产品说明
应用
4E1RCat was used to inhibit new protein synthesis in transformed primary chicken embryo fibroblasts.
包装
5, 25 mg in glass bottle
生化/生理作用
4E1RCat ilnhibits the eIF4F translation initiation complex by binding to IF4E b and inhibiting the interaction between IF4E:eIF4G (IC50 = 3.2 μM). In in vitro translation experiments using MDA-MB-231 cells, 4E1RCat dose dependently inhibited cap-dependent translation, led to a decrease in polysome and 80S ribosomal subunits and reduced levels of the eIF4F-dependant proteins Mcl-1 and c-Myc.
特点和优势
This compound is featured on the MAPKAPs page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Merck & Co., Inc., Kenilworth, NJ, U.S.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
This compound is a featured product for Gene Regulation research. Click here to discover more featured Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
基本信息
经验(实验)分子式 | C28H18N2O6 |
分子量 | 478.45 |
MDL编号 | MFCD01931282 |
PubChem化学物质编号 | 329825222 |
NACRES | NA.77 |
产品性质
质量水平 | 100 |
测定 | ≥97% (HPLC) |
形式 | powder |
颜色 | faint brown to dark brown-red |
溶解性 | DMSO: ≥5 mg/mL |
创始人 | Merck & Co., Inc., Kenilworth, NJ, U.S. |
储存温度 | 2-8℃ |
SMILES string | OC(=O)c1ccc(cc1)N2C(=O)\C(=C\c3ccc(o3)-c4ccc(cc4)[N+]([O-])=O)C=C2c5ccccc5 |
InChI | 1S/C28H18N2O6/c31-27-21(16-24-14-15-26(36-24)19-6-12-23(13-7-19)30(34)35)17-25(18-4-2-1-3-5-18)29(27)22-10-8-20(9-11-22)28(32)33/h1-17H,(H,32,33)/b21-16+ |
InChI key | BBQRBOIMSKMFFO-LTGZKZEYSA-N |
安全信息
储存分类代码 | 13 - Non Combustible Solids |
WGK | WGK 3 |
闪点(F) | Not applicable |
闪点(C) | Not applicable |