相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
- 库存:
货期:询盘
- 供应商:
MedChemExpress LLC
- CAS号:
2408406-89-1
- 规格:
询盘
MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。
P-gp inhibitor 2
CAS No. : 2408406-89-1
MCE 国际站:P-gp inhibitor 2
产品活性:P-gp inhibitor 2 是一种有效的 P-gp 抑制剂。P-gp Inhibitor 2 在过表达 P-gp 的人结肠直肠癌细胞 (SW600 Ad300) 中显示出阿霉素耐药的逆转作用(IC50=0.22 µM)。
研究领域:Membrane Transporter/Ion Channel
作用靶点:P-glycoprotein
In Vitro: P-gp inhibitor 2 (compound 2) exhibits no cytotoxicity (IC50>30 µM) toward human carcinoma (SW600) cells.
相关产品:Verapamil | Elacridar | Glibenclamide | Tariquidar | Zosuquidar trihydrochloride | CP-100356 hydrochloride | Piperine | Risperidone | Limonin | Valspodar | Trifluoperazine dihydrochloride | Atazanavir sulfate | Paris saponin VII | Encequidar | Solamargine | Dofequidar fumarate | Sinapine | Selamectin | (20S)-Protopanaxadiol | Reversan | Isosinensetin | TTT-28 | Coniferyl ferulate | Polyoxyethylene stearate | AZD-5672
热门产品线:重组蛋白 | 化合物库 | 天然产物 | 荧光染料 | PROTAC | 同位素标记物
Trending products:Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Dye Reagents | PROTAC | Isotope-Labeled Compounds
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Methods for Studying the Interaction of Barnase with Its Inhibitor Barstar
Barnase is a 110-residue extracellular ribonuclease produced by Bacillus amyloliquefaciens . The same organism produces an 89-residue polypeptide, barstar, which binds tightly to barnase and inhibits its potentially lethal RNase activity
(Table 1 ). The enzymatic activity of MMP family members is controlled by a group of inhibitor proteins known as the Tissue Inhibitors of Metalloproteinases (TIMPs), which consist of four family members (Table 2 ). Whereas all four TIMPs can inhibit
Screening for P-Glycoprotein (Pgp) Substrates and Inhibitors
the absorption, distribution, excretion, and toxicity of many drugs, P-gp is the potential locus of a number of pharmacokinetic drug-drug interactions when two drugs, one a substrate and the other a substrate or inhibitor of the transporter, are co-administered
技术资料暂无技术资料 索取技术资料


















