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H-L-Lys(N3-Gly)-OH

  CAS No.: 1198617-82-1   Cat No.: BADC-01714   Purity: >99% 4.5  

H-L-Lys(N3-Gly)-OH is an azide-functionalized lysine-based ADC linker intermediate designed for site-specific click chemistry conjugation in antibody-drug conjugates. It supports precise payload attachment and controlled drug release in targeted cancer therapies. Keywords: ADC linker, azide linker, lysine derivative, click chemistry, targeted delivery.

H-L-Lys(N3-Gly)-OH

Structure of 1198617-82-1

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ADC Linker
Molecular Formula
C8H15N5O3
Molecular Weight
229.24
Shipping
Store at 2-8 °C

* For research and manufacturing use only. We do not sell to patients.

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Synonyms
N6-(2-Azidoacetyl)-L-lysine; (S)-2-Amino-6-(2-azidoacetamido)hexanoic acid; (2S)-2-Amino-6-(2-azidoacetamido)hexanoic acid; Azidoacetyl-L-Lysine; N6-(2-Azidoacetyl)-lysine; H-Lys(N3-Gly); Lys(N3-Gly); H-Lys(N3-Gly)-OH
IUPAC Name
(2S)-2-amino-6-[(2-azidoacetyl)amino]hexanoic acid
Canonical SMILES
C(CCNC(=O)CN=[N+]=[N-])C[C@@H](C(=O)O)N
InChI
InChI=1S/C8H15N5O3/c9-6(8(15)16)3-1-2-4-11-7(14)5-12-13-10/h6H,1-5,9H2,(H,11,14)(H,15,16)/t6-/m0/s1
InChIKey
JHBRZAKVPNZDFK-LURJTMIESA-N
Sequence
Lys(N3-Gly)
Storage
Store at 2-8 °C

H-L-Lys(N3-Gly)-OH, a compound with distinctive peptide modifications, finds specialized applications in bioscience. Here are four key applications:

Protein Labeling: Utilizing H-L-Lys(N3-Gly)-OH in bioconjugation techniques, researchers employ it as a foundational component for tagging proteins with fluorescent markers or other labels. This peptide alteration enables selective attachment, facilitating intricate studies on the dynamics of protein localization and interactions within cellular environments. This method plays a critical role in advanced imaging and proteomics research, unlocking new insights into the complex world of cellular biology.

Click Chemistry: The presence of an azide group in H-L-Lys(N3-Gly)-OH makes it ideal for click chemistry reactions, enabling the efficient coupling of diverse biomolecules. This innovative technique offers a versatile and high-yield approach to constructing complex molecular structures under gentle conditions. Scientists widely apply this method in synthesizing novel peptides, nucleic acids, and other bioactive compounds, advancing the frontier of molecular chemistry research.

Drug Delivery Systems: By incorporating H-L-Lys(N3-Gly)-OH into drug delivery systems, researchers enhance the targeting specificity and efficiency of therapeutic agents. This modified peptide facilitates the precise delivery of drugs to specific cells or tissues, improving treatment efficacy while minimizing side effects. This application proves invaluable in the development of targeted therapies for conditions like cancer.

Biocompatible Hydrogels: Introducing H-L-Lys(N3-Gly)-OH into hydrogel materials enables the modification of their mechanical and biological properties for applications in tissue engineering and regenerative medicine. These tailored hydrogels support cell growth, differentiation, and tissue repair, mimicking the natural extracellular environment. This crucial application lays the foundation for creating scaffolds and matrices that replicate the intricacies of biological systems, offering promising solutions for various biomedical challenges.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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