021-51111890
购物车（）
sales@molnova.cn
Propargyl-PEG13-bromide
CAS No. 2055105-25-2
Propargyl-PEG13-bromide ( —— )
产品货号. M27787 CAS No. 2055105-25-2
Propargyl-PEG13-bromide is a PEG derivative containing a propargyl group.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ￥616 | 有现货 |
|
| 5MG | ￥786 | 有现货 |
|
| 10MG | ￥1272 | 有现货 |
|
| 25MG | ￥2292 | 有现货 |
|
| 50MG | ￥3216 | 有现货 |
|
| 100MG | ￥4666 | 有现货 |
|
| 200MG | ￥6334 | 有现货 |
|
| 500MG | ￥9501 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Propargyl-PEG13-bromide
-
注意事项本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
-
产品简述Propargyl-PEG13-bromide is a PEG derivative containing a propargyl group.
-
产品描述Propargyl-PEG13-bromide is a PEG derivative containing a propargyl group. The propargyl group can be reacted with azide-bearing compounds or biomolecules via copper-catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. The bromide (Br) can be used in nucleophilic substitution reactions.(In Vitro):PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体p53/MDM2;Apoptosis
-
研究领域——
-
适应症——
化学信息
-
CAS Number2055105-25-2
-
分子量691.7
-
分子式C29H55BrO13
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESBrCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCC#C
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Wang H, et al. A small-molecule p53 activator induces apoptosis through inhibiting MDMX expression in breast cancer cells. Neoplasia. 2011 Jul;13(7):611-9.
产品手册
关联产品
-
Orientin-2-O-p-trans...
Orientin-2''-O-p-trans-coumarate can strongly promote 2BS cell proliferation induced by H(2)O(2).
-
Lipofermata
Lipofermata is a fatty acid transport protein (FATP) inhibitor that prevents lipid transport to melanoma cells and reduces melanoma growth and invasion.
-
(-)-Maackiain
(-)-Maackiain, a phytoalexin, which is an anti-allergic compound that suppresses the up-regulation of the histamine H1 receptor (H1R) gene.
