors with opioids as ligands.

Products for  Opioid Receptor

  1. Cat.No. Product Name Information
  2. GC13688 Naltrindole hydrochloride

    δ opioid antagonist

    Naltrindole hydrochloride  Chemical Structure
  3. GC15408 Neuropeptide AF (human) Endogenous antiopioid peptide implicated in pain modulation and endocrine functions Neuropeptide AF (human)  Chemical Structure
  4. GC17325 Nociceptin Endogenous ligand for the NOP opioid receptor Nociceptin  Chemical Structure
  5. GC63115 Nociceptin (1-13), amide TFA Nociceptin (1-13), amide TFA is a potent ORL1 receptor (opioid receptor-like 1 receptor, OP4) agonist with a pEC50 of 7.9 for mouse vas deferens and a Ki of 0.75 nM for binding to rat forebrain membranes. Nociceptin (1-13), amide TFA  Chemical Structure
  6. GC13645 nor-Binaltorphimine dihydrochloride κ-opioid receptor antagonist nor-Binaltorphimine dihydrochloride  Chemical Structure
  7. GC31250 Opioid receptor modulator 1

    Opioid receptor modulator 1 is a opioid receptor modulator extracted from patent WO2014072809A2, Compound RA11 in EXAMPLE 7.

    Opioid receptor modulator 1  Chemical Structure
  8. GC31127 ORL1 antagonist 1 ORL1 antagonist 1 is an opioid receptor-like 1 (ORL1) antagonist with an IC50 of 61 nM. ORL1 antagonist 1  Chemical Structure
  9. GC10807 PL 017 Selective μ opioid receptor agonist PL 017  Chemical Structure
  10. GC36947 Porcine dynorphin A(1-13) Porcine dynorphin A (1-13) is a potent, endogenous κ opioid receptor agonist and is antinociceptive at physiological concentrations. Porcine dynorphin A(1-13)  Chemical Structure
  11. GC30771 PZM21 A µ-opioid receptor agonist PZM21  Chemical Structure
  12. GC38842 Ro 64-6198 Ro 64-6198 is a potent, selective, nonpeptide, high-affinity, high cellular permeability and brain penetration N/OFQ receptor (NOP) agonist with an EC50 value of 25.6 nM. Ro 64-6198  Chemical Structure
  13. GC13910 Salvinorin A Non-nitrogenous κ-opioid selective agonist Salvinorin A  Chemical Structure
  14. GC18679 Salvinorin B

    Salvinorin B is an analytical reference standard categorized as a diterpene.

    Salvinorin B  Chemical Structure
  15. GC13581 SB 205607 dihydrobromide non-peptide δ1 opioid receptor agonist SB 205607 dihydrobromide  Chemical Structure
  16. GC39619 SB-612111 SB-612111 is a novel and potent opiate receptor-like orphan receptor (ORL-1) antagonist with a high affinity for hORL-1 (Ki=0.33 nM). SB-612111  Chemical Structure
  17. GC10011 SDM25N hydrochloride δ receptor antagonist SDM25N hydrochloride  Chemical Structure
  18. GN10135 Sec-O-Glucosylhamaudol Sec-O-Glucosylhamaudol  Chemical Structure
  19. GN10213 Sinomenine Hydrochloride Sinomenine Hydrochloride  Chemical Structure
  20. GC12041 SNC 162 δ-opioid receptor agonist SNC 162  Chemical Structure
  21. GC11355 SNC 80 A δ-opioid agonist SNC 80  Chemical Structure
  22. GC63200 Spiradoline Spiradoline  Chemical Structure
  23. GC50558 TAN 452

    Potent and selective peripherally acting δ opioid antagonist; antianalgesic.

    TAN 452  Chemical Structure
  24. GC10702 Trimebutine Antimuscarinic Trimebutine  Chemical Structure
  25. GC37829 Trimebutine maleate Trimebutine maleate is a drug with antimuscarinic and weak mu opioid agonist effects. Trimebutine maleate  Chemical Structure
  26. GC30816 Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) regulates human immune function and inhibits tumor growth via binding to the opioid receptor. Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin)  Chemical Structure
  27. GC15512 U-54494A hydrochloride κ-opioid agonist and NMDA antagonist U-54494A hydrochloride  Chemical Structure
  28. GC61586 UFP-101 TFA UFP-101 TFA is a potent, selective, and competitive antagonist of the N/OFQ peptide (NOP) receptor, with a pKi of 10.24. UFP-101 TFA  Chemical Structure
  29. GC31126 Valorphin Valorphin is an endogenous hemoglobin β-chain (33-39) fragment with opioid analgesic activity, binds to rat mu-opioid receptor, with an IC50 of 14 nM; Valorphin also shows anti-tumor activity. Valorphin  Chemical Structure
  30. GC30994 Vanilpyruvic acid (Vanylpyruvic acid) Vanilpyruvic acid (Vanylpyruvic acid) is a catecholamine metabolite and precursor to vanillactic acid. Vanilpyruvic acid (Vanylpyruvic acid)  Chemical Structure
  31. GC31006 ZT 52656A hydrochloride ZT 52656A is a selective kappa opioid agonist, used for the prevention or alleviation of pain in the eye. ZT 52656A hydrochloride  Chemical Structure
  32. GC11848 [D-Ala2]-Deltorphin II [D-Ala2]-Deltorphin II is a selective peptide agonist for the δ opioid receptor. [D-Ala2]-Deltorphin II  Chemical Structure
  33. GC33081 [D-Ala2]leucine-enkephalin [D-Ala2]leucine-enkephalin, a delta opioid agonist, is a degradation resistant long-acting Leu-enkephalin. [D-Ala2]leucine-enkephalin  Chemical Structure
  34. GC11236 [Leu5]-Enkephalin Endogenous opioid agonist peptide [Leu5]-Enkephalin  Chemical Structure
  35. GC35017 [Leu5]-Enkephalin, amide [Leu5]-Enkephalin, amide is a δ opioid receptor agonist. [Leu5]-Enkephalin, amide  Chemical Structure
  36. GC31138 [Met5]-Enkephalin, amide (5-Methionine-enkephalin amide) [Met5]-Enkephalin, amide (5-Methionine-enkephalin amide) is an agonist for δ opioid receptors as well as putative ζ (zeta) opioid receptors. [Met5]-Enkephalin, amide (5-Methionine-enkephalin amide)  Chemical Structure
  37. GC35018 [Met5]-Enkephalin, amide TFA [Met5]-Enkephalin, amide TFA is an agonist for δ opioid receptors as well as putative ζ (zeta) opioid receptors. [Met5]-Enkephalin, amide TFA  Chemical Structure

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