70386-06-0

Y-590 Chemical Structure
70386-06-0

Chemical Structure

Y-590

  • CAS No.: 70386-06-0
  • Formula:C15H17N3O2
  • Molecular Weight:271.31

IUPAC Name: 1-methyl-6-(4-methyl-6-oxo-1,4,5,6-tetrahydropyridazin-3-yl)-3,4-dihydroquinolin-2(1H)-one

InChIKey: JHPWSIOCWUJGJE-UHFFFAOYSA-N

SMILES: O=C1NN=C(C(C1)C)C2=CC(CCC(N3C)=O)=C3C=C2

Biological Activity: Y-590 is an orally active platelet cyclic adenosine monophosphate phosphodiesterase (cAMP-PDE) inhibitor with an IC50 of 0.9 nM against rabbit cAMP-PDE. Y-590 inhibits platelet aggregation, disaggregates aggregated platelets, suppresses collagen-induced platelet release, reduces platelet retention and inhibits cAMP degradation in platelets. Y-590 enhances PGI2-mediated elevation of intracellular cAMP in platelets and exerts a synergistic effect with PGI2 on ADP-induced platelet aggregation. Y-590 can be used in studies related to thrombotic diseases and thrombosis[1][2].

Cat. No. 상품명 Purity 제품 설명 Pricing
HY-123366
Y-590 Y-590 is an orally active platelet cyclic adenosine monophosphate phosphodiesterase (cAMP-PDE) inhibitor with an IC50 of 0.9 nM against rabbit cAMP-PDE. Y-590 inhibits platelet aggregation, disaggregates aggregated platelets, suppresses collagen-induced platelet release, reduces platelet retention and inhibits cAMP degradation in platelets. Y-590 enhances PGI2-mediated elevation of intracellular cAMP in platelets and exerts a synergistic effect with PGI2 on ADP-induced platelet aggregation. Y-590 can be used in studies related to thrombotic diseases and thrombosis.
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