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Products for Wnt/β-catenin

  1. Cat.No. Product Name Information
  2. BCC7790 Cardiogenol C hydrochloride Cardiogenol C hydrochloride is a potent cell-permeable pyrimidine inducer which prompts the differentiation of ESCs into cardiomyocytes (EC50=100 nM). Cardiogenol C hydrochloride also acts cardiomyogenic on already lineage-committed progenitor cell types with a limited degree of plasticity. Cardiogenol C hydrochloride is a useful cardiomyogenic agent and can be used as a tool to improve cardiac repair by cell transplantation therapy in animal models. Cardiogenol C hydrochloride
  3. BCC1573 FH535 FH535 is an inhibitor of Wnt/β-catenin and PPAR, with anti-tumor activities. FH535
  4. BCC3628 KY 02111 KY02111 is a small molecule which can promote differentiation of hPSCs to cardiomyocytes. KY 02111
  5. BCC5507 WAY-262611 WAY-262611 is a wingless β-Catenin agonist that increases bone formation rate with an EC50 of 0.63 μM in TCF-Luciferase assay. WAY-262611
  6. BCC5102 IWR-1-endo IWR-1 is a tankyrase inhibitor which inhibits Wnt/β-catenin signaling pathway. IWR-1-endo
  7. BCC7823 exo-IWR 1 exo-IWR 1
  8. BCC6099 IDE 2 IDE 2
  9. BCC7704 PNU 74654 PNU-74654 is an inhibitor of Wnt/β-catenin pathway with an IC50 of 129.8 μM in NCI-H295 cell. PNU 74654
  10. BCC7841 IDE 1 IDE1 is an inducer of definitive endoderm 1. IDE 1
  11. BCC7798 TCS 2210 TCS 2210
  12. BCC6258 CCT 031374 hydrobromide CCT 031374 hydrobromide
  13. BCC3965 Wnt-C59 Wnt-C59 (C59) is a highly potent and oral porcupine (PORCN) inhibitor with an IC50 of 74 pM. Wnt-C59
  14. BCC5103 LGK-974 LGK974 (WNT974) is an orally bioavailable and specific Porcupine (PORCN) inhibitor with an IC50 of 0.1 nM. LGK-974
  15. BCC5101 IWP-L6 IWP L6 (Porcn Inhibitor III) is a Porcn inhibitor with an EC50 of 0.5 nM. IWP-L6
  16. BCC6487 CCT251545 CCT251545 is an orally bioavailable and potent inhibitor of WNT signaling with an IC50 of 5 nM in 7dF3 cells. CCT251545
  17. BCC6486 Windorphen Windorphen
  18. BCC6334 Shz 1 Shz 1
  19. BCC7965 IQ 1 IQ 1 has many functions such as decreasing Wnt-stimulated phosphorylation, maintaining the pluripotency of murine ESCs, preventing PP2A/Nkd interaction and so on. IQ 1
  20. BCC6251 JW 67 JW 67
  21. BCC6211 Kartogenin Kartogenin is an inducer of differentiation of human mesenchymal stem cells into chondrocytes. Kartogenin
  22. BCC1916 Salinomycin Salinomycin (Procoxacin), a polyether potassium ionophore antibiotic, selectively inhibits the growth of gram-positive bacteria. Salinomycin is a potent inhibitor of Wnt/β-catenin signaling, blocks Wnt-induced LRP6 phosphorylation. Salinomycin (Procoxacin) shows selective activity against human cancer stem cells. Salinomycin
  23. BCC6199 Cardionogen 1 Cardionogen 1
  24. BCC5401 iCRT 14 iCRT 14 is a novel potent inhibitor of β-catenin-responsive transcription (CRT), with IC50 of 40.3 nM against Wnt responsive STF16 luciferase. iCRT 14
  25. BCC1665 IWP-2 IWP-2 is an inhibitor of Wnt processing and secretion with an IC50 of 27 nM. IWP-2 targets the membrane-bound O-acyltransferase porcupine (Porcn) and thus preventing a crucial Wnt ligand palmitoylation. IWP-2 is also an ATP-competitive CK1δ inhibitor with an IC50 of 40 nM for the gatekeeper mutant M82FCK1δ. IWP-2
  26. BCC5602 IWP 4 IWP-4 is a small molecule Wnt inhibitor with an IC50 of 25 nM. IWP 4
  27. BCC6181 ISX 9 ISX-9 is a small molecule inducer of adult neural stem cell differentiation. ISX 9
  28. BCC3632 ICG 001 ICG-001 antagonizes Wnt/β-catenin/TCF-mediated transcription and specifically binds to CREB-binding protein (CBP) with IC50 of 3 μM, but is not the related transcriptional coactivator p300. ICG 001
  29. BCC7738 Neurodazine Neurodazine is an imidazole-based small molecule, serve as a promoter of neurogenesisin pluripotent cells. Neurodazine promotes neurogenesis by activating Wnt and Shh signaling pathways. Neurodazine selectively suppresses astrocyte differentiation of P19 cells. Neurodazine
  30. BCC7648 QS 11 ARFGAP1 inhibitor; modulates Wnt signaling pathway,QS11 is a GTPase activating protein of ADP-ribosylation factor 1 (ARFGAP1) inhibitor. QS 11

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