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Generation of the First Structure-Based Pharmacophore Model Containing a Selective “Zinc Binding Group” Feature to Identify Potential Glyoxalase-1 Inhibitors

Within this study, a unique 3D structure-based pharmacophore model of the enzyme glyoxalase-1 (Glo-1) has been revealed. Glo-1 is considered a zinc metalloenzyme in which the inhibitor binding with zinc atom at the active site is crucial. To our knowledge, this is the first pharmacophore model that...

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Detalles Bibliográficos
Autores principales: Al-Balas, Qosay, Hassan, Mohammad, Al-Oudat, Buthina, Alzoubi, Hassan, Mhaidat, Nizar, Almaaytah, Ammar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268171/
https://www.ncbi.nlm.nih.gov/pubmed/23174893
http://dx.doi.org/10.3390/molecules171213740