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 15

  1. Cat.No. Product Name Information/Activity
  2. BCN5499 Genistein Genistein, a soy isoflavone, is a multiple tyrosine kinases (e.g., EGFR) inhibitor which acts as a chemotherapeutic agent against different types of cancer, mainly by altering apoptosis, the cell cycle, and angiogenesis and inhibiting metastasis. Genistein chemical structure
  3. BCC7300 GW 583340 dihydrochloride 1173023-85-2 GW 583340 dihydrochloride chemical structure
  4. BCC7441 HDS 029 881001-19-0 HDS 029 chemical structure
  5. BCC6046 HKI 357 HKI-357 is an irreversible dual inhibitor of EGFR and ERBB2 with IC50s of 34 nM and 33 nM, respectively. HKI-357 suppresses EGFR autophosphorylation (at Y1068), and AKT and MAPK phosphorylation. HKI 357 chemical structure
  6. BCN2173 Gefitinib Gefitinib (ZD1839) is a potent, selective and orally active EGFR tyrosine kinase inhibitor with an IC50 of 33 nM. Gefitinib selectively inhibits EGF-stimulated tumor cell growth (IC50 of 54 nM) and that blocks EGF-stimulated EGFR autophosphorylation in tumor cells. Gefitinib also induces autophagy. Gefitinib has antitumour activity. Gefitinib chemical structure
  7. BCC7662 JNJ 28871063 hydrochloride 944342-90-9 JNJ 28871063 hydrochloride chemical structure
  8. BCN1808 Lavendustin A Lavendustin A (RG-14355), isolated from Streptomyces Griseolavendus, is a potent, specific and ATP-competitive inhibitor of tyrosine kinase, with an IC50 of 11 ng/mL for EGFR-associated tyrosine kinase. It suppresses VEGF-induced angiogenesis and blocks the induction of LTPGABA-A. Lavendustin A chemical structure
  9. BCC6702 Methyl 2,5-dihydroxycinnamate 63177-57-1 Methyl 2,5-dihydroxycinnamate chemical structure
  10. BCC7434 PD 158780 PD158780 is a potent EGFR family inhibitor with IC50s of 8 pM, 49, 52, 52 nM for EGFR, ErbB2, ErbB3, and ErbB4, respectively. PD 158780 chemical structure
  11. BCC7486 PP 3 5334-30-5 PP 3 chemical structure

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