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 86

  1. Cat.No. Product Name Information/Activity
  2. BCC3963 NVP-BHG712 NVP-BHG712 is an oral active EphB4 kinase autophosphorylation inhibitor, with IC50 values of 3.3 nM and 3.0 nM for EphA2 and EphB4, respectively. NVP-BHG712 chemical structure
  3. BCC6104 5'-Fluoroindirubinoxime 5'-Fluoroindirubinoxime (5’-FIO, compound 13), an Indirubin (HY-N0117) derivative, is a potent FLT3 inhibitor, with an IC50 of 15 nM. 5'-Fluoroindirubinoxime chemical structure
  4. BCC1183 TCS 359 TCS 359, a 2-acylaminothiophene-3-carboxamide, is a potent inhibitor of FLT3 with IC50 of 42 nM. TCS 359 chemical structure
  5. BCC1177 BMS-536924 BMS-536924 is an orally active, competitive and selective insulin-like growth factor receptor (IGF-1R) kinase and insulin receptor (IR) inhibitor with IC50s of 100 nM and 73 nM, respectively. BMS-536924 has anti-cancer activity. BMS-536924 chemical structure
  6. BCC4553 NVP-ADW742 NVP-ADW742 (ADW742) is an orally active, selective IGF-1R tyrosine kinase inhibitor with an IC50 of 0.17 μM. NVP-ADW742 inhibits insulin receptor (InsR) with an IC50 of 2.8 μM. NVP-ADW742 induces pleiotropic antiproliferative/proapoptotic biologic sequelae in tumor cells. NVP-ADW742 chemical structure
  7. BCC1388 Beta-Apopicropodophyllin Selective IGF1R inhibitor,Linsitinib (OSI-906) is a selective inhibitor of IGF-1R with IC50 of 35 nM in cell-free assays; modestly potent to InsR with IC50 of 75 nM, and no activity towards Abl, ALK, BTK, EGFR, FGFR1/2, PKA etc. Phase 3. Beta-Apopicropodophyllin chemical structure
  8. BCC1159 PQ 401 PQ401 is a potent inhibitor of IGF-IR signaling. PQ401 inhibits IGF-I-stimulated IGF-IR autophosphorylation with an IC50 of 12.0 μM in a series of studies in MCF-7 cells. PQ401 is effective at inhibiting IGF-I-stimulated growth of MCF-7 cells (IC50, 6 μM). PQ401 is a potential agent for breast and other IGF-I-sensitive cancers. PQ401 induces caspase-mediated apoptosis. PQ 401 chemical structure
  9. BCC7189 Demethylasterriquinone B1 78860-34-1 Demethylasterriquinone B1 chemical structure
  10. BCC7689 human Insulin expressed in yeast Insulin (human) is a polypeptide hormone that regulates the level of glucose. human Insulin expressed in yeast chemical structure
  11. BCC8021 HNGF6A 1093111-54-6 HNGF6A chemical structure

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