3095-48-5Relevant articles and documents
Photoinduced properties of methyl ester of 2,6-dimethyl-1-amino-4-benzoic acid: Evidence of charge transfer emission from a weak primary amino donor
Ghosh, Shalini,Chakraborty, Amrita,Kar, Samiran,Guchhait, Nikhil
, p. 320 - 324 (2010)
Photophysical properties of methyl ester of 2,6-dimethyl-1-amino-4-benzoic acid (M26DMB) have been investigated using steady state absorption and emission spectroscopy and time-resolved emission spectroscopy. Interestingly, not only in polar solvents, the molecule M26DMB having a weak primary amino donor group shows broad red-shifted emission band even in non-polar environment which in all probability arises from closely spaced local and charge transfer (CT) states. Clear dual fluorescence in polar protic solvents comprises of less intense local emission band and strong red-shifted CT band. The position of the red-shifted emission band is dependent on both the polarity and the hydrogen-bonding ability of the solvent.
Discovery of substituted-2,4-dimethyl-(naphthalene-4-carbonyl)amino-benzoic acid as potent and selective EP4 antagonists
Blanco, Maria-Jesus,Vetman, Tatiana,Chandrasekhar, Srinivasan,Fisher, Matthew J.,Harvey, Anita,Mudra, Daniel,Wang, Xu-Shan,Yu, Xiao-Peng,Schiffler, Matthew A.,Warshawsky, Alan M.
, p. 105 - 109 (2015/12/18)
A novel series of EP4 antagonists, based on a quinoline scaffold, has been discovered. Medicinal chemistry efforts to optimize the potency of the initial hit are described. A highly potent compound in a clinically relevant human whole blood assay was iden
DIMETHYL-BENZOIC ACID COMPOUNDS
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Sheet 18; 19, (2014/01/17)
The present invention provides a compound of the Formula II: wherein A is: * R 1 is CH3, CF 3, or F; * R 2 is H, CH3, or F; * R 3 is CH3, OCH 3, OH, F; R 4 is OH or CH 20H; and *