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 70

  1. Cat.No. Product Name Information/Activity
  2. BCC7652 NPEC-caged-(S)-3,4-DCPG 1257323-85-5 NPEC-caged-(S)-3,4-DCPG chemical structure
  3. BCC6578 O-Phospho-L-serine O-Phospho-L-serine is the immediate precursor to L-serine in the serine synthesis pathway, and an agonist at the group III mGluR receptors (mGluR4, mGluR6, mGluR7, and mGluR8); O-Phospho-L-serine also acts as a weak antagonist for mGluR1 and a potent antagonist for mGluR2. O-Phospho-L-serine chemical structure
  4. BCC6975 (RS)-PPG (RS)-PPG is a potent and selective agonist for group III mGluRs. The EC50s of 5.2 μM, 4.7 μM, 185 μM, and 0.2 μM for hmGluR4a, hmGluR6, hmGluR7b, and hmGluR8a, respectively. Anticonvulsive and neuroprotective activity. (RS)-PPG chemical structure
  5. BCC7615 VU 0155041 1093757-42-6 VU 0155041 chemical structure
  6. BCC7642 VU 0155041 sodium salt 1259372-69-4 VU 0155041 sodium salt chemical structure
  7. BCC7616 Z-Cyclopentyl-AP4 103439-17-4 Z-Cyclopentyl-AP4 chemical structure
  8. BCC6872 CPPG CPPG ((RS)-CPPG) is a potent group II/III mGlu receptor antagonist. CPPG exhibits some selectivity (approximately 20 fold) for group III (IC50=2.2 nM) over group II (IC50=46.2 nM) mGlu receptors in the rat cerebral cortex. CPPG has weak effects at group I mGlu receptors. CPPG chemical structure
  9. BCC7528 MMPIP hydrochloride 479077-02-6 MMPIP hydrochloride chemical structure
  10. BCC6818 MPPG 169209-65-8 MPPG chemical structure
  11. BCC7033 UBP1112 339526-74-8 UBP1112 chemical structure

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