Artículo
An ab initio conformational study on captopril
Zamarbide, Graciela Nidia; Estrada, Mario Rinaldo; Zamora, Miguel Angel; Torday, Ladislaus L.; Enriz, Ricardo Daniel
; Vert, Francisco Tomás; Csizmadia, Imre Gyula
Fecha de publicación:
12/2003
Editorial:
Elsevier Science
Revista:
Journal of Molecular Structure Theochem
ISSN:
0166-1280
Idioma:
Inglés
Tipo de recurso:
Artículo publicado
Clasificación temática:
Resumen
Captopril can interact regio- and stereo-specifically with various functional groups present at the active site of angiotensin converting enzyme (ACE). Since no X-ray structure of ACE is available, Captopril, as an ACE inhibitor may be used as a 'molecular caliper', to estimate upper and lower bound values for separation d, where the mercaptidic terminal group of the molecule is linked to the enzyme Zn2+ cofactor, while the carboxylate links via an hydrogen bond to the guanidine moiety of an arginine side chain. As the results of this Ab Initio study, the conformations of the dianionic form of the full captopril molecule are reported here.
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Articulos(IMIBIO-SL)
Articulos de INST. MULTIDICIPLINARIO DE INV. BIO. DE SAN LUIS
Articulos de INST. MULTIDICIPLINARIO DE INV. BIO. DE SAN LUIS
Citación
Zamarbide, Graciela Nidia; Estrada, Mario Rinaldo; Zamora, Miguel Angel; Torday, Ladislaus L.; Enriz, Ricardo Daniel; et al.; An ab initio conformational study on captopril; Elsevier Science; Journal of Molecular Structure Theochem; 666-667; 12-2003; 599-608
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