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ACETOHEXAMIDE

    
99.14%

ACETOHEXAMIDE

源叶(MedMol)
S87581 一键复制产品信息
968-81-0
C15H20N2O4S
324.4
醋磺环已脲;1[(对乙酰苯)磺酰]-3-环已脲;1[(对乙酰苯)磺酰]-3-环己脲;醋磺环己脲;4-乙酰-N-[(环己氨基)羰基]苯磺酰胺;乙酸己脲;醋磺己脲;4-乙酰基-N-[(环己胺基)羰基]苯磺酰胺;4-ACETYL-N-[(CYCLOHEXYLAMINO)-CARBONYL]BENZENESULFONAMIDE;ACETOHEXAMIDE
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S87581-25mg促销
99.14%

¥224.00 ¥140.00

6 - - - -
S87581-100mg促销
99.14%

¥360.00 ¥290.00

5 - - - -
S87581-500mg
≥98%

¥640.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Acetohexamide is an intermediate-acting, first-generation sulfonylurea with hypoglycemic activity. It inhibits sulfonylurea receptor 1 (SUR1) linked to the inwardly rectifying potassium channel (KIR6.2) with Ki values of 22.9 and 14.2 μM in HEK293 cells transfected with the human receptor and in rat brain, respectively. Acetohexamide is metabolized in the liver to its active metabolite hydroxyhexamide.
靶点: NADPH;Potassium Channel;PotassiumChannel; NADPH
体内研究: Acetohexamide (Compound AH) (100 mg/kg 悬浮于水中,口服,单剂量) 与苯丁诺酮 (PBZ) 联合使用可增强兔模型中的降血糖作用。
参考文献: 1. Gopalakrishnan M, et al. Pharmacology of human sulphonylurea receptor SUR1 and inward rectifier K(+) channel Kir6.2 combination expressed in HEK-293 cells. Br J Pharmacol. 2000 Apr;129(7):1323-32. 2. Imamura Y, et al. Hypoglycemic effect of S(-)-hydroxyhexamide, a major metabolite of acetohexamide, and its enantiomer R(+)-hydroxyhexamide. Life Sci. 2001 Sep 7;69(16):1947-55. 3. Aldawsari H, et al. Int J Pharm. 2013 Sep 10;453(2):315-21. 4. McMahon RE, et al. The nature of the metabolites of acetohexamide in the rat and in the human. J Pharmacol Exp Ther. 1965 Aug;149(2):272-9.
溶解性: Soluble  in  DMSO
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.083 ml 15.413 ml 30.826 ml
5 mM 0.617 ml 3.083 ml 6.165 ml
10 mM 0.308 ml 1.541 ml 3.083 ml
50 mM 0.062 ml 0.308 ml 0.617 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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