Cell Cycle Inhibitor

Cell cycle inhibitors slow or stop cell cycle progression through various mechanisms. Cell cycle arrest can be induced at different stages, decreasing the rate of cell division and the number of actively cycling cells.

Products for Cell Cycle Inhibitor

  1. Cat.No. Product Name Information/Activity
  2. BCC4914 Itraconazole Itraconazole (R51211) is a triazole antifungal agent and a potent and orally active Hedgehog (Hh) signaling pathway antagonist with an IC50 of ~800 nM. Itraconazole potently inhibits lanosterol 14α-demethylase (cytochrome P450 enzyme), thereby inhibits the oxidative conversion of lanosterol to ergosterol. Itraconazole has anticancer and antiangiogenic effects. Itraconazole chemical structure
  3. BCC1050 10058-F4 10058-F4 is a c-Myc inhibitor that prevents c-Myc-Max dimerization and transactivation of c-Myc target gene expression. 10058-F4 chemical structure
  4. BCC1085 ABT-751 (E7010) ABT-751(E 7010) is a novel bioavailable tubulin-binding and antimitotic sulfonamide agent with IC50 of about 1.5 and 3.4 μM in neuroblastoma and non-neuroblastoma cell lines, respectively. ABT-751 (E7010) chemical structure
  5. BCC3689 AZD-5438 AZD-5438 is a potent CDK1, CDK2, and CDK9 inhibitor, with IC50s of 16 nM, 6 nM, and 20 nM in cell-free assays, respectively. AZD-5438 shows less inhibition activity against GSK3β, CDK5 and CDK6 . AZD-5438 chemical structure
  6. BCN5599 Baicalein Baicalein (5,6,7-Trihydroxyflavone) is a xanthine oxidase inhibitor with an IC50 value of 3.12 mM. Baicalein chemical structure
  7. BCC8017 CFM 4 331458-02-7 CFM 4 chemical structure
  8. BCC7935 8-Chloroadenosine 34408-14-5 8-Chloroadenosine chemical structure
  9. BCC4099 CPI-203 CPI-203 is a novel potent, selective and cell permeable inhibitor of BET bromodomain, with an IC50 value of appr 37 nM (BRD4 α-screen assay). CPI-203 chemical structure
  10. BCN5590 Daidzein Daidzein is a soy isoflavone, which acts as a PPAR activator. Daidzein chemical structure
  11. BCC1306 3,3'-Diindolylmethane 3,3'-Diindolylmethane is a strong, pure androgen receptor (AR) antagonist. 3,3'-Diindolylmethane chemical structure

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