Pomalidomide-PEG3-C2-NH2
CAS No. 2093416-31-8
Pomalidomide-PEG3-C2-NH2( Cereblon Ligand-Linker Conjugates 5 | E3 ligase Ligand-Linker Conjugates 30 )
Catalog No. M26944 CAS No. 2093416-31-8
Pomalidomide-PEG3-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate incorporating the Pomalidomide based cereblon ligand and 3-unit PEG linker.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 393 | Get Quote |
|
10MG | 590 | Get Quote |
|
25MG | 1060 | Get Quote |
|
50MG | 1591 | Get Quote |
|
100MG | 2387 | Get Quote |
|
200MG | 3580 | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NamePomalidomide-PEG3-C2-NH2
-
NoteResearch use only, not for human use.
-
Brief DescriptionPomalidomide-PEG3-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate incorporating the Pomalidomide based cereblon ligand and 3-unit PEG linker.
-
DescriptionPomalidomide-PEG3-C2-NH2 is a synthesized E3 ligase ligand-linker conjugate incorporating the Pomalidomide based cereblon ligand and 3-unit PEG linker.
-
In Vitro——
-
In Vivo——
-
SynonymsCereblon Ligand-Linker Conjugates 5 | E3 ligase Ligand-Linker Conjugates 30
-
PathwayOthers
-
TargetOther Targets
-
RecptorMRCK| ROCK1| ROCK2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2093416-31-8
-
Formula Weight448.476
-
Molecular FormulaC21H28N4O7
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESNCCOCCOCCOCCNc1cccc2C(=O)N(C3CCC(=O)NC3=O)C(=O)c12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Yen Ting Chen, et al. Asymmetric synthesis of potent chroman-based Rho kinase (ROCK-II) inhibitors. Med.Chem.Commun., 2011, 2, 73-75.
molnova catalog
related products
-
ASCORBYL GLUCOSIDE
ASCORBYL GLUCOSIDE is a glucoside derivative of ascorbic acid shows anti-cancer activity after enzymatic hydrolysis to ascorbic acid.
-
Ingenol-5,20-acetoni...
Ingenol-5,20-acetonide is a natural product.
-
Trimethoxystilbene
3, 5, 4'-Trimethoxystilbene, a natural methoxylated analog of resveratrol, inhibits breast Y cell invasiveness by downregulation of PI3K/Akt and Wnt/β-catenin signaling cascades and reversal of epithelial-mesenchymal transition.