Maleimide-PEG2-hydrazide TFA

Maleimide-PEG2-hydrazide TFA Catalog number: BADC-01270

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Category
ADCs Linker
Product Name
Maleimide-PEG2-hydrazide TFA
Catalog Number
BADC-01270
Molecular Formula
C16H23F3N4O8
Molecular Weight
456.37
Purity
≥95%

Ordering Information

Catalog Number Size Price Quantity
BADC-01270 -- $-- Inquiry
Solubility
10 mm in DMSO
Shelf Life
-20°C 3 years powder; -80°C 2 years in solvent
Shipping
Room temperature
Storage
Store at -20 °C, keep in dry and avoid sunlight.

Maleimide-PEG2-hydrazide TFA is a versatile compound commonly used in bioconjugation and targeted drug delivery systems. The maleimide group is highly reactive with thiol groups on proteins, peptides, or antibodies, enabling the formation of stable covalent bonds. The PEG2 spacer, a short polyethylene glycol chain, provides enhanced solubility, reduces immunogenicity, and improves the pharmacokinetics of the conjugate. The hydrazide functional group is useful for further conjugation reactions, such as linking the compound to aldehydes or ketones on biomolecules. The trifluoroacetic acid (TFA) salt form ensures stability and ease of handling during synthesis and storage. This structure makes Maleimide-PEG2-hydrazide TFA ideal for creating highly specific and stable conjugates for therapeutic, diagnostic, and research applications.

One key application of Maleimide-PEG2-hydrazide TFA is in the development of targeted antibody-drug conjugates (ADCs) for cancer therapy. By conjugating cytotoxic drugs to antibodies through the maleimide linkage, the compound allows for the selective delivery of drugs directly to tumor cells. The PEG2 spacer enhances the solubility and stability of the conjugate, which is crucial for maintaining its effectiveness during circulation. The hydrazide group can further be used to attach the cytotoxic agent or imaging probe to the antibody, enhancing targeting specificity and reducing off-target toxicity. This method is particularly useful for therapies where traditional chemotherapy fails to target specific cancer cells.

Maleimide-PEG2-hydrazide TFA is also widely employed in the synthesis of diagnostic probes, particularly for cancer imaging. The hydrazide functionality allows for the efficient conjugation of imaging agents, such as fluorescent dyes or radiolabeled compounds, to antibodies or peptides that specifically bind to tumor antigens. The maleimide group facilitates selective conjugation to thiol groups on the targeting molecules, ensuring that the probe is directed precisely to the site of interest. This application is valuable for non-invasive imaging techniques like positron emission tomography (PET) or fluorescence imaging, which provide critical information for early detection, tumor localization, and treatment monitoring.

In addition to drug delivery and diagnostic applications, Maleimide-PEG2-hydrazide TFA is also utilized in the study of protein interactions and biomolecular engineering. The hydrazide group is a useful tool for labeling proteins, peptides, or nucleic acids with aldehyde- or ketone-functionalized molecules, enabling the tracking and analysis of biomolecular interactions. This can be particularly valuable in proteomics, where understanding protein-protein interactions or cellular localization is critical for studying disease mechanisms. The PEG2 spacer reduces steric hindrance and enhances the solubility of the conjugates, making it easier to study interactions in complex biological environments. This versatility makes Maleimide-PEG2-hydrazide TFA an important reagent in biomolecular research and diagnostics.

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: Maleimide-PEG2-hydrazide TFA
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