1 thesis of the nonsteroidal anti-inflammatory diflunisal.

2 zation by the potential therapeutic compound diflunisal.

3 n applied to a highly efficient synthesis of diflunisal.

4 ain III of human serum albumin (HSA-III) and diflunisal, a cyclooxygenase inhibitor with antiinflamma

5                                 Analogues of diflunisal, an FDA-approved nonsteroidal antiinflammator

6 -derived binding constants were obtained for diflunisal and closely related analogues to develop a st

7  studies indicate that the aromatic rings of diflunisal are involved in extensive and specific intera

8                       The carboxylic acid of diflunisal forms electrostatic interactions with the pro

9 inity for TTR was unchanged by halogenation, diflunisal gradually improves binding up to 1 order of m

10 ke peptide 1 (GLP-1) was functionalized with diflunisal, indomethacin, or both.

11 armacological chaperones, Tafamidis((R)) and diflunisal, inhibit TTR misfolding by stabilizing native

12                                              Diflunisal itself appears to occupy both orientations ba