Difenoximide hydrochloride

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol ( HY-14616 ), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cellsIn Vitro(E)-[6]-Dehydroparadol (M15) (5-80 µM: 24 h)

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol ( HY-14616 ), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cellsIn Vitro(E)-[6]-Dehydroparadol (M15) (5-80 µM: 24 h)

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol ( HY-14616 ), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cellsIn Vitro(E)-[6]-Dehydroparadol (M15) (5-80 µM: 24 h)

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol ( HY-14616 ), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cellsIn Vitro(E)-[6]-Dehydroparadol (M15) (5-80 µM: 24 h)

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol ( HY-14616 ), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cellsIn Vitro(E)-[6]-Dehydroparadol (M15) (5-80 µM: 24 h)

(E)-[6]-Dehydroparadol, an oxidative metabolite of [6]-Shogaol ( HY-14616 ), is a potent Nrf2 activator. (E)-[6]-Dehydroparadol can inhibit the growth and induce the apoptosis of human cancer cellsIn Vitro(E)-[6]-Dehydroparadol (M15) (5-80 µM: 24 h)

1-Hydroxyibuprofen is one of the metabolites of ibuprofen, which is classified under the non-steroidal anti-inflammatory drugs (NSAIDs) group of compounds. Application 1-Hydroxyibuprofen has been used as an analytical reference standard for the

Description2,2-Di(4-tert-octylphenyl)-1-picrylhydrazyl (DPPH) is classified as a “stable” free radical since it has a long shelf life and can be synthesized and stored under normal laboratory

Application：2,4-Difluoropyrimidine can be used as a starting material to synthesize:·3-Pyrimidin-4-yl-oxazolidin-2-one derivatives as mutant isocitrate dehydrogenase (IDH1) inhibitors.·N,N′-(1,4-phenylenebis(methylene))bis(2-fluoropyrimidin-4-amine)

Application：2,4-Difluoropyrimidine can be used as a starting material to synthesize:·3-Pyrimidin-4-yl-oxazolidin-2-one derivatives as mutant isocitrate dehydrogenase (IDH1) inhibitors.·N,N′-(1,4-phenylenebis(methylene))bis(2-fluoropyrimidin-4-amine)

Application：2,4-Difluoropyrimidine can be used as a starting material to synthesize:·3-Pyrimidin-4-yl-oxazolidin-2-one derivatives as mutant isocitrate dehydrogenase (IDH1) inhibitors.·N,N′-(1,4-phenylenebis(methylene))bis(2-fluoropyrimidin-4-amine)

2,5-Diamino-4,6-dihydroxypyrimidine Hydrochloride.