webinar
Oct. 27-28, 2025, Boston, MA, USA - Booth 114.
Read More

Mal-amido-PEG2-Val-Cit-PAB-OH

  CAS No.:   Cat No.: BADC-01267   Purity: ≥95% 4.5  

Mal-amido-PEG2-Val-Cit-PAB-OH is a maleimide cleavable ADC linker with PEG2 spacer and Val-Cit-PABC peptide for enzymatic drug release. Enhances stability and conjugation efficiency in ADCs.

Mal-amido-PEG2-Val-Cit-PAB-OH

Structure of

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C32H47N7O10
Molecular Weight
689.76
Shipping
Room temperature
Shipping
-20°C

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

Size Price Stock Quantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

Popular Publications Citing BOC Sciences Products
IUPAC Name
Solubility
10 mm in DMSO
Shelf Life
≥ 2 years
Shipping
Room temperature
Storage
-20°C

Mal-amido-PEG2-Val-Cit-PAB-OH is a chemical linker commonly used in the development of antibody-drug conjugates (ADCs) and other drug delivery systems. Here are some key applications of Mal-amido-PEG2-Val-Cit-PAB-OH:

Antibody-Drug Conjugates (ADCs): Mal-amido-PEG2-Val-Cit-PAB-OH is integral in the design of ADCs, where it acts as a stable yet cleavable linker between the antibody and therapeutic agent. This linker ensures the stable delivery of the drug to the target site and releases the drug upon internalization into target cells. The valine-citrulline dipeptide sequence is responsible for the linker’s cleavage inside lysosomes, ensuring controlled drug release and minimizing off-target effects.

Targeted Cancer Therapy: By facilitating the conjugation of cytotoxic drugs to targeting antibodies, Mal-amido-PEG2-Val-Cit-PAB-OH plays a crucial role in the development of targeted cancer therapies. Its design allows for precise delivery of potent chemotherapeutic agents to cancer cells, sparing healthy cells and reducing systemic toxicity. This approach enhances the therapeutic index of anticancer drugs, improving efficacy and patient outcomes.

Bioconjugation Research: Researchers use Mal-amido-PEG2-Val-Cit-PAB-OH in bioconjugation applications to study complex biological processes. Its bifunctional nature allows for precise attachment of biomolecules to proteins, facilitating the creation of bioconjugates for mechanistic studies and biomarker identification. This approach is valuable for both in vitro and in vivo studies, advancing our understanding of molecular interactions.

Drug Delivery Systems: In the broader field of drug delivery, Mal-amido-PEG2-Val-Cit-PAB-OH is employed to create versatile delivery platforms. Its PEG (polyethylene glycol) moiety provides solubility and biocompatibility, while the cleavable linker ensures drug activation at the target site. This is essential for developing advanced delivery technologies that improve drug pharmacokinetics, reduce side effects, and enhance therapeutic outcomes.

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

Related Products

Contact our experts today for pricing and comprehensive details on our ADC offerings.

You May Also Be Interested In

From cytotoxin synthesis to linker design, discover our specialized services that complement your ADC projects.

ADC Linker Development Enzyme Cleavable Linker Cathepsin B Cleavable Linker/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker/Hydrazone Linker

Unlock Deeper ADC Insights

Learn more about payload design, linker strategies, and integrated CDMO support through our curated ADC content.

Linkers - A Crucial Factor in Antibody–Drug Conjugates In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress New Structural Insights Solve Instability Issues of Maleimide Linkers in ADCs PEG Linkers in Antibody-Drug Conjugates Peptide Linkers in Antibody-Drug Conjugates Disulfide Linkers in Antibody-Drug Conjugates Biotinylation Reagents in Antibody-Drug Conjugates Maleimide Linkers in Antibody-Drug Conjugates Current ADC Linker Chemistry SPDB Linkers in Antibody-Drug Conjugates

Explore More ADC Products

Find exactly what your project needs from our expanded range of ADCs, offering flexible options to fit your timelines and goals.

ADC Cytotoxin

Powerful Targeted Cancer Solutions

ADC  Cytotoxin with Linker

Enhanced Stability And Efficacy

ADC Linker

Precise Conjugation For Success

Antibody-Drug  Conjugates (ADCs)

Maximized Therapeutic Performance

Auristatins

Next-Level Tubulin Inhibition

Calicheamicins

High-Impact DNA Targeting

Camptothecins

Advanced Topoisomerase Inhibition

Daunorubicins / Doxorubicins

Trusted Anthracycline Payloads

Duocarmycins

Potent DNA Alkylation Agents

Maytansinoids

Superior Microtubule Disruption

Pyrrolobenzodiazepines

Ultra-Potent DNA Crosslinkers

Traditional Cytotoxic Agents

Proven Chemotherapy Solutions

Cleavable Linker

Precise Intracellular Drug Release

Non-Cleavable Linker

Exceptional Long-Term Stability

Historical Records: perfluorophenyl 3-(2-(2-(2-(1,3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)ethoxy)propanoate | Fmoc-Phe-Lys(Trt)-PAB | perfluorophenyl 1-(1,3-dioxoisoindolin-2-yloxy)-3,6,9,12-tetraoxapentadecan-15-oate | PDdB-Pfp | Pladienolide D | Mal-PEG4-VC-PAB-DMEA | perfluorophenyl 1-(cyclooct-2-ynyloxy)-2-oxo-6,9,12,15-tetraoxa-3-azaoctadecan-18-oate | perfluorophenyl 3-(2-(2-(2-(cyclooct-2-ynyloxy)acetamido)ethoxy)ethoxy)propanoate | perfluorophenyl 3-(2-(4-formylbenzamido)ethoxy)propanoate | Ald-Ph-amido-PEG2-C2-Pfp ester | Mal-amido-PEG2-Val-Cit-PAB-OH
Send Inquiry
Verification code
Inquiry Basket