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Antitumor Potential of Conjugable Valinomycins Bearing Hydroxyl Sites: In Vitro Studies
[Image: see text] Following our pioneering studies on the direct and efficient introduction of derivatizable hydroxyl handles into the valinomycin (VLM, 1) structure, a K(+)-ionophore with potent antitumor activity, the ensuing conjugable analogues (HyVLMs 2, 3, and 4) have herein been compared to t...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Chemical
Society
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4027489/ https://ncbi.nlm.nih.gov/pubmed/24900628 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ml400300q |
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