Synthesis and Serotonergic Activity of Substituted 2,N-Benzylcarboxamido-5-(2-ethyl-1-dioxoimidazolidinyl)-N,N-dimethyltrypt- amine Derivatives: Novel Antagonists for the Vascular 5-HT1B-like Receptor-Reference-Cited by-同舟云学术

Synthesis and Serotonergic Activity of Substituted 2,N-Benzylcarboxamido-5-(2-ethyl-1-dioxoimidazolidinyl)-N,N-dimethyltrypt- amine Derivatives: Novel Antagonists for the Vascular 5-HT1B-like Receptor

Published:1999-06-17 Issue:14 Volume:42 Page:2504-2526
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Moloney Gerard P.¹,Martin Graeme R.¹,Mathews Neil¹,Milne Aynsley¹,Hobbs Heather¹,Dodsworth Susan¹,Sang Pang Yih¹,Knight Cameron¹,Williams Marnie¹,Maxwell Miles¹,Glen Robert C.¹

Affiliation:

1. Department of Medicinal Chemistry, Victorian College of Pharmacy, Monash University, 381 Royal Parade, Parkville, Victoria 3052, Australia, Department of Molecular Pharmacology, Neurobiology Unit, Roche Bioscience, 3401 Hillview Avenue, R2-101, Palo Alto, California 94304, Department of Medicinal Chemistry and Systems Pharmacology Unit, GlaxoWellcome Research Group, Gunnels Road, Stevenage, Hertfordshire SG1 2NY, U.K., and Tripos Inc., 1699 South Hanley Road, St. Louis, Missouri 63144

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm9706325

Reference45 articles.

1. 5-HT Receptor Classification and Nomenclature: Towards a Harmonization with the Human Genome

2. Alignment of receptor nomenclature with the human genome: classification of 5-HT1B and 5-HT1D receptor subtypes

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