Identification of PR-SET7 and EZH2 selective inhibitors inducing cell death in human leukemia U937 cells was written by Valente, Sergio;Lepore, Ilaria;Dell’Aversana, Carmela;Tardugno, Maria;Castellano, Sabrina;Sbardella, Gianluca;Tomassi, Stefano;Di Maro, Salvatore;Novellino, Ettore;Di Santo, Roberto;Costi, Roberta;Altucci, Lucia;Mai, Antonello. And the article was included in Biochimie in 2012.Related Products of 108940-96-1 This article mentions the following:
Chem. manipulations undertaken on some bis(bromo- and dibromo-phenol) compounds previously reported by us as wide-spectrum epigenetic inhibitors let us to identify bis (bromo- and dibromo-methoxyphenyl) derivatives highly selective for PR-SET7 and EZH2 (compounds 4, 5, 9, and 10). Western blot analyses were carried out in U937 cells to determine the effects of such compounds on the Me marks related to the tested enzymes (H3K4me1, H3K9me2, H4H20me1, and H3K27me3). The 1,5-bis(3-bromo-4-methoxyphenyl)penta-1,4-dien-3-one 4 (EC50 vs EZH2 = 74.9 娓璏), tested in U937 cells at 50 娓璏, induced massive cell death and 28% of granulocytic differentiation, highlighting the potential use of EZH2 inhibitors in cancer. In the experiment, the researchers used many compounds, for example, 3,5-Dibromo-4-methoxybenzaldehyde (cas: 108940-96-1Related Products of 108940-96-1).
3,5-Dibromo-4-methoxybenzaldehyde (cas: 108940-96-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.Related Products of 108940-96-1
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary