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 49

  1. Cat.No. Product Name Information/Activity
  2. BCC7335 WEB 2086 Apafant (WEB 2086), a potent platelet-activating factor (PAF) antagonist, inhibits PAF binding to human PAF receptors with a Ki of 9.9 nM. WEB 2086 chemical structure
  3. BCC7381 (±)-AC 7954 hydrochloride 477313-09-0 (±)-AC 7954 hydrochloride chemical structure
  4. BCC5796 Urotensin II (human) Urotensin II (114-124), human, an 11-amino acid residue peptide, is a potent vasoconstrictor and agonist for the orphan receptor GPR14. Urotensin II (human) chemical structure
  5. BCC8010 GSK 1562590 hydrochloride 1003878-07-6 GSK 1562590 hydrochloride chemical structure
  6. BCC6257 SB 611812 345892-71-9 SB 611812 chemical structure
  7. BCC7713 SB 657510 SB-657510 is a selective urotensin II (UII) receptor (UT) antagonist. The Ki values are 61, 17, 30, 65 and 56 nM for human, monkey, cat, rat and mouse receptors, respectively. SB-657510 exerts anti-inflammatory effects by inhibiting UII-induced upregulation of inflammatory mediators such as adhesion molecules, cytokines, and tissue factor in human vascular endothelial cells. SB 657510 chemical structure
  8. BCC6256 SB 706375 733734-61-7 SB 706375 chemical structure
  9. BCC5917 UFP 803 879497-82-2 UFP 803 chemical structure
  10. BCC5985 [Orn5]-URP 782485-03-4 [Orn5]-URP chemical structure
  11. BCC7705 3-Bromocytisine 3-Bromocytisine (3-Br-cytisine) is a potent nACh receptors agonist, with IC50s are 0.28, 0.30 and 31.6 nM for hα4β4, hα4β2, and hα7-nACh, respectively. 3-Bromocytisine (3-Br-cytisine) shows different effects on high (HS) and low (LS) ACh sensitivity α4β2 nAChRs with EC50s are 8 and 50 nM, respectively. 3-Bromocytisine chemical structure

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