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SGI-110

CAS No. 929901-49-5

SGI-110 ( SGI 110 | SGI110 | Guadecitabine )

产品货号. M16656 CAS No. 929901-49-5

一种新型 DNA 低甲基化二核苷酸,可抑制 DNA 甲基转移酶 (DNMT)。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
100MG 获取报价 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    SGI-110
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    一种新型 DNA 低甲基化二核苷酸,可抑制 DNA 甲基转移酶 (DNMT)。
  • 产品描述
    A novel DNA hypomethylating dinucleotide that inhibits DNA methyltransferase (DNMT); induces/up-regulates the expression of investigated cancer/testis antigens in broad cancer cell lines, both at mRNA and at protein levels; reduces the stem-like properties of ALDH(+) ovarian cancer stem-like cells, including their tumor-initiating capacity, resensitizes these OCSCs to platinum; induces hypomethylation and CTA gene expression in a dose dependent manner both in vitro and in vivo.Blood Cancer Phase 3 Clinical.
  • 体外实验
    Exposure to Guadecitabine induces the expression of investigated cancer/testis antigens (CTA) in CTA-negative cancer cells.Results show that Guadecitabine induces and/or strongly up-regulates the constitutive levels of MAGE-A3- and NY-ESO-1-specific mRNA expression in neoplastic cells of all histotypes investigated. Exposure to Guadecitabine significantly (p<0.05) up-regulates the constitutive levels of expression of HLA class I antigens, HLA-A2 allospecificity, and of the co-stimulatory molecule ICAM-1, on Mel 275 melanoma cells.Results show that treatment with Guadecitabine induces a significant (p<0.01) reduction in the constitutive methylation levels of CTA promoters in investigated cancer cells. Mean values of the percentage of demethylation induced by Guadecitabine in MAGE-A1 and NY-ESO-1 promoters are 57 and 30 %, in Mel 195, and 22 and 33 % in MZ-1257 RCC cells, respectively.
  • 体内实验
    Guadecitabine (S110) is effective at retarding tumor growth. While the tumors do not shrink in size with Guadecitabine treatment, they experience very minimal growth while the tumors treated with PBS only show substantial growth. In addition, Guadecitabine induces much less toxicity as determined by mouse weight changes when given subcutaneously (SQ) compare to that with IP injections.
  • 同义词
    SGI 110 | SGI110 | Guadecitabine
  • 通路
    Chromatin/Epigenetic
  • 靶点
    DNMT
  • 受体
    DNMT
  • 研究领域
    Cancer
  • 适应症
    Blood cancer

化学信息

  • CAS Number
    929901-49-5
  • 分子量
    557.41
  • 分子式
    C18H24N9O10P
  • 纯度
    >98% (HPLC)
  • 溶解度
    H2O
  • SMILES
    O=P(OC[C@@H]1O[C@@H](N2C=NC3=C2N=C(N)NC3=O)C[C@H]1O)(O[C@@H]4[C@@H](CO)O[C@@H](N5C(N=C(N)N=C5)=O)C4)O
  • 化学全称
    (2R,3S,5R)-5-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)-2-(hydroxymethyl)tetrahydrofuran-3-yl (((2S,3R,5R)-5-(2-amino-6-oxo-1H-purin-9(6H)-yl)-3-hydroxytetrahydrofuran-2-yl)methyl) hydrogen phosphate

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Wang Y, et al. Cancer Res. 2014 Sep 1;74(17):4922-36. 2. Srivastava P, et al. Epigenetics. 2015;10(3):237-46. 3. Srivastava P, et al. Leuk Res. 2014 Nov;38(11):1332-41. 4. Fang F, et al. Clin Cancer Res. 2014 Dec 15;20(24):6504-16.
产品手册
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