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dc.contributor.author | Abarca González, Belén | |
dc.contributor.author | Ballesteros Campos, Rafael | |
dc.contributor.author | Elmasnaouy, Mostafá | |
dc.contributor.author | D'Ocon Navaza, María Pilar | |
dc.contributor.author | Ivorra Insa, María Dolores | |
dc.contributor.author | Valiente Bautista, Miguel | |
dc.date.accessioned | 2010-06-08T10:32:58Z | |
dc.date.available | 2010-06-08T10:32:58Z | |
dc.date.issued | 2002 | |
dc.identifier.citation | ABARCA GONZALEZ, Belen ; Ballesteros Campos,Rafael ; Elmasnaouy, Mostafá ; D’Ocón, Pilar ; Ivorra Insa, Maria Dolores ; Valiente Bautista, Miguel, 2002, Evaluation and synthesis of 7-arylhydroxymethyltriazolopyridines as potential cardiovascular agents, Arkivoc, vol. 2002, no. X, p. 9-13 | en |
dc.identifier.uri | http://hdl.handle.net/10550/12904 | |
dc.description.abstract | 7-Arylhydroxymethyltriazolopyridines 3a-c and 4a-d were synthesized by regioselective lithiation of [1,2,3]triazolo[1,5-a]pyridines 1 and 2 and subsequent trapping of the 7-lithioderivatives formed using aryl aldehydes as electrophiles. The structural relationship between compounds 3a-c and 4a-d and arylethanolamines suggested their consideration as potential cardiovascular agents. A preliminary evaluation as vascular smooth muscle relaxants was carried out. These compounds did not act as α1-adrenoceptor antagonists and were unable to block calcium entry through voltage-dependent calcium channels. | en |
dc.language.iso | en | en |
dc.subject | Triazolopyridines ; Lithiation reaction ; α1-adrenoceptor antagonism ; Calcium channels blockade | en |
dc.title | Evaluation and synthesis of 7-arylhydroxymethyltriazolopyridines as potential cardiovascular agents | en |
dc.type | journal article | es_ES |
dc.subject.unesco | UNESCO::QUÍMICA | en |
dc.subject.unesco | UNESCO::QUÍMICA::Química orgánica | en |
dc.identifier.idgrec | 003661 | en |
dc.type.hasVersion | VoR | es_ES |
dc.identifier.url | http://www.arkat-usa.org/get-file/19233/ | en |