Mocetinostat产品图

Mocetinostat

收藏
  • ¥363 - 4300
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-12164
  • 2025年07月11日
    avatar
    品牌商
    14钻石会员
  • 企业认证

    点击 QQ 联系

    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.

    • 英文名

      MGCD0103

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      726169-73-9

    • 规格

      10 mM * 1 mL/1 mg/5 mg/10 mg/50 mg/100 mg

    规格:10 mM * 1 mL产品价格:¥880.0
    规格:1 mg产品价格:¥363.0
    规格:5 mg产品价格:¥800.0
    规格:10 mg产品价格:¥1100.0
    规格:50 mg产品价格:¥2700.0
    规格:100 mg产品价格:¥4300.0

    MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。

    Mocetinostat

    CAS No. : 726169-73-9

    MCE 国际站:Mocetinostat

    产品活性:Mocetinostat (MGCD0103)是一种有效,可口服和同种型选择性的 HDAC (Class I/IV) 抑制剂,抑制HDAC1HDAC2HDAC3HDAC11IC50分别为0.15,0.29,1.66 和 0.59 μM。 Mocetinostat对HDAC4,HDAC5,HDAC6,HDAC7或HDAC8没有抑制作用。

    研究领域:Cell Cycle/DNA Damage  |  Epigenetics  |  Autophagy  |  Apoptosis

    作用靶点:HDAC  |  Autophagy  |  Apoptosis

    In Vitro: Mocetinostat is a potent, orally active and isotype-selective HDAC (Class I/IV) inhibitor with IC50s of 0.15, 0.29, 1.66 and 0.59 μM for HDAC1, HDAC2, HDAC3 and HDAC11, respectively. Mocetinostat shows no inhibition on HDAC4, HDAC5, HDAC6, HDAC7, or HDAC8. Mocetinostat (MGCD0103) exhibits potent and selective antiproliferative activities against a broad spectrum of human cancer cell lines in vitro, and HDAC inhibitory activity is required for these effects. In all cell lines tested, Mocetinostat (MGCD0103) partially inhibits cellular HDAC enzyme activity although the maximal inhibition of activity varies among cell lines from 75% to 85% of total activity. The IC50 of Mocetinostat in intact cancer cells is independent of tissue origin. In A549 cells, MGCD0103 shows dose-dependent inhibition of HDAC activity in whole cells. At high concentrations in A549 cells, Mocetinostat inhibits a maximum of 80% of total activity. In HCT116 cells, Mocetinostat induces a significant S-phase depletion and both G1 and G2-M accumulation.

    In Vivo: Mocetinostat (MGCD0103) significantly inhibits growth of human tumor xenografts in nude mice in a dose-dependent manner and the antitumor activity correlated with induction of histone acetylation in tumors. The p.o. administration of Mocetinostat (MGCD0103) (2HBr salt) significantly reduces growth of implanted advanced A549 tumors in nude mice in a dose-dependent manner after 13 days of daily administration. Mocetinostat (170 mg/kg for 2HBr salt, corresponding to 120 mg/kg of free base) significantly blocks growth of tumors compared with vehicle treatment alone (P<0.05 in post-ANOVA Dunnett's test) with no change in body weight.

    相关产品:Drug Repurposing Compound Library Plus  |  FDA-Approved Drug Library Plus  |  FDA-Approved Drug Library Mini  |  Bioactive Compound Library Plus  |  Apoptosis Compound Library  |  Cell Cycle/DNA Damage Compound Library  |  Epigenetics Compound Library  |  FDA-Approved Drug Library  |  Histone Modification Research Compound Library  |  Anti-Cancer Compound Library  |  Autophagy Compound Library  |  Anti-Aging Compound Library  |  Drug Repurposing Compound Library  |  Reprogramming Compound Library  |  Oxygen Sensing Compound Library  |  Anti-COVID-19 Compound Library  |  Orally Active Compound Library  |  FDA Approved & Pharmacopeial Drug Library  |  Anti-Breast Cancer Compound Library  |  Anti-Pancreatic Cancer Compound Library  |  Anti-Blood Cancer Compound Library  |  Anti-Liver Cancer Compound Library   |  Rare Diseases Drug Library  |  FDA-Approved Anticancer Drug Library  |  Human Metabolite Library  |  Anti-Prostate Cancer Compound Library  |  Anti-Pulmonary Fibrosis Compound Library  |  Osteogenesis Compound Library  |  Off-patent Drug Library  |  Highly Selective Inhibitors Library  |  Highly Selective Activators Library  |  Cell Death Library  |  MG-132  |  Doxorubicin hydrochloride  |  Bafilomycin A1  |  LY294002  |  Tamoxifen  |  Paclitaxel  |  Y-27632  |  Acetylcysteine  |  Angiotensin II human  |  2-Deoxy-D-glucose  |  Staurosporine  |  SB-431542  |  Actinomycin D  |  Deferoxamine mesylate  |  Bortezomib  |  5-Fluorouracil  |  Trametinib  |  Sorafenib  |  Oxaliplatin  |  Gemcitabine  |  Temozolomide  |  Rotenone  |  Mdivi-1  |  Elesclomol  |  Ruxolitinib  |  Decitabine  |  SP600125  |  MK-2206 dihydrochloride  |  Etoposide  |  Trichostatin A

    热门产品线:重组蛋白  |  化合物库  |  天然产物  |  荧光染料  |  PROTAC  |  同位素标记物

    Trending products:Recombinant Proteins  |  Bioactive Screening Libraries  |  Natural Products  |  Dye Reagents  |  PROTAC  |  Isotope-Labeled Compounds

    类药多样性化合物库
    顾客使用MCE产品发表的科研文献
    一站式药筛新体验
    MCE 您身边的生物活性分子大师 | 抑制剂、激动剂、化合物库
    重组蛋白 | 高纯度、高稳定性
    磁珠
    MCE Hotline: 4008203792 | 中国现货 - 全球文献引用 - 高纯度高品质 - 全方位技术支持

    风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。

    图标文献和实验
    相关实验
    • IF:29!华西刘玉、陈崇伉俪报道染色体缺失促进肿瘤发生的新机制,除了P53还有它

      又发挥怎样的作用呢?研究人员通过 shRNA 降低了 Sin3a 在 shPhf23 淋巴瘤 / 白血病细胞和 Ba/F3 细胞中的表达,结果显示,Sin3a 敲低特异性地损害了 Phf23 缺失组淋巴瘤 / 白血病细胞的生长,但对 Ba/F3 细胞影响轻微,Sin3b 的敲低亦得到相似的结果。此外,与 shRen 相比,Hdac1 shRNAs 显著降低了 Phf23 缺失组淋巴瘤 / 白血病的存活。另外,HDAC 抑制剂 Entinostat、Mocetinostat 和 Chidamide

    图标技术资料

    暂无技术资料 索取技术资料

    同类产品报价

    产品名称
    产品价格
    公司名称
    报价日期
    ¥2160
    上海麦克林生化科技股份有限公司
    2026年05月28日询价
    询价
    上海瑶韵生物科技有限公司
    2025年07月04日询价
    ¥10584
    北京孚博生物科技有限公司
    2025年07月12日询价
    ¥3840
    Proteintech中国公司
    2024年11月04日询价
    ¥2433.20
    深圳欣博盛生物科技有限公司
    2023年10月25日询价
    Mocetinostat
    ¥363 - 4300