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 93

  1. Cat.No. Product Name Information/Activity
  2. BCC4001 NH125 NH125 is a potent and selective inhibitor of eukaryotic elongation factor 2 kinase (eEF-2K/CaMKIII), also can induce eEF2 phosphorylation, with an IC50 of 60 nM for eEF-2K. NH125 chemical structure
  3. BCC7112 STO-609 acetate 1173022-21-3 STO-609 acetate chemical structure
  4. BCC5614 CKI 7 dihydrochloride 1177141-67-1 CKI 7 dihydrochloride chemical structure
  5. BCC4246 LH846 LH846 is a selective inhibitor of CKIδ, with an IC50 of 290 nM, and less potently inhibits CKIα and CKIε, with IC50s of 2.5 μM and 1.3 μM, respectively. LH846 chemical structure
  6. BCC7904 PF 4800567 hydrochloride 1391052-28-0 PF 4800567 hydrochloride chemical structure
  7. BCC1856 PF-670462 PF-670462 is a potent and selective inhibitor of casein kinase (CK1ε and CK1δ), with IC50s of 7.7 nM and 14 nM, respectively. PF-670462 chemical structure
  8. BCC3968 TAK-715 TAK-715 is a p38 MAPK inhibitor for p38α with IC50 of 7.1 nM, 28-fold more selective for p38α over p38β, no inhibition to p38γ/δ, JNK1, ERK1, IKKβ, MEKK1 or TAK1. TAK-715 chemical structure
  9. BCC1988 TBB TBB is a cell-permeable and ATP-competitive CK2 inhibitor with an IC50 of 0.15 μM for rat liver CK2. TBB chemical structure
  10. BCC7745 TMCB 905105-89-7 TMCB chemical structure
  11. BCC2017 TTP 22 TTP 22 is a potent CK2 inhibitor, with an IC50 of 100 nM and a Ki of 40 nM. TTP 22 chemical structure

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