29 Results for "

ORL1 receptor

" in MedChemExpress (MCE) Product Catalog:
Products (29)

29 Results for "ORL1 receptor" in MCE Product Catalog:

7
7 Publications Verification
Cat. No.: HY-13274
CAS No.: 244218-51-7
Purity:  98.91%
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

JTC-801 is a selective opioid receptor-like1 (ORL1) receptor antagonist, binding to ORL1 receptor with a Ki value of 8.2 nM.
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2
2 Cited Publications
Cat. No.: HY-18618A
SB-612111 hydrochloride hydrochloride 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 hydrochloride exhibits selectivity for μ-,?κ- and?δ-receptors with Ki values of?57.6 nM, 160.5 nM and 2109 nM, respecticely. SB-612111 hydrochloride effectively antagonizes the pronociceptive action of Nociceptin (HY-P0183) in an acute pain model .
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1
1 Cited Publications
Cat. No.: HY-13101
CAS No.: 1108147-88-1
Purity:  99.98%
MCOPPB trihydrochloride is a NOP/ORL1 G protein-coupled receptor agonist and autophagy inhibitor that can cross the blood-brain barrier. MCOPPB trihydrochloride clears senescent cells, regulates locomotion, lipid storage and immune responses, and inhibits fibrosis and angiogenesis. MCOPPB trihydrochloride blocks autophagic flux, induces changes in locomotion and lipid storage, and activates the stress-responsive immune transcription network, thereby improving post-infarction cardiac function and exerting anxiolytic effects. MCOPPB trihydrochloride can be applied to research fields such as aging-related diseases and ischemic heart failure .
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Cat. No.: HY-107721
CAS No.: 217461-40-0
Purity:  98.59%
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

(±)-J-113397 is a potent and selective non-peptidyl ORL1 receptor antagonist with a Ki of 1.8 nM for cloned human ORL1. J-113397 inhibited nociceptin/orphanin FQ-stimulated GTPγS binding to CHO cells expressing ORL1 with an IC50 value of 5.3 nM. J-113397 can be used for researching the physiological roles of nociceptin/orphanin FQ .
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Cat. No.: HY-114072
CAS No.: 256640-45-6
Purity:  ≥99.0%
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

J-113397 is the first potent and selective nonpeptidyl ORL1 receptor antagonist (Ki: cloned human ORL1=1.8 nM) without any agonistic effects on other opioid receptors .
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Cat. No.: HY-P1302
CAS No.: 178249-41-7
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Orphanin FQ(1-11), a orphanin FQ or nociceptin (OFQ/N) fragment, is a potent NOP receptor (ORL-1; OP4) agonist, with a Ki of 55 nM. Orphanin FQ(1-11) has no affinity for μ, δ, κ1 and κ3 receptors (Ki>1000 nM). Orphanin FQ(1-11) is analgesic in CD-1 mice .
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Cat. No.: HY-P1317A
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

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 .
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Cat. No.: HY-106234
CAS No.: 383123-18-0
ZP 120C is a potent and partial ORL1 receptor agonist. ZP 120C inhibits electrically induced contraction. ZP 120C can be used in the research of hyponatremia/hypokalemia .
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Cat. No.: HY-120385
CAS No.: 1357348-09-4
Synonyms: GRT-6006
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Lexanopadol (GRT-6006) is a μ-opioid receptor and nociceptor receptor (ORL-1 receptor) agonist. Lexanopadol can be used to study pain .
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Cat. No.: HY-14124
CAS No.: 919482-44-3
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

MK-5757 is a Nociceptin/Orphanin FQ Peptide Receptor antagonist. ORL1 antagonist 3 can improve cerebral blood flow disorders and ischemic damage, and alleviate abnormal neurological symptoms. ORL1 antagonist 3can be used for the research of neurological disease, such as traumatic brain injury .
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Cat. No.: HY-W001874
CAS No.: 353-07-1
Synonyms: 3-Hydrazinylpropanenitrile
2-Cyanoethylhydrazine (3-Hydrazinylpropanenitrile) is a drug synthesis intermediate that can be used to synthesize an antagonist of opioid receptor-like 1 (ORL1) .
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Cat. No.: HY-P1319
CAS No.: 178249-42-8
Target:  

Opioid Receptor

Research Areas:  

Inflammation/Immunology

Nociceptin (1-7) is the N-terminal bioactive fragment of nociceptin (HY-P0183). Nociceptin (1-7) is a potent ORL1 (NOP) receptor agonist with antinociceptive activity. Nociceptin (1-7) combines with nociceptin reduces hyperalgesia in vivo .
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Cat. No.: HY-P1316A
CAS No.: 408305-09-9
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Ac-RYYRWK-NH2 is a potent and selective partial agonist for the nociceptin receptor (NOP), [ 3H]Ac-RYYRWK-NH2 binds to rat cortical membranes ORL1 with a Kd of 0.071 nM, but has no affinity for μ-, κ- or δ-opioid receptors .
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Cat. No.: HY-P1302A
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Orphanin FQ(1-11) TFA, a orphanin FQ or nociceptin (OFQ/N) fragment, is a potent NOP receptor (ORL-1; OP4) agonist, with a Ki of 55 nM. Orphanin FQ(1-11) TFA has no affinity for μ, δ, κ1 and κ3 receptors (Ki>1000 nM). Orphanin FQ(1-11) TFA is analgesic in CD-1 mice .
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Cat. No.: HY-18617
CAS No.: 371980-94-8
rel-SB-612111 hydrochloride is a novel and potent human opiate receptor-like orphan receptor (ORL-1) antagonist with a high affinity for hORL-1 (Ki=0.33 nM). rel-SB-612111 hydrochloride exhibits selectivity for μ-, κ- and δ-receptors with Ki values of 57.6 nM, 160.5 nM and 2109 nM, respecticely. rel-SB-612111 hydrochloride effectively antagonizes the pronociceptive action of Nociceptin (HY-P0183) in an acute pain model .
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Cat. No.: HY-112263
CAS No.: 1174985-59-1
Target:  

Opioid Receptor

ORL1 antagonist 1 is an opioid receptor-like 1 (ORL1) antagonist with an IC50 of 61 nM.
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Cat. No.: HY-13274A
CAS No.: 244218-93-7
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

JTC-801 free base is a selective opioid receptor-like1 (ORL1) receptor antagonist, binding to ORL1 receptor with a Ki value of 8.2?nM.
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Cat. No.: HY-158236
CAS No.: 1169982-72-2
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

ORL1 antagonist 2 (1B) is an opioid receptor-Like 1 (ORL1) antagonist, usd in P-glycoprotein (P-gp) research .
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Cat. No.: HY-138984
CAS No.: 228246-34-2
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

GRT2932Q is a nonpeptidic opioid receptor-like 1 (ORL1) agonist .
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Cat. No.: HY-P0192
CAS No.: 213130-17-7
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 is a nociceptin receptor (ORL1) agonist. [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 strongly depresses the nociceptive flexor reflex in rats. [Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2 can be used for analgesia research .
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