Pain and Inflammation Research

Although separate conditions, pain and inflammation are nearly always associated with each other. Pain is defined by the International Association for the Study of Pain (IASP) as 'an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage'. Inflammation is the tissue's immunologic response to injury, characterized by mobilization of white blood cells and antibodies, swelling, and fluid accumulation.

Pain and Inflammation Research Products Areas

Products for Pain and Inflammation Research - Page 9

  1. Cat.No. Product Name Information/Activity
  2. BCC7310 FPL 55712 40785-97-5 FPL 55712 chemical structure
  3. BCC7334 MK 571 MRP1 inhibitor; also CysLT<sub>1</sub> (LTD<sub>4</sub>) inverse agonist MK 571 chemical structure
  4. BCC4680 Montelukast Sodium Montelukast (sodium) (MK0476) is a potent, selective CysLT1 receptor antagonist. Montelukast Sodium chemical structure
  5. BCC4827 Pranlukast Pranlukast is a highly potent, selective and competitive antagonist of peptide leukotrienes. Pranlukast inhibits [3H]LTE4, [3H]LTD4, and [3H]LTC4 bindings to lung membranes with Kis of 0.63±0.11, 0.99±0.19, and 5640±680 nM, respectively. Pranlukast chemical structure
  6. BCC7180 SR 2640 hydrochloride 146662-42-2 SR 2640 hydrochloride chemical structure
  7. BCC6274 Gue 1654 397290-30-1 Gue 1654 chemical structure
  8. BCN2215 Arachidonic acid Arachidonic acid is an essential fatty acid and a major constituent of biomembranes. Arachidonic acid chemical structure
  9. BCC6038 BAY-X 1005 Veliflapon (BAY X 1005; DG-031) is an orally active and selective 5-lipoxygenase activating protein (FLAP) inhibitor. Veliflapon inhibits the synthesis of the leukotrienes B4 and C4. BAY-X 1005 chemical structure
  10. BCC7457 Cilastatin sodium 81129-83-1 Cilastatin sodium chemical structure
  11. BCC7017 MK 886 MK886 is a potent 5-lipoxygenase activating protein inhibitor (FLAP) also a non-competitive inhibitor of PPAR alpha. a potent inhibitor of leukotriene (LT) biosynthesis in intact human polymorphonuclear leukocytes with IC 50 of 2.5 nM. Block the synthessis of leukotrien intact activate leukocyte. MK 886 chemical structure

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