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

DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM

  CAS No.:   Cat No.: BADC-00761 4.5  

DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM is a drug-linker conjugate for ADC by using Duocarmycin DM (a potent antitumor antibiotic), linked via DBCO-PEG4-vc-PAB-(PEG2).

DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM

Structure of

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Cytotoxin with Linker
Molecular Formula
C83H103ClN12O18
Molecular Weight
1592.25
Shipping
Room temperature
Storage
-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

DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM, a bioconjugation molecule utilized in targeted cancer therapies, presents a multitude of applications. Here are four key applications:

Targeted Drug Delivery: The utilization of DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM in targeted cancer therapies involves the conjugation of this bioconjugation molecule to antibodies that exhibit specificity towards cancer cells. This groundbreaking approach facilitates the precise delivery of duocarmycin, a potent cytotoxic agent, directly to tumor cells. By minimizing off-target effects and enhancing therapeutic efficacy, this innovative strategy heightens the selectivity and potency of cancer treatments, reshaping the landscape of targeted drug delivery with remarkable precision.

Preclinical Oncology Research: Within the realm of preclinical oncology research, this compound assumes a pivotal role in evaluating the effectiveness of antibody-drug conjugates (ADCs). Researchers leverage the unique properties of DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM to investigate the pharmacokinetics, biodistribution, and antitumor activity of experimental ADCs. These studies yield indispensable data essential for advancing ADC candidates into clinical trials, propelling forward groundbreaking advancements in the field of oncology research with profound insights.

Biochemical Assays: In the domain of biochemical assays, DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM serves as a cornerstone for monitoring the internalization and intracellular processing of ADCs. Leveraging the click chemistry potential of DBCO, researchers can seamlessly conjugate this molecule to a diverse range of biological targets, facilitating a deeper comprehension of the underlying mechanisms of action. These assays not only unravel the intricacies of biological processes but also aid in optimizing the design of ADCs to achieve enhanced therapeutic outcomes, pushing the boundaries of biochemical research with unparalleled precision.

Combination Therapy Research: Embarking on studies exploring combination therapies, researchers leverage the versatility of this molecule by conjugating it with other therapeutic agents. By merging targeted delivery with complementary treatments, novel synergistic strategies are devised to combat resistance mechanisms and amplify anti-cancer effects.

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 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: DBCO-PEG4-vc-PAB-Duocarmycin SA | C-lock-PEG4-MMAE | DBCO-PEG4-vc-PAB-Duocarmycin TM | OSu-PEG4-vc-PAB-DMEA-Duocarmycin SA | OSu-PEG4-vc-PAB-DMEA-Duocarmycin TM | Me-Tet-PEG3-NH2 | MPB-MMAF | DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin SA | Me-Tet-PEG8-NH2 hydrochloride | DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin DM
Send Inquiry
Verification code
Inquiry Basket