3027617-37-1

Zanubrutinib-d<sub>5</sub> Chemical Structure
3027617-37-1

Chemical Structure

Zanubrutinib-d5

Synonym(s): BGB-3111-d5

  • CAS No.: 3027617-37-1
  • Formula:C27H24D5N5O3
  • Molecular Weight:476.58

IUPAC Name: (S)-7-(1-acryloylpiperidin-4-yl)-2-(4-(phenoxy-d5)phenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide

InChIKey: RNOAOAWBMHREKO-LRUCMAMWSA-N

SMILES: NC(C1=C2N(N=C1C3=CC=C(OC4=C([2H])C([2H])=C([2H])C([2H])=C4[2H])C=C3)[C@H](C5CCN(C(C=C)=O)CC5)CCN2)=O

Biological Activity: Zanubrutinib-d5 is deuterium labeled Zanubrutinib. Zanubrutinib is a selective Bruton tyrosine kinase (Btk) inhibitor[1].

Cat. No. Product Name Purity Description Pricing
HY-101474S
Zanubrutinib-d5 99.0% Zanubrutinib-d5 is deuterium labeled Zanubrutinib. Zanubrutinib is a selective Bruton tyrosine kinase (Btk) inhibitor.
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HY-101474R
(±)-Zanubrutinib (Standard) ≥98% (±)-Zanubrutinib (Standard) is the analytical standard of (±)-Zanubrutinib (HY-101474). This product is intended for research and analytical applications. (±)-Zanubrutinib ((±)-BGB-3111) is the racemate of Zanubrutinib (HY-101474A). (±)-Zanubrutinib inhibits Bruton's tyrosine kinase (Btk) with an IC50 of 0.63 nM.
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HY-101474
(±)-Zanubrutinib 99.41% (±)-Zanubrutinib ((±)-BGB-3111) is the racemate of Zanubrutinib (HY-101474A). (±)-Zanubrutinib inhibits Bruton's tyrosine kinase (Btk) with an IC50 of 0.63 nM.
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References