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首页-小分子抑制剂&激动剂-Epigenetics-Histone Methyltransferase (HMTase)-KMI169
KMI169

Chemical Structure : KMI169

CAS No.:

KMI169 (KMI-169, KMI 169)

货号: PC-21606Not For Human Use, Lab Use Only.

KMI169 (KMI-169) is a potent and selective lysine methyltransferase 9 (KMT9) inhibitor with ITC Kd of 25 nM and enzymatic IC50 of 50 nM.

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

    生物&药学活性

    KMI169 (KMI-169) is a potent and selective lysine methyltransferase 9 (KMT9) inhibitor with ITC Kd of 25 nM and enzymatic IC50 of 50 nM.
    KMI169 displays high selectivity for KMT9 against a large panel of SET domain- or Rossmann fold-containing methyltransferases as well as protein kinases.
    KMI169 dispalys a linear dependence upon increasing SAM or substrate concentrations corroborating a competitive inhibition mode.
    KMI169 demonstrates cell membrane permeability and cellular target engagement, impairs tumour cell proliferation with GI50 of 120 nM in PC-3M cells, as well as in other prostate, bladder, lung, and colon tumour cells.
    KMI169 also impairs proliferation of castration- and enzalutamide-resistant prostate cancer cell lines such as PC-3M, DU145, LNCaP-abl, and LNCaP-abl EnzaR.
    KMI169 affects expression of genes involved in cell cycle regulation, including MYB proto-oncogene (MYB), aurora kinase B (AURKB), forkhead box A2 (FOXA2), cyclin dependent kinase 2 (CDK2), baculoviral iap repeat containing 5 (BIRC5), E2F transcription factor 1 (E2F1), E2F transcription factor 8 (E2F8), cell division cycle 6 (CDC6), and DNA ligase 1 (LIG1).
    KMI169 is a suitable tool to study cellular KMT9 functions.

    物理化学性质&存储条件

    分子量 604.54
    分子式 C31H31Cl2N7O2
    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

    (1R,2S,3R,5R)-3-(4-amino-5-(1-benzyl-4-chloro-1H-pyrazol-3-yl)-2-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-5-(3-(azetidin-1-ylmethyl)phenyl)cyclopentane-1,2-diol

    参考文献

    1. Sheng Wang, et al. Nat Commun. 2024 Jan 2;15(1):43.

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