Naltrexone hydrochloride
CAS No. 16676-29-2
Naltrexone hydrochloride( NIH 8503 )
Catalog No. M12543 CAS No. 16676-29-2
A potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of 0.0825 nM, 0.509 nM, and 8.02 nM, for MOR, KOR, and DOR, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 37 | In Stock |
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| 25MG | 29 | In Stock |
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| 50MG | 34 | In Stock |
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| 100MG | 47 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 105 | In Stock |
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| 1G | 154 | In Stock |
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Biological Information
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Product NameNaltrexone hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of 0.0825 nM, 0.509 nM, and 8.02 nM, for MOR, KOR, and DOR, respectively.
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DescriptionA potent, competitive antagonist for μ, κ, δ, and σ-opioid receptors with Ki of 0.0825 nM, 0.509 nM, and 8.02 nM, for MOR, KOR, and DOR, respectively; also inhibits IL-6 and TNFα production in human immune cell subsets following stimulation with ligands for intracellular TLRs; a TLR-4 antognist that inhibits LPS-induced TLR4 downstream NO production in microglia BV-2 cells (IC50=105 uM).Alcoholism Approved.
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In Vitro——
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In Vivo——
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SynonymsNIH 8503
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PathwayEndocrinology/Hormones
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TargetOpioid Receptor
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RecptorOpioidReceptor
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Research AreaNeurological Disease
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IndicationAlcoholism
Chemical Information
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CAS Number16676-29-2
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Formula Weight377.8618
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Molecular FormulaC20H24ClNO4
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 33 mg/mL
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SMILESC1CC1CN2CC[C@]34[C@@H]5C(=O)CC[C@]3([C@H]2CC6=C4C(=C(C=C6)O)O5)O.Cl
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Chemical NameMorphinan-6-one, 17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-, hydrochloride (1:1), (5α)-
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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[Arg14,Lys15]Nocicep...
Highly potent and selective NOP receptor agonist (EC50 = 1 nM). Displays > 875-fold selectivity over opioid receptors (IC50 values are 0.32, 280, > 10000 and 1500 for NOP, μ, δ and κ receptors respectively). Longer lasting and 30-fold more potent than nociceptin in vivo; pronociceptive and inhibits locomotor activity.
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Hemorphin-7
Hemorphin-7 binds to the angiotensin IV receptor, triggering multiple effects including cellular proliferation and memory enhancement. Hemorphins are endogenous peptides belonging to the family of atypical opioid peptides released from hydrolyzed hemoglobin. Hemorphin-7 is investigated as a potential biomarker for breast cancer.
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Bevenopran
Bevenopran is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.
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