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首页-小分子抑制剂&激动剂-PI3K/Akt/mTOR Pathway-PI3K-LP-182
LP-182

Chemical Structure : LP-182

CAS No.: 2172343-43-8

LP-182 (LP182)

货号: PC-49266Not For Human Use, Lab Use Only.

LP-182 (LP182) is a potent, selective and orally bioavailable multi-functional kinase inhibitor, specifically targets PI3K and MAPK signaling pathways.

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

    生物&药学活性

    LP-182 (LP182) is a potent, selective and orally bioavailable multi-functional kinase inhibitor, specifically targets PI3K and MAPK signaling pathways.
    LP-182 displays >100-fold selectivity against a broad panel of 321 human protein kinases.
    LP-182 ameliorated of splenomegaly and fibrotic disease phenotypes, and extended overall survival in the myeloproliferative leukemia oncogene (MPL W515L) mouse model of myelofibrosis (MF).
    Oral treatment of MPLW515L mice with LP-182 also resulted in renormalization of blood cell populations and attenuation of downstream protein kinase B (PKB/AKT) and extracellular signalregulated protein kinase 1/2 (ERK1/2) signaling activity in bone marrow and isolated splenocytes.

    物理化学性质&存储条件

    分子量 1093.287
    分子式 C45H42ClF4IN8O8S
    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

    N-(2-(2-(2-(3-(4-(7-(6-chloro-5-((4-fluorophenyl)sulfonamido)pyridin-3-yl)quinoxalin-2-yl)piperazin-1-yl)-3-oxopropoxy)ethoxy)ethoxy)ethoxy)-3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)benzamide

    参考文献

    1. Brian D Ross, et al. Nat Commun. 2022 Aug 17;13(1):4730.

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