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].
Molecular Weight:
433.47
CAS Number:
[121083-05-4]
Formula:
C22H21F2NO4S
Target:
Prostaglandin Receptor
Application Notes:
MCE Product type: Reference compound
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