Anticancer Activity of Ferrocenylthiosemicarbazones
- Авторы: Sandra C.1, Elena K.2, Marcos F.3, Elena M.4, Arturo R.5, Teresa R.6, Marcos M.7
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Учреждения:
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- Выпуск: Том 14, № 3 (2014)
- Страницы: 459-465
- Раздел: Oncology
- URL: https://kld-journal.fedlab.ru/1871-5206/article/view/695063
- DOI: https://doi.org/10.2174/18715206113136660365
- ID: 695063
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Аннотация
Aliphatic and aromatic ferrocenylthiosemicarbazones were synthesized. The characterization of the new ferrocenylthiosemicarbazones was done by IR, 1H-NMR and 13C-NMR spectroscopy, elemental analysis and X-ray diffraction studies. The biological activity of the obtained compounds was assessed in terms of anticancer activity. Their activity against U251 (human glyoblastoma), PC-3 (human prostatic adenocarcinoma), K562 (human chronic myelogenous leukemia), HCT-15 (human colorectal adenocarcinoma), MCF-7 (human mammary adenocarcinoma) and SKLU-1 (human lung adenocarcinoma) cell lines was studied and compared with cisplatin. All tested compounds showed good activity and the aryl-chloro substituted ferrocenylthiosemicarbazones showed the best anticancer activity.
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Об авторах
Cortez-Maya Sandra
aff1
Email: info@benthamscience.net
Klimova Elena
aff2
Email: info@benthamscience.net
Flores-Alamo Marcos
aff3
Email: info@benthamscience.net
Martínez-Klimova Elena
aff4
Email: info@benthamscience.net
Ramírez-Ramírez Arturo
aff5
Email: info@benthamscience.net
Ramírez Teresa
aff6
Email: info@benthamscience.net
Martínez-García Marcos
aff7
Email: info@benthamscience.net
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