(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH

Modify Date: 2024-01-10 10:50:11

(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH Structure
(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH structure
Common Name (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH
CAS Number 2086301-47-3 Molecular Weight 754.98
Density N/A Boiling Point N/A
Molecular Formula C39H58N6O7S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH


(S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH (VH032-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH) is a E3 ligase ligand-linker conjugate that contains on one end a VHL ligand. (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH is used in PROTAC technology[1].

 Names

Name (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH

  Biological Activity

Description (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH (VH032-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH) is a E3 ligase ligand-linker conjugate that contains on one end a VHL ligand. (S,R,S)-AHPC-Boc-trans-3-aminocyclobutanol-Pip-CH2COOH is used in PROTAC technology[1].
Related Catalog
Target

VHL

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[2].
References

[1]. Yimin Qian, et al. Compounds and methods for the targeted degradation of bromodomain-containing proteins. WO2017030814A1.

[2]. Nalawansha DA, et al. PROTACs: An Emerging Therapeutic Modality in Precision Medicine. Cell Chem Biol. 2020;27(8):998-991.

 Chemical & Physical Properties

Molecular Formula C39H58N6O7S
Molecular Weight 754.98
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