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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-Ras-SRJ23
SRJ23

Chemical Structure : SRJ23

CAS No.: 908130-69-8

SRJ23 (SRJ-23, SRJ 23)

货号: PC-70353Not For Human Use, Lab Use Only.

SRJ23 is a semisynthetic derivative of andrographolide that directly target Ras to block the exchange of GDP for GTP and thus prevent Ras activation.

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

    生物&药学活性

    SRJ23 is a semisynthetic derivative of andrographolide that directly target Ras to block the exchange of GDP for GTP and thus prevent Ras activation.
    SRJ23 significantly suppresses K-Ras GTP loading, whereas H-Ras and N-Ras GTP loading are much less sensitive.
    SRJ23 reduceds K-RasG12V GTP, phosphorylated ERK (ppERK) levels in K-RasG12V-transformed cells.
    SRJ23 induces G1 arrest and apoptosis in MCF-7 and HCT-116 cells, respectively.

    物理化学性质&存储条件

    分子量 491.00
    分子式 C27H32ClFO5
    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(3H)-Furanone, 3-[2-[(4aR,6aS,7R,10aS,10bR)-3-(3-chloro-4-fluorophenyl)decahydro-6a,10b-dimethyl-8-methylene-1H-naphtho[2,1-d][1,3]dioxin-7-yl]ethylidene]dihydro-4-hydroxy-, (3E,4S)-

    参考文献

    1. Hocker HJ, et al. Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):10201-6.

    2. Jada SR, et al. Br J Pharmacol. 2008 Nov;155(5):641-54.

    3. Wong HC, et al. Cell Biol Toxicol. 2014 Oct;30(5):269-88.

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