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.
- 英文名:
SC 204330
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
491871-58-0
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥507.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥283.0 |
| 规格: | 5 mg | 产品价格: | ¥627.0 |
| 规格: | 10 mg | 产品价格: | ¥1004.0 |
| 规格: | 25 mg | 产品价格: | ¥2000.0 |
| 规格: | 50 mg | 产品价格: | ¥3000.0 |
| 规格: | 100 mg | 产品价格: | ¥4500.0 |
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。
TCS PIM-1 1
CAS No. : 491871-58-0
MCE 国际站:TCS PIM-1 1
产品活性:TCS PIM-1 1 (SC 204330) 是一种有效的,具有选择性和 ATP 竞争性的 Pim-1 激酶抑制剂,IC50 为 50 nM,对 Pim-2 和 MEK1/MEK2 表现出良好的选择性 (IC50 >20000 nM)。
研究领域:JAK/STAT Signaling
作用靶点:Pim
In Vitro: TCS PIM-1 1 (compound 1), a substituted pyridone scaffold, binds convincingly within the ATP-binding site of Pim-1 suggesting an ATP-competitive inhibitory mechanism. Preliminary data further suggests that TCS PIM-1 1 lacked in vitro inhibitory activity toward related serine/threonine kinases Pim-2 and MEK1/2. Hence, small molecules similar to TCS PIM-1 1 may serve as useful starting scaffolds for the development of other improved yet selective Pim-1 inhibitors. TCS PIM-1 1 serves both as a starting point for SAR chemical syntheses and was used for co-crystallization with Pim-1 protein.
相关产品:Covalent Screening Library Plus | Bioactive Compound Library Plus | Epigenetics Compound Library | Immunology/Inflammation Compound Library | JAK/STAT Compound Library | Kinase Inhibitor Library | Anti-Cancer Compound Library | Covalent Screening Library | Anti-Pancreatic Cancer Compound Library | Anti-Cancer Metabolism Compound Library | Anti-Obesity Compound Library | Targeted Diversity Library | Cancer Stem Cells Compound Library | Membrane Protein-targeted Compound Library | Highly Selective Inhibitors Library | AZD1208 | Hispidulin | PIM-447 dihydrochloride | TP-3654 | Pim1/AKK1-IN-1 | SGI-1776 free base | CX-6258 | Quercetagetin | SMI-16a | GDC-0339 | Uzansertib phosphate | CK2/ERK8-IN-1 | CX-6258 hydrochloride | SMI-4a | M-110 | SEL24-B489 | HTH-01-091 TFA | PIM1-IN-1 | HTH-01-091 | 10-DEBC | CDK6/PIM1-IN-1 | CK2/PIM1-IN-1 | FD1024 | GSK-3β inhibitor 13 | HJ-PI01 | HS56
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, GAB2, GNG2, GRB2, HRAS, INDO, KRAS2, KSR, MADH1, MADH2, MADH3, MADH4, MADH5, MADH6, MADH7, MADH9, MAPK8IP1, MCM5, MIZ1, NRAS, OSM, PAK1, PAK3, PIAS1, PIAS3, PIASY, PIM1, PREX1, PTPN1, PTPNS1, PTPRC, RAC1, RAC2, SOCS1, SOCS2, SOCS3, SOCS4, SOCS5, SOCS
From In Vitro to In Vivo: Imaging from the Single Cell to the Whole Organism
) Thermoregulated Lucite chamber (Vestavia Scientific) Confocal microscope system (e. g., Leica TCS SP2, Leica Microsystem
(2)CTL的识别机制:多种粘附分子参与CTL对靶细胞的识别和粘附,主要有:①LFA-1/ICAM-1、ICAM-2、ICAM-3,可溶性ICAM-1(sICAM-1)可抑制CTL杀伤肿瘤细胞;②CD2/LFA-3(CD58),抗CD2McAb或抗CD58 McAb均可抑制CTL效应细胞对靶细胞的杀伤;③CD8/MHc I类抗原的非多态性结构域。 (3)CTL的杀伤机制:TCL杀伤靶细胞的机理目前认为主要通过释放多种的介质和因子介导的。 ①穿孔素(perforin):又称成孔蛋白
技术资料暂无技术资料 索取技术资料

















