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Guanethidine Monosulfate

    
99.6%

Guanethidine Monosulfate

源葉(MedMol)
S86078 一鍵復制產品信息
645-43-2
C10H24N4O4S
296.39
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S86078-50mg
99.6% ¥168.00 7 - - -
S86078-100mg
99.6% ¥320.00 3 - - -
S86078-500mg
≥98% ¥800.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

Guanethidine sulfate (Guanethidine monosulfate) ia an antihypertensive agents. Guanethidine is also an adrenergic neurone blocking drug, enters noradrenergic nerve terminals by the neuronal amine carrier

產品描述: Guanethidine sulfate (Guanethidine monosulfate) ia an antihypertensive agents. Guanethidine is also an adrenergic neurone blocking drug, enters noradrenergic nerve terminals by the neuronal amine carrier
靶點: Norepinephrine
體內研究: Guanethidine (5-40 mg/kg; intraperitoneal injection; daily; for 4-28 days; male Wistar rats) treatment for 28 days by 40 mg/kg results in an incomplete sympathectomy accompanied by a partially irreversible hypersensitivity to noradrenaline, whereas 5 mg/kg does not induce histological or permanent haemodynamic changes
參考文獻: 1. Mitchell JR, et al. Antagonism of the antihypertensive action of guanethidine sulfate by desipramine hydrochloride. JAMA. 1967 Dec 4;202(10):973-6. 2. Nielsen GD. Guanethidine induced sympathectomy in the adult rat. I. Functional effects following subacute administration. Acta Pharmacol Toxicol (Copenh). 1977 Sep;41(3):203-8. 3. Fabiani ME, et al. Inhibition of sympathetic noradrenergic transmission by guanabenz and guanethidine in rat isolated mesenteric artery: involvement of neuronal potassium channels. Pharmacol Res. 1996 Mar;33(3):171-80.
溶解性: Soluble  in  H2O
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.374 ml 16.87 ml 33.739 ml
5 mM 0.675 ml 3.374 ml 6.748 ml
10 mM 0.337 ml 1.687 ml 3.374 ml
50 mM 0.067 ml 0.337 ml 0.675 ml
注意: 部分產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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請輸入貨號和一個與之匹配的批號。
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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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