20 Results for "

Orphanin

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "Orphanin" 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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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-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-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-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-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-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-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-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-P1301
CAS No.: 236098-40-1
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

[Arg14,Lys15]Nociceptin is a highly potent and selective NOP receptor (ORL1; OP4) agonist, with an EC50 of 1 nM. [Arg14,Lys15]Nociceptin displays high selectivity over opioid receptors, with IC50s of 0.32, 280, >10000 and 1500 nM for NOP, μ, δ and κ receptors, respectively .
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Cat. No.: HY-P1301A
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

[Arg14,Lys15]Nociceptin TFA is a highly potent and selective NOP receptor (ORL1; OP4) agonist, with an EC50 of 1 nM. [Arg14,Lys15]Nociceptin TFA displays high selectivity over opioid receptors, with IC50s of 0.32, 280, >10000 and 1500 nM for NOP, μ, δ and κ receptors, respectively .
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Cat. No.: HY-13101B
CAS No.: 1108147-70-1
Purity:  98.97%
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

(S)-MCOPPB is the S-form of MCOPPB (HY-13101). 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 can be used for anxiety disorders study .
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Cat. No.: HY-13222A
CAS No.: 475150-69-7
Target:  

Opioid Receptor

Research Areas:  

Cancer

BAN ORL 24 free base is a nociceptin/orphanin FQ (N/OFQ) peptide receptor (NOP) antagonist. BAN ORL 24 free base has antagonistic effect for nociceptin (NOP) receptor with KI value of 0.24 nM in CHO cell. BAN ORL 24 free base can be used for the research of cancer and analgesic .
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Cat. No.: HY-P1318
CAS No.: 200959-48-4
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Ac-RYYRIK-NH2 is a potent and partial agonist on ORL1 transfected in CHO cells (Kd=1.5 nM) and behaves as a endogenous ligand of ORL1. Ac-RYYRIK-NH2 is a specific antagonist for the activation of G protein and competitively antagonizes the stimulation of [ 35S]-GTPgS binding to G proteins by nociceptin/orphanin FQ (noc/OFQ) in membranes and sections of rat brain .
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Cat. No.: HY-P1318A
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Ac-RYYRIK-NH2 TFA is a potent and partial agonist on ORL1 transfected in CHO cells (Kd=1.5 nM) and behaves as a endogenous ligand of ORL1. Ac-RYYRIK-NH2 is a specific antagonist for the activation of G protein and competitively antagonizes the stimulation of [ 35S]-GTPgS binding to G proteins by nociceptin/orphanin FQ (noc/OFQ) in membranes and sections of rat brain .
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Cat. No.: HY-P1320A
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-184490
CAS No.: 3118558-91-8
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

BPR1M492 is a brain-penetrant μ-opioid receptor (MOR) agonist an in vitro EC50 of 0.93 nM in the cAMP inhibition assay and 0.004 nM in the FLIPR Ca 2+ assay without a clear signaling bias between cAMP and β-arrestin-2 pathway. BPR1M492 is a cAMP-biased nociceptin-orphanin FQ opioid peptide agonist. BPR1M492 is a weak cAMP-biased δ/κ-opioid receptor agonist. BPR1M492 demonstrates potent in vivo antinociception and can be used for pain research .
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