| Literature DB >> 12110307 |
Eddy Sotelo1, Nuria Fraiz, Matilde Yáñez, Vicente Terrades, Reyes Laguna, Ernesto Cano, Enrique Raviña.
Abstract
A series of 6-phenyl-3(2H)-pyridazinones with a diverse range of substituents in the 5-position have been prepared and evaluated in the search for new antiplatelet agents. A significant dependence of the substituent on the inhibitory effect has been observed. The pharmacological study of these compounds confirms that modification of the chemical group at position 5 of the 6-phenyl-3(2H)-pyridazinone system influences both variations in the antiplatelet activity and the mechanism of action.Entities:
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Year: 2002 PMID: 12110307 DOI: 10.1016/s0968-0896(02)00146-3
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641