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(±)-Zanubrutinib

Chemical Structure : (±)-Zanubrutinib

CAS No.: 1633350-06-7

(±)-Zanubrutinib ((±)-BGB-3111;(±)-BGB 3111;(±)-BGB3111)

Catalog No.: PC-42396Not For Human Use, Lab Use Only.

The active enantiomer of Zanubrutinib, a potent, selective and orally available Btk inhibitor.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

The active enantiomer of Zanubrutinib (BGB3111), 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.

Blood Cancer

Phase 3 Clinical

Physicochemical Properties

M.Wt 471.55086
Formula C27H29N5O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Pyrazolo[1,5-a]pyrimidine-3-carboxamide, 4,5,6,7-tetrahydro-7-[1-(1-oxo-2-propen-1-yl)-4-piperidinyl]-2-(4-phenoxyphenyl)-

References

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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