
Journal of Medicinal Chemistry p. 160 - 164 (1985)
Update date:2022-08-05
Topics:
Bailey
DeGrazia
Alexander
Powles
Johnson
Patrick
Heerdt
Fairbain
Pruden
The syntheses of 4-(2-phenyl-1H-indol-3-yl)cyclohexane-1-carboxylic acids are described. These compounds express potent in vitro inhibition of the human classical complement pathway, and qualitative SAR have been determined. Several of the in vitro active
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