(S,R,S)-AHPC-PEG4-N3
CAS No. 1797406-81-5
(S,R,S)-AHPC-PEG4-N3 ( VH032-PEG4-N3; VHL Ligand-Linker Conjugates 5; E3 ligase Ligand-Linker Conjugates 4 )
Catalog No. M26950 CAS No. 1797406-81-5
(S,R,S)-AHPC-PEG4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 45 | Get Quote |
|
5MG | 75 | Get Quote |
|
10MG | 107 | Get Quote |
|
25MG | 177 | Get Quote |
|
50MG | 266 | Get Quote |
|
100MG | 410 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product Name(S,R,S)-AHPC-PEG4-N3
-
NoteResearch use only, not for human use.
-
Brief Description(S,R,S)-AHPC-PEG4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology.
-
Description(S,R,S)-AHPC-PEG4-N3 is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 4-unit PEG linker used in PROTAC technology.(In Vitro):E3?ligase Ligand-Linker Conjugates 4 together with JQ1 triggers the intracellular destruction of BET proteins.
-
SynonymsVH032-PEG4-N3; VHL Ligand-Linker Conjugates 5; E3 ligase Ligand-Linker Conjugates 4
-
PathwayOthers
-
TargetOther Targets
-
RecptorATP-sensitive potassium (KATP) channels
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1797406-81-5
-
Formula Weight689.8
-
Molecular FormulaC32H47N7O8S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(N[C@@H](C(C)(C)C)C(N(C[C@H](O)C1)[C@@H]1C(NCC2=CC=C(C(SC=N3)=C3C)C=C2)=O)=O)COCCOCCOCCOCCN=[N+]=[N-]
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.L?ffler C, et al. Pharmacological characterization of the sulphonylurea receptor in rat isolated aorta. Br J Pharmacol. 1997 Feb;120(3):476-80.
molnova catalog
related products
-
CH 5450
CH 5450 (Z-Ile-Glu-Pro-Phe-Ome) is a short peptide inhibitor of chymase in the human heart.
-
N-(3-methoxybenzyl)-...
N-(3-methoxybenzyl)-octadecanamide deverts from Maca (Lepidium meyenii Walp.).
-
Glycodeoxycholic aci...
Glycodeoxycholic Acid induces apoptosis in hepatocytes by a mechanism associated with DNA cleavage by endonucleases. It is a secondary bile acid produced by the action of enzymes existing in the microbial flora of the colonic environment.