Ligustrazine derivatives. Part 5: Design, synthesis and biological evaluation of novel ligustrazinyloxy-cinnamic acid derivatives as potent cardiovascular agents
ARTICLE;
CELL PROLIFERATION;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG DETERMINATION;
DRUG SCREENING;
DRUG SYNTHESIS;
IN VITRO STUDY;
NONHUMAN;
OXIDATIVE STRESS;
STRUCTURE ACTIVITY RELATION;
THROMBOCYTE AGGREGATION INHIBITION;
Atherothrombosis: A widespread disease with unpredictable and life-threatening consequences
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A selective thromboxane A2 (TXA2) synthase inhibitor, ozagrel, attenuates lung injury and decreases monocyte chemoattractant protein-1 and interleukin-8 mRNA expression in oleic acid-induced lung injury in guinea pigs
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Synthesis of ligustrazine-aromatic acid derivatives and their inhibitory effect on platelet aggregation
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Ligustrazine inhibits lipopolysaccharide-induced proliferation by affecting P27, Bcl-2 expression in rat mesangial cells
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