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 8

  1. Cat.No. Product Name Information/Activity
  2. BCC6115 GSK 9027 1229096-88-1 GSK 9027 chemical structure
  3. BCC2256 Methylprednisolone Methylprednisolone is a synthetic corticosteroid with anti-inflammatory and immunomodulating properties. Methylprednisolone chemical structure
  4. BCC4801 Mometasone furoate Mometasone furoate, prodrug of the free form mometasone, is a agent with high affinity for the glucocorticoid receptor. Mometasone furoate chemical structure
  5. BCC4486 Mifepristone Mifepristone is a progesterone receptor (PR) and glucocorticoid receptor (GR) antagonist with IC50s of 0.2 nM and 2.6 nM in in vitro assay. Mifepristone chemical structure
  6. BCC4767 Budesonide Budesonide is a glucocortical steroid with potent anti-inflammatory activity. Budesonide chemical structure
  7. BCC1184 Dexamethasone (DHAP) Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist. Dexamethasone also significantly decreases CD11b, CD18, and CD62L expression on neutrophils, and CD11b and CD18L expression on monocytes. Dexamethasone (DHAP) chemical structure
  8. BCN2192 Hydrocortisone Hydrocortisone is a steroid hormone or glucocorticoid produced by the adrenal gland. Hydrocortisone chemical structure
  9. BCC1659 IRAK-1-4 Inhibitor I IRAK-1-4 Inhibitor I is an inhibitor of interleukin-1 receptor-associated kinase 1/4 (IRAK 1/4) with IC50s of 0.2 μM and 0.3 μM, respectively. IRAK-1-4 Inhibitor I chemical structure
  10. BCC7576 BAY-u 9773 Dual CysLT<sub>1</sub> and CysLT<sub>2</sub> antagonist BAY-u 9773 chemical structure
  11. BCC7244 Cinalukast 128312-51-6 Cinalukast chemical structure

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