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 195

  1. Cat.No. Product Name Information/Activity
  2. BCC7760 K858 K858 Racemic is an ATP-uncompetitive inhibitor of kinesin Eg5 with an IC50 of 1.3 μM. K858 chemical structure
  3. BCC7978 Paprotrain Paprotrain is a cell-permeable inhibitor of the kinesin MKLP-2, inhibits the ATPase activity of MKLP-2 with an IC50 of 1.35 μM and a Ki of 3.36 μM and shows a moderate inhibition activity on DYRK1A with an IC50 of 5.5 μM. Paprotrain chemical structure
  4. BCC4559 SB743921 SB-743921 is a potent inhibitor of the mitotic kinesin KSP (Eg5), with a Ki of 0.1 nM. SB743921 chemical structure
  5. BCC2911 H-Cys(Trt)-OH 2799-07-7 H-Cys(Trt)-OH chemical structure
  6. BCC4375 (-)-Blebbistatin (-)-Blebbistatin is a selective inhibitor of the ATPase activity of non-muscle myosin II. (-)-Blebbistatin chemical structure
  7. BCC7195 (R)-(+)-Blebbistatin (+)-Blebbistatin is the inactive enantiomer of (–)-Blebbistatin. (–)-Blebbistatin is a selective inhibitor of myosin II ATPase. (R)-(+)-Blebbistatin chemical structure
  8. BCC7169 (±)-Blebbistatin Blebbistatin is a selective non-muscle myosin II (NMII) inhibitor, promotes directional migration of corneal endothelial cells (CECs) and accelerates wound healing, and better preserves cell junctional integrity and barrier function. (±)-Blebbistatin chemical structure
  9. BCC5425 BTS BTS is a potent inhibitor of Ca2+-stimulated myosin S1 ATPase (IC50 ~ 5 μM) and reversibly blocks the gliding motility. BTS chemical structure
  10. BCC3987 ML 239 ML239 is a potent and selective inhibitor of breast cancer stem cells, with an IC50 of 1.16 μM. ML 239 chemical structure
  11. BCC7880 SC 26196 SC-26196 is a potent, orally active Delta6 desaturase (D6D) inhibitor (IC50=0.2 µM in a rat liver microsomal assay). Antiinflammatory properties. SC 26196 chemical structure

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