Journal of Medicinal Chemistry p. 2087 - 2093 (1990)
Update date:2022-07-29
Topics:
Macor
Burkhart
Heym
Ives
Lebel
Newman
Nielsen
Ryan
Schulz
Torgersen
Koe
The synthesis and in vitro and in vivo characteristics of 3-(1,2,5,6-tetrahydropyrid-4-yl)pyrrolo[3,2-b]pyrid-5-one (1, CP-93,129) are described. This rotationally restricted phenolic analogue of RU-24,969 is a potent (15 nM) and selective (200x vs the 5-
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(2011)