A series of xanthone 1,4-dihydropyridine derivatives bearing a 2,3-lactone ring and a 2-acetoxymethyl group were prepared. The compounds were evaluated for inotropic, chronotropic and calcium antagonist properties. The introduction of a 2,3-lactone ring improved the negative inotropic activity and selectivity.

Structure-activity relationship studies in the field of calcium antagonists. Xanthone 1,4-dihydropyridines bearing a 2,3-lactone ring / Rampa A.; Budriesi R.; Bisi A.; Fabbri G.; Barili P.L.; Chiarini A.; Valenti P.. - In: ARZNEIMITTEL-FORSCHUNG. - ISSN 0004-4172. - STAMPA. - 45:9(1995), pp. 957-962.

Structure-activity relationship studies in the field of calcium antagonists. Xanthone 1,4-dihydropyridines bearing a 2,3-lactone ring

Rampa A.;Budriesi R.;Bisi A.;Fabbri G.;Chiarini A.;Valenti P.
1995

Abstract

A series of xanthone 1,4-dihydropyridine derivatives bearing a 2,3-lactone ring and a 2-acetoxymethyl group were prepared. The compounds were evaluated for inotropic, chronotropic and calcium antagonist properties. The introduction of a 2,3-lactone ring improved the negative inotropic activity and selectivity.
1995
Structure-activity relationship studies in the field of calcium antagonists. Xanthone 1,4-dihydropyridines bearing a 2,3-lactone ring / Rampa A.; Budriesi R.; Bisi A.; Fabbri G.; Barili P.L.; Chiarini A.; Valenti P.. - In: ARZNEIMITTEL-FORSCHUNG. - ISSN 0004-4172. - STAMPA. - 45:9(1995), pp. 957-962.
Rampa A.; Budriesi R.; Bisi A.; Fabbri G.; Barili P.L.; Chiarini A.; Valenti P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/911650
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