ONO4057

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Reagent Code: #62105
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CAS Number 134578-96-4

science Other reagents with same CAS 134578-96-4

blur_circular Chemical Specifications

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Weight 470.55 g/mol
Formula C₂₇H₃₄O₇
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

ONO-4057 (also known as Tirabrutinib) is a potent, selective, covalent inhibitor of Bruton's Tyrosine Kinase (BTK), a critical enzyme in B-cell receptor (BCR) signaling pathways. It is primarily used in medical research for investigating B-cell malignancies such as lymphomas, autoimmune diseases, and inflammatory disorders. By irreversibly binding to BTK, it disrupts aberrant signaling, aiding in the study of disease mechanisms and preclinical evaluation of targeted therapies. Its high specificity makes it a valuable tool in drug development for precision immunomodulation.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿192,000.00
inventory 5mg
10-20 days ฿480,000.00

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ONO4057
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ONO-4057 (also known as Tirabrutinib) is a potent, selective, covalent inhibitor of Bruton's Tyrosine Kinase (BTK), a critical enzyme in B-cell receptor (BCR) signaling pathways. It is primarily used in medical research for investigating B-cell malignancies such as lymphomas, autoimmune diseases, and inflammatory disorders. By irreversibly binding to BTK, it disrupts aberrant signaling, aiding in the study of disease mechanisms and preclinical evaluation of targeted therapies. Its high specificity makes

ONO-4057 (also known as Tirabrutinib) is a potent, selective, covalent inhibitor of Bruton's Tyrosine Kinase (BTK), a critical enzyme in B-cell receptor (BCR) signaling pathways. It is primarily used in medical research for investigating B-cell malignancies such as lymphomas, autoimmune diseases, and inflammatory disorders. By irreversibly binding to BTK, it disrupts aberrant signaling, aiding in the study of disease mechanisms and preclinical evaluation of targeted therapies. Its high specificity makes it a valuable tool in drug development for precision immunomodulation.

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