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| Cat. No. : | HY-108561 |
| M.Wt: | 433.47 |
| Formula: | C22H21F2NO4S |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
L-670596 is an orally active and selective thrombsxane A2 receptor/prostaglandin receptor antagonist. L-670596 inhibits arachidonic acid (HY-109590) and U-44069 induced bronchoconstriction in the guinea pig. L-670596 also inhibits the aggregation of human platelet rich plasma induced by U-44069[1][2].
In Vitro:L-670596 inhibits the aggregation of human platelet rich plasma induced by U-44069[1].
In Vivo:L-670596 (0.03mg/kg ; i.v.; single) inhibits arachidonic acid and U-44069 induced bronchoconstriction in the guinea pig[1].
L-670596 (2 mg/kg; i.v.; single) inhibits platelet aggregation to collagen in pigs[2].
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