N3-Aca-Aca-OH is a bifunctional azide-containing ADC linker precursor designed for modular assembly of antibody-drug conjugates. It facilitates precise and stable payload attachment, improving therapeutic index in cancer treatment. Keywords: ADC linker, azide linker, bifunctional linker, drug conjugation.
Structure of 866363-71-5
* For research and manufacturing use only. We do not sell to patients.
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Capabilities & Facilities
N3-Aca-Aca-OH, a versatile small molecule with immense potential in various bioscience applications, plays a pivotal role in peptide synthesis, protease inhibition, drug development, and diagnostics.
Peptide Synthesis: Acting as a fundamental building block in peptide synthesis, N3-Aca-Aca-OH is indispensable for constructing complex peptide chains using solid-phase techniques. Its unique chemical properties facilitate crucial coupling reactions required for tailoring peptides with precise sequences tailored for therapeutic and biochemical studies.
Protease Inhibition: Embracing its role as a protease inhibitor, N3-Aca-Aca-OH emerges as a key player in biochemical research, binding to specific classes of proteases and disrupting their active sites. This mechanism sheds light on protease function and regulation, particularly in diseases marked by protease dysregulation.
Drug Development: Spearheading innovations in pharmaceutical research, N3-Aca-Aca-OH contributes significantly to the design and refinement of novel therapeutics. Its intricate structure enables the modification of lead compounds to enhance pharmacokinetics and bioavailability, amplifying the efficacy of drugs aimed at combatting diverse diseases like cancer and infectious ailments.
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