Propargyl-PEG13-bromide
CAS No. 2055105-25-2
Propargyl-PEG13-bromide ( —— )
产品货号. M27787 CAS No. 2055105-25-2
Propargyl-PEG13-bromide 是一种含有炔丙基的 PEG 衍生物。
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 是一种含有炔丙基的 PEG 衍生物。
-
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.
-
体外实验——
-
体内实验——
-
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691.65
-
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
-
Deferasirox
一种口服铁螯合剂,用于减少慢性铁超负荷;还通过靶向 caspase 诱导骨髓性白血病细胞凋亡。
-
Lucidumol A
Lucidumol A has relatively good effect against aldose reductase with IC50 of 19.1uM. Lucidumol A has cytotoxic activity, it reduced cell growth in three human carcinoma cells (Caco-2, HepG2, and HeLa cells) dose dependently with LC50s from 20.87 to 84.36 uM.
-
116-9e
116-9e (MAL2-11B) 是一种 Hsp70 共伴侣 DNAJA1 抑制剂。116-9e 抑制猿猴病毒40 (SV40) 的复制和 DNA 合成。116-9e 抑制肿瘤抗原 (TAg) 内源性 ATP 酶活性和 TAg 介导的 Hsp70 激活。
021-51111890
购物车()
sales@molnova.cn

