5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-Based Potent and Selective CCK1 Receptor Antagonists: Structural Modifications at the Tryptophan Domain-Reference-Cited by-同舟云学术

5-(Tryptophyl)amino-1,3-dioxoperhydropyrido[1,2-c]pyrimidine-Based Potent and Selective CCK1 Receptor Antagonists: Structural Modifications at the Tryptophan Domain

Published:1999-10-07 Issue:22 Volume:42 Page:4659-4668
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Bartolomé-Nebreda José M.¹,Gómez-Monterrey Isabel¹,García-López M. Teresa¹,González-Muñiz Rosario¹,Martín-Martínez Mercedes¹,Ballaz Santiago¹,Cenarruzabeitia Edurne¹,LaTorre Miriam¹,Del Río Joaquín¹,Herranz Rosario¹

Affiliation:

1. Insituto de Química Médica (CSIC), Juan de la Cierva 3, E-28006 Madrd, Spain, and Departamento de Farmacología, Universidad de Navarra, Irunlarrea 1, E-31080 Pamplona, Spain

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm991078x

Reference43 articles.

1. Biological actions of cholecystokinin

2. Cholecystokinin-dopamine intearctions

3. The role of CCK, caerulein, and CCK antagonists in nociception

4. Evidence that decreased feeding induced by systemic injection of cholecystokinin is mediated by CCK-A receptors

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