Chemical Structure : BAY 61-3606 dihydrochloride
CAS No.: 648903-57-5
货号: 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.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥1280 | In stock | |
10 mg | ¥1880 | In stock | |
25 mg | ¥3280 | In stock | |
50 mg | ¥5280 | In stock | |
100 mg | Get quote |
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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.
分子量 | 463.3172 | |
分子式 | C20H20Cl2N6O3 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: ≥ 4.6 mg/mL |
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Chemical Name/SMILES |
3-Pyridinecarboxamide, 2-[[7-(3,4-dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-yl]amino]-, hydrochloride (1:2) |
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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