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Structure-toxicity relationship of phenolic analogs as anti-melanoma agents: An enzyme directed prodrug approach

The aim of this study was to identify a phenolic prodrug compound that is minimally metabolized by rat liver microsomes, but yet could form quinone reactive intermediates in melanoma cells as a result of its bioactivation by tyrosinase. In current work, we investigated 24 phenolic compounds for thei...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Vad, Nikhil M., Kandala, Prabodh K., Srivastava, Sanjay K., Moridani, Majid Y.
التنسيق: Artigo
اللغة:Inglês
منشور في: 2009
الموضوعات:
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC2821678/
https://ncbi.nlm.nih.gov/pubmed/19944085
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cbi.2009.11.020
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