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Fenebrutinib, MedChemExpress
Description
Fenebrutinib (GDC-0853) is a potent, selective, orally available, and noncovalent bruton's tyrosine kinase (Btk) inhibitor with Kis of 0.91 nM, 1.6, 1.3, 12.6, and 3.4 nM for WT Btk, and the C481S, C481R, T474I, T474M mutants. Fenebrutinib has the potential for rheumatoid arthritis and systemic lupus erythematosus research.
Specifications
Specifications
| Kemiskt namn eller material | Fenebrutinib |
| CAS | 1434048-34-6 |
| Färg | Off-White |
| Anteckningar om renhetsgrad | Research |
| Molekylformel | C37H44N8O4 |
| Kvantitet | 5 mg |
| Synonym | GDC-0853 |
| Löslighetsinformation | DMSO : ≥ 23 mg/mL (34.60 mM) |
| LEDER | O=C1C(NC(C=C2)=NC=C2N3CCN(C4COC4)C[C@@H]3C)=CC(C5=CC=NC(N6C(C7=CC(CC(C)(C)C8)=C8N7CC6)=O)=C5CO)=CN1C |
| Molekylvikt (g/mol) | 664.8 |
| Show More |
Research purposes only
Product Title
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