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Ro 41-1049 (hydrochloride)

    
≥99%

Ro 41-1049 (hydrochloride)

源葉(MedMol)
S82705 一鍵復制產(chǎn)品信息
127917-66-2
C12H13ClFN3OS
301.7675
N-(2-Aminoethyl)-5-(3-fluorophenyl)-4-thiazolecarboxamide hydrochloride; Ro 41-1049 hydrochloride; UNII-19Z49HUF4G;
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S82705-5mg
≥99% ¥660.00 貨期:2-3天 - - -
S82705-10mg
≥99% ¥990.00 貨期:2-3天 - - -
S82705-50mg
≥99% ¥2700.00 貨期:2-3天 - - -
S82705-100mg
≥99% ¥4500.00 貨期:2-3天 - - -
產(chǎn)品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產(chǎn)品

產(chǎn)品介紹

Ro 41-1049 hydrochloride is a reversible and selective inhibitor of monoamine oxidase-A (MAO-A). An homogeneous population of high affinity binding sites for [3H]Ro 41-1049 is found in membrane preparations from human frontal cortex and placenta (Kd values of 16.5 and 64.4 nM, respectively)

產(chǎn)品描述: Ro 41-1049 hydrochloride is a reversible and selective inhibitor of monoamine oxidase-A (MAO-A). An homogeneous population of high affinity binding sites for [3H]Ro 41-1049 is found in membrane preparations from human frontal cortex and placenta (Kd values of 16.5 and 64.4 nM, respectively)
靶點: MAO-A;MAO
體內研究: Ro 41-1049 (1-50 mg/kg; intraperitoneal injection; for 3 hours; Sprague-Dawley rats) treatment inhibits dopamine metabolite formation and increases dopamine levels in a dose-dependent fashion. Pretreatment with Ro 41-1049 (20 mg/kg) significantly increases dopamine formation following L-dopa administration (100 mg/kg IP) while decreasing formation of 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA). Animal Model: Sprague-Dawley rats (200-240 g) Dosage: 1 mg/kg, 5 mg/kg, 10 mg/kg, 20 mg/kg, or 50 mg/kg Administration: Intraperitoneal injection; for 3 hours Result: Inhibited dopamine metabolite formation and increased dopamine levels in a dose-dependent fashion. Pretreatment with the concentration of 20 mg/kg significantly increased dopamine formation following L-dopa administration while decreasing formation of DOPAC and HVA.
參考文獻: 1. Cesura AM, et al. Characterization of the binding of [3H]Ro 41-1049 to the active site of human monoamine oxidase-A. Mol Pharmacol. 1990 Mar;37(3):358-66. 2. Brannan T, et al. Effect of a selective MAO-A inhibitor (Ro 41-1049) on striatal L-dopa and dopamine metabolism: an in vivo study. J Neural Transm Park Dis Dement Sect. 1994;8(1-2):99-105.
溶解性: Soluble  in  DMSO、H2O
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.314 ml 16.569 ml 33.138 ml
5 mM 0.663 ml 3.314 ml 6.628 ml
10 mM 0.331 ml 1.657 ml 3.314 ml
50 mM 0.066 ml 0.331 ml 0.663 ml
注意: 部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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