46 Results for "

Nociceptin

" in MedChemExpress (MCE) Product Catalog:
Products (46)

46 Results for "Nociceptin" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-P0183
CAS No.: 170713-75-4
Synonyms: Orphanin FQ
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Nociceptin, a heptadecapeptide, is the endogenous ligand of the nociceptin receptor, acting as a potent anti-analgesic.
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2
2 Cited Publications
Cat. No.: HY-114452
CAS No.: 1307245-86-8
Purity:  99.91%
Synonyms: BTRX-246040
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

LY2940094 (BTRX-246040) is a potent, selective and orally available nociceptin receptor (NOP receptor) antagonist with high affinity (Ki=0.105 nM) and antagonist potency (Kb=0.166 nM). LY2940094 reduces ethanol self-administration in animal models .
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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-13222
CAS No.: 1401463-54-4
Purity:  99.68%
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease Cancer

BAN ORL 24 is a nociceptin/orphanin FQ (N/OFQ) peptide receptor (NOP) antagonist. BAN ORL 24 has antagonistic effect for nociceptin (NOP) receptor with KI value of 0.24 nM in CHO cell. BAN ORL 24 can be used for the research of cancer and analgesic .
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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-128865
CAS No.: 2059904-66-2
Purity:  98.32%
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

BPR1M97 is a dual-acting mu opioid receptor (MOP) and nociceptin-orphanin FQ peptide (NOP) receptor agonist with Ki values of 1.8 and 4.2 nM, respectively. BPR1M97 shows high potency and blood-brain barrier penetration, and produces potent antinociceptive effects .
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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-107722
CAS No.: 322473-89-2
Purity:  99.00%
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

SCH 221510 is a potent, orally active and selective NOP (nociceptin opioid receptor) agonist, with an EC50 of 12 nM and Ki of 0.3 nM. SCH 221510 shows an anxiolytic-like effect .
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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-P1320
CAS No.: 267234-08-2
Target:  

Opioid Receptor

Research Areas:  

Inflammation/Immunology

[Nphe1]Nociceptin(1-13)NH2, a novel nociceptin/orphanin FQ (NC) endogenous ligand, is a selective and competitive ociceptin receptor antagonist without any residual agonist activity. [Nphe1]nociceptin(1-13)NH2 binds selectively to recombinant nociceptin receptors (pKi=8.4) and antagonizes the inhibitory effects of nociceptin on cyclic AMP accumulation in CHO cells (pA2=6.0). [Nphe1]Nociceptin(1-13)NH2 has the potential to act as an analgesic agent .
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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-156972
CAS No.: 2099681-43-1
Target:  

Opioid Receptor

Research Areas:  

Metabolic Disease

NOP agonist-1(compound 4) is a nociceptin opioid receptor (NOP) partial agonist. NOP agonist-1attenuate parkinsonian disabilities in 6-OHDA hemilesioned rats .
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Cat. No.: HY-P3839
CAS No.: 207392-60-7
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Nocistatin, a neuropeptide, is an endogenous ligand for the orphan opioid receptor-like receptor. Nocistatin is also a functional antagonist of neuropeptide nociceptin or orphanin FQ (Noc/OFQ). Nocistatin inhibits 5-HT release via a Gi/o proteinmediated pathway. Nocistatin blocks Nociceptin (Nociceptin)-induced allodynia and hyperalgesia .
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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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Cat. No.: HY-10886
CAS No.: 1028969-49-4
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

MCOPPB is an orally active and selective agonist of Nociceptin/Orphanin FQ–Receptor. MCOPPB inhibits signaling through the NOP receptor in the mouse brain. MCOPPB is used in anxiety disorders research .
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Cat. No.: HY-122681
CAS No.: 857262-16-9
Synonyms: SR-16435 free base
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

SR-16434 is a nociceptin/orphanin FQ (NOP)/μ-opioid receptor partial agonist, with high binding affinity (NOP receptor Ki=7.49; μ-Opioid receptor Ki=2.70). SR-16434 can relieve pain .
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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-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-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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