Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride

Modify Date: 2024-04-02 21:44:29

Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride Structure
Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride structure
Common Name Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride
CAS Number 1416771-72-6 Molecular Weight 373.78
Density N/A Boiling Point N/A
Molecular Formula C13H24ClNO9 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride


Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride is a cleavable PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Amino-Tri-(carboxyethoxymethyl)-methan hydrochloride is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1][2].

 Names

Name Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride

  Biological Activity

Description Amino-Tri-(carboxyethoxymethyl)-methane hydrochloride is a cleavable PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Amino-Tri-(carboxyethoxymethyl)-methan hydrochloride is also a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1][2].
Related Catalog
In Vitro ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker[1]. 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]. Markus Ribbert, et al. Self coupling recombinant antibody fusion proteins. WO2009013359A2.

[2]. David Margulies, et al. Fluorescent molecular sensor for targeting changes in protein surfaces, and methods of use thereof. WO2015166491A2.

 Chemical & Physical Properties

Molecular Formula C13H24ClNO9
Molecular Weight 373.78