Synthesis of some guanylhydrazones and imidazolinylhydrazones as thromboxane-synthase and platelet aggregation inhibitors

DOI: 10.1002/ardp.19923251206

Source and publish data:

Archiv der Pharmazie p. 773 - 777 (1992)

Update date:2022-08-04

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Authors:

Desideri

Sestili Sestili

Piccardoni

Rotondo Rotondo

Cerletti

Stein Stein

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Article abstract of DOI:10.1002/ardp.19923251206

The imidazolinylhydrazones of (3-pyridinyloxy)-acetaldehyde and of 6-[3(2-formyl-pyridinyl)oxy]hexanoic acid were synthesized as cyclic analogues of the corresponding guanylhydrazones which were found to be selective inhibitors of human thromboxane-syntha

Full text of DOI:10.1002/ardp.19923251206

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