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UNC7467

    
99.20%

UNC7467

源叶(MedMol)
S89691 一键复制产品信息
C20H13NO3
315.32
3-([1,1'-biphenyl]-4-yl)benzo[c]isoxazole-5-carboxylic acid
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S89691-5mg买3赠1
99.20%

¥900.00

8 - - - -
S89691-10mg促销
99.20%

¥1600.00 ¥1280.00

7 - - - -
S89691-25mg促销
99.20%

¥3610.00 ¥2880.00

5 - - - -
S89691-100mg促销
≥98%

¥13500.00 ¥10800.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: UNC7467 is a potent IP6K inhibitor with values of 4.9, 8.9 and 1320 nM for IP6K2, IP6K1 and IP6K6, respectively. UNC7467 reduces levels of inositol pyrophosphates. UNC7467 can be used for obesity research
靶点: IC50: 4.9 nM (IP6K2), 8.9 nM (IP6K1), 1320 nM (IP6K3)
体外研究: UNC7467 (2.5 μM; 3 hours; HCT116 cells) reduces levels of inositol pyrophosphates. UNC7467 reduces 5-InsP7 levels by 81% and 5-InsP8 levels by 63%.
体内研究: UNC7467 (5 mg/kg; i.p.; daily, for 4 weeks; diet-induced obesity mice) ameliorated diet induced obesity, insulin resistance, and hepatic steatosis.
UNC7467 (1-5 mg/kg; i.v. and i.p.; diet-induced obesity mice) exhibits low clearance (13.7 (mL/min)/kg) and large AUClast (6054 h•ng/mL for intra venous (i.v.) and 2527 h•ng/mL for intraperitoneal (i.p.)) in mice at 5 mg/kg dose.
参考文献: 1. Zhou Y, et, al. Development of Novel IP6K Inhibitors for the Treatment of Obesity and Obesity-Induced Metabolic Dysfunctions. J Med Chem. 2022 May 12;65(9):6869-6887.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.171 ml 15.857 ml 31.714 ml
5 mM 0.634 ml 3.171 ml 6.343 ml
10 mM 0.317 ml 1.586 ml 3.171 ml
50 mM 0.063 ml 0.317 ml 0.634 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

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