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Description: CDDO-Im (CDDO-imidazolide; TP235; RTA403) is a novel and ptent activator of Nrf2 and PPAR signaling with Kis of 232 and 344 nM for PPARalpha and PPARgamma. It is able to increase Nrf2 protein expression and enhances Nrf2-dependentcytoprotective gene expression. It inhibits cell growth and inducesapoptosis of pancreatic cancer cells in vitro and also reducesacetaminophen-induced liver injury in mice.
References:
1. PlaceAE, et al. The novel synthetic triterpenoid, CDDO-imidazolide, inhibitsinflammatory response and tumor growth in vivo. Clin Cancer Res. 2003Jul; 9(7):2798-806.
2. LibyK, et al. The synthetic triterpenoids, CDDO and CDDO-imidazolide, arepotent inducers of heme oxygenase-1 and Nrf2/ARE signaling. Cancer Res.2005 Jun 1; 65(11):4789-98.
3. SoJY, et al. A synthetic triterpenoid CDDO-Im inhibits tumorsphereformation by regulating stem cell signaling pathways in triple-negativebreast cancer. PLoS One. 2014 Sep 17; 9(9):e107616.
Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.
All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.
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