Huntington's Disease Research

Huntington's disease is a neurodegenerative disease characterized by cognitive decline and motor dysfunction. It is a genetic disorder which results in the production of mutant huntingtin protein (mHtt). This protein aggregates in the cell cytoplasm and nucleus, affecting cellular function.

Huntington's Disease Research Products Targets

Products for Huntington's Disease Research - Page 20

  1. Cat.No. Product Name Information/Activity
  2. BCC6978 2-APB 2-Aminoethyl diphenylborinate (2-APB) is a cell-permeable inhibitor of IP3R. 2-Aminoethyl diphenylborinate also inhibits the store-operated Ca2+ (SOC) channel and activates some TRP channels (V1, V2 and V3). 2-APB chemical structure
  3. BCC7002 (-)-Xestospongin C 88903-69-9 (-)-Xestospongin C chemical structure
  4. BCC6940 ATPA ATPA is a selective glutamate receptor GluR5 activator with EC50s of 0.66, 9.5, 1.4, 23, 32, 18, and 14 μM for GluR5wt, GluR5(S741M), GluR5(S721T), GluR5(S721T, S741M), GluR5(S741A), GluR5(S741L), and GluR5(S741V), respectively. ATPA chemical structure
  5. BCC6586 Domoic acid 14277-97-5 Domoic acid chemical structure
  6. BCC6597 (S)-(-)-5-Iodowillardiine 140187-25-3 (S)-(-)-5-Iodowillardiine chemical structure
  7. BCC6572 Kainic acid Kainic acid is a potent agonist at excitatory amino acid receptor subtypes in the CNS. Kainic acid chemical structure
  8. BCC7297 MNI caged kainic acid 1315378-75-6 MNI caged kainic acid chemical structure
  9. BCC7462 ACET 936095-50-0 ACET chemical structure
  10. BCC6569 CNQX CNQX (FG9065) is a potent AMPA/kainate receptor antagonist. CNQX chemical structure
  11. BCC6908 CNQX disodium salt 479347-85-8 CNQX disodium salt chemical structure

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