Literature DB >> 15038061

Antiaggregating and antithrombotic activities of new 1, 2, 3-triazolecarboxamides.

Anke Cwiklicki1, Klaus Rehse.   

Abstract

Twenty five new triazolecarboxamides related to YC-1 were prepared and tested for their antiplatelet (in vitro) and antithrombotic (in vivo) activities. Five of them inhibited the aggregation of blood platelets (Born test, inducer collagen) with IC50 values between 90 and 130 microM. Nine compounds exhibited significant antithrombotic properties with an inhibition of thrombus formation between 11 and 7%. Only one compound (8c) showed both, in vitro and in vivo effects. In vitro, the most active compounds were 11c and 12d. They inhibit platelet aggregation with IC50 = 90 and 95 microM. In vivo, 10a showed the strongest inhibition of thrombus formation with 11% in arterioles (5% in venules) after a single oral dose of 60 mg/kg. With serotonin as inducer both, 11c and 12d, showed lower IC50 values namely 25 or 30 microM, respectively. Additional antiplatelet activities were found for 11c against adrenaline (IC50 = 25 microM) and for 12d against platelet activating factor (PAF) (IC50 = 15 microM) as inducer.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15038061     DOI: 10.1002/ardp.200300837

Source DB:  PubMed          Journal:  Arch Pharm (Weinheim)        ISSN: 0365-6233            Impact factor:   3.751


  2 in total

1.  A study of the scope and regioselectivity of the ruthenium-catalyzed [3 + 2]-cycloaddition of azides with internal alkynes.

Authors:  Max M Majireck; Steven M Weinreb
Journal:  J Org Chem       Date:  2006-10-27       Impact factor: 4.354

2.  New Members of the Cinchona Alkaloids Family: Assembly of the Triazole Heterocycle at the 6' Position.

Authors:  Catalin Vasile Maftei; Martin Heiko Franz; Christian Kleeberg; Ion Neda
Journal:  Molecules       Date:  2021-06-02       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.