
Journal of Medicinal Chemistry p. 212 - 215 (1995)
Update date:2022-08-04
Topics:
Bernstein
Gomes
Kosmider
Vacek
Williams
Further modification of the 3-amino substituent in a trifluoromethyl ketone-based series of 3-amino-6-phenylpyridin-2-ones that had been optimized for oral activity led to analogs that were potent intratracheal inhibitors in a model of HLE-induced lung da
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