Nociception

Nociception is the sensory process that provides the signals that lead to pain. This occurs through nociceptors, primary sensory neurons that are activated by stimuli that cause tissue damage. Stimuli can include tissue injury, extremes of heat and noxious chemicals. Unlike other sensory neurons that detect vision or taste, nociceptors are located all around the body, particularly under the skin, however, they are notably absent from the brain.

Nociception Products Targets

Products for Nociception - Page 73

  1. Cat.No. Product Name Information/Activity
  2. BCC4527 Cimetidine Cimetidine is a histamine-2 (H2) receptor antagonist. Cimetidine chemical structure
  3. BCC6808 ICI 162,846 84545-30-2 ICI 162,846 chemical structure
  4. BCC4533 Ranitidine Hydrochloride Ranitidine hydrochloride is a histamine H2-receptor antagonist that inhibits stomach acid production. Ranitidine Hydrochloride chemical structure
  5. BCC5676 Tiotidine Tiotidine (ICI 125211) is a potent and selective antagonist of histamine H2-receptor (pA2=7.3-7.8 for guinea-pig right atrium). Tiotidine has low affinity for both the H1 and the H3 receptors. Tiotidine chemical structure
  6. BCC6922 Zolantidine dimaleate 104076-39-3 Zolantidine dimaleate chemical structure
  7. BCC6768 Imetit dihydrobromide Imetit dihydrobromide (VUF 8325 dihydrobromide) is a high affinity and potent agonist of histamine H3 and H4 receptors, with Ki values of 0.3 and 2.7 nM, respectively. Imetit mimics histamine effect in triggering a shape change in eosinophils (EC50=25 nM). Imetit dihydrobromide chemical structure
  8. BCC6853 Immepip dihydrobromide 164391-47-3 Immepip dihydrobromide chemical structure
  9. BCC7524 Methimepip dihydrobromide 817636-54-7 Methimepip dihydrobromide chemical structure
  10. BCC5665 (R)-(-)-α-Methylhistamine dihydrobromide (R)-(-)-α-Methylhistamine dihydrobromide is a potent and selective H3 histamine receptor agonist with a Kd of 50.3 nM. (R)-(-)-α-Methylhistamine dihydrobromide can cross the blood-brain barrier, and can enhance memory retention, attenuates memory impairment in rats. (R)-(-)-α-Methylhistamine dihydrobromide chemical structure
  11. BCC6700 (S)-(+)-α-Methylhistamine dihydrobromide 75614-93-6 (S)-(+)-α-Methylhistamine dihydrobromide chemical structure

Items 721 to 730 of 957 total