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Discovery of 5,6-diaryl-1,2,4-triazines hybrids as potential apoptosis inducers
A series of 5,6-diaryl-1,2,4-triazines hybrids bearing a 1,2,3-triazole linker were synthesized by molecular hybridization strategy and evaluated for antiproliferative activity against three selected cancer cell lines (MGC-803, EC-109 and PC-3). The first structure-activity relationship (SAR) for th...
Tallennettuna:
| Julkaisussa: | Eur J Med Chem |
|---|---|
| Päätekijät: | , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5975277/ https://ncbi.nlm.nih.gov/pubmed/28763643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ejmech.2017.07.011 |
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