相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- CAS号:
246529-22-6
- 规格:
1mg/1mLx10mM(inDMSO)/5mg/10mg/25mg/50mg/100mg
| 规格: | 1mg | 产品价格: | ¥214.0 |
|---|---|---|---|
| 规格: | 1mLx10mM(inDMSO) | 产品价格: | ¥716.0 |
| 规格: | 5mg | 产品价格: | ¥462.0 |
| 规格: | 10mg | 产品价格: | ¥713.0 |
| 规格: | 25mg | 产品价格: | ¥1456.0 |
| 规格: | 50mg | 产品价格: | ¥2120.0 |
| 规格: | 100mg | 产品价格: | ¥2920.0 |
Product Introduction
Bioactivity
| 名称 | Aramchol |
| 描述 | Aramchol (C20-FABAC), also known as arachidyl amido cholanoic acid, is a conjugate of arachidic acid and cholic acid. It reduces ex vivo cholesterol crystallization in native human bile and dissolves pre-formed cholesterol crystals in a dose-dependent manner. |
| 动物实验 | Performed a randomized, double-blind, placebo-controlled trial of 60 patients with biopsy-confirmed NAFLD (6 with nonalcoholic steatohepatitis) at 10 centers in Israel. Patients were given Aramchol (100 or 300 mg) or placebo once daily for 3 months (n = 20/group). The main end point was the difference between groups in the change in liver fat content according to magnetic resonance spectroscopy. The secondary end points focused on the differences between groups in alterations of liver enzyme levels, levels of adiponectin, homeostasis model assessment scores, and endothelial function[1]. |
| 体内活性 | 连续三个月给予脂肪酸-胆汁酸结合物Aramchol能显著降低非酒精性脂肪肝(NAFLD)患者的肝脂肪含量。肝脂肪含量的减少呈剂量依赖性,并伴有新陈代谢改善的趋势,表明Aramchol可能用于治疗脂肪肝疾病[1]。 |
| 存储条件 | Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | 10% DMSO+40% PEG300+5% Tween-80+45% Saline : 2.5 mg/mL (3.56 mM), Sonication is recommended. DMSO : 53.33 mg/mL (75.96 mM), Sonication is recommended. |
| 关键字 | Inhibitor | inhibit | Aramchol |
| 相关产品 | MK-8245 | Sesamin | SC-26196 | SLC13A5-IN-1 | SCD1 inhibitor-4 | SW209049 | PluriSIn 1 | (-)-Asarinin | GSK1940029 | SCD1 inhibitor-3 | T-3364366 | Elemicin |
| 相关库 | Bioactive Compound Library | Bioactive Compounds Library Max | Bioactive Lipid Compound Library | ReFRAME Related Library | Failed Clinical Trials Compound Library | Anti-Fibrosis Compound Library | NO PAINS Compound Library | Clinical Compound Library | Immunology/Inflammation Compound Library | Drug Repurposing Compound Library |
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验体系,可与质子结合,故其碱性(PKb=8.8)较吡咯(pKb=13.6)强,也比苯胺(pKb=9.3)强,能与强酸作用生成较稳定的盐。但比氨(pKb=4.75)弱,也比脂肪叔胺(三甲胺的pKb=4.22)弱。原因在于吡啶环上未参与共轭体系的这一对未共用电子对处于sp2杂化轨道上,其s成分较sp3杂化轨道多,受原子核束缚强,因而较难与H+结合。 吡啶与水能以任意比例混溶,同时又能溶解大多数极性及非极性有机化合物,它是一个良好的溶剂。吡啶具有高水溶性的原因,除分子极性外,是由于其氮原子上一对未参与环
分子中具有高能键的化合物。在生物体内主要有上式(Ⅰ)和(Ⅱ)两种结构的高能化合物。其作用为贮藏能量(例如 ATP、肌酸磷酸)和作为产生 ATP源的中间代谢产物(例如磷酸烯醇丙酮酸)以及合成反应的中间物质(例如酰基辅酶 A),在蛋白质的结构( conformation)变化周期的第一阶段上(例如钠钾 ATP酶的羧基磷酸中间体)也具有重要作用。多数高等化合物具有磷酸基,但也有例外。
由不同种元素组成的纯净物叫做化合物。化合物一般有固定的组成。化合物的组成一般可用化学式表示。化合物具有确定的物理性质和化学性质,不同于其组成元素的性质。化合物中的元素不能用简单的机械方法或物理方法分开,而必须用化学方法才能分离。
技术资料暂无技术资料 索取技术资料










