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2,4-Diamino-5-(2′-arylpropargyl)pyrimidine derivatives as new nonclassical antifolates for human dihydrofolate reductase inhibition

Dihydrofolate reductase (DHFR) has been a well-recognized target for the development of therapeutics for human cancers for several decades. Classical inhibitors of DHFR use an active transport mechanism to gain access to the cell; disabling this mechanism creates a pathway for resistance. In respons...

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Detalhes bibliográficos
Main Authors: Algul, Oztekin, Paulsen, Janet L., Anderson, Amy C.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3073677/
https://ncbi.nlm.nih.gov/pubmed/21146434
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jmgm.2010.11.004
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