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S83686

INDIRUBIN-3'-MONOXIME

源叶(MedMol) 99%
  • 英文名:
  • INDIRUBIN-3'-MONOXIME
  • 别名:
  • 靛玉红-3' -单肟;靛玉红-3'-肟;3-[1,3-DIHYDRO-3-(HYDROXYIMINO)-2H-INDOL-2-YLIDENE]-1,3-DIHYDRO-2H-INDOL-2-ONE;INDIRUBIN-3'-MONOXIME;INDIRUBIN-3'-OXIME;Indirubine-3'-oxime;INDIRUBIN-3’-MONOOXIME;Indirubin-3'
  • CAS号:
  • 160807-49-8
  • 分子式:
  • C16H11N3O2
  • 分子量:
  • 277.277
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S83686-5mg 99% ¥367.20元 9 - - - EA 加入购物车
源叶(MedMol) S83686-10mg 99% ¥578.00元 7 - - - EA 加入购物车
源叶(MedMol) S83686-25mg 99% ¥1258.00元 10 - - - EA 加入购物车
源叶(MedMol) S83686-50mg 99% ¥2312.00元 9 - - - EA 加入购物车
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产品介绍

参考文献(1篇)

质检证书(COA)

摩尔浓度计算器

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  • 提示:详情请下载说明书。
  • 产品描述: Indirubin-3'-monoxime is a potent GSK-3β inhibitor, and weakly inhibits 5-Lipoxygenase, with IC50s of 22 nM and 7.8-10 µM, respectively; Indirubin-3'-monoxime also shows inhibitory activities against CDK5/p25 and CDK1/cyclin B, with IC50s of 100 and 180 nM.
  • 靶点: GSK-3β:22 nM (IC50);CDK5/p25:100 nM (IC50);CDK1/cyclin B:180 nM (IC50);5-LOX:7.8-10 μM (IC50);GSK-3; Lipoxygenase; CDK
  • 体内研究:
    Indirubin-3'-monoxime (0.1, 0.2 and 0.4 mg/kg, i.p) dose dependently reverses the cognitive impairment and combats the elevated oxidative stress markers in HFD fed mice. Indirubin-3'-monoxime also dose dependently lowers the serum glucose, TGs, TC and insulin levels, and improves the β-cell functioning in HFD fed mice. Moreover, Indirubin-3'-monoxime treatment significantly decreases HOMA-IR levels compared to HFD group. Indirubin-3'-monoxime (0.4 mg/kg) significantly attenuates the increased EL in the HFD group
  • 参考文献:
    1. Leclerc S, et al. Indirubins inhibit glycogen synthase kinase-3 beta and CDK5/p25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. A property common to most cyclin-dependent kinase inhibitors? J Biol Chem. 2001 Jan 5;2 2. Sharma S, et al. Neuroprotective role of Indirubin-3'-monoxime, a GSKβ inhibitor in high fat diet induced cognitive impairment in mice. Biochem Biophys Res Commun. 2014 Oct 3;452(4):1009-15. 3. Blazevic T, et al. Indirubin-3'-monoxime exerts a dual mode of inhibition towards leukotriene-mediated vascular smooth muscle cell migration. Cardiovasc Res. 2014 Mar 1;101(3):522-32. 4. Cao Z, et al. Indirubin Derivatives as Dual Inhibitors Targeting Cyclin-Dependent Kinase and Histone Deacetylase for Treating Cancer [published online ahead of print, 2021 Oct 8]. J Med Chem. 2021;10.1021/acs.jmedchem.1c01311.
  • 溶解性: DMSO  :  ≥  37  mg/mL  (133.44  mM)
  • 保存条件: 2-8℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 3.607 ml 18.033 ml 36.065 ml
    5 mM 0.721 ml 3.607 ml 7.213 ml
    10 mM 0.361 ml 1.803 ml 3.607 ml
    50 mM 0.072 ml 0.361 ml 0.721 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)


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