Methoxyphenamine Hydrochloride
CAS No. 5588-10-3
Methoxyphenamine Hydrochloride ( 2-methoxy-N-methylamphetamine Hydrochloride;OMMA Hydrochloride;Orthoxine )
Catalog No. M19816 CAS No. 5588-10-3
Methoxyphenamine is a β-adrenergic receptor agonist of the amphetamine class used as a bronchodilator.
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
10MG | 49 | In Stock |
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25MG | 76 | In Stock |
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50MG | 115 | In Stock |
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100MG | Get Quote | In Stock |
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200MG | Get Quote | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameMethoxyphenamine Hydrochloride
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NoteResearch use only not for human use.
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Brief DescriptionMethoxyphenamine is a β-adrenergic receptor agonist of the amphetamine class used as a bronchodilator.
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DescriptionMethoxyphenamine is a β-adrenergic receptor agonist of the amphetamine class used as a bronchodilator.
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Synonyms2-methoxy-N-methylamphetamine Hydrochloride;OMMA Hydrochloride;Orthoxine
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PathwayAngiogenesis
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TargetAdrenergic Receptor
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Recptorβ-adrenergic receptor
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Research AreaMetabolic Disease
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IndicationCough and respiratory infection
Chemical Information
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CAS Number5588-10-3
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Formula Weight215.72
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Molecular FormulaC11H18ClNO
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Purity>98% (HPLC)
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SolubilityDMSO: 30 mg/mL;Ethanol: 30 mg/mL
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SMILESCl.CNC(C)Cc1ccccc1OC
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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
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JP1302 dihydrochlori...
JP1302 dihydrochloride is a selective, high affinity antagonist of the alpha2C-adrenoceptor (α2C-adrenoceptor), with a Ki (binding affinity) value of 28 nM and a Kb value (antagonist activity) of 16 nM.
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Ajmalicine
Ajmalicine (Raubasine) is a potent adrenolytic agent which preferentially blocks α1-adrenoceptor. Ajmalicine is an reversible but non-competitive nicotine receptor full inhibitor, IC50 = 72.3 μM. Ajmalicine also can be used as anti-hypertensive, and serpentine, with sedative activity。
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DL-071-IT
DL 071-IT is a potent non-selective beta-adrenoceptor antagonist. DL 071 IT showed intrinsic sympathomimetic activity and weak membrane stabilizing activity.