Please use this identifier to cite or link to this item: http://idr.niser.ac.in:8080/jspui/handle/123456789/1006
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dc.contributor.authorDash, Tapan Kumar-
dc.contributor.authorKonkimalla, V. Badireenath-
dc.date.accessioned2024-11-25T14:53:05Z-
dc.date.available2024-11-25T14:53:05Z-
dc.date.issued2011-10-26-
dc.identifier.citationDharmaraja, A. T., Dash, T. K., Konkimalla, V. B., & Chakrapani, H. (2012). Synthesis, thiol-mediated reactive oxygen species generation profiles and anti-proliferative activities of 2,3-epoxy-1,4-naphthoquinones. MedChemComm, 3(2), 219–224.en_US
dc.identifier.urihttps://doi.org/10.1039/C1MD00234A-
dc.identifier.urihttp://idr.niser.ac.in:8080/jspui/handle/123456789/1006-
dc.description.abstractHere, we report that thiol-mediated decomposition of 2,3-epoxy-1,4-naphthoquinones to generate peroxide, a reactive oxygen species (ROS), could be modulated by changing the substitution pattern on the aryl ring and the epoxide. Epoxides which generated higher amounts of peroxide upon reaction with thiols were better inhibitors of human leukaemia (THP1) cell proliferation.en_US
dc.language.isoenen_US
dc.publisherMedChemCommen_US
dc.titleSynthesis, thiol-mediated reactive oxygen species generation profiles and anti-proliferative activities of 2,3-epoxy-1,4-naphthoquinonesen_US
dc.typeArticleen_US
Appears in Collections:Journal Papers

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