N-[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines: Synthesis and Wide Range of Antagonism at the Human 5-HT1A Receptor-Reference-Cited by-同舟云学术

N-[2-[(Substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines: Synthesis and Wide Range of Antagonism at the Human 5-HT1A Receptor

Published:1997-04-01 Issue:8 Volume:40 Page:1252-1257
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Yasunaga Tomoyuki¹,Naito Ryo¹,Kontani Toru¹,Tsukamoto Shin-ichi¹,Nomura Tamako¹,Yamaguchi Tokio¹,Mase Toshiyasu¹

Affiliation:

1. Institute for Drug Discovery Research, Yamanouchi Pharmaceutical Company, Ltd., 21 Miyukigaoka, Tsukuba, Ibaraki 305, Japan

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm960760d

Reference24 articles.

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3. Olivier, B.; Mos, J.; van der Heyden, J. A. M.; Molewijk, H. E.; van Dijken, H. H.; Zethof, T.; Hest, A. v.; Tulp, M. Th. M.; Slangen, J. L. Functional Correlates of 5-HT Receptors, Clinical Applications and Possibilities of Serotonergic Drugs. InTrends in Drug Research; Claassen, V., Ed.; Elsevier Science Publishers: Amsterdam, 1993; Pharmacochemistry Library Vol. 20, pp 97−122.

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