PCI-29732

CAS No. 330786-25-9

PCI-29732( PCI29732 | PCI 29732 )

Catalog No. M14102 CAS No. 330786-25-9

A selective and irreversible Btk inhibitor with biochemical Ki of 8.2 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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2MG 43 In Stock
5MG 72 In Stock
10MG 115 In Stock
25MG 227 In Stock
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Biological Information

  • Product Name
    PCI-29732
  • Note
    Research use only, not for human use.
  • Brief Description
    A selective and irreversible Btk inhibitor with biochemical Ki of 8.2 nM.
  • Description
    A selective and irreversible Btk inhibitor with biochemical Ki of 8.2 nM; also inhibits Lck and Lyn with Ki of 4.6 and 2.5 nM.(In Vitro):PCI29732 shows cytotoxicity in different cells. The IC50 values are 7.94 μM for S1, 7.79 μM for S1-MI-80, 6.55 μM for H460, 6.34 μM for H460/MX20, 6.14 μM for KB, 6.02 μM for KBv200, 12.45 μM for HEK293/pcDNA3, 14.58 μM for HEK293-ABCG2-482-R2, and 13.24 μM for HEK293-ABCG2-482-T7 cells.PCI-29732 blocks the transcriptional up-regulation of a panel of B-cell activation genes in human CD20+ B cells stimulated at the B-cell antigen receptor (BCR).(In Vivo):PCI 29732 inhibits the function of ABCG2 by competitively binding to the ATP-binding site of ABCG2 and enhances the anti-tumor efficacy of substrate chemotherapeutic agents.PCI 29732 (20 mg/kg; p.o.; every 3 d × 5 times) enhances the anticancer efficacy of Topotecan in the H460/MX20 cell xenograft nude mice model.
  • In Vitro
    PCI29732 shows cytotoxicity in different cells. The IC50 values are 7.94 μM for S1, 7.79 μM for S1-MI-80, 6.55 μM for H460, 6.34 μM for H460/MX20, 6.14 μM for KB, 6.02 μM for KBv200, 12.45 μM for HEK293/pcDNA3, 14.58 μM for HEK293-ABCG2-482-R2, and 13.24 μM for HEK293-ABCG2-482-T7 cells.PCI-29732 blocks the transcriptional up-regulation of a panel of B-cell activation genes in human CD20+ B cells stimulated at the B-cell antigen receptor (BCR).
  • In Vivo
    PCI 29732 inhibits the function of ABCG2 by competitively binding to the ATP-binding site of ABCG2 and enhances the anti-tumor efficacy of substrate chemotherapeutic agents.PCI 29732 (20 mg/kg; p.o.; every 3 d × 5 times) enhances the anticancer efficacy of Topotecan in the H460/MX20 cell xenograft nude mice model. Animal Model:5-6 weeks old athymic nude mice (bearing H460/MX20 cells)Dosage:20 mg/kg (combination with Topotecan; every 3 d × 5 times, i.p., 3 mg/kg; topotecan was given 1 h after PCI29732 administration)Administration:P.o.; every 3 d × 5 times Result:Significant reductions in tumor weight and volume were observed in the group treated with PCI29732 in combination with Topotecan.
  • Synonyms
    PCI29732 | PCI 29732
  • Pathway
    Tyrosine Kinase
  • Target
    BTK
  • Recptor
    BTK|Itk
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    330786-25-9
  • Formula Weight
    371.435
  • Molecular Formula
    C22H21N5O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 53 mg/mL
  • SMILES
    NC1=C2C(N(C3CCCC3)N=C2C4=CC=C(OC5=CC=CC=C5)C=C4)=NC=N1
  • Chemical Name
    1H-Pyrazolo[3,4-d]pyrimidin-4-amine, 1-cyclopentyl-3-(4-phenoxyphenyl)-

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Pan Z, et al. ChemMedChem. 2007 Jan;2(1):58-61. 2. Honigberg LA, et al. Proc Natl Acad Sci U S A. 2010 Jul 20;107(29):13075-80.
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