The Reactions of Mitomycin C with Dithiols I. Reductive Activation

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Orgánicagl
dc.contributor.authorPaz Castañal, Manuel María
dc.date.accessioned2021-08-19T11:08:15Z
dc.date.available2021-08-19T11:08:15Z
dc.date.issued2010
dc.descriptionThe 14th International Electronic Conference on Synthetic Organic Chemistry session Natural Products Chemistrygl
dc.description.abstractWe report that the clinically used antitumor drug mitomycin C is reductively activated in vitro by simple thiols; a mechanism for this activation is proposed based on kinetic data and the identification of mitosene metabolites. The biological implications of these findings are discussedgl
dc.identifier.citationProceedings of the 14th International Electronic Conference on Synthetic Organic Chemistry, 1–30 November 2010, MDPI: Basel, Switzerland, doi:10.3390/ecsoc-14-00482gl
dc.identifier.doi10.3390/ecsoc-14-00482
dc.identifier.isbn3-906980-24-3
dc.identifier.urihttp://hdl.handle.net/10347/26882
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.ispartofseriesElectronic Conference on Synthetic Organic Chemistry;14
dc.relation.publisherversionhttps://doi.org/10.3390/ecsoc-14-00482gl
dc.rights© 2010 The author(s). Published by MDPI, Basel, Switzerland. Open Accessgl
dc.rights.accessRightsopen accessgl
dc.titleThe Reactions of Mitomycin C with Dithiols I. Reductive Activationgl
dc.typebook partgl
dspace.entity.typePublication
relation.isAuthorOfPublication70589fec-3154-40e1-bcc7-1d1cc6e6f25a
relation.isAuthorOfPublication.latestForDiscovery70589fec-3154-40e1-bcc7-1d1cc6e6f25a

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