Decrypt The Mystery Of 40400-13-3

If you want to learn more about this compound(1-(Bromomethyl)-2-iodobenzene)Application In Synthesis of 1-(Bromomethyl)-2-iodobenzene, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(40400-13-3).

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 40400-13-3, is researched, Molecular C7H6BrI, about Discovery of Dihydro-1,4-Benzoxazine Carboxamides as Potent and Highly Selective Inhibitors of Sirtuin-1, the main research direction is hydrobenzoxazine carboxamide sirtuin 1 selective inhibitor.Application In Synthesis of 1-(Bromomethyl)-2-iodobenzene.

Sirtuins are signaling hubs orchestrating the cellular response to various stressors with roles in all major civilization diseases. Sirtuins remove acyl groups from lysine residues of proteins, thereby controlling their activity, turnover, and localization. The seven human sirtuins, SirT1-7, are closely related in structure, hindering the development of specific inhibitors. Screening 170,000 compounds, we identify and optimize SirT1-specific benzoxazine inhibitors, Sosbo, which rival the efficiency and surpass the selectivity of selisistat (EX527). The compounds inhibit the deacetylation of p53 in cultured cells, demonstrating their ability to permeate biol. membranes. Kinetic anal. of inhibition and docking studies reveal that the inhibitors bind to a complex of SirT1 and NAD, similar to selisistat. These new SirT1 inhibitors are valuable alternatives to selisistat in biochem. and cell biol. studies. Their greater selectivity may allow the development of better targeted drugs to combat SirT1 activity in diseases such as cancer, Huntington’s chorea, or anorexia.

If you want to learn more about this compound(1-(Bromomethyl)-2-iodobenzene)Application In Synthesis of 1-(Bromomethyl)-2-iodobenzene, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(40400-13-3).

Reference:
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate