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

MC-vc-PAB-(PEG2)-duocarmycin TM

  CAS No.:   Cat No.: BADC-00744 4.5  

MC-vc-PAB-(PEG2)-duocarmycin TM is a drug-linker conjugate for ADC by using Duocarmycin TM (a potent antitumor antibiotic), linked via MA-MC-vc-PAB-(PEG2).

MC-vc-PAB-(PEG2)-duocarmycin TM

Structure of

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Cytotoxin with Linker
Molecular Formula
C62H77ClN10O16
Molecular Weight
1253.80
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
Shipping
Room temperature
Storage
-20°C

MC-vc-PAB-(PEG2)-duocarmycin TM is a powerful peptide-drug conjugate (PDC) that combines the targeting specificity of a peptide with the potent cytotoxicity of duocarmycin TM. One key application is in targeted cancer therapy. The conjugate uses a valine-citrulline (vc) linker to ensure selective cleavage by enzymes found in the tumor microenvironment. This enables the release of duocarmycin TM directly within the cancer cells, leading to efficient DNA damage and cell death while minimizing exposure to healthy tissues. This highly targeted approach reduces systemic toxicity and enhances therapeutic efficacy.

Another important application of MC-vc-PAB-(PEG2)-duocarmycin TM is in enhancing pharmacokinetics and stability. The addition of PEG2 (polyethylene glycol) to the conjugate improves its solubility, stability, and circulation time in the bloodstream. PEGylation helps to evade recognition by the immune system, thus preventing rapid clearance and allowing for prolonged drug exposure. This modification optimizes the drug’s bioavailability and improves its accumulation in the tumor site, which is essential for maximizing the therapeutic benefit of duocarmycin TM.

MC-vc-PAB-(PEG2)-duocarmycin TM also shows promise in combination therapies. The conjugate can be used alongside other anticancer treatments, such as immunotherapies or chemotherapy agents, to enhance the overall therapeutic response. By delivering duocarmycin TM directly to the tumor, it can work synergistically with other drugs to increase the likelihood of overcoming resistance mechanisms and achieving sustained tumor regression. This multi-pronged therapeutic approach offers a promising strategy to improve treatment outcomes in complex cancer cases.

Lastly, MC-vc-PAB-(PEG2)-duocarmycin TM is well-suited for personalized medicine applications. The peptide component of the conjugate can be tailored to bind to specific receptors or biomarkers expressed on various cancer types. This customization allows for the design of highly targeted therapies, providing an opportunity for more effective and personalized treatment regimens. By aligning the drug delivery with the unique molecular profile of a patient's cancer, MC-vc-PAB-(PEG2)-duocarmycin TM holds potential for advancing precision oncology and improving patient 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 Payload Development Biological Payload ADC Linker–Payload Conjugation ADC Linker Development Chemical Payload Enzyme Cleavable Linker Cathepsin B Cleavable Linker/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker

Unlock Deeper ADC Insights

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

Maytansine and Its Analogues Linkers - A Crucial Factor in Antibody–Drug Conjugates Cytotoxic Agents Used in Antibody–Drug Conjugates Exatecan Mesylate in ADCs: A New Topo I Inhibitor What is Calicheamicin? What is Monomethyl Auristatin E (MMAE)? What is Monomethyl Auristatin F (MMAF)? What is Pyrrolobenzodiazepine (PBD)? Antiviral Potential of Thapsigargin in COVID-19 Research In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress

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: Trastuzumab emtansine | PF-06380101 | Trastuzumab-MC-MMAE | Trastuzumab duocarmazine | PF-06380101 D8 | Moxetumomab pasudotox | Glembatumumab vedotin | Mirvetuximab-MMAE | Loncastuximab tesirine | Oportuzumab monatox | MC-vc-PAB-(PEG2)-duocarmycin TM
Send Inquiry
Verification code
Inquiry Basket