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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T4351 | DAMGO | Dagol,DAGO,RX-783006 | Opioid Receptor |
DAMGO (DAGO) is an opioid receptor agonist with the ability to affect the locomotive activity in rodents. Possible analgesic agent due to μ-opiod receptor interaction. | |||
T8991 | BMS986187 | Opioid Receptor | |
BMS986187 is a novel Potent and Selective Positive Allosteric Modulators of the delta-Opioid Receptor. | |||
T1242 | Alvimopan | Opioid Receptor | |
Alvimopan (LY 246736) is a synthetic trans-3, 4-dimethyl-4-(3-hydroxyphenyl) piperidine with peripherally selective opioid mu receptor antagonist activity. Alvimopan is a selective and competitive antagonist at mu-opioid... | |||
T4691 | Asimadoline hydrochloride | EMD-61753 hydrochloride | Opioid Receptor |
Asimadoline hydrochloride (EMD-61753 hydrochloride) is a κ-opioid receptor agonist potentially for the treatment of pruritus. Asimadoline hydrochloride has also been shown to be used in the treatment of irritable bowel s... | |||
T79430 | μ opioid receptor agonist 3 | Opioid Receptor | |
Compound 20, identified as μ opioid receptor agonist 3, is a potent µOR agonist that exhibits an EC50 value of 0.87 nM. It holds promise for research into pain management and neuropsychiatric disorders [1]. | |||
T62025 | μ opioid receptor agonist 2 | ||
μ opioid receptor agonist 2 (Compound H-3)is a MOR receptor agonist. μ opioid receptor agonist 2 can be used for the research of pain and pain related diseases. | |||
T62268 | μ opioid receptor agonist 1 | ||
μ opioid receptor agonist 1 (Compound H-1a) is an optically pure oxyheterocyclic substituted pyrroloxypyrazole derivative and an MOR receptor agonist that can be used in the study of pain and pain-related disorders. | |||
T61901 | σ1 Receptor/μ Opioid receptor modulator 1 | ||
σ 1 Receptor/ μ Opioid receiver modulator 1 (Compound 44) is an effective σ 1 receptor antagonist (Ki=1.86 nM) and μ Opioid receptor agonists (Ki=2.1 nM). Opioid receptor modulator 1 shows potent analgesic activity, and ... | |||
T4633 | Asimadoline | EMD-61753 | Opioid Receptor |
Asimadoline (EMD-61753) is a proprietary small molecule therapeutic, originally discovered by Merck KGaA of Darmstadt, Germany. Asimadoline was originally developed to treat peripheral pain such as arthritis. Asimadoline... | |||
T7567L | Adrenorphin 3TFA(88377-68-8(free base)) | Metorphamide | Opioid Receptor |
Adrenorphin 3TFA(88377-68-8(free base)) (Metorphamide) is an agonist of μ-opioid receptor(Ki :12 nM). | |||
T4386 | PZM21 | Opioid Receptor | |
PZM21 is an effective and selective μ opioid receptor agonist (EC50: 1.8 nM). | |||
T23002 | ML-335 | Opioid Receptor | |
ML-335 is a μ-δ isomer-targeted agonist, a μOR-δOR-biased ligand that can serve as a scaffold for the development of unique types of (isomer-biased) drugs.ML-335 is a MOR (μ-opioid receptor)/DOR (δ-opioid receptor) heter... | |||
T7173L | [Leu5]-Enkephalin acetate(58822-25-6 free base) | Leucine enkephalin,Leu-enkephalin,Leucyl-enkephalin | Opioid Receptor , Endogenous Metabolite |
[Leu5]-Enkephalin acetate(58822-25-6 free base) is an endogenous neuropeptide involved in nociception and an agonist of δ-opioid and μ-opioid receptors (Kis = 4.0 and 3.4 nM, respectively) | |||
TP1832 | Gluten Exorphin C | Opioid Receptor | |
Gluten exorphin C is an opioid peptide derived from wheat gluten. Its IC50 values are 40 μM and 13.5 μM for μ opioid and δ opioid activities in the GPI and MVD assays, respectively.Gluten Exorphin C, isolated from the pe... | |||
T6175 | ADL-5859 | ADL5859 Hydrochloride,ADL5859 HCl | Opioid Receptor |
ADL-5859 (ADL5859 Hydrochloride) is a selective δ-opioid receptor agonist ( Ki: 0.8 nM), selectivity against opioid receptor κ, μ, and little inhibition for the hERG channel. | |||
T5167 | Cebranopadol | GRT6005 | Opioid Receptor |
Cebranopadol (GRT6005) is an analgesic NOP and opioid receptor agonist with Kis of 0.9 nM, 0.7 nM, 2.6 nM, 18 nM for human NOP, μ-opioid (MOP), κ-opioid (KOP) and δ-opioid (DOP) receptor, respectively. | |||
T39284 | EST73502 HCl | Opioid Receptor | |
EST73502 is an agonist of μ-opioid receptor(Ki = 64 nM) agonist and an antagonist of σ1 receptor (Ki = 118 nM). EST73502 displays antinociceptive activity. | |||
T4407 | SR17018 | Opioid Receptor | |
SR17018 is an mu-opioid-receptor (MOR) agonist, binding with GTPγS, with an EC50 of 97 nM. | |||
T14551 | Bevenopran | CB-5945,ADL-5945 | Opioid Receptor |
Bevenopran (CB-5945) is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction. | |||
T67888L | Samidorphan HCl | Samidorphan HCl(852626-89-2 free base) | Opioid Receptor |
Samidorphan HCl is an orally active and highly potent modulator of the opioid system that binds to μ‐opioid, κ‐opioid, and delta-opioid receptors. Samidorphan HCl is a novel μ-opioid receptor antagonist, a partial agonis... |