Cart
sales@molnova.com
Boc-NH-PEG8-CH2CH2NH2
CAS No. 1052207-59-6
Boc-NH-PEG8-CH2CH2NH2 ( —— )
Catalog No. M26928 CAS No. 1052207-59-6
Boc-NH-PEG8-CH2CH2NH2 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 |
| 10MG | 26 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameBoc-NH-PEG8-CH2CH2NH2
-
NoteResearch use only, not for human use.
-
Brief DescriptionBoc-NH-PEG8-CH2CH2NH2 is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
-
DescriptionBoc-NH-PEG8-CH2CH2NH2 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.
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorBombesin Receptor; GPR
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1052207-59-6
-
Formula Weight512.6
-
Molecular FormulaC23H48N2O10
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESCC(C)(C)OC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCN
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Mihara S, et al. Non-peptide bombesin receptor antagonists, kuwanon G and H, isolated from mulberry. Biochem Biophys Res Commun. 1995 Aug 15;213(2):594-9.
molnova catalog
related products
-
Ginsenoside Rg1
Ginsenosides are a class of steroid glycosides, and triterpene saponins found exclusively in the plant genus Panax (ginseng).
-
Nootkatone
Nootkatone can prevent obesity and improve physical performance through AMPK activation in skeletal muscle and liver.
-
Norchlorcyclizine
Norchlorcyclizine is a partially selective NPR-B inhibitor. It also is an inhibitor of human tyrosyl-DNA phosphodiesterase 1.
