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Opioid Receptor

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Opioid Receptor

Chemical Structure Cat. No. Product Name CAS No.
EST73502 HCl Chemical Structure
BCP37164 EST73502 HCl 2307458-82-6
EST73502 is a Dual μ?Opioid Receptor Agonist and σ1 Receptor Antagonist Clinical Candidate for the Treatment of Pain.
LY-2795050 Chemical Structure
BCP33958 LY-2795050 1346133-08-1
LY2795050 is a nobel kappa opioid receptor selective antagonist.
Aticaprant Chemical Structure
BCP32123 Aticaprant 1174130-61-0
Aticaprant is a potent and centrally-penetrant kappa opioid receptor antagonist with a Ki of 0.807 nM.
BTRX-335140 Chemical Structure
BCP32121 BTRX-335140 2244614-14-8
BTRX-335140 (CYM-53093) is a potent and selective, orally active κ opioid receptor (KOR) antagonist, has antagonist activity for κOR, μOR and δOR with IC50 values of 0.8 nM, 110 nM, and 6500 nM, respectively. BTRX-335140 endows with favorable in vitro ADMET and in vivo pharmacokinetic profiles and medication-like duration of action in rats.
JDTic Chemical Structure
BCP31607 JDTic 361444-66-8
JDTic is a highly selective antagonist for the κ-opioid receptor; without affecting the μ- or δ-opioid receptors.
Mitragynine Chemical Structure
BCP31518 Mitragynine 6202-22-8
Mitragynine is an indole alkaloid isolated from the plant Mitragyna speciosa, and acts as an opioid receptor agonist with preference for μ-opioid receptor. It is a neurochemical that exhibits stimulatory, antinociceptive, and opiate-like effects.
Mitragynine Chemical Structure
BCP31324 Mitragynine 4098-40-2
Mitragynine is an indole alkaloid from the plant Mitragyna speciosa. It has stimulatory, antinociceptive, and opiate-like effects, acting through noradrenergic, serotonergic, and opioid receptors.
JDTic dihydrochloride Chemical Structure
BCP21083 JDTic dihydrochloride 785835-79-2
JDTic (dihydrochloride) is a potent antagonist of kappa-opioid receptors (KOR), blocking the κ-agonist U50, 488-induced antinociception.
U69593 Chemical Structure
BCP23063 U69593 96744-75-1
U69593 is a selective kappa opioid receptor agonist.
Trap101 HCl Chemical Structure
BCP23061 Trap101 HCl 873567-76-1
Trap 101 is a potent and selective nociceptin/orphanin FQ (NOP) receptor antagonist (pA2 = 7.75).
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