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dc.contributor.author | Núñez-Navarro, Nicolás E. | |
dc.contributor.author | Segovia, Gerardine F. | |
dc.contributor.author | Burgos, Renato A. | |
dc.contributor.author | Lagos, Carlos F. | |
dc.contributor.author | Fuentes-Ibacache, Nataly | |
dc.contributor.author | Faúndez, Mario A. | |
dc.contributor.author | Zacconi, Flavia C. | |
dc.date.accessioned | 2024-09-26T00:28:51Z | |
dc.date.available | 2024-09-26T00:28:51Z | |
dc.date.issued | 2017-02 | |
dc.identifier.issn | 0103-5053 | |
dc.identifier.uri | https://repositorio.uss.cl/handle/uss/12288 | |
dc.description | Publisher Copyright: ©2017 Sociedade Brasileira de Química. | |
dc.description.abstract | A series of six-membered lactam derivatives containing C, O and S atoms in position 4 were synthesized using microwave methodology through coupling reactions. The novel compounds were synthesized following two step reaction to yield fifteen derivatives. The final derivative N-(4-(3-oxotiomorpholin)phenyl) hexanamide was selectively toxic to the HCT-116 cell line over the HeLa cancerous and HEK-293 human non-malignant control cells with low inhibition Factor Xa (FXa) activity. The new products were characterized by spectral data including 1H and 13C nuclear magnetic resonance (NMR), infrared (IR) and high-resolution mass spectrometry (HRMS). Cytotoxicity of products on HCT-116, HeLa, HEK-293 cell lines and FXa activity assays are also reported. | en |
dc.language.iso | eng | |
dc.relation.ispartof | vol. 28 Issue: no. 2 Pages: 203-207 | |
dc.source | Journal of the Brazilian Chemical Society | |
dc.title | Microwave assisted synthesis of novel six-membered 4-C, 4-O and 4-S lactams derivatives : Characterization and in vitro biological evaluation of cytotoxicity and anticoagulant activity | en |
dc.type | Artículo | |
dc.identifier.doi | 10.21577/0103-5053.20160292 | |
dc.publisher.department | Facultad de Medicina y Ciencia |
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