Neuroscience Research

Neuroscience is the study of the nervous system - one of the major mammalian systems responsible for sustaining life. The central nervous system (CNS) and peripheral nervous system (PNS) work in concert to coordinate basic functions such as moving and breathing, as well as 'higher order' functions including thought, speech and emotion.

Neuroscience Research Products Areas

Products for Neuroscience Research - Page 6

  1. Cat.No. Product Name Information/Activity
  2. BCC6565 L-(-)-threo-3-Hydroxyaspartic acid 7298-99-9 L-(-)-threo-3-Hydroxyaspartic acid chemical structure
  3. BCC6804 (±)-threo-3-Methylglutamic acid 63088-04-0 (±)-threo-3-Methylglutamic acid chemical structure
  4. BCC6873 MPDC MPDC is a potent and competitive inhibitor of the Na+-dependent high-affinity glutamate transporter in forebrain synaptosomes. MPDC chemical structure
  5. BCC6595 L-trans-2,4-PDC 64769-66-0 L-trans-2,4-PDC chemical structure
  6. BCC6840 SYM 2081 SYM 2081 is a high-affinity ligand and potent, selective agonist of kainate receptors, inhibits [3H]-kainate binding with an IC50 of 35 nM, almost 3000- and 200-fold selectivity for kainate receptors over AMPA and NMDA receptors respectively. SYM 2081 chemical structure
  7. BCC5735 DL-TBOA DL-TBOA is a potent non-transportable inhibitor of excitatory amino acid transporters with IC50s of 70 μM, 6 μM and 6 μM for excitatory amino acid transporter-1 (EAAT1), EAAT2 and EAAT3, respectively. DL-TBOA inhibits the uptake of [14C]glutamate in COS-1 cells expressing the human EAAT1 and EAAT2 with Ki valuesof 42 μM and 5.7 μM, respectively. DL-TBOA blocks EAAT4 and EAAT5 in a competitive manner with Ki values of 4.4 μM and 3.2 μM, respectively. DL-TBOA chemical structure
  8. BCC5919 TFB-TBOA 480439-73-4 TFB-TBOA chemical structure
  9. BCC7692 UCPH 101 UCPH-101 is an excitatory amino acid transporter subtype 1 (EAAT1) inhibitor with an IC50 of 0.66 μM. UCPH 101 chemical structure
  10. BCC7442 WAY 213613 WAY-213613 is a potent, selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 with IC50 of 85 nM EAAT2. It displays 59- and 44-fold selectivity over EAAT1 and EAAT3 (IC50s are 5 and 3.8 μM, respectively). WAY-213613 shows no activity at ionotropic and metabotropic glutamate receptors. It is a potential tool for the elucidation of EAAT2 function. WAY 213613 chemical structure
  11. BCC5896 MNI-caged-D-aspartate 845555-94-4 MNI-caged-D-aspartate chemical structure

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