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| Product | Description | |
|---|---|---|
| Zanubrutinib | Zanubrutinib (BGB-3111) is a selective and orally active Bruton tyrosine kinase ( Btk ) inhibitor ( IC 50 : 0.3 nM) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BGB-3111. CAS No. 1691249-45-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101474A. |  |
| Zanubrutinib | Zanubrutinib. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1691249-45-2. Molecular formula: C27H29N5O3. Mole weight: 471.56. Catalog: APB1691249452. |  |
| Zanubrutinib Impurity 1 | Zanubrutinib Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1691249-44-1. Molecular formula: C27H24D5N5O4. Mole weight: 476.59. Catalog: APB1691249441. | |
| (±)-Zanubrutinib | (±)-Zanubrutinib ((±)-BGB-3111) is the racemate of Zanubrutinib (HY-101474A). (±)-Zanubrutinib inhibits Bruton's tyrosine kinase (Btk) with an IC 50 of 0.63 nM [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-BGB-3111. CAS No. 1633350-06-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-101474. | |
| (±)-Zanubrutinib | (±)-Zanubrutinib is a potent, selective and orally available Bruton's tyrosine kinase (Btk) inhibitor that demonstrates superior oral bioavailability, achieving higher exposure and more complete target inhibition in the tissues than ibrutinib. Uses: Antineoplastic agents. Synonyms: 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)-; 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; 7-(1-Acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxamide; DL-Zanubrutinib; (±)-BGB-3111. CAS No. 1633350-06-7. Molecular formula: C27H29N5O3. Mole weight: 471.55. |  |
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