Journal of Medicinal Chemistry p. 2635 - 2640 (1990)
Update date:2022-07-30
Topics:
Von Angerer
Knebel
Kager
Ganss
A number of 1-(ω-aminoalkyl)-5-hydroxy-2-(4-hydroxyphenyl)indoles were synthesized and studied for their binding affinities for the calf uterine estrogen receptor and estrogen antagonistic activities. Highest binding affinities were found with derivatives
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Doi:10.1002/ejic.201500756
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(1989)Doi:10.1021/jo00301a043
(1990)Doi:10.1021/jo1024927
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