BAR502
目录号: PL01204 纯度: ≥98%
CAS No. :1612191-86-2
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PL01204-1mg 1mg ¥1174.55 请登录
PL01204-5mg 5mg ¥3585.45 请登录
PL01204-10mg 10mg ¥5192.73 请登录
PL01204-50mg 50mg ¥15825.45 请登录
PL01204-100mg 100mg 询价 询价
PL01204-200mg 200mg 询价 询价
PL01204-10mM*1mLinEthanol 10mM*1mLinEthanol ¥3944.00 请登录
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中文名称
BAR502
英文名称
BAR502
英文别名
BAR502;BAR-502;BAR 502;BDBM50028027;(3R,5S,6R,7R,8S,9S,10S,13R,14S,17R)-6-Ethyl-17-[(2R)-4-hydroxybutan-2-yl]-10,13-dimethyl-2,3,4,5,6,7
Cas No.
1612191-86-2
分子式
C25H44O3
分子量
392.62
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
BAR502是FXR和GPBAR1的双重激动剂,IC50值分别为2 μM 和0.4 μM。
生物活性
BAR502 is a dual FXR and GPBAR1 agonist with IC 50 values of 2 μM and 0.4 μM, respectively.
性状
Solid
IC50 & Target[1][2]
IC50: 2 μM (FXR), 0.4 μM (GPBAR1)
体外研究(In Vitro)
BAR502 is a truncated side chain alcohol with both substituents on ring B in α-configuration. At the concentration of 10 μM, BAR502 fails to transactivate GR, PPARγ, and LXR, respectively, but it transactivates the nuclear receptor PXR. BAR502 is able to induce the expression of pro-glucagon mRNA in GLUTAg cells, an intestinal endocrine cell line, as well as to increase cAMP concentrations in THP-1 cells. BAR502 induces the expression of OSTα, BSEP, and SHP in HepG2 cells. BAR502 shows a very potent activity in the recruitment of SRC-1 coactivator and high affinity to FXR. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Treatment with BAR502 causes a 10% reduction of b.w., increases insulin sensitivity and circulating levels of HDL, while reduces steatosis, inflammatory and fibrosis scores and liver expression of SREPB1c, FAS, PPARγ, CD36 and CYP7A1 mRNA. BAR502 increases the expression of SHP and ABCG5 in the liver and SHP, FGF15 and GLP1 in intestine. BAR502 promotes the browning of epWAT and reduces liver fibrosis induced by CCl4. In models of non-obstructive cholestasis, BAR502 attenuates liver injury without causing itching. Co-treatment with BAR502 increases survival, attenuates serum alkaline phosphatase levels and robustly modulates the liver expression of canonical FXR target genes including OSTα, BSEP, SHP and MDR1, without inducing pruritus. has not independently confirmed the accuracy of these methods. They are for referen
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Festa C, et al. Exploitation of cholane scaffold for the discovery of potent and selective farnesoid X receptor (FXR) and G-protein coupled bile acid receptor 1 (GP-BAR1) ligands. J Med Chem. 2014 Oct 23;57(20):8477-95.
[2]. Carino A, et al. BAR502, a dual FXR and GPBAR1 agonist, promotes browning of white adipose tissue and reverses liver steatosis and fibrosis. Sci Rep. 2017 Feb 16;7:42801.
溶解度数据
In Vitro: DMF : 50 mg/mL (127.35 mM; Need ultrasonic)Ethanol : ≥ 50 mg/mL (127.35 mM)
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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