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(S,R,S)-AHPC-C5-COOH

(S,R,S)-AHPC-C5-COOH
(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized conjugate for E3 ligase ligand-linker applications, combining the VH032 VHL-based ligand with a linker for PROTAC development. VH-032 is a selective and potent VHL/HIF-1α interaction inhibitor with a dissociation constant (Kd) of 185 nM, offering potential in anemia and ischemic diseases research[1].
Catalog No. T18667Cas No. 2267282-19-7
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(S,R,S)-AHPC-C5-COOH

Catalog No. T18667Cas No. 2267282-19-7
(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized conjugate for E3 ligase ligand-linker applications, combining the VH032 VHL-based ligand with a linker for PROTAC development. VH-032 is a selective and potent VHL/HIF-1α interaction inhibitor with a dissociation constant (Kd) of 185 nM, offering potential in anemia and ischemic diseases research[1].
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Product Introduction

Bioactivity
Description
(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized conjugate for E3 ligase ligand-linker applications, combining the VH032 VHL-based ligand with a linker for PROTAC development. VH-032 is a selective and potent VHL/HIF-1α interaction inhibitor with a dissociation constant (Kd) of 185 nM, offering potential in anemia and ischemic diseases research[1].
In vitro
PROTACs are bifunctional molecules consisting of two ligands linked together; one binds to an E3 ubiquitin ligase, and the other targets a specific protein. Through the utilization of the cell's ubiquitin-proteasome system, PROTACs achieve the selective degradation of target proteins. Notably, the von Hippel–Lindau (VHL) tumor suppressor protein functions as the substrate-binding component of the VHL E3 ubiquitin ligase, targeting the hydroxylated α subunit of hypoxia-inducible factors (HIFs) for ubiquitination and subsequent proteasomal degradation.
AliasVH032-C5-COOH
Chemical Properties
Molecular Weight558.73
FormulaC29H42N4O5S
Cas No.2267282-19-7
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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