H-L-Lys(N3-Gly)-OH - CAS 1198617-82-1

H-L-Lys(N3-Gly)-OH - CAS 1198617-82-1 Catalog number: BADC-01714

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H-L-Lys(N3-Gly)-OH is a click chemistry containing an azide group, a lysine derivative.

Category
ADCs Linker
Product Name
H-L-Lys(N3-Gly)-OH
CAS
1198617-82-1
Catalog Number
BADC-01714
Molecular Formula
C8H15N5O3
Molecular Weight
229.24

Ordering Information

Catalog Number Size Price Quantity
BADC-01714 -- $-- Inquiry
Description
H-L-Lys(N3-Gly)-OH is a click chemistry containing an azide group, a lysine derivative.
IUPAC Name
(2S)-2-amino-6-[(2-azidoacetyl)amino]hexanoic acid
Canonical SMILES
C(CCNC(=O)CN=[N+]=[N-])CC(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

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

Historical Records: H-L-Lys(N3-Gly)-OH
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