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Bisacodyl 603-50-9

简要描述:Bisacodyl 603-50-9
Bisacodyl (INN) is a stimulant laxative drug that works directly on the colon to produce a bowel movement.

  • 产品型号:abs47028375
  • 厂商性质:生产厂家
  • 更新时间:2026-02-02
  • 访  问  量:962

详细介绍

品牌absinCAS603-50-9
分子式C22H19NO4纯度>98%
分子量361.39货号abs47028375
规格50mg供货周期现货
主要用途is a stimulant laxative drug应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

Bisacodyl 603-50-9

产品描述
描述

Bisacodyl (INN) is a stimulant laxative drug that works directly on the colon to produce a bowel movement.

纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
比sha可啶
外观
白色或类白色结晶性粉末
可溶性/溶解性
DMSO : 67 mg/mL (185.4 mM)
生物活性
In vitro(体外研究)
Bisacodyl (10 μg/mL) increases mRNA expression level of TNF-α, COX2 and PGE2 in Raw264.7 cells.
In vivo(体内研究)
Bisacodyl (20 mg/kg) results in a decrease in AQP3 protein expression and increased mRNA expression level of TNF-α in the colon of rats. Bisacodyl inhibits water absorption in rat jejunum, ileum, and colon, the degree of inhibition is linearly related to the logarithm of the bisacodyl concentration over the range of 0.05 mg to 2.0 mg per 100 mL. Bisacodyl (10 mg/kg, intragastrically) induces a significant decrease in jejunal NOS activity in rats. Bisacodyl (10 mg/kg, intragastrically) increases the distance traveled by the marker in all time periods. Bisacodyl (5.9 mg/kg) decreases significantly jejunal and colonic (Na + K) ATPase activity as compared to saline-treated rats. Bisacodyl (5.9 mg/kg) increases significantly jejunal and colonic PGE2 content and stimulates jejunal and colonic adenyl cyclase activity as compared to those in control rats without affecting cAMP content. Bisacodyl (4.3 mg/kg) coupled with AOM increases the number of crypt per focus, but not the number of tumors in rats. Bisacodyl (43 mg/kg) significantly increases the number of crypt per focus and tumors in rats.
参考文献
参考文献
研究领域
研究领域
Metabolism
Drug DiscoverySmall Molecule DrugLead Compound Discovery
Bisacodyl 603-50-9温馨提示:本产品仅作科研实验使用,不支持临床等研究

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