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1.
J Proteome Res ; 13(9): 4205-10, 2014 Sep 05.
Artículo en Inglés | MEDLINE | ID: mdl-25102069

RESUMEN

Panorama is a web application for storing, sharing, analyzing, and reusing targeted assays created and refined with Skyline,1 an increasingly popular Windows client software tool for targeted proteomics experiments. Panorama allows laboratories to store and organize curated results contained in Skyline documents with fine-grained permissions, which facilitates distributed collaboration and secure sharing of published and unpublished data via a web-browser interface. It is fully integrated with the Skyline workflow and supports publishing a document directly to a Panorama server from the Skyline user interface. Panorama captures the complete Skyline document information content in a relational database schema. Curated results published to Panorama can be aggregated and exported as chromatogram libraries. These libraries can be used in Skyline to pick optimal targets in new experiments and to validate peak identification of target peptides. Panorama is open-source and freely available. It is distributed as part of LabKey Server,2 an open source biomedical research data management system. Laboratories and organizations can set up Panorama locally by downloading and installing the software on their own servers. They can also request freely hosted projects on https://panoramaweb.org , a Panorama server maintained by the Department of Genome Sciences at the University of Washington.


Asunto(s)
Bases de Datos de Proteínas , Bases del Conocimiento , Proteómica/métodos , Programas Informáticos , Internet , Espectrometría de Masas
2.
Org Biomol Chem ; 8(3): 529-32, 2010 Feb 07.
Artículo en Inglés | MEDLINE | ID: mdl-20090966

RESUMEN

The newly discovered natural product bacillamide C and several derivatives were convergently synthesized for the first time and in only three steps. The key transformation constitutes a thiazole Ugi multicomponent reaction. These compounds will serve to elucidate chemical biology and SAR of this potent anti-algae natural product and shows the synthetic pathway to related natural products.


Asunto(s)
Tiazoles/química , Tiazoles/síntesis química , Triptaminas/química , Triptaminas/síntesis química , Productos Biológicos/síntesis química , Productos Biológicos/química , Cinética , Estereoisomerismo , Especificidad por Sustrato
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