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Opioid Receptor Opioid Receptor

Cat.No.  Name Information
M4808 TRV130 hydrochloride TRV130 (Oliceridine) hydrochloride is a novel μ-opioid receptor (MOR) G protein-biased ligand.
M1579 Naloxone Naloxone is an opioid inverse agonist drug used to counter the effects of opiate overdose.
M9615 DAMGO DAMGO is an opioid receptor agonist with the ability to affect the locomotive activity in rodents, Kd value is 3.46 nM for native μ-OPR.
M41893 Deltorphin Deltorphin (Deltorphin A; Dermenkephalin) is a biological active peptide.
M41892 TIPP TIPP is a potent and selective δ-opioid antagonist with a Ki value of 1.22 nM.
M41891 DSLET DSLET ([D-Ser2, Leu5, Thr6]-enkephalin) is a highly specific agonist of the δ-receptor.
M41890 ICI 154129 ICI 154 129 is a delta-opioid receptor antagonist and can be used for seizure research.
M41889 DALDA TFA DALDA TFA is a potent and highly selective μ-opioid receptor agonist with a Ki of 1.69 nM.
M41888 BAN ORL 24 free base BAN ORL 24 free base is a nociceptin/orphanin FQ (N/OFQ) peptide receptor (NOP) antagonist.
M41887 DALDA acetate DALDA acetate is a potent and highly selective μ-opioid receptor agonist with a Ki of 1.69 nM.
M41886 MOR agonist-2 MOR agonist-2 is a antagonist of D3R and agonist of MOR (Ki: 7.26 nM and 564 nM, respectively).
M41885 GR 89696 free base GR 89696 free base is a highly selective κ2 opioid receptor agonist with potential to prevent pruritus.
M41884 SR16835 SR16835 has high affinity for both NOPr and MOPr, with full agonist activity for NOPr and partial agonist activity for MOPr.
M40713 ASP8062 ASP8062 is an orally active GABAB receptor-positive altered modulator (PAM) that can be used in studies related to opioid-related disorder (OUD).
M38964 Akuammidine Akuammidine, isolated from the seeds of Picralima nitida, shows a preference for μ-opioid binding sites with Ki values of 0.6, 2.4 and 8.6 μM at μ-, σ- and κ-opioid binding sites, respectively. Akuammidine possesses anti-inflammatory and anti-asthmatic properties.
M31391 TRV734 TRV734 is an orally bioavailable G-protein-biased ligand for the μ-opioid receptor and an agonist for the μ-opioid receptor.
M31390 TRV250 TRV250 is a novel delta-like opioid receptor (DOR) small molecule agonist that preferentially selects G-protein signaling with relatively little activation of the β-arrestin2 post-receptor signaling pathway.
M31388 TRV-130 fumarate TRV-130 fumarate is a biased agonist of the mu-opioid receptor (MOR) and can be used in studies related to acute pain.
M30898 Naldemedine Naldemedine (S-297995) is an orally active μ-opioid receptor antagonist (PAMORA). Naldemedine shows potent binding affinities (Ki=0.34, 0.43, 0.94 nM, respectively) and antagonist activities (IC50=25.57, 7.09, 16.1 nM, respectively) for recombinant human μ-, δ-, and κ- opioid receptors. Naldemedine can be used in opioid-induced constipation (OIC) research. Naldemedine is predicted to bind to 3CLpro encoded by SARS-CoV2 genome.
M30824 TAN-452  TAN-452 is an orally active, selective peripherally acting δ-opioid receptor (DOR) antagonist with a Ki of 0.47 nM and a Kb of 0.21 nM. TAN-452 is an antagonist for μ-opioid receptor (MOR; Ki=36.56 nM and Kb=9.43 nM) and κ-opioid receptor (KOR; Ki=5.31 nM and Kb=7.18 nM). TAN-452, a derivative of Naltrindole, demonstrates low brain penetrability and attenuates morphine-induced side effects without affecting pain control.
M30799 Naloxonazine dihydrochloride  Naloxonazine dihydrochloride is a specific μ-opioid receptor antagonist with an IC50 of 5.4 nM. Naloxonazine dihydrochloride also shows anti-leishmanial activity.
M30655 Naloxonazine  Naloxonazine is a potent and selective opiate mu-1 antagonist that can also affect leishmania by regulating host coding function.
M30361 MT-7716 free base MT-7716 free base (W-212393) is a selective non-peptide nociceptin receptor (NOP) agonist and promising potential treatment drug for alcohol abuse and relapse prevention.




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