Evaluation and synthesis of 7-arylhydroxymethyltriazolopyridines as potential cardiovascular agents
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Evaluation and synthesis of 7-arylhydroxymethyltriazolopyridines as potential cardiovascular agents

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Evaluation and synthesis of 7-arylhydroxymethyltriazolopyridines as potential cardiovascular agents

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Abarca González, Belén; Ballesteros Campos, Rafael; Elmasnaouy, Mostafá; D'Ocon Navaza, Pilar; Ivorra Insa, María Dolores; Valiente Bautista, Miguel
This document is a artículo publicadoDate2002

Este documento está disponible también en : http://hdl.handle.net/10550/12904
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.

    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
http://www.arkat-usa.org/get-file/19233/

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