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首页-抗体药物偶连体和PROTACs-E3 Ligase Ligand-GH501
GH501

Chemical Structure : GH501

CAS No.: 1333205-84-7

GH501 (GCBH-110)

货号: PC-24401Not For Human Use, Lab Use Only.

GH501 is a small molecule inhibitor of Skp1-Skp2 interaction, may bind Skp1 and disrupts the physical interaction between Skp1 and S-phase kinase-associated protein 2 (Skp2) within the Skp1-Cullin1-F-box protein ubiquitin ligase complexes (SCF).

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

    生物&药学活性

    GH501 is a small molecule inhibitor of Skp1-Skp2 interaction, may bind Skp1 and disrupts the physical interaction between Skp1 and S-phase kinase-associated protein 2 (Skp2) within the Skp1-Cullin1-F-box protein ubiquitin ligase complexes (SCF).
    GH501 affects multiple oncogenic signals in mCRPC cells, affects multiple oncogenic signals implicated in mCRPC progression, including p21, p27, β-catenin, cyclin D1, enhancer of zeste homolog 2 (EZH2), c-Myc, and survivin.
    GH501 monotherapy inhibits the in vivo growth of mCRPC in multiple xenograft models.

    物理化学性质&存储条件

    分子量 605.79
    分子式 C39H44FN3O2
    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

    (S)-3-([1,1'-biphenyl]-4-yl)-2-((R)-2-(2-fluoro-[1,1'-biphenyl]-4-yl)propanamido)-N-(2,2,6,6-tetramethylpiperidin-4-yl)propanamide

    参考文献

    1. Li X, et al. Br J Cancer. 2025 Apr 19. doi: 10.1038/s41416-025-02993-8.

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