Products for BTK

  1. Cat.No. Product Name Information
  2. BCC5125 Btk inhibitor 1 R enantiomer IBT6A is an impurity of Ibrutinib. IBT6A can be used in synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a selective, irreversible Btk inhibitor with an IC50 of 0.5 nM. Btk inhibitor 1 R enantiomer
  3. BCC1385 AVL-292 Spebrutinib (AVL-292; CC-292) is a covalent, orally active, and highly selective with an IC50 of 0.5 nM. AVL-292
  4. BCC4394 CNX-774 CNX-774 is a potent, selective, and orally available small molecule inhibitor of Btk (IC50< 1 nM) that forms a ligand-directed covalent bond with Cys-481, a non-conserved amino acid within the active site of the enzyme. CNX-774
  5. BCC3921 RN486 RN486 is a selective Btk inhibitor with an IC50 Value of 4.0 nM. RN486
  6. BCC6463 ONO-4059 ONO-4059 analog is the analog of ONO-4059, ONO-4059 is a highly potent and selective Btk inhibitor. ONO-4059
  7. BCC4238 Btk inhibitor 1 (Rac)-IBT6A is a racemate of IBT6A. IBT6A is an impurity of Ibrutinib. IBT6A can be used in synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is a selective, irreversible Btk inhibitor with an IC50 of 0.5 nM. Btk inhibitor 1
  8. BCC3920 QL47 QL47 is a potent, selective and irreversible BTK kinase inhibitor with IC50 of 7 nM. QL47
  9. BCC6472 LFM-A13 LFM-A13 is a potent BTK, JAK2, PLK inhibitor, inhibits recombinant BTK, Plx1 and PLK3 with IC50s of 2.5 μM, 10 μM and 61 μM; LFM-A13 shows no effects on JAK1 and JAK3, Src family kinase HCK, EGFR and IRK. LFM-A13
  10. BCC4100 PCI 29732 PCI 29732 is a selective and irreversible Btk inhibitor with IC50 of 8.2 nM in a FRET based biochemical enzymology assay. PCI 29732
  11. BCC1473 CGI-1746 CGI-1746 is a potent and highly selective inhibitor of the Btk with IC50 of 1.9 nM. CGI-1746
  12. BCC5124 PCI-32765 Racemate Ibrutinib Racemate (PCI-32765 Racemate) is the racemate of Ibrutinib. Ibrutinib is a selective, irreversible Btk inhibitor with IC50 value of 0.5 nM. PCI-32765 Racemate
  13. BCC1266 PCI-32765 (Ibrutinib) Ibrutinib (PCI-32765) is a selective, irreversible Btk inhibitor with an IC50 of 0.5 nM. Ibrutinib can be used as a Btk ligand in the synthesis of a series of PROTACs, such as P13I. P13I induces 73% degradation of Btk at 10 nM and 89% at 100 nM in human Burkitt’s lymphoma, RAMOS cells. PCI-32765 (Ibrutinib)

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