dc.creator | dos Santos | |
dc.creator | Eric F. S.; Cury | |
dc.creator | Nathalia M.; do Nascimento | |
dc.creator | Tainara A.; Raminelli | |
dc.creator | Cristiano; Casagrande | |
dc.creator | Gleison A.; Pereira | |
dc.creator | Claudio M. P.; Simionatto | |
dc.creator | Euclesio; Yunes | |
dc.creator | Jose A.; Pizzuti | |
dc.creator | Lucas | |
dc.date | 2017 | |
dc.date | fev | |
dc.date | 2017-11-13T13:54:30Z | |
dc.date | 2017-11-13T13:54:30Z | |
dc.date.accessioned | 2018-03-29T06:07:53Z | |
dc.date.available | 2018-03-29T06:07:53Z | |
dc.identifier | Journal Of The Brazilian Chemical Society. Soc Brasileira Quimica, v. 28, p. 217 - 224, 2017. | |
dc.identifier | 0103-5053 | |
dc.identifier | 1678-4790 | |
dc.identifier | WOS:000394031600003 | |
dc.identifier | 10.5935/0103-5053.20160166 | |
dc.identifier | http://www.scielo.br/scielo.php?script=sci_abstract&pid=S0103-50532017000200217&lng=en&nrm=iso&tlng=en | |
dc.identifier | http://repositorio.unicamp.br/jspui/handle/REPOSIP/329412 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1366437 | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | 3-(Thiophen-2-yl)-4,5-dihydro-1H-pyrazole-1-carboximidamides were efficiently prepared through a cyclocondensation of thiophenylchalcones with aminoguanidine hydrochloride under ultrasonic conditions in the presence of KOH and ethanol as a green solvent in short reaction times (15-35 min) and good yields (62-95%). All compounds produced were evaluated against the human Jurkat and RS4; 11 acute lymphoblastic leukemia cell lines of T- and B-cell origin, respectively, and the K562 myelogenous leukemia cell line. Six compounds presented half maximal inhibitory concentration (IC50) values around 15 mu mol L-1 and five compounds presented IC50 values around 40 mu mol L-1 for at least one of the three cell lines analyzed. One compound was not significantly cytotoxic, presenting IC50 value > 100 mu mol L- 1. | |
dc.description | 28 | |
dc.description | 2 | |
dc.description | 217 | |
dc.description | 224 | |
dc.description | Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [483021/2013-0] | |
dc.description | Fundacao de Apoio ao Desenvolvimento do Ensino, Ciencia e Tecnologia do Estado de Mato Grosso do Sul (FUNDECT) [0180/12] | |
dc.description | Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [12/12802-1] | |
dc.description | Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) | |
dc.description | FAPESP | |
dc.description | CNPq | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) | |
dc.description | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.language | English | |
dc.publisher | Soc Brasileira Quimica | |
dc.publisher | São Paulo | |
dc.relation | Journal of the Brazilian Chemical Society | |
dc.rights | aberto | |
dc.source | WOS | |
dc.subject | Amidinopyrazole | |
dc.subject | Pyrazoline | |
dc.subject | Cytotoxic Activity | |
dc.subject | Leukemia | |
dc.subject | Ultrasonic Irradiation | |
dc.title | Ultrasound-promoted Synthesis Of 3-(thiophen-2-yl)-4,5-dihydro-1h-pyrazole-1carboximidamides And Anticancer Activity Evaluation In Leukemia Cell Lines | |
dc.type | Artículos de revistas | |