1. Epigenetics
  2. Histone Demethylase
  3. CBB1007 hydrochloride

CBB1007 hydrochloride 

目录号: HY-15313B 纯度: ≥98.0%
COA 产品使用指南 技术支持

CBB1007 hydrochloride 是一种可逆、选择性的 LSD1 抑制剂,对人 LSD1 的 IC50 为 5.27 µM。CBB1007 hydrochloride 可显著抑制 LSD1 对 H3K4Me2 和 H3K4Me 的去甲基化酶活性。CBB1007 hydrochloride 对 LSD1 的选择性高于 LSD2 或 JARID1A,并可诱导多能细胞中的分化相关基因。CBB1007 hydrochloride 目前已在非多能性癌症研究中开展研究,靶向畸胎癌、胚胎癌和精原瘤。

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CBB1007 hydrochloride

CBB1007 hydrochloride Chemical Structure

CAS No. : 2070014-96-7

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CBB1007 hydrochloride 的其他形式现货产品:

Other Forms of CBB1007 hydrochloride:

MCE 顾客使用本产品发表的 1 篇科研文献

WB

    CBB1007 hydrochloride purchased from MCE. Usage Cited in: BMC Neurosci. 2022 Nov 10;23(1):63.  [Abstract]

    CBB1007 (CBB) elevates H3K4me2 expression in RGC-5 cells, after which miR-21-5p expression levels are increased .

    查看 Histone Demethylase 亚型特异性产品:

    • 生物活性

    • 纯度 & 产品资料

    • 参考文献

    生物活性

    CBB1007 hydrochloride is a reversible and selective LSD1 inhibitor with an IC50 of 5.27 µM for human LSD1. CBB1007 hydrochloride significantly blocks the demethylase activity of LSD1 on H3K4Me2 and H3K4Me. CBB1007 hydrochloride shows selectivity for LSD1 over LSD2 or JARID1A, and induces differentiation-related genes in pluripotent cells. CBB1007 hydrochloride is studied in  non-pluripotent cancer research, targeting teratocarcinoma, embryonic carcinoma, and seminoma[1][2].

    IC50 & Target[2]

    KDM1/LSD1

    5.27 μM (IC50)

    体外研究
    (In Vitro)

    CBB1007(0-100 μM;30 小时;F9) hydrochloride 抑制 F9 细胞生长[2]
    CBB1007 (5-20 μM;;14 天;hESCs) hydrochloride 在脂肪分化过程中增加 hESCs 中的脂滴形成[1]
    CBB1007 (5-20 μM;14 天;hESCs) hydrochloride 可降低人胚胎干细胞 (hESC) 中的 LSD1 和组蛋白 H3 水平,同时增加 H3K4me2 水平[1]
    CBB1007 (5-20 μM;14 天;hESC) hydrochloride 可上调 hESC 中的脂肪细胞标志基因 PPARγ-2 和 C/EBPα[1]
    CBB1007 (0.5-20 μM;24 小时; F9) hydrochloride 激活 CHRM4 和 SCN3A 基因的表达[1]
    CBB1007 (10 μM) hydrochloride 可显著抑制 LSD1 对单甲基化和二甲基化 H3K4 的去甲基化酶活性,但对三甲基化 H3K4 或二甲基化 H3K9 的去甲基化酶活性无效[2]

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    Cell Proliferation Assay[2]

    Cell Line: F9 cell
    Concentration: 1 μM, 5 μM, 10 μM, 50 μM, 100 μM
    Incubation Time: 30 h
    Result: Cell growth was significantly inhibited.

    Cell Differentiation Assay[1]

    Cell Line: hESCs
    Concentration: 5 μM, 10 μM, 20 μM
    Incubation Time: 14 days
    Result: Lipid droplet density increased, and droplets fused due to high density.

    Western Blot Analysis[1]

    Cell Line: hESCs
    Concentration: 5 μM, 10 μM, 20 μM
    Incubation Time: 14 days
    Result: LSD1 and histone H3 expression decreased, while H3K4me2 levels increased with higher doses.

    Real Time qPCR[1]

    Cell Line: hESCs
    Concentration: 5 μM, 10 μM, 20 μM
    Incubation Time: 14 days
    Result: PPARγ-2 and C/EBPα expression increased with increasing doses.

    Real Time qPCR[2]

    Cell Line: F9
    Concentration: 0.5 μM, 1 μM, 5 μM, 20 μM
    Incubation Time: 24 h
    Result: The expression of CHRM4 and SCN3A genes were activated. And markedly induced the expression of genes for differentiation, such as FOXA2.
    分子量

    716.91

    Formula

    C27H39Cl5N8O4

    CAS 号
    性状

    固体

    颜色

    White to off-white

    运输条件

    Room temperature in continental US; may vary elsewhere.

    储存方式

    4°C, sealed storage, away from moisture

    *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

    纯度 & 产品资料
    参考文献
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    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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    产品名称:
    CBB1007 hydrochloride
    目录号:
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