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MCOPPB trihydrochlride
CAS No. 1108147-88-1
MCOPPB trihydrochlride( MCOPPB-trihydrochloride | MCOPPB tri-HCl )
Catalog No. M10404 CAS No. 1108147-88-1
MCOPPB 3hydrochloride is a nociceptin receptor agonist with pKi of 10.07.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 50 | In Stock |
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| 2MG | 28 | In Stock |
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| 5MG | 44 | In Stock |
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| 10MG | 75 | In Stock |
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| 25MG | 158 | In Stock |
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| 50MG | 249 | In Stock |
|
| 100MG | 367 | In Stock |
|
| 200MG | 524 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameMCOPPB trihydrochlride
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NoteResearch use only, not for human use.
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Brief DescriptionMCOPPB 3hydrochloride is a nociceptin receptor agonist with pKi of 10.07.
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DescriptionMCOPPB 3hydrochloride is a nociceptin receptor agonist with pKi of 10.07; weaker activity at other opioid receptors.
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In Vitro——
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In Vivo——
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SynonymsMCOPPB-trihydrochloride | MCOPPB tri-HCl
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PathwayEndocrinology/Hormones
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TargetOpioid Receptor
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RecptorOpioid Receptor
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number1108147-88-1
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Formula Weight518.01
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Molecular FormulaC26H43Cl3N4
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM
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SMILESCC1(N2CCC(N3C4=CC=CC=C4N=C3[C@H]5CNCCC5)CC2)CCCCCCC1.[H]Cl.[H]Cl.[H]Cl
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Chemical Name1-[1-(1-Methylcyclooctyl)piperidin-4-yl]-2-[(3R)-piperidin-3-yl]benzimidazole trihydrochloride
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Gluten Exorphin C
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 pepsin-trypsin-chymotrypsin digest of wheat gluten, was considered as a δ-opioid receptor-selective ligand.Gluten exorphin C, a novel opioid peptide, is isolated from the pepsin-trypsin-chymotrypsin digest of wheat gluten.
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Endomorphin 2?
Endomorphins-2 (EM-2) could decrease both the frequency and amplitude of the sEPSC of the motoneurons in lamina IX which was reversed by the MOR antagonist CTOP.??
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Calenduloside E
Calenduloside E exhibits hypoglycemic activities by suppressing the transfer of glucose from the stomach to the small intestine and by inhibiting glucose transport at the brush border of the small intestine in oral glucose-loaded rats.
