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dc.contributor.authorUchôa, Paula Karina S.-
dc.contributor.authorSilva Jr., José Nunes da-
dc.contributor.authorSilveira, Edilberto Rocha-
dc.contributor.authorLima, Mary Anne S.-
dc.contributor.authorBraz-Filho, Raimundo-
dc.contributor.authorCosta-Lotufo, Letícia Veras-
dc.contributor.authorAraújo, Ana Jérsia-
dc.contributor.authorMoraes Filho, Manoel Odorico de-
dc.contributor.authorPessoa, Claudia do Ó-
dc.date.accessioned2014-01-29T16:38:42Z-
dc.date.available2014-01-29T16:38:42Z-
dc.date.issued2013-
dc.identifier.citationUCHÔA, P. K. S. et al. Trachylobane and kaurane diterpenes from Croton floribundus Spreng. Química Nova, São Paulo, v. 36, n. 6, p. 778-782, 2013.pt_BR
dc.identifier.issn0100-4042-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/7193-
dc.description.abstractA new trachylobane diterpene ent-trachyloban-18,19-diol (1) was isolated from root bark of Croton floribundus, along with known diterpenes ent-trachyloban-19-oic acid (2), 15b-hydroxy-ent-trachyloban-19-oic acid (3), ent-trachyloban-19-ol (4), ent-kaur-16-en- 19-oic acid (5), ent-kaur-16-ene-6a,19-diol (6) and ent-16a-hydroxykaur-11-en-19-oic acid (7). ent-trachyloban-18,19-diol (1) was submitted to derivatization reactions affording four new compounds (8-11). Cytotoxic activity of diterpenes 1, 3, 4, 7-11 against three human cancer cell lines was evaluated. No compounds showed cytotoxic potential with IC50 values greater than 25 mg/mL. Compound 6 was evaluated against five human cancer cell lines, showing moderate effect against three cancer cell lines, MDA-MB-435, HCT-8 and HCT-116, with IC50 values of 14.32, 13.47 and 12.1 mg/mL, respectively.pt_BR
dc.language.isoenpt_BR
dc.publisherQuímica Novapt_BR
dc.subjectDiterpenospt_BR
dc.subjectEuphorbiaceaept_BR
dc.titleTrachylobane and kaurane diterpenes from Croton floribundus Sprengpt_BR
dc.typeArtigo de Periódicopt_BR
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