Neural Development

Neural development describes the growth and development of the nervous system starting from embryogenesis and continuing throughout life.

Neural Development Products Targets

Products for Neural Development - Page 58

  1. Cat.No. Product Name Information/Activity
  2. BCC6556 Dihydrokainic acid 52497-36-6 Dihydrokainic acid chemical structure
  3. BCC7295 (±)-HIP-B 227619-65-0 (±)-HIP-B chemical structure
  4. BCC6565 L-(-)-threo-3-Hydroxyaspartic acid 7298-99-9 L-(-)-threo-3-Hydroxyaspartic acid chemical structure
  5. BCC6804 (±)-threo-3-Methylglutamic acid 63088-04-0 (±)-threo-3-Methylglutamic acid chemical structure
  6. BCC6873 MPDC MPDC is a potent and competitive inhibitor of the Na+-dependent high-affinity glutamate transporter in forebrain synaptosomes. MPDC chemical structure
  7. BCC6595 L-trans-2,4-PDC 64769-66-0 L-trans-2,4-PDC chemical structure
  8. 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
  9. BCC5919 TFB-TBOA 480439-73-4 TFB-TBOA chemical structure
  10. 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
  11. 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

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