Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid

Muriel Amblard; Marc Rodriguez; Marie Francoise Lignon; Marie Christine Galas; Nicole Bernad; Anne Marie Artis-Noel; Leticia Hauad; Jeanine Laur; Jean Christophe Califano

doi:10.1021/jm00072a024

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Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid

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Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid

Muriel Amblard, Marc Rodriguez, Marie Francoise Lignon, Marie Christine Galas, Nicole Bernad, Anne Marie Artis-Noel, Leticia Hauad, Jeanine Laur et Jean Christophe Califano

Journal of medicinal chemistry, Vol.36(20), pp.3021-3028

01/10/1993

DOI: https://doi.org/10.1021/jm00072a024

PMID: 7692048

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Titre: Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid
Créateurs - sans rôle: Muriel Amblard
Marc Rodriguez
Marie Francoise Lignon
Marie Christine Galas
Nicole Bernad
Anne Marie Artis-Noel
Leticia Hauad
Jeanine Laur
Jean Christophe Califano
Détails de publication: Journal of medicinal chemistry, Vol.36(20), pp.3021-3028
Éditeur: American Chemical Society
Nombre de pages: 8
Identifiants: 99138632309311
Unité académique: Institut des Biomolécules Max Mousseron - IBMM
Langue: English
Type de ressource: Journal article