Authors:
BIAGI G
GIORGI I
LIVI O
SCARTONI V
LUCACCHINI A
MARTINI C
TACCHI P
Citation: G. Biagi et al., N(6)-SUBSTITUTED 2-PHENYL-9-BENZYL-8-AZAADENINES - AFFINITY FOR ADENOSINE A(1)-RECEPTOR AND A(2)-RECEPTOR - A COMPARISON WITH 2-N-BUTYL ANALOGOUS DERIVATIVES .5., Il Farmaco, 49(3), 1994, pp. 187-191
Authors:
BIAGI G
GIORGI I
LIVI O
SCARTONI V
LUCACCHINI A
MARTINI C
TACCHI P
Citation: G. Biagi et al., 2-ARYL-8-AZAADENOSINES - STRUCTURE-ACTIVITY-RELATIONSHIPS IN THE BINDING WITH A(1) AND A(2) RECEPTORS - A COMPARISON WITH THE CORRESPONDING9-BENZYL-8-AZAADENINES .III, Il Farmaco, 49(2), 1994, pp. 93-96
Authors:
BIAGI G
GIORGI I
LIVI O
LUCACCHINI A
MARTINI C
SCARTONI V
Citation: G. Biagi et al., STUDIES ON SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME C-BENZOYL-1,2,3-TRIAZOLE DERIVATIVES, Journal of pharmaceutical sciences, 82(9), 1993, pp. 893-896
Authors:
BIAGI G
GIORGI I
LIVI O
SCARTONI V
TONETTI I
LUCACCHINI A
Citation: G. Biagi et al., XANTHINE-OXIDASE (XO) - RELATIVE CONFIGURATION OF COMPLEXES FORMED BYTHE ENZYME, 2-N-ALKYL-HYPOXANTHINE OR 8-N-ALKYL-HYPOXANTHINE AND 2-N-ALKYL-8-AZAHYPOXANTHINES .12., Il Farmaco, 48(3), 1993, pp. 357-374