2-Pyridinealdoxime methochloride
CAS No. 51-15-0
2-Pyridinealdoxime methochloride( 2-PAM )
Catalog No. M14766 CAS No. 51-15-0
Pralidoxime chloride is a useful agent in the treatment of organophosphate poisoning.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 32 | In Stock |
|
| 100MG | 45 | In Stock |
|
| 200MG | 61 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product Name2-Pyridinealdoxime methochloride
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NoteResearch use only, not for human use.
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Brief DescriptionPralidoxime chloride is a useful agent in the treatment of organophosphate poisoning.
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DescriptionPralidoxime chloride is a useful agent in the treatment of organophosphate poisoning. Pralidoxime binds to organophosphate-inactivated acetylcholinesterase, used to combat poisoning by organophosphates or acetylcholinesterase inhibitors (nerve agents) in conjunction with atropine and diazepam.(In Vivo):Pralidoxime chloride (10-150 mg/kg; intramuscular administration, once) reverses paraoxon-induced respiratory toxicity in mice.
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In Vitro——
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In VivoPralidoxime chloride (10-150 mg/kg; intramuscular administration, once) reverses paraoxon-induced respiratory toxicity in mice. Animal Model:F1B6D2 mice (male, administered subcutaneously diethylparaoxon)Dosage:10, 50, 100, and 150 mg/kg Administration:Intramuscular administration, once Result:Induced a partial, albeit complete, reversal of respiratory toxicity at 50 mg/kg, and completely reversed diethylparaoxon-induced respiratory toxicity in mice at 150 mg/kg.
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Synonyms2-PAM
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PathwayEndocrinology/Hormones
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TargetAChR
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RecptorAchE
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number51-15-0
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Formula Weight172.61
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Molecular FormulaC7H9ClN2O
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM
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SMILESCN1C=CC=CC1=C[NH+]=O.[Cl-]
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Chemical Name[(E)-(1-methylpyridin-2-ylidene)methyl]-oxoazanium;chloride
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.Jokanovi? M, Prostran M. Curr Med Chem. 2009;16(17):2177-88.
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