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Inecalcitol

CAS No. 163217-09-2

Inecalcitol ( TX-522 | TX 522 | TX522 )

产品货号. M27771 CAS No. 163217-09-2

Inecalcitol 是人类乳腺癌细胞的生长抑制剂。 Inecalcitol 是一种独特的维生素 D3 类似物,Kd 为 0.53 nM。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥6278 有现货
5MG ¥9639 有现货
10MG ¥12879 有现货
25MG ¥19359 有现货
50MG ¥26082 有现货
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
    Inecalcitol
  • 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
    Inecalcitol 是人类乳腺癌细胞的生长抑制剂。 Inecalcitol 是一种独特的维生素 D3 类似物,Kd 为 0.53 nM。
  • 产品描述
    Inecalcitol is the growth inhibitor of human breast cancer cells. Inecalcitol is a unique vitamin D3 analog with Kd of 0.53 nM.(In Vitro):A xenograft model of LNCaP cells was developed in immunodeficient mice treated with inecalcitol. The tumors of the diluent-treated control mice increased in size but those in the inecalcitol treatment group did not grow.(In Vivo):Inecalcitol maximal tolerated dose (MTD) by intraperitoneal (i.p.) administration was 30 μg/mouse (1,300 μg/kg) three times per week, while we previously found that the MTD of 1,25(OH)(2) D(3) is 0.0625 μg/mouse; therefore, inecalcitol is 480 times less hypercalcemic than 1,25OH2 D3. Inecalcitol inhibits androgen-responsive prostate cancer growth in vivo.
  • 体外实验
    Western Blot Analysis Cell Line:LNCaP cells Concentration:0.1 nM, 1 nM, 10 nM Incubation Time:48 hours Result:Resulted in decreased expression of both protein and mRNA of Pim-1 in a dose-dependent manner.
  • 体内实验
    Animal Model:Male BNX nu/nu mice (8 weeks of age) injected with LNCaP cells.Dosage:1.3 mg/kg Administration:i.p.; 3 times per week; for 42 days Result:Inhibited androgen-responsive prostate cancer growth in vivo.
  • 同义词
    TX-522 | TX 522 | TX522
  • 通路
    Apoptosis
  • 靶点
    Apoptosis
  • 受体
    HIPK2
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    163217-09-2
  • 分子量
    400.603
  • 分子式
    C26H40O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (249.63 mM)
  • SMILES
    C[C@H](CC#CC(C)(C)O)[C@H]1CC[C@@H]2\C(CCC[C@]12C)=C\C=C1C[C@@H](O)C[C@H](O)C1
  • 化学全称
    ——

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.Ruijie Liu, et al. A Novel Inhibitor of Homeodomain Interacting Protein Kinase 2 Mitigates Kidney Fibrosis through Inhibition of the TGF-β1/Smad3 Pathway. J Am Soc Nephrol. 2017 Feb 20. pii: ASN.2016080841.
产品手册
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