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Tubulin inhibitor 11

CAS No. 2366260-33-3

Tubulin inhibitor 11 ( —— )

产品货号. M36093 CAS No. 2366260-33-3

Tubulin inhibitor 11 是一种有效的具有口服活性的微管蛋白 (tubulin) 抑制剂。Tubulin inhibitor 11 靶向微管蛋白上的秋水仙碱结合位点,抑制微管蛋白聚合,促进有丝分裂阻断和细胞凋亡 (apoptosis)。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥646 有现货
5MG ¥985 有现货
10MG ¥1591 有现货
25MG ¥3558 有现货
50MG ¥5255 有现货
100MG ¥7313 有现货
500MG ¥14688 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Tubulin inhibitor 11
  • 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
    Tubulin inhibitor 11 是一种有效的具有口服活性的微管蛋白 (tubulin) 抑制剂。Tubulin inhibitor 11 靶向微管蛋白上的秋水仙碱结合位点,抑制微管蛋白聚合,促进有丝分裂阻断和细胞凋亡 (apoptosis)。
  • 产品描述
    Tubulin inhibitor 11 is a potent and orally active tubulin inhibitor. Tubulin inhibitor 11 targets the Colchicine binding site on tubulin, inhibits tubulin polymerization, promotes mitotic blockade and apoptosis.
  • 体外实验
    Tubulin inhibitor 11 (Compound 48; 0.03-0.1 μM; 12 hours) causes cell cycle arrest at G2/M phase. Tubulin inhibitor 11 reduces cdc2 phosphorylation and increases cyclin B1 and phosphorylation of histone H3 at Ser10 in cells.Tubulin inhibitor 11 (Compound 48; 0.03-0.3 μM; 48 hours) causes cancer cell apoptosis.Tubulin inhibitor 11 (Compound 48) demonstrates favorable antiproliferative activities in DU145 cells with an IC50 of 8 nM.Tubulin inhibitor 11 (Compound 48; 0.03-0.3 μM) significantly reduces the expression levels of acetyl-α-tubulin and α-tubulin in a dose-dependent manner.Cell Cycle Analysis Cell Line:DU145 cells Concentration:0.01 μM, 0.03 μM, and 0.1 μM Incubation Time:12 hours Result:Caused cell cycle arrest at G2/M phase.Apoptosis Analysis Cell Line:DU145 cells Concentration:0.03 μM, 0.1 μM, and 0.3 μM Incubation Time:48 hours Result: Induced cancer cell apoptosis.Western Blot Analysis Cell Line:DU145 cells Concentration:0.01 μM, 0.03 μM, and 0.1 μM Incubation Time:12 hours Result:Reduced cdc2 phosphorylation and increased cyclin B1 and phosphorylation of histone H3 at Ser10 in cells.
  • 体内实验
    Tubulin inhibitor 11 (Compound 48; 5-10 mg/kg; p.o; once daily) shows robust in vivo antitumor efficacies.Animal Model:Male athymic BALB/c nude mice (18-20 g) injected with DU145, NCI-H1299 or A549R cells Dosage:5 mg/kg, 10 mg/kg Administration:p.o; once dailyResult:Effectively suppressed tumor growth.
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Microtubule Associated | Apoptosis
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    2366260-33-3
  • 分子量
    409.5
  • 分子式
    C22H23N3O3S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO 中的溶解度 : 100 mg/mL (244.20 mM; 超声助溶 )
  • SMILES
    N(S(=O)(=O)C1=CC=C(C)C=C1)C2=CC(C(NCC=3C=CC(C)=NC3)=O)=CC=C2C
  • 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. Songwen Lin, et al. Optimization of Benzamide Derivatives as Potent and Orally Active Tubulin Inhibitors Targeting the Colchicine Binding Site. J Med Chem. 2022 Dec 22;65(24):16372-16391. ?
产品手册
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