A new synthetic route of 16588-26-4

In some applications, this compound(16588-26-4)HPLC of Formula: 16588-26-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

HPLC of Formula: 16588-26-4. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 3-Bromo-4-chloronitrobenzene, is researched, Molecular C6H3BrClNO2, CAS is 16588-26-4, about Optimization of Potent ATAD2 and CECR2 Bromodomain Inhibitors with an Atypical Binding Mode. Author is Lucas, Simon C. C.; Atkinson, Stephen J.; Bamborough, Paul; Barnett, Heather; Chung, Chun-wa; Gordon, Laurie; Mitchell, Darren J.; Phillipou, Alexander; Prinjha, Rab K.; Sheppard, Robert J.; Tomkinson, Nicholas C. O.; Watson, Robert J.; Demont, Emmanuel H..

Most bromodomain inhibitors mimic the interactions of the natural acetylated lysine (KAc) histone substrate through key interactions with conserved asparagine and tyrosine residues within the binding pocket. Herein we report the optimization of a series of Ph sulfonamides that exhibit a novel mode of binding to non-bromodomain and extra terminal domain (non-BET) bromodomains through displacement of a normally conserved network of four water mols. Starting from an initial hit mol., we report its divergent optimization toward the ATPase family AAA domain containing 2 (ATAD2) and cat eye syndrome chromosome region, candidate 2 (CECR2) domains. This work concludes with the identification of (R)-55 (GSK232)(I), a highly selective, cellularly penetrant CECR2 inhibitor with excellent physicochem. properties.

In some applications, this compound(16588-26-4)HPLC of Formula: 16588-26-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

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