Epilepsy Research

Epilepsy is a group of neurological conditions consisting of recurrent, usually unprovoked epileptic seizures. Epileptic seizures have recently been defined as "a transient occurrence of signs and/or symptoms due to abnormal, excessive or synchronous neuronal activity in the brain". Epilepsy is one of the most common disorders of the brain, with one in 10 people suffering at least one seizure in their lifetime. There are over 40 different types of epilepsy, each of which presents with its own unique combination of seizure type, typical age of onset, EEG findings, treatment, and prognosis.

Epilepsy Research Products Targets

Products for Epilepsy Research - Page 7

  1. Cat.No. Product Name Information/Activity
  2. BCC6078 (E)-FeCP-oxindole 884338-18-5 (E)-FeCP-oxindole chemical structure
  3. BCC6079 (Z)-FeCP-oxindole 1137967-28-2 (Z)-FeCP-oxindole chemical structure
  4. BCC1116 Ki8751 Ki8751 is a potent VEGFR2 inhibitor with an IC50 of 0.9 nM. Ki8751 chemical structure
  5. BCC7073 SU 4312 5812-07-7 SU 4312 chemical structure
  6. BCC1974 SU5416 Semaxinib (SU5416) is a potent and selective inhibitor of VEGFR (Flk-1/KDR) with an IC50 of 1.23 μM. SU5416 chemical structure
  7. BCC3664 Sunitinib malate Sunitinib Malate (SU 11248 Malate) is a multi-targeted receptor tyrosine kinase inhibitor with IC50s of 80 nM and 2 nM for VEGFR2 and PDGFRβ, respectively. Sunitinib Malate, an ATP-competitive inhibitor, effectively inhibits autophosphorylation of Ire1α by inhibiting autophosphorylation and consequent RNase activation. Sunitinib malate chemical structure
  8. BCC2005 Toceranib Toceranib phosphate (SU11654 phosphate) is an orally active receptor tyrosine kinase (RTK) inhibitor, and it potently inhibits PDGFR, VEGFR, and Kit with Kis of 5 and 6 nM for PDGFRβ and Flk-1/KDR, respectively. Toceranib phosphate (SU11654 phosphate) has antitumor and antiangiogenic activity, and used in the treatment of canine mast cell tumors. Toceranib chemical structure
  9. BCC1264 Cabozantinib (XL184, BMS-907351) Cabozantinib is a potent multiple receptor tyrosine kinases (RTKs) inhibitor that inhibits VEGFR2, c-Met, Kit, Axl and Flt3 with IC50s of 0.035, 1.3, 4.6, 7 and 11.3 nM, respectively. Cabozantinib (XL184, BMS-907351) chemical structure
  10. BCC5098 ZM 323881 HCl ZM323881 hydrochloride is a potent and selective VEGFR2 inhibitor with an IC50 of less than 2 nM. ZM 323881 HCl chemical structure
  11. 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

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