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Solid Phase Synthesis of a Metronidazole Oligonucleotide Conjugate

Direct, solid phase synthesis of an oligonucleotide conjugate of the antibiotic drug metronidazole was accomplished by the phosphoramidite method. Removal of protecting groups and cleavage from the controlled pore glass (CPG) solid support was successful using mild conditions (20% Et(3)N in pyridine...

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Detalles Bibliográficos
Publicado en:Molecules
Main Authors: Walsh, Andrew J., Davis, Michael L., Fraser, William
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2006
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6148672/
https://ncbi.nlm.nih.gov/pubmed/17962782
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/11060486
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