全部分类
  • VERU-111
VERU-111的可视化放大

VERU-111

VERU-111 (ABI-231) 是一种有效且具有口服活性的 α和β tubulin 抑制剂,具有很强的抗增殖活性,对黑色素瘤和前列腺癌细胞系的平均 IC50 为 5.2 nM。 VERU-111 (ABI-231) 通过靶向 HPV E6 和 E7 抑制宫颈癌细胞的肿瘤生长和转移表型,具有治疗前列腺癌的潜力。

此产品仅用于科学研究,我们不为任何个人用途提供产品和服务

VERU-111的二维码
  • 库存: 现货
可选规格
  • 包装
    价格
    促销价
    数量
  • 100mg
    ¥0.00
    0.00
    - +
  • 250mg
    ¥0.00
    0.00
    - +
  • 500mg
    ¥0.00
    0.00
    - +
已选 0 0
金额: ¥0.00
首页 收藏
  • 货号: ajce60040
  • CAS: 1332881-26-1
  • 别名: VERU-111; ABI-231
  • 分子式: C21H19N3O4
  • 分子量: 377.39
  • 纯度: >98%
  • 溶解度: Soluble in DMSO
  • 储存: 4°C, away from moisture and light
  • 库存: 现货

Background

VERU-111 (ABI-231) is a potent and orally bioavailable α and β tubulin inhibitor, which displays strong antiproliferative activity, with an average IC50 of 5.2 nM against panels of melanoma and prostate cancer cell lines. VERU-111 (ABI-231) suppresses tumor growth and metastatic phenotypes of cervical cancer cells via targeting HPV E6 and E7, and has potential for the treatment of prostate cancer[1][2][3]. tubulin[1]


VERU-111 (2.5-80 nM; 24-48 hours) inhibits Panc-1, AsPC-1 and HPAF-II cells growth in a dose and time-dependent manner (24 hours: IC50s of 25, 35 and 35 nM, respectively; 48 hours: IC50s of 11.8, 15.5, and 25 nM, respectively)[4].VERU-111 (5-20 nM; 24 hours) arrests Panc-1 and AsPC-1 cells in G2/M phase in a dose-dependent manner[4]. VERU-111 (5-20 nM; 24 hours) shows dose-dependent inhibition of pro-Caspase 3 and 9 and activation of Caspase-3 and 9, induces the expression of Bax and Bad, and inhibits the expression of Bcl-2 and Bcl-xl proteins in both AsPC-1 and Panc-1 cells[4]. Cell Proliferation Assay[4] Cell Line: Panc-1, AsPC-1, HPAF-II cells


VERU-111 (50 μg/mouse; intra-tumorally; 3 times per week for 3 weeks) effectively inhibits tumor growth as compared to vehicle-treated group. None of the mouse showed any apparent toxicity as constant increase of body weight in VERU-111 treated mice[4]. Animal Model: Six-week-old female athymic nude mice (bearing AsPC-1 cells)


[1]. Wang Q, et al. Structure-Guided Design, Synthesis, and Biological Evaluation of (2-(1H-Indol-3-yl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl) Methanone (ABI-231) Analogues Targeting the Colchicine Binding Site in Tubulin. J Med Chem. 2019 Jul 12. [2]. Qinghui Wang, et al. Discovery of ABI-231 analogs targeting the colchicine site in tubulin for advanced melanoma. Cancer Research 76(14 Supplement):4848-4848. [3]. Vivek Kashyap, et al. ABI-231: A novel small molecule suppresses tumor growth and metastatic phenotypes of cervical cancer cells via targeting Human papilloma virus (HPV) E6 and E7. Cancer Research 78(13 Supplement):679-679. [4]. Kashyap VK, et al. Therapeutic efficacy of a novel βIII/βIV-tubulin inhibitor (VERU-111) in pancreatic cancer. J Exp Clin Cancer Res. 2019 Jan 23;38(1):29.

没有评价数据

温馨提示 ×
商品已成功加入购物车!
购物车共 0 件商品
去购物车结算