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Design, synthesis, and evaluation of novel heteroaromatic analogs of curcumin as anti-cancer agents
To improve the potential of curcumin to treat advanced hormone-refractory prostate cancer, three series (A–C) of heteroaromatic analogs (thirty two compounds) with different monoketone linkers have been synthesized and evaluated for cytotoxicity against two human androgen-independent prostate cancer...
Tallennettuna:
| Julkaisussa: | Eur J Med Chem |
|---|---|
| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5971660/ https://ncbi.nlm.nih.gov/pubmed/24531225 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ejmech.2014.01.041 |
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