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Chk2 Inhibitor II hydrate

Chk2 抑制剂 II 水合物

品牌
Sigma-Aldrich
CAS
516480-79-8
货号
C3742
规格纯度
≥98% (HPLC)
参考价格
2587.35 *本价格含增值税费
促销
服务
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  • 包邮
  • 增值税票
数量
-+
产品名称:
516480-79-8
Chk2 Inhibitor II hydrate
2-(4-(4-Chlorophenoxy)phenyl)-1H-benzimidazole-5-carboxamide hydrate
Chk2 抑制剂 II 水合物
产品介绍:

产品说明

包装

5, 25 mg in glass bottle

生化/生理作用

Chk2 Inhibitor II is a checkpoint kinase 2 inhibitor, which controls the p53 response to DNA breaks induced by radiation, leading to apoptosis. Protection of T-cells from apoptosis implies use as an adjuvant for radiation therapy in cancer. IC50 = 15 nM; Ki = 37 nM. Chk2 Inhibitor II shows 1000-fold greater selectivity for the Chk2 serine/threonine kinase than for the Cdk1/B and CK1 kinases (for which IC50 = 12 μM and 17 μM, respectively). Chk2 Inhibitor II weakly inhibits a panel of 31 other kinases (<25% inhibition at a concentration of 10 μM and prevents apoptosis of human CD4+ and CD8+ T-cells subjected to ionizing radiation (EC50 = 3 μM and 7.6 μM, respectively).

特点和优势

This compound was developed by Johnson & Johnson. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

基本信息

经验(实验)分子式C20H14ClN3O2 · xH2O
分子量363.80 (anhydrous basis)
MDL编号MFCD08276917
PubChem化学物质编号24724438
NACRESNA.77

产品性质

质量水平100
测定≥98% (HPLC)
形式solid
颜色 off-white to tan
溶解性DMSO: ≥2 mg/mL (warmed)
创始人Johnson & Johnson
储存温度2-8℃
SMILES stringO=C(C1=CC=C2C(N=C(C3=CC=C(OC4=CC=C(Cl)C=C4)C=C3)N2)=C1)N
InChI1S/C20H14ClN3O2/c21-14-4-8-16(9-5-14)26-15-6-1-12(2-7-15)20-23-17-10-3-13(19(22)25)11-18(17)24-20/h1-11H,(H2,22,25)(H,23,24)
InChI keyUXGJAOIJSROTTN-UHFFFAOYSA-N
Gene Informationhuman ... CHEK2(11200)

安全信息

储存分类代码13 - Non Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable

Sigma-Aldrich

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