欢迎访问ProbeChem中文网站,英文网站请访问www.probechem.com

首页-小分子抑制剂&激动剂-Cell Cycle/DNA Damage-Polo-like Kinase (PLK)-BI-2536
BI-2536

Chemical Structure : BI-2536

CAS No.: 755038-02-9

BI-2536 (BI 2536;BI2536)

货号: PC-45847Not For Human Use, Lab Use Only.

BI-2536 is a potent and selective inhibitor of PLK1 with IC50 of 0.83 nM.

规格 价格 库存 数量
10 mg ¥880 In stock
25 mg ¥1380 In stock
50 mg ¥2180 In stock
100 mg Get quote

大包装,大折扣!

E-mail: sales@probechem.com

Tech Support: tech@probechem.com

纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

BI-2536 is a potent and selective inhibitor of PLK1 with IC50 of 0.83 nM.
BI-2536 also weakly inhibits the activities of PLK2 and PLK3 (IC50=3.5 nM and 9.0 nM, respectively), displays >1,000-fold selectivity to a panel of 63 other protein kinases.
BI-2536 causes a mitotic arrest and induces apoptosis in human cancer cell lines, inhibits growth of human tumor xenografts in nude mice and induces regression of large tumors with well-tolerated intravenous dose regimens.
BI-2536 also inhibits BRD4 with IC50 of 25 nM.

物理化学性质&存储条件

分子量 521.6544
分子式 C28H39N7O3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Benzamide, 4-[[(7R)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-pteridinyl]amino]-3-methoxy-N-(1-methyl-4-piperidinyl)-

参考文献

1. Steegmaier M, et al. Curr Biol. 2007 Feb 20;17(4):316-22. Epub 2007 Feb 8.

2. Chen L, et al. ACS Med Chem Lett. 2015 May 18;6(7):764-9.

3. Nappi TC, et al. Cancer Res. 2009 Mar 1;69(5):1916-23.

备案号:沪ICP备16042516号-1 Copyright © 2022 probechem.com. All Rights Reserved. probechem Copyright

联系我们 sales@probechem.com

Bulk Inquiry

* Indicates a Required FieldYour information is safe with us.

  • *Product name:
  • *Applicant name:
  • *Email address:
  • *Organization name:
  • *Requested quantity:
  • *Country:
  • *Additional Information:

询单

  • *产品名称:
  • *姓名:
  • *邮箱:
  • *公司名称:
  • *询单数量:
  • *国籍:
  • 询单信息: