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首页 > 产品中心 > 生化试剂 > 小分子化合物 > abs47028179Alpha-D-galactose 218600-44-3

Alpha-D-galactose 218600-44-3

简要描述:Alpha-D-galactose 218600-44-3
CDDO is a synthetic oleanane triterpenoid that blocks the cellular synthesis of inducible nitric oxide synthase and inducible COX-2 in INF-γ-activated mouse macrophages

  • 产品型号:abs47028179
  • 厂商性质:生产厂家
  • 更新时间:2026-01-22
  • 访  问  量:662

详细介绍

品牌absinCAS218600-44-3
分子式C31H41NO4纯度98%
分子量491.70货号abs47028179
规格10mg供货周期现货
主要用途is a synthetic oleanane triterpenoid应用领域化工,生物产业,农林牧渔,制药/生物制药,综合

Alpha-D-galactose 218600-44-3

产品描述
描述

CDDO is a synthetic oleanane triterpenoid that blocks the cellular synthesis of inducible nitric oxide synthase and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.4 nM.By suppressing reactive oxygen and nitrogen species (ROS/RNS) formation, it promotes the cellular control of ROS/RNS levels that would lead to DNA damage associated with tumorigenesis.In various cancer cell lines, CDDO has been shown to specifically inhibit proliferation and induce apoptosis. Mechanism studies revealed that CDDO is a ligand for peroxisome proliferator-activated receptor γ, and also that it induces genes regulated by Nrf2, including heme oxygenase-1 and eotaxin-1, which play a role in antioxidant response element signaling activity。

纯度
98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
可溶性/溶解性
DMSO:Soluble
生物活性
靶点
Keap1-Nrf2
In vitro(体外研究)
Bardoxolone methyl, a novel synthetic triterpenoid and antioxidant inflammation modulator, potently induces Nrf2 and inhibits NF-κB and Janus-activated kinase/STAT signaling. Bardoxolone methyl has been shown to induce differentiation, inhibit proliferation, and induce apoptosis in cancer cell lines.
In vivo(体内研究)
Kidney sections from Bardoxolone methyl-treated monkeys demonstrates decreased megalin protein expression despite similar mRNA expression across groups. The visualized decrease in megalin protein expression is confirmed by densitometry analyses, which demonstrated that Bardoxolone methyl administration significantly decreased megalin protein expression in the monkey kidney. Bardoxolone methyl administration does not affect the protein expression of cubilin in the kidney or the mRNA expression of cubilin in the kidney. The creatinine clearance in monkeys administered Bardoxolone methyl significantly differed from that at baseline and in vehicle-treated animals on day 28. After 28 days of Bardoxolone methyl administration, urinary albumin-to-creatinine ratios (UACRs), determined from the 24-hour urine collections, are significantly increased compared with those in animals receiving vehicle. Of note, UACRs decreases 53.3% in vehicle-treated animals and increased 27.9% in Bardoxolone methyl-treated monkeys. Male C57BL/6J mice are administered oral BARD during HFD feeding (HFD/BARD), only fed a high-fat diet (HFD), or fed low-fat diet (LFD) for 21 weeks. Compared with LFD mice, HFD mice have a marked increase in the number of F4/80 crown-like structures (+95%; p.
参考文献
参考文献
1. Reisman SA, et al. J Am Soc Nephrol. 2012 Oct;23(10):1663-73. 2. Thomas M, et al. Expert Opin Drug Metab Toxicol. 2012 Aug;8(8):1015-22.3. Rojas-Rivera J, et al. Int J Nephrol. 2012;2012:321714.
研究领域
研究领域
CancerCancer Metabolism
Drug DiscoverySmall Molecule DrugLead Compound Discovery
Alpha-D-galactose 218600-44-3温馨提示:本产品仅作科研实验使用,不支持临床等研究

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