Cbz-NH-PEG1-CH2COOH
CAS No. 1260092-43-0
Cbz-NH-PEG1-CH2COOH( —— )
Catalog No. M26934 CAS No. 1260092-43-0
Cbz-NH-PEG1-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 53 | Get Quote |
|
| 200MG | 77 | Get Quote |
|
| 500MG | 139 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameCbz-NH-PEG1-CH2COOH
-
NoteResearch use only, not for human use.
-
Brief DescriptionCbz-NH-PEG1-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
-
DescriptionCbz-NH-PEG1-CH2COOH is a PEG-based PROTAC linker that 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.
-
In VitroPROTACs 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.
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
Recptoranandamide cellular uptake| CB1| Human Endogenous Metabolite| TRPV1
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1260092-43-0
-
Formula Weight253.254
-
Molecular FormulaC12H15NO5
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (394.87 mM)
-
SMILESOC(=O)COCCNC(=O)OCc1ccccc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Ortar G, et al. Novel selective and metabolically stable inhibitors of anandamide cellular uptake. Biochem Pharmacol. 2003 May 1;65(9):1473-81.
molnova catalog
related products
-
RSV604
RSV-604 is an inhibitor of respiratory syncytial virus (RSV) that binds to RSV nucleoprotein (Kd = 1.31 μM).
-
pep2-EVKI
Inhibitor peptide that selectively disrupts binding of the AMPA receptor subunit GluA2 (at the C-terminal PDZ site) to protein interacting with C kinase (PICK1). Does not affect binding of GluA2 to GRIP or ABP and does not increase AMPA current amplitude or affect long term depression (LTD).
-
Dymanthine
Dymanthine is an agent of veterinary anthelmintic.
Cart
sales@molnova.com