191096-30-7Relevant academic research and scientific papers
Benzoxazinones as PPARγ agonists. Part 1: SAR of three aromatic regions
Rybczynski, Philip J.,Zeck, Roxanne E.,Combs, Donald W.,Turchi, Ignatius,Burris, Thomas P.,Xu, Jun Z.,Yang, Maria,Demarest, Keith T.
, p. 2359 - 2362 (2007/10/03)
A series of benzoxazinones was synthesized as PPARγ agonists. The compounds were obtained in seven steps, and SAR was developed by variations to the core shown below. The compounds were tested as functional agonists in the induction of the aP2 gene in preadipocytes, and the most potent compound in the series has an EC50=0.51 μM. The potency was further confirmed through a PPAR-Gal4 construct. Efficacy has been demonstrated in the db/db mouse model of hyperglycemia.
The preparation of 2-hydroxyethyl-2,3-dihydro-2H-1,4-benzoxazin-3(4H)- one derivatives
Frechette, Roger F.,Beach, Michael J.
, p. 3471 - 3478 (2007/10/03)
An efficient synthesis of 2-hydroxyethyl-2,3-dihydro-2H-1,4-benzoxazin- 3(4H)-one derivatives is described using α-bromo-γ-butyrolactone as a bis- electrophile containing a latent hydroxyethyl functional group.
