L-670596

CAT:
804-HY-108561
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
L-670596 - image 1

L-670596

  • Description :

    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].
  • UNSPSC :

    12352005
  • Target :

    Prostaglandin Receptor
  • Type :

    Reference compound
  • Related Pathways :

    GPCR/G Protein
  • Applications :

    Neuroscience-Neuromodulation
  • Field of Research :

    Others
  • Assay Protocol :

    https://www.medchemexpress.com/l-670596.html
  • Solubility :

    10 mM in DMSO
  • Smiles :

    O=C(O)CC1C(N(CC2=CC=C(S(=O)(C)=O)C=C2)C3=C4C=C(F)C=C3F)=C4CCC1
  • Molecular Formula :

    C22H21F2NO4S
  • Molecular Weight :

    433.47
  • References & Citations :

    [1]Ford-Hutchinson AW, et al. The pharmacology of L-670,596, a potent and selective thromboxane/prostaglandin endoperoxide receptor antagonist. Can J Physiol Pharmacol. 1989 Sep;67 (9) :989-93.|[2]Nuttall GA, et al. Protamine-heparin-induced pulmonary hypertension in pigs: effects of treatment with a thromboxane receptor antagonist on hemodynamics and coagulation. Anesthesiology. 1991 Jan;74 (1) :138-45.
  • Shipping Conditions :

    Room temperature
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [121083-05-4]

Featured Selection

Popular Products

Discover our most sought-after biotechnology products, trusted by researchers worldwide