Academic Journal

New Chiral Inhibitors of Induced Platelet Aggregation: the Enantiomeric Specificity of (R)- and (S)-Methyl and Ethyl Esters of 1-{p-[(1-Hydroxycarbonyl)-ethyloxy]-benzyl}-1H-1,2,3-triazole as a Tool for Determining their Biological Target.

التفاصيل البيبلوغرافية
العنوان: New Chiral Inhibitors of Induced Platelet Aggregation: the Enantiomeric Specificity of (R)- and (S)-Methyl and Ethyl Esters of 1-{p-[(1-Hydroxycarbonyl)-ethyloxy]-benzyl}-1H-1,2,3-triazole as a Tool for Determining their Biological Target.
المؤلفون: Biagi G, Catalani R, Gervasi O, Livi O, Scartoni V., GIORGI, IRENE
المساهمون: Biagi, G, Giorgi, Irene, Catalani, R, Gervasi, O, Livi, O, Scartoni, V.
سنة النشر: 1996
المجموعة: ARPI - Archivio della Ricerca dell'Università di Pisa
الوصف: The synthesis of title enantiomers was accomplished and their biological behaviour as inhibitors of rabbit platelet aggregation process induced by ADP and arachidonic acid was determined. Structure-activity comparison with that of SM-12502 [(2R,5S)-(+)3,5-dimethyl-2-(3-pyridyl)-thiazolidin-4-one hydrochloride] and Dazoxiben {4-[2-(1H-imidazol-1-yl)-ethoxy]-benzoic acid} allowed us to formulate the possible capability for the synthesized compounds to interact with the biological targets of the model molecules.
نوع الوثيقة: article in journal/newspaper
اللغة: English
Relation: info:eu-repo/semantics/altIdentifier/wos/A1996WG66200001; volume:51; firstpage:761; lastpage:766; numberofpages:6; journal:IL FARMACO; http://hdl.handle.net/11568/45415; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0030485477
الاتاحة: http://hdl.handle.net/11568/45415
رقم الانضمام: edsbas.A7FBF487
قاعدة البيانات: BASE