Cancer Research

Cancer is a term used to define a group of diseases in which abnormal cells divide without control, are able to invade neighboring tissues/organs and metastasize. Cancer has been characterized by six hallmarks; self sufficiency in proliferative growth signals, insensitivity to growth inhibitors, evasion of apoptosis, limitless replicative potential, ability to develop blood vessels (angiogenesis), and tissue invasion and metastasis.

Cancer Research Products Areas

Products for Cancer Research - Page 96

  1. Cat.No. Product Name Information/Activity
  2. BCC6074 TCS 2002 1005201-24-0 TCS 2002 chemical structure
  3. BCC5817 2B-(SP) 186901-17-7 2B-(SP) chemical structure
  4. BCC5747 Phospho-Glycogen Synthase Peptide-2 (substrate) 851366-97-7 Phospho-Glycogen Synthase Peptide-2 (substrate) chemical structure
  5. BCC5899 TCS 184 1315378-71-2 TCS 184 chemical structure
  6. BCC1659 IRAK-1-4 Inhibitor I IRAK-1-4 Inhibitor I is an inhibitor of interleukin-1 receptor-associated kinase 1/4 (IRAK 1/4) with IC50s of 0.2 μM and 0.3 μM, respectively. IRAK-1-4 Inhibitor I chemical structure
  7. BCC1424 BMS-509744 BMS-509744 is a potent, selective and ATP competitive Itk inhibitor with an IC50 of 19 nM. BMS-509744 chemical structure
  8. BCN5539 Damnacanthal Damnacanthal is an anthraquinone isolated from the root of Morinda citrifolia. Damnacanthal is a highly potent, selective inhibitor of p56lck tyrosine kinase activity. Natural Damnacanthal inhibits p56 lck autophosphorylation and phosphorylation of exogenous substrates with IC50s of 46 nM and 220 nM, respectively. Damnacanthal is a potent inducer of apoptosis with anticancer activity. Damnacanthal also has antinociceptive, anti-inflammatory effects in mice and anti-fungal activity against Candida albicans. Damnacanthal chemical structure
  9. BCC7972 LIMKi 3 BMS-5 (LIMKi 3) is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, respectively. LIMKi 3 chemical structure
  10. BCC5617 T 5601640 T56-LIMKi is a selective inhibitor of LIMK2; inhibits the growth of Panc-1 cells with an IC50 of 35.2 μM. T 5601640 chemical structure
  11. BCC6218 CZC 54252 hydrochloride CZC-54252 is a potent inhibitor of LRRK2 with IC50s of 1.28 nM and 1.85 nM for wild-type and G2019S LRRK2 respectively. CZC 54252 hydrochloride chemical structure

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