Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Laurent Gouilleux"'
Publikováno v:
ChemInform. 28
The synthesis of chiral 3-substituted quinazoline-2,4-diones was performed starting from N-urethane anthranilamides. This synthetic pathway was applied in solid phase, from commercially available anthranilic acid that was bound to hydroxymethyl polys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28591b8898bf31f14baa3414582d71ec
https://doi.org/10.1002/chin.199710133
https://doi.org/10.1002/chin.199710133
Autor:
Luis Moroder, Véronique Gigoux, Chantal Escrieut, Jean-Alain Fehrentz, Danielle Gully, Nicole Vaysse, Daniel Fourmy, Laurent Gouilleux, Bernard Maigret, Sandrine Silvente-Poirot
Publikováno v:
HAL
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 1998, 273 (23), pp.14380-14386
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 1998, 273 (23), pp.14380-14386
Sulfation of the tyrosine at the seventh position from the C terminus of cholecystokinin (CCK) is crucial for CCK binding to the CCK-A receptor. Using three-dimensional modeling, we identified methionine 195 of the CCK-A receptor as a putative amino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9ed1a110116250c249cc48242e20b8f
https://hal.archives-ouvertes.fr/hal-00357491
https://hal.archives-ouvertes.fr/hal-00357491
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 1996, 37 (39), pp.7031-7034
Tetrahedron Letters, Elsevier, 1996, 37 (39), pp.7031-7034
The synthesis of chiral 3-substituted quinazoline-2,4-diones was performed starting from N-urethane anthranilamides. This synthetic pathway was applied in solid phase, from commercially available anthranilic acid that was bound to hydroxymethyl polys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1485db19870cf461facd0079775ddb72
https://hal.archives-ouvertes.fr/hal-00357388
https://hal.archives-ouvertes.fr/hal-00357388