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 99

  1. Cat.No. Product Name Information/Activity
  2. BCC5729 MDL 29,913 135721-56-1 MDL 29,913 chemical structure
  3. BCC7133 MEN 10376 Men 10376 is a selective tachykinin NK-2 receptor antagonist, with a Ki of 4.4 μM for rat small intestine NK-2 receptor. MEN 10376 chemical structure
  4. BCC6921 Senktide Senktide is a tachykinin NK3 receptor agonist. Senktide chemical structure
  5. BCC7037 SB 218795 174635-53-1 SB 218795 chemical structure
  6. BCC1926 SB-222200 SB 222200 is a selective, reversible and competitive antagonist of human NK-3 receptor(Ki=4.4 nM) that effectively crosses the blood-brain barrier. SB-222200 chemical structure
  7. BCC1981 Talnetant Talnetant (SB 223412) is a potent and selective NK3 receptor antagonist (ki=1.4 nM, hNK-3-CHO); 100-fold selective for the hNK-3 versus hNK-2 receptor, with no affinity for the hNK-1 at concentrations up to 100 uM. Talnetant chemical structure
  8. BCC7635 SSR 146977 hydrochloride 264618-38-4 SSR 146977 hydrochloride chemical structure
  9. BCC7413 ZK 756326 874911-96-3 ZK 756326 chemical structure
  10. BCC7572 BMS CCR2 22 BMS CCR2 22 is a potent, specific and high affinity CC-type chemokine receptor 2 (CCR2) antagonist with excellent binding affinity (binding IC50 of 5.1 nM) and potent functional antagonism (calcium flux IC50 of 18 nM and chemotaxis IC50 of 1 nM). BMS CCR2 22 chemical structure
  11. BCC6029 BX 471 BX471 (ZK-811752) is an orally active, potent and selective non-peptide CCR1 antagonist with a Ki of 1 nM, and exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4. BX 471 chemical structure

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