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BAY-1816032

    
10mM in DMSO

BAY-1816032

源叶(MedMol)
T96643 一键复制产品信息
1891087-61-8
C27H24F2N6O4
534.51
Ethanol,2-​[3,​5-​difluoro-​4-​[[3-​[5-​methoxy-​4-​[(3-​methoxy-​4-​pyridinyl)​amino]​-​2-​pyrimidinyl]​-​1H-​indazol-​1-​yl]​methyl]​phenoxy]​-
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T96643-1ml促销
10mM in DMSO

¥720.00 ¥648.00

5 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: 丝氨酸/苏氨酸激酶抑制剂;Serine/threonin kinase Inhibitors;;InformationBAY-1816032 BAY-1816032 is a potent and oral available inhibitor of budding uninhibited by benzimidazoles 1 (BUB1) kinase with IC50 of 6.1 nM for recombinant catalytic domain of human BUB1. BAY-1816032 has antitumor activity.TargetsBUB1 (Cell-free assay) 6.1 nMIn vitroBAY 1816032 is a novel, bioavailable inhibitor of the catalytical activity of the mitotic checkpoint protein BUB1, which is involved in centromere cohesion and attachment error correction. Inhibition of BUB1 sensitizes tumor cells towards paclitaxel and docetaxel, and towards ATR inhibitors and PARP inhibitiors.In vivoIn xenograft models of triple-negative breast cancer BAY 1816032 in combination with paclitaxel or olaparib strongly delays outgrowth of tumors under treatment as compared to paclitaxel or olaparib single agents.Cell Research(from reference)Cell lines:HeLa, SUM-149, MDA-MB-436, NCI-H1299, 22RV1, H4 cells. Concentrations:0.1 μM to 10 μM Incubation Time:4 h, 24 h, 48 h, 72 h, 96 h 
靶点: IC50: 7 nM (BUB1)
体内研究: 在肿瘤异种移植研究中,BAY 1816032 作为单一药物在口服给药时仅略微抑制肿瘤生长,然而,与紫杉醇或多西紫杉醇联合使用后,与各自的单一疗法相比,观察到肿瘤大小有显著减小。
参考文献: 1. Siemeister G, et al. BAY 1816032, a novel BUB1 kinase inhibitor with potent antitumor activity [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Ishington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 287. doi:10.1158/1538-7445.AM2017-287
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.871 ml 9.354 ml 18.709 ml
5 mM 0.374 ml 1.871 ml 3.742 ml
10 mM 0.187 ml 0.935 ml 1.871 ml
50 mM 0.037 ml 0.187 ml 0.374 ml
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参考文献

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摩尔浓度计算器

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