Mal-PEG4-Val-Cit-PAB - CAS 1949793-41-2

Mal-PEG4-Val-Cit-PAB - CAS 1949793-41-2 Catalog number: BADC-01023

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Category
ADCs Linker
Product Name
Mal-PEG4-Val-Cit-PAB
CAS
1949793-41-2
Catalog Number
BADC-01023
Molecular Formula
C36H55N7O12
Molecular Weight
777.86
Purity
>98.0%

Ordering Information

Catalog Number Size Price Quantity
BADC-01023 -- $-- Inquiry
Canonical SMILES
CC(C)C(C(=O)NC(CCCNC(=O)N)C(=O)NC1=CC=C(C=C1)CO)NC(=O)CCOCCOCCOCCOCCNC(=O)CCN2C(=O)C=CC2=O
InChI
InChI=1S/C36H55N7O12/c1-25(2)33(35(50)41-28(4-3-13-39-36(37)51)34(49)40-27-7-5-26(24-44)6-8-27)42-30(46)12-16-52-18-20-54-22-23-55-21-19-53-17-14-38-29(45)11-15-43-31(47)9-10-32(43)48/h5-10,25,28,33,44H,3-4,11-24H2,1-2H3,(H,38,45)(H,40,49)(H,41,50)(H,42,46)(H3,37,39,51)/t28-,33-/m0/s1
InChIKey
PEGLOOGTSQEDBL-UVMMSNCQSA-N
Solubility
10 mm in DMSO
Appearance
Solid
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature, or blue ice upon request.
Storage
Store at -20 °C, keep in dry and avoid sunlight.
Form
Solid

Mal-PEG4-Val-Cit-PAB is a bioconjugation reagent designed for use in targeted drug delivery systems, especially in the context of antibody-drug conjugates (ADCs). The compound consists of a maleimide (Mal) group, a polyethylene glycol (PEG4) spacer, and a Val-Cit-PAB (valine-citrulline-p-aminobenzyloxycarbonyl) linker. The maleimide group facilitates conjugation with thiol-containing biomolecules, such as antibodies or peptides, while the PEG4 spacer enhances solubility, stability, and pharmacokinetics. The Val-Cit-PAB linker is particularly useful for selective drug release, as it is cleaved by specific enzymes, making this compound ideal for controlled and targeted delivery of therapeutic agents.

One of the primary applications of Mal-PEG4-Val-Cit-PAB is in the development of antibody-drug conjugates (ADCs) for cancer therapy. The maleimide group enables the attachment of cytotoxic drugs to antibodies, allowing for the targeted delivery of therapeutics to cancer cells that express specific surface markers. The PEG4 spacer ensures the stability and solubility of the conjugate, improving circulation time and enhancing the pharmacokinetics of the ADC. The Val-Cit-PAB linker provides enzyme-sensitive cleavage, which ensures that the drug is released selectively in the tumor microenvironment, where the linker is typically cleaved by tumor-associated proteases. This mechanism minimizes systemic toxicity and improves the therapeutic index, making ADCs a powerful tool in precision medicine for cancer treatment.

Mal-PEG4-Val-Cit-PAB is also used in the design of targeted delivery systems for other therapeutic agents, such as small molecule drugs or RNA-based therapies. The PEG4 spacer enhances the solubility and bioavailability of the conjugate, while the Val-Cit-PAB linker allows for drug release under specific conditions. This feature makes Mal-PEG4-Val-Cit-PAB ideal for use in developing drugs that require targeted release at specific sites in the body, such as tumors or infected tissues. The ability to control drug release based on enzymatic activity allows for greater precision in treatment, reducing off-target effects and improving patient outcomes.

Another important application of Mal-PEG4-Val-Cit-PAB is in the field of peptide and protein conjugation for research and diagnostic purposes. The maleimide group facilitates the covalent attachment of peptides or proteins to other biomolecules, while the PEG4 spacer ensures that the conjugated molecules remain soluble and stable in aqueous environments. The Val-Cit-PAB linker enables selective cleavage, which is useful in creating controlled release systems for various bioactive agents. This compound is valuable in proteomics, immunoassays, and targeted delivery of imaging agents, offering high specificity and efficiency in conjugation and release applications.

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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