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 52

  1. Cat.No. Product Name Information/Activity
  2. BCC6182 SEN 12333 874450-44-9 SEN 12333 chemical structure
  3. BCC7394 TC 1698 dihydrochloride 787587-06-8 TC 1698 dihydrochloride chemical structure
  4. BCC7264 α-Bungarotoxin 11032-79-4 α-Bungarotoxin chemical structure
  5. BCC1047 COG 133 ApoE peptide fragment; <span class='symbol'>&#945;</span>7 nAChR antagonist COG 133 chemical structure
  6. BCC5974 α-Conotoxin ImI 156467-85-5 α-Conotoxin ImI chemical structure
  7. BCC6897 Methyllycaconitine citrate 112825-05-5 Methyllycaconitine citrate chemical structure
  8. BCC7028 MG 624 77257-42-2 MG 624 chemical structure
  9. BCC4027 Tropisetron Hydrochloride Tropisetron Hydrochloride (SDZ-ICS-930) is a selective 5-HT3 receptor antagonist and α7-nicotinic receptor agonist with an IC50 of 70.1 ± 0.9 nM for 5-HT3 receptor. Tropisetron Hydrochloride chemical structure
  10. BCC1324 A-867744 A-867744 is a highly potent and selective type II positive allosteric modulator (PAM) of the alpha7 nicotinic acetylcholine receptors (nAChR) with an EC50 of 1.0 μM. A-867744 chemical structure
  11. BCC7788 CCMI CCMI is a potent and selective α7 nAChR-positive allosteric modulator, does not bind to or activate α7 nAChRs via the orthosteric site, and causes significant positive modulation of agonist-induced currents at α7 nAChRs. CCMI has potential in CNS diseases with cognitive dysfunction. CCMI chemical structure

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