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 32

  1. Cat.No. Product Name Information/Activity
  2. BCC7867 Salermide Salermide is an inhibitor of Sirt1 and Sirt2; can cause strong cancer-specific apoptotic cell death. Salermide chemical structure
  3. BCC6513 SirReal2 SirReal2 is a potent, isotype-selective Sirt2 inhibitor with an IC50 value of 140 nM and has very little effect on the activities of Sirt3-5. SirReal2 leads to tubulin hyperacetylation in HeLa cells and induces destabilization of the checkpoint protein BubR1. SirReal2 chemical structure
  4. BCC2224 Sirtinol Sirtinol is a sirtuin (SIRT) inhibitor, with IC50s of 48 μM, 57.7 μM and 131 μM for ySir2, hSIRT2 and hSIRT2, respectively. Sirtinol chemical structure
  5. BCC3652 Splitomicin Splitomicin (Splitomycin) is a selective Sir2p inhibitor. Splitomicin inhibits NAD+-dependent HDAC activity of Sir2 protein. Splitomicin induces dose-dependent inhibition of HDAC in the yeast extract with an IC50 of 60 μM. Splitomicin chemical structure
  6. BCC5033 Amitriptyline HCl Amitriptyline hydrochloride is a dibenzocycloheptene-derivative tricyclic antidepressant (TCA). Amitriptyline HCl chemical structure
  7. BCC5944 BDNF (human) 218441-99-7 BDNF (human) chemical structure
  8. BCC6072 7,8-Dihydroxyflavone 7,8-Dihydroxyflavone is a potent and selective TrkB agonist that mimics the physiological actions of Brain-derived neurotrophic factor (BDNF). Displays therapeutic efficacy toward various neurological diseases. 7,8-Dihydroxyflavone chemical structure
  9. BCC6239 LM 22A4 LM22A-4 is a specific agonist of tyrosine kinase receptor B, used for neurological disease research. LM 22A4 chemical structure
  10. BCC6287 ANA 12 ANA-12 is a potent and selective TrkB antagonist with IC50s of 45.6 nM and 41.1 μM for the high and low affinity sites, respectively. ANA 12 chemical structure
  11. BCC6357 Cyclotraxin B 1203586-72-4 Cyclotraxin B chemical structure

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