Literature DB >> 9923191

New NO donors with antithrombotic and vasodilating activities, Part 26. Amidoximes and their prodrugs.

K Rehse1, F Brehme.   

Abstract

Seventeen amidoximes (2a-q) comprising aliphatic (2a-d), aromatic (2e-n), and bis compounds (2o-q) have been synthesized. In the Born test 4-chlorophenylethenecarboxamidoxime (21) was most active and inhibited the blood platelet aggregation induced by collagen with an IC50 = 3 microM. After oral administration to rats (60 mg/kg) fourteen compounds significantly inhibited the formation of thrombi in arterioles and venules. The strongest effect was observed with ethene-bis-carboxamidoxime (2q) (31% in arterioles and 18% in venules). The O-ethoxycarbonylderivatives 3 and the corresponding 1,2,4-oxadiazol-5-ones 4, which had been synthesized as prodrugs, showed smaller antithrombotic effects.

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Year:  1998        PMID: 9923191     DOI: 10.1002/(sici)1521-4184(199812)331:12<375::aid-ardp375>3.0.co;2-f

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


  1 in total

1.  Theoretical investigation of tautomerism in N-hydroxy amidines.

Authors:  Hossein Tavakol; Sattar Arshadi
Journal:  J Mol Model       Date:  2009-01-06       Impact factor: 1.810

  1 in total

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