Application of 144875-48-9, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 144875-48-9, Name is Resiquimod, SMILES is CC(O)(C)CN1C(COCC)=NC2=C1C3=CC=CC=C3N=C2N, belongs to indole-building-block compound. In a article, author is Lu, Fangliu, introduce new discover of the category.
Piperlongumine, a natural alkaloid, is reported to possess various biological activities. In this study, six analogs with indole moiety have been designed and synthesized using scaffold hopping strategy. They exhibited better antitumor activities than the parent piperlongumine without apparent toxicity in normal cells. Among them, 3-chloro-1-(5,6,7-trimethoxy-1-methyl-1H-indole-2-carbonyl)-5,6-dihydropyridin-2(1H)-one showed the best in vitro antitumor activity with the IC50 value improved in 4-8-fold against four cancer cell lines. In an A549 lung cancer xenograft model, it exhibited a tumor growth inhibition of 54.6%, which is much higher than that of parent piperlongumine (38.3%) and comparable to the positive drug doxorubicin (53.3%). The indole-piperlongumine provides a novel lead compound for anticancer drug discovery. [GRAPHICS] .
Application of 144875-48-9, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 144875-48-9 is helpful to your research.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles