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APS6-45

CAS No. 2188236-41-9

APS6-45 ( —— )

产品货号. M23989 CAS No. 2188236-41-9

APS6-45 抑制 RAS/MAPK 信号传导并表现出抗肿瘤活性。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1442 有现货
10MG ¥2341 有现货
25MG ¥4277 有现货
50MG ¥6229 有现货
100MG ¥8748 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
    APS6-45
  • 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
    APS6-45 抑制 RAS/MAPK 信号传导并表现出抗肿瘤活性。
  • 产品描述
    APS6-45 inhibits RAS/MAPK signaling and exhibits anti-tumor activity.
  • 体外实验
    APS6-45 (3-30 nM; 3 weeks) strongly suppresses TT human Medullary Thyroid Carcinoma (MTC) cells colony formation in a soft agar assay.APS6-45 (1 μM; 1 h) strongly inhibits RAS pathway activity signaling in human MTC cell lines TT and MZ-CRC-1.
  • 体内实验
    APS6-45 (10 mg/kg; p.o. daily for 30 d) inhibits growth of TT tumors in mice and does not affect body weight.APS6-45 (0.1-160 mg/kg; a single p.o.) does not cause detectable toxic effects in mice.APS6-45 (20 mg/kg; a single p.o.) exhibits long half-life (5.6 h), Cmax (9.7 μM) and AUC0-24 (123.7 μM?h) in mice. Animal Model:Female nude mice (6 weeks) are implanted with TT cellsDosage:10 mg/kgAdministration:P.o. daily for 30 days Result:Led to partial or complete responses in 75% and was well tolerated.Animal Model:Male ICR mice (6 weeks of age)Dosage:20 mg/kg (Pharmacokinetic Analysis)Administration:A single p.o.Result:T1/2=5.6 h, Cmax=9.7 μM,AUC0-24=123.7 μM?h.
  • 同义词
    ——
  • 通路
    MAPK/ERK Signaling
  • 靶点
    p38 MAPK
  • 受体
    MAPK|Ras
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    2188236-41-9
  • 分子量
    548.4
  • 分子式
    C23H16F8N4O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:240mg/mL (437.67mM)
  • SMILES
    O=C(NC)C1=NC=CC(OC2=CC=C(NC(NC3=CC(C(C(F)(F)F)(F)C(F)(F)F)=CC=C3F)=O)C=C2)=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.Sonoshita M, Scopton AP, Ung PMU, et al. A whole-animal platform to advance a clinical kinase inhibitor into new disease space. Nat Chem Biol. 2018;14(3):291-298. doi:10.1038/nchembio.2556
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