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dc.contributor.authorOliveira, Ana M. A. G.-
dc.contributor.authorCampos, Ana M. F. Oliveira-
dc.contributor.authorRaposo, M. Manuela M.-
dc.contributor.authorMachado, António E. H.-
dc.contributor.authorPuapairoj, Prapawadee-
dc.contributor.authorPedro, Madalena-
dc.contributor.authorNascimento, Maria São José-
dc.contributor.authorPortela, César-
dc.contributor.authorAfonso, Carlos A. M.-
dc.contributor.authorPinto, Madalena-
dc.date.accessioned2006-06-26T15:34:15Z-
dc.date.available2006-06-26T15:34:15Z-
dc.date.issued2006-03-
dc.identifier.citationOliveira, A. M. A. G., Raposo, M. M. M., Oliveira-Campos, A. M. F., Machado, A. E. H., Puapairoj, P., Pedro, M., . . . Pinto, M. (2006). Psoralen analogues: synthesis, inhibitory activity of growth of human tumor cell lines and computational studies. European Journal of Medicinal Chemistry, 41(3), 367-372. doi: https://doi.org/10.1016/j.ejmech.2005.10.016eng
dc.identifier.issn0223-5434eng
dc.identifier.urihttps://hdl.handle.net/1822/5168-
dc.description.abstractEight psoralens have been evaluated for their ability to inhibit the in vitro growth of three human turner cell lines representing different tumor types, MCF-7 (breast cancer), NCI-14460 (non-small cell lung cancer) and SF-268 (CNS cancer). The synthesis of four new psoralens (benzofur-ocournarins) is presented as well as the results of the ab initio calculations to find the parameters that relate the structure with the antitumor activity. This work provides supplementary information that could allow the development of new psoralen analogues with this type of biological activity.eng
dc.description.sponsorshipFor financial support from Fundação para a Ciência e Tecnologia, Portugal (I&D no. 226/9 and to CQ-UM), POCTI and FEDER; Ph.D. grants from FCT: Ana M.A.G. Oliveira (PRAXIS XXI/BD/19707/99), Madalena Pedro (SFRH/BD/1456/2000) and César Portela (SFRH/BD/3036/2000). For financial support and research grants to FAPEMIG (Fundação de Amparo à Pesquisa do Estado de Minas Gerais) and CNPq (Conselho Nacional do Desenvolvimento Científico e Tecnológico, Brazil). The authors thank National Cancer Institute, Bethesda, MD (USA) for kindly providing the tumor cell lines and Elisa Pinto for obtaining 1H-NMR and 13C-NMR spectra and elemental analyses.por
dc.description.sponsorshipPOCTI.por
dc.language.isoengeng
dc.publisherElsevier 1eng
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F1456%2F2000/PT-
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F3036%2F2000/PT-
dc.rightsopenAccesseng
dc.subjectFurocoumarinseng
dc.subjectBenzopsoralenseng
dc.subjectAntitumoreng
dc.subjectComputational studieseng
dc.titlePsoralen analogues: synthesis, inhibitory activity of growth of human tumor cell lines and computational studieseng
dc.typearticlepor
dc.peerreviewedyeseng
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0223523405003090eng
sdum.number3eng
sdum.pagination367-372eng
sdum.publicationstatuspublishedeng
sdum.volume41eng
oaire.citationStartPage367por
oaire.citationEndPage372por
oaire.citationIssue3por
oaire.citationVolume41por
dc.identifier.doi10.1016/j.ejmech.2005.10.016por
dc.identifier.pmid16439037por
dc.subject.wosScience & Technologypor
sdum.journalEuropean Journal of Medical Chemistrypor
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