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首页-小分子抑制剂&激动剂-Tyrosine Kinase-Syk-JTE-852
JTE-852

Chemical Structure : JTE-852

CAS No.: 909283-40-5

JTE-852 (JTE852)

货号: PC-63130Not For Human Use, Lab Use Only.

JTE-852 is a novel potent, selective, ATP-competitive Syk kinase inhibitor with IC50 of 1.25/1.28 nM for human/rat Syk, respectively.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

    生物&药学活性

    JTE-852 is a novel potent, selective, ATP-competitive Syk kinase inhibitor with IC50 of 1.25/1.28 nM for human/rat Syk, respectively.
    JTE-852 is less potent for Lck (IC50=80 nM), and has IC50 of >300 nM against a kinase panel screenings;.
    JTE-852 inhibits the kinase activity of Syk in an intracellular condition, suppresses the secretion of histamine, LTC4/D4/E4, TXA2, PGD2, and IL-13 from mast cells stimulated by IgE-crosslinking with IC50 of 40-100 nM.
    JTE-852 attenuates IgG-mediated responses and signs in animal model of autoimmune diseases.

    物理化学性质&存储条件

    分子量 437.562
    分子式 C23H27N5O2S
    外观性状 Solid
    CAS No.
    储存条件
    固体粉末
    -20 °C 12 个月; 4°C 6 个月
    配置液
    -80 °C 6 个月; -20°C 6 个月
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    2-methyl-2-(1-{5-[6-(4-methylpyridin-2-ylamino)pyridin-2-yl]thiazol-2-yl}piperidin-4-yl)propanoic acid

    参考文献

    1. Kato T, et al. Eur J Pharmacol. 2017 Apr 15;801:1-8.

    2. Kato T, et al. Life Sci. 2017 Dec 15;191:166-174.

    3. Kato T, et al. J Vet Med Sci. 2018 Jan 26. doi: 10.1292/jvms.17-0659.

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