SWP-BX528
                        Yes
                        Customized
                        GMP, HSE, ISO 9001, USP, BP, SGS
                        Adult
                        Powder
                        >99%
                        Ibrutinib
                        White Powder
                        936563-96-1
                        C25h24n6o2
                        440.50
                        100g
                        HPLC
                        Available
                        Pharmaceutical Grade
                        2 Years
                        Cool and Dry Place
                        Sonwu
                        Vacuum Sealed Foil Bag
                        100g/bag
                        Shaanxi, China
                        
                        Product Description
                    
                                
| Product Name | Ibrutinib | 
| CAS | 936563-96-1 | 
| Formula | C25h24n6o2 | 
| MW | 440.50 | 
| Purity | 99% | 
| Appearance | White powder | 
| Shelf life | 2 years | 
| Storage | Cool and dry place | 
Ibrutinib is a highly selective Bruton's tyrosine kinase (Btk) irreversible inhibitor.PCI-32765 (Ibrutinib) is a selective and irreversible pyrrolopyrimidine-based inhibitor of BTK with IC50 of 0.5 nM. [1] PCI-32765 binds irreversibly to Cys-481 in BTK and thus is only active with other kinases with such a modifiable cysteine residue. In DOHH2 cells, in which the BCR pathway can be activated by anti-IgG, PCI-32765 inhibits autophosphorylation of BTK (IC50, 11 nM), BTK's physiological substrate, PLCg (IC50, 29 nm), and downstream ERK (IC50, 13 nm)


Ibrutinib is a kind of Bruton tyrosine kinase (BTK) inhibitor, it could be used for the chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL). MCL and CLL are belonged to the B-cell non-Hodgkin's lymphoma, which is difficult to easy to recurrent. Common chemical immunotherapy does not have the targeting, often occurs 3 or 4 adverse reactions. Ibrutinib and B lymphocytes could target with BTK which is necessary for formation, differentiation, and transmission of information, inhibit BTK activity irreversibly, and inhibit cell proliferation and survival effectively. Ibrutinib could be rapidly absorbed after oral administration, during 1~2h reach maximum blood concentration, adverse reactions belong to one or two, therefore, Ibrutinib will become a new choice for the CLL and MCL.| Similiar product recommendation | |||
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