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Hyodeoxycholic acid

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纯度: 98.82%

货号 T2968Cas号 83-49-8

别名 猪去氧胆酸, α-Hyodeoxycholic Acid, NSC 60672, HDCA

Hyodeoxycholic acid (NSC 60672) 是由肠道菌群在小肠中形成的次级胆汁酸,是TGR5(GPCR19)的激动剂, CHO 细胞中的EC50=31.6 µM。它已用于研究高胆固醇血症的治疗。

Hyodeoxycholic acid
其他形式的 “Hyodeoxycholic acid”:

Hyodeoxycholic acid

一键复制产品信息
Rating icon 很棒

纯度: 98.82%

货号 T2968 别名 猪去氧胆酸, α-Hyodeoxycholic Acid, NSC 60672, HDCACas号 83-49-8

Hyodeoxycholic acid (NSC 60672) 是由肠道菌群在小肠中形成的次级胆汁酸,是TGR5(GPCR19)的激动剂, CHO 细胞中的EC50=31.6 µM。它已用于研究高胆固醇血症的治疗。

规格价格库存数量
25 mg
¥ 140
现货
50 mg
¥ 190
现货
100 mg
¥ 328
现货
500 mg
¥ 797
现货
1 g
¥ 969
现货
1 mL x 10 mM (in DMSO)
¥ 163
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产品介绍


Hyodeoxycholic acid AI Summary
Hyodeoxycholic acid exhibits diverse biological activities across multiple domains. It shows strong binding affinity (210,000 Kb M-1) and a sensitivity change (0.4) towards cyclodextrin-conjugated peptide (with pyrene) at 25°C. Notably, it inhibits glucuronosyltransferase activity in human colon cancer cell line HT-29 at 5 µM concentration with 75.2% activity. The compound is highly soluble in water (15,000 nM) and forms micelles at a Critical Micellar Concentration of 14.0 mM with pH stability varying at a pKa of 5.0 and a critical micellar pH of 8.1. It has high lipophilicity with a logP of 4.27 and a relative lipophilicity value of 0.89. In terms of receptor activity, Hyodeoxycholic acid acts as an agonist at human TGR5 in CHO cells (EC50 of 31,600 nM) with 79.7% efficacy relative to lithocholic acid. It exhibits cytotoxic effects in human HET-1A and HuH7 cells (500 µM) with 0.882% and 0.738% activity, respectively. The compound demonstrates varying activities against different isoforms of UDP-glucuronosyltransferases (UGTs), showing higher activity with UGT1A8 and UGT2B7. It is also a substrate for Oatp1 transport protein with a Km value of 17,500 nM in Oatp1-expressing HeLa cells. Hyodeoxycholic acid exhibits antiplasmodial activity against Plasmodium falciparum 3D7, antitrypanosomal activity against Trypanosoma brucei brucei, and cytotoxicity against human WI38 cells. It has agonistic and antagonistic activities based on VDR-LBD and VP16 tagged-VDR-LBD assays, with EC50 and IC50 values greater than 150,000 nM and 50,000 nM, respectively. Additionally, it demonstrates antibacterial activity against Clostridium difficile NAP1 with 500 µM required for inhibition, antiviral efficacy against SARS-CoV-2 by reducing cytotoxicity in VERO-6 and Caco-2 cells at 10 µM, and inhibiting the SARS-CoV-2 3CL-Pro protease by -1.852% at 20 µM. Lastly, it shows weak inhibitory activity on human HDAC6 with commercial and custom peptide substrates (-3.31% and -1.14%)..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Hyodeoxycholic acid (NSC 60672) has been used in trials studying the treatment of Hypercholesterolemia.
靶点活性
TGR5/GPCR19:31.6 µM(EC50)
别名猪去氧胆酸, α-Hyodeoxycholic Acid, NSC 60672, HDCA
化学信息
分子量392.57
分子式C24H40O4
CAS No.83-49-8
Smiles[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])C[C@H](O)[C@]2([H])C[C@H](O)CC[C@]12C
密度0.9985 g/cm3 (Estimated)
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 50 mg/mL (127.37 mM), Sonication is recommended.
Ethanol: 72 mg/mL (183.41 mM), Sonication is recommended.
H2O: < 1 mg/mL (insoluble or slightly soluble)
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.09 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO/Ethanol
1mg5mg10mg50mg
1 mM2.5473 mL12.7366 mL25.4732 mL127.3658 mL
5 mM0.5095 mL2.5473 mL5.0946 mL25.4732 mL
10 mM0.2547 mL1.2737 mL2.5473 mL12.7366 mL
20 mM0.1274 mL0.6368 mL1.2737 mL6.3683 mL
50 mM0.0509 mL0.2547 mL0.5095 mL2.5473 mL
100 mM0.0255 mL0.1274 mL0.2547 mL1.2737 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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