Thalidomide-O-amido-C6-NH2 hydrochloride
CAS No. 2376990-31-5
Thalidomide-O-amido-C6-NH2 hydrochloride ( —— )
产品货号. M27019 CAS No. 2376990-31-5
Thalidomide-O-amido-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker. It can be used in the synthesis of PROTACs.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥3038 | 有现货 |
|
10MG | ¥4512 | 有现货 |
|
25MG | ¥7266 | 有现货 |
|
50MG | ¥9963 | 有现货 |
|
100MG | ¥13365 | 有现货 |
|
500MG | ¥26649 | 有现货 |
|
1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Thalidomide-O-amido-C6-NH2 hydrochloride
-
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Thalidomide-O-amido-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker. It can be used in the synthesis of PROTACs.
-
产品描述Thalidomide-O-amido-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker. It can be used in the synthesis of PROTACs.(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P450
-
研究领域——
-
适应症——
化学信息
-
CAS Number2376990-31-5
-
分子量466.9
-
分子式C21H27ClN4O6
-
纯度>98% (HPLC)
-
溶解度——
-
SMILESCl.NCCCCCCNC(=O)COc1cccc2C(=O)N(C3CCC(=O)NC3=O)C(=O)c12
-
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.Levron, J.C., et al. Pharmacokinetic study of 2,3-dichloro 4- (2-thienyl keto14C) phenoxyacetic acid (tienilic acid) in animals. European Journal of Drug Metabolism and Pharmacokinetics 2, 107–120 (1977).
产品手册
关联产品
-
Methyl Icosanoate
Methyl Icosanoate is an esterified form of arachidic acid.
-
Arvenin III
Arvenin III is a useful organic compound for research related to life sciences.
-
Methyl nomilinate
Methyl nomilinate from citrus can modulate cell cycle regulators to induce cytotoxicity in human colon cancer (SW480) cells in vitro.