- ￥3000
- MedChemExpress(MCE)
- 美国
- HY-143715
- 2025年12月05日
企业认证
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：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
2672489-14-2
- 规格：
1 mg
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。
Cereblon inhibitor 1
CAS No. : 2672489-14-2
MCE 国际站：Cereblon inhibitor 1
产品活性：Cereblon inhibitor 1 是一种异吲哚啉衍生物，一种 cereblon E3 泛素连接酶调节活性分子。 Cereblon inhibitor 1 具有用于癌症研究的潜力。
研究领域：PROTAC
作用靶点：Ligands for E3 Ligase
In Vitro: Cereblon inhibitor 1 (compound CM-48) suppresses MM.1S cell proliferation (IC50=0.0365 nM).
相关产品：Lenalidomide | Pomalidomide | CC-885 | Eragidomide | Iberdomide | Thalidomide | VH-298 | VH032 | ALV2 | Cemsidomide | (S,R,S)-AHPC monohydrochloride | (S,S,S)-AHPC hydrochloride | (S,R,S)-AHPC-Me hydrochloride | Golcadomide | VH032-cyclopropane-F | Lenalidomide-Br | Thalidomide-5-OH | Thalidomide 4-fluoride | BC-1215 | ALV1 | ZXH-1-161 | Thalidomide-NH-CH2-COOH | Lenalidomide-5-Br | Thalidomide-O-COOH | VL285 | (S,R,S)-AHPC-propargyl
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14-3-3 is a potent inhibitor of protein kinase C, but the N-terminal domain does not inhibit PKC activity. Site-specific mutagenesis of several regions in the tau isoform of 14-3-3, including the mutation of a putative pseudosubstrate site
Introduction of human 14-3-3 proteins
inhibitor of protein kinase C,but the N-terminal domain does not inhibit PKC activity.Site-specific mutagenesis of several regions in the tau isoform of 14-3-3,including the mutation of a putative pseudosubstrate site to a potential substrate sequence
Methods for Studying the Interaction of Barnase with Its Inhibitor Barstar
complex, with K d =10−14 M , half-life of about 2 d and an association rate constant of 4�108 M −1 /s. The kinetic and thermodynamics of the barnase-barstar interaction were investigated in detail (12 –20 ). High affinity is maintained at pH 7.0–
技术资料暂无技术资料 索取技术资料
