Naloxone hydrochloride
CAS No. 357-08-4
Naloxone hydrochloride( N-Allyldihydro-14-hydroxynormorphinone | NIH 7890 )
Catalog No. M14225 CAS No. 357-08-4
Naloxone hydrochloride is an opioid inverse agonist drug used to counter the effects of opiate overdose.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 37 | In Stock |
|
| 200MG | 56 | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameNaloxone hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionNaloxone hydrochloride is an opioid inverse agonist drug used to counter the effects of opiate overdose.
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DescriptionNaloxone hydrochloride is an opioid inverse agonist drug used to counter the effects of opiate overdose.
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In Vitro——
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In VivoNaloxone (2.0 mg/kg with constant infusion of 1.7 mg/kg/h) causes a significant improvement in neurobehavioral outcome which persists up to 4 weeks postinjury in rat. Naloxone treatment causes a modest and nonsignificant increase in mean arterial blood pressure (MAP). Naloxone (0.4 mg/kg) causes memory facilitation and antagonizes the amnestic effect of ACTH and epinephrine in rat. Naloxone treatment diminishes the strength of the initial tetanus in a dose-related manner in cats. Naloxone (5 or 10 mg/kg, i.v.) causes subsequent doses of morphine to produce less PTP depression but has no effect on maximal twitch depression.
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SynonymsN-Allyldihydro-14-hydroxynormorphinone | NIH 7890
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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 Number357-08-4
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Formula Weight363.84
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Molecular FormulaC19H21NO4·HCl
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Purity>98% (HPLC)
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SolubilityWater: 73 mg/mL (200.63 mM); DMSO: 73 mg/mL (200.63 mM)
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SMILESC=CCN1CC[C@]23[C@@H]4C(=O)CC[C@]2([C@H]1CC5=C3C(=C(C=C5)O)O4)O.Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Liu B, et al. J Pharmacol Exp Ther, 2000, 293(2), 607-617.
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