Cholic acid sodium (Synonyms: 胆酸钠; Sodium cholate)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物,专注于信号通路和疾病研究领域。
Cholic acid sodium  (Synonyms: 胆酸钠; Sodium cholate) 纯度: 99.41%

Cholic acid sodium 是肝脏中产生的主要胆汁酸,通常与甘氨酸或牛磺酸缀合,有助于脂肪吸收和胆固醇排泄。Cholic acid sodium 具有口服活性。

Cholic acid sodium                                          (Synonyms: 胆酸钠; Sodium cholate)

Cholic acid sodium Chemical Structure

CAS No. : 361-09-1

规格 价格 是否有货 数量
10 mM * 1 mL in Water ¥660 In-stock
100 mg ¥600 In-stock
200 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

Cholic acid sodium 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Drug Repurposing Compound Library Plus
  • FDA-Approved Drug Library Plus
  • FDA-Approved Drug Library Mini
  • Bioactive Compound Library Plus
  • Metabolism/Protease Compound Library
  • Natural Product Library
  • FDA-Approved Drug Library
  • Human Endogenous Metabolite Compound Library
  • Drug Repurposing Compound Library
  • NMPA-Approved Drug Library
  • Medicine Food Homology Compound Library
  • Orally Active Compound Library
  • Traditional Chinese Medicine Active Compound Library
  • FDA Approved & Pharmacopeial Drug Library
  • Drug-Induced Liver Injury (DILI) Compound Library
  • Neurodegenerative Disease-related Compound Library
  • Food Additive Library
  • Food-Sourced Compound Library
  • Rare Diseases Drug Library
  • EMA-Approved Drug Library
  • Human Metabolite Library
  • Off-patent Drug Library
  • Animal-Sourced Natural Product Library
  • FDA-Approved Traditional Chinese Medicine Active Compound Library

同靶点产品:

同靶点蛋白产品:

生物活性

Cholic acid sodium is a major primary bile acid produced in the liver and usually conjugated with glycine or taurine. It facilitates fat absorption and cholesterol excretion. Cholic acid sodium is orally active[1][2].

IC50 & Target

Human Endogenous Metabolite

 

体外研究
(In Vitro)

Cholic acid sodium (1 mg/mL,30 分钟) 竞争性结合 HepG2 细胞上的 Na+/牛磺胆酸盐协同转运多肽 (NTCP),并显著抑制 Cholic acid sodium (CA)-纳米脂质体 (LP)-多柔比星的摄取 (DOX)-HCl,这表明 CA-LPs-DOX-HCl 也通过 NTCP 介导的内吞途径被摄取[1]

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Cholic acid sodium 相关抗体:

体内研究
(In Vivo)

Cholic acid sodium (1% (w/w) 胆酸补充饮食;口服;14 天) 可能通过上调 miR142-3p 降低 SHP (小异二聚体伴侣) 蛋白表达。胆酸增加 CYP2D6 的表达和活性[2]

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Tg-CYP2D6 adult male mice (8 weeks of age and weighing 20–25 g)[2]
Dosage: 1% (w/w) Cholic acid-supplemented diet
Administration: Oral, 14 days
Result: Decreases SHP expression and increased CYP2D6 activity.

Clinical Trial

分子量

430.55

Formula

C24H39NaO5

CAS 号

361-09-1

性状

固体

颜色

White to off-white

中文名称

胆酸钠

结构分类
  • Steroids
初始来源
  • 内源性代谢物
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

H2O 中的溶解度 : ≥ 250 mg/mL (580.65 mM)

* “≥” means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3226 mL 11.6131 mL 23.2261 mL
5 mM 0.4645 mL 2.3226 mL 4.6452 mL
10 mM 0.2323 mL 1.1613 mL 2.3226 mL

查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

* 备注:如您选择水作为储备液,请稀释至工作液后,再用 0.22 μm 的滤膜过滤除菌后使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量

=

浓度

×

体积

×

分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×

体积 (start)

V1

=

浓度 (final)

C2

×

体积 (final)

V2

In Vivo:

以下溶解方案,请直接配置工作液。建议现用现配,在短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在您配制终溶液中的体积占比; 如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶。

  • 方案 一

    请依序添加每种溶剂: PBS

    Solubility: 100 mg/mL (232.26 mM); 澄清溶液; 超声助溶

扫码获得
动物溶解方案

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量

计算结果
工作液所需浓度 : mg/mL

该产品水溶性佳,请具体参考实测 水 / PBS / Saline 中的溶解度数据。
免费服务热线:021-50837765
E-mail:sales@jinpanbio.com
技术支持电话:021-50837765
技术支持邮箱:sales@jinpanbio.com

纯度 & 产品资料

纯度: 99.41%

Data Sheet (618 KB) SDS (0 KB)

COA (197 KB) RP-HPLC (178 KB)

产品使用指南 (1538 KB)

参考文献
  • [1]. Li Y, et al. Mechanism of hepatic targeting via oral administration of DSPE-PEG-Cholic acid-modified nanoliposomes. Int J Nanomedicine. 2017 Feb 28;12:1673-1684.  [Content Brief]

    [2]. Pan X, et al. Cholic acid Feeding Leads to Increased CYP2D6 Expression in CYP2D6-Humanized Mice. Drug Metab Dispos. 2017 Apr;45(4):346-352.  [Content Brief]

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务