H-L-Ser(Propargyl)-OH hydrochloride is a serine-based ADC linker building block featuring a propargyl group for site-selective click conjugation. It improves antibody-drug conjugate stability and targeted payload delivery efficiency. Keywords: ADC linker, propargyl linker, serine derivative, click chemistry, bioconjugation.
Structure of 1379006-45-7
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Capabilities & Facilities
H-L-Ser(Propargyl)-OH hydrochloride, a versatile chemical compound utilized in peptidomimetics and drug design, boasts a diverse range of applications in bioscience. Here are four key applications:
Peptide Synthesis: H-L-Ser(Propargyl)-OH hydrochloride contributes to the synthesis of peptides adorned with terminal alkyne groups, facilitating click chemistry reactions. This innovative approach empowers researchers to construct intricate peptide structures with unparalleled efficiency. These tailored peptides find utility in investigations pertaining to protein interactions and functionality, offering a window into the intricate web of molecular biology.
Drug Development: H-L-Ser(Propargyl)-OH hydrochloride acts as a fundamental building block in the creation of novel compounds with promising therapeutic potentials. Its integration into peptidomimetics elevates the stability and binding affinity of lead compounds, paving the way for the development of next-generation drugs with enhanced pharmacokinetic attributes.
Chemical Biology: A linchpin in the domain of chemical biology, H-L-Ser(Propargyl)-OH hydrochloride finds application in studying post-translational modifications of proteins. By introducing alkyne handles, researchers can selectively label and monitor specific proteins within live cellular environments. This technique offers a unique insight into the dynamic nature and functional intricacies of proteins within their biological milieu.
Bioorthogonal Chemistry: The alkyne moiety within H-L-Ser(Propargyl)-OH hydrochloride stands as a critical tool in the toolbox of bioorthogonal chemistry, empowering researchers to modify biomolecules covalently without disrupting native cellular processes. This strategic capability opens avenues for precise imaging and probing of biological systems in a highly selective and efficient manner.
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