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Antiproliferative chromone derivatives induce K562 cell death through endogenous and exogenous pathways
A series of furoxan derivatives of chromone were prepared. The antiproliferative activities were tested against five cancer cell lines HepG2, MCF-7, HCT-116, B16, and K562, and two normal human cell lines L-02 and PBMCs. Among them, compound 15a exhibited the most potent antiproliferative activity....
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| Pubblicato in: | J Enzyme Inhib Med Chem |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Taylor & Francis
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7144234/ https://ncbi.nlm.nih.gov/pubmed/32183548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/14756366.2020.1740696 |
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