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BAY 61-3606 dihydrochloride

Chemical Structure : BAY 61-3606 dihydrochloride

CAS No.: 648903-57-5

BAY 61-3606 dihydrochloride (BAY61-3606 dihydrochloride;BAY 61-3606)

Catalog No.: PC-44143Not For Human Use, Lab Use Only.

BAY 61-3606 dihydrochloride is a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase with Ki of 7.5 nM, displays no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

BAY 61-3606 dihydrochloride is a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase with Ki of 7.5 nM, displays no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
BAY 61-3606 inhibits not only degranulation (IC50=5-46 nM) but also lipid mediator and cytokine synthesis in mast cells.
BAY 61-3606 suppresses B cell receptor activation and receptors for Fc portion of IgG signaling in eosinophils and monocytes.
BAY 61-3606 suppresses antigen-induced passive cutaneous anaphylactic reaction, bronchoconstriction, and bronchial edema at 3 mg/kg in rats; orally bioavailable.

Physicochemical Properties

M.Wt 463.3172
Formula C20H20Cl2N6O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 4.6 mg/mL

Chemical Name/SMILES

3-Pyridinecarboxamide, 2-[[7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-yl]amino]-, hydrochloride (1:2)

References

1. Yamamoto N, et al. J Pharmacol Exp Ther. 2003 Sep;306(3):1174-81.

2. Tabeling C, et al. Allergy. 2017 Jul;72(7):1061-1072.

3. Perova T, et al. Sci Transl Med. 2014 May 14;6(236):236ra62.

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