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J Comb Chem ; 7(5): 697-702, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16153064

RESUMO

As part of our program to identify novel small molecules with interesting biological activity, we have designed and synthesized a library of end-capped dipeptides with an emphasis on compound diversity, complexity, and membrane permeability. An approximately 1500-member library was synthesized manually on large polystyrene beads using the mix-and-split method. The final compounds were cleaved into 384-well plates to generate individual stock solutions for input into high-throughput biological screens. Individual compounds were decoded using a combination of mass spectrometry and microflow NMR spectroscopy. In principle, this approach to deconvolution obviates the need for complicated binary encoding-decoding strategies for one-bead-one-compound libraries.


Assuntos
Dipeptídeos/química , Microquímica/métodos , Ressonância Magnética Nuclear Biomolecular/métodos , Biblioteca de Peptídeos , Aminoimidazol Carboxamida/química , Microfluídica , Poliestirenos/química , Sulfonamidas/química
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