On the ground of the evidentiated choleretic activity of 3-[2- benzylbenzimidazol-1-yl]butanoic acid, 28 new acids were prepared in order to evaluate the influence of suitable substitutions in either C5 of heteroring or C3', C4', C5' of benzyl group in position 2 on the choleretic activity. Pharmacological results after i.v. administration of 0.5 mmol/Kg in rats confirmed a general high choleretic activity that in eleven cases showed during the first 4 hours an increase of bile volume higher than 80%, that is superior to that produced by dehydrocholic acid. Only in a few cases the bile volume increase was less than 37% of basal value.

Synthesis and choleretic activity of 3-[2-(3-R', 4-R'', 5R'''-Benzyl)-5-R-Benzimidazol-1-YL]- Butanoic acids / G., Grella; G., Paglietti; F., Sparatore; M., Satta; P., Manca; Peana, Alessandra Tiziana. - In: IL FARMACO. - ISSN 0014-827X. - 47:1(1992), pp. 21-35.

Synthesis and choleretic activity of 3-[2-(3-R', 4-R'', 5R'''-Benzyl)-5-R-Benzimidazol-1-YL]- Butanoic acids

PEANA, Alessandra Tiziana
1992-01-01

Abstract

On the ground of the evidentiated choleretic activity of 3-[2- benzylbenzimidazol-1-yl]butanoic acid, 28 new acids were prepared in order to evaluate the influence of suitable substitutions in either C5 of heteroring or C3', C4', C5' of benzyl group in position 2 on the choleretic activity. Pharmacological results after i.v. administration of 0.5 mmol/Kg in rats confirmed a general high choleretic activity that in eleven cases showed during the first 4 hours an increase of bile volume higher than 80%, that is superior to that produced by dehydrocholic acid. Only in a few cases the bile volume increase was less than 37% of basal value.
1992
Synthesis and choleretic activity of 3-[2-(3-R', 4-R'', 5R'''-Benzyl)-5-R-Benzimidazol-1-YL]- Butanoic acids / G., Grella; G., Paglietti; F., Sparatore; M., Satta; P., Manca; Peana, Alessandra Tiziana. - In: IL FARMACO. - ISSN 0014-827X. - 47:1(1992), pp. 21-35.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11388/45020
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