(S)-Zanubrutinib

CAS No. 1691249-45-2

(S)-Zanubrutinib( S)-Zanubrutinib | BGB3111 | BGB 3111 )

Catalog No. M12579 CAS No. 1691249-45-2

(S)-Zanubrutinib (BGB3111)?is a potent, selective and orally available Btk inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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10MG 237 In Stock
25MG 537 In Stock
50MG 767 In Stock
100MG 1053 In Stock
500MG 2115 In Stock
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Biological Information

  • Product Name
    (S)-Zanubrutinib
  • Note
    Research use only, not for human use.
  • Brief Description
    (S)-Zanubrutinib (BGB3111)?is a potent, selective and orally available Btk inhibitor.
  • Description
    (S)-Zanubrutinib (BGB3111)?is a potent, selective and orally available Btk inhibitor; shows much more restricted off-target activities against a panel of kinases, including ITK, compared with Ibrutinib; demonstrates nanomolar BTK inhibition activity, inhibits BCR aggregation-triggered BTK autophosphorylation, blocks downstream PLC-γ2 signaling, and potently inhibits cell proliferation in several MCL and DLBCL cell lines; demonstrates better anti-tumor activity than ibrutinib in TMD-8 subcutaneous xenograft model.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    S)-Zanubrutinib | BGB3111 | BGB 3111
  • Pathway
    Tyrosine Kinase
  • Target
    BTK
  • Recptor
    BTK
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1691249-45-2
  • Formula Weight
    471.561
  • Molecular Formula
    C27H29N5O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 56.75 mg/mL 120.35 mM; Ethanol : < 1 mg/mL
  • SMILES
    C=CC(=O)N1CCC(CC1)C2CCNC3=C(C(=NN23)C4=CC=C(C=C4)OC5=CC=CC=C5)C(=O)N
  • Chemical Name
    (7S)-4,5,6,7-Tetrahydro-7-[1-(1-oxo-2-propen-1-yl)-4-piperidinyl]-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Shipping & Storage Information

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

Reference

1. Na Li, et al. Abstract 2597: BGB-3111 is a novel and highly selective Bruton's tyrosine kinase (BTK) inhibitor. AACR.
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