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

DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA)

  CAS No.:   Cat No.: BADC-01422 4.5  

DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA) is a click-reactive drug-linker conjugate used in the synthesis of antibody-drug conjugates (ADCs).

DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA)

Structure of

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Cytotoxin with Linker
Molecular Formula
C79H95ClN12O20
Molecular Weight
1568.14

* 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
InChI
InChI=1S/C79H95ClN12O20/c1-48(2)68(88-65(94)27-32-107-34-36-109-38-39-110-37-35-108-33-29-82-64(93)25-26-66(95)91-45-52-16-10-9-14-50(52)21-22-51-15-11-12-18-60(51)91)74(97)87-57(17-13-28-83-77(81)100)73(96)84-55-23-19-49(20-24-55)47-111-78(101)89(3)30-31-90(4)79(102)112-62-43-61-67(56-42-59(76(99)106-8)86-70(56)62)54(44-80)46-92(61)75(98)58-40-53-41-63(103-5)71(104-6)72(105-7)69(53)85-58/h9-12,14-16,18-20,23-24,40-43,48,54,57,68,85-86H,13,17,25-39,44-47H2,1-8H3,(H,82,93)(H,84,96)(H,87,97)(H,88,94)(H3,81,83,100)/t54-,57+,68+/m1/s1
InChIKey
LRCRYXKCKKVMDA-CJHYWFRCSA-N

DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA) is a complex molecule used in targeted drug delivery and cancer therapy. Here are some key applications of DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA):

Antibody-Drug Conjugates (ADCs): This compound is utilized in the design of ADCs, which are engineered to target and destroy cancer cells specifically. The DBCO group enables site-specific conjugation to antibodies, ensuring precise delivery of the cytotoxic payload. By selectively targeting cancer cells, ADCs minimize off-target effects and improve the therapeutic index.

Cellular Imaging: DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA) can be used in cellular imaging applications to study cell surface proteins and internalization mechanisms. The DBCO moiety reacts with azide-modified biomolecules in a bioorthogonal fashion, allowing for the visualization of molecular interactions. This helps researchers to track the localization and fate of the compound within living cells.

Drug Delivery Systems: This molecule is fundamental in developing advanced drug delivery systems such as polymeric nanoparticles and liposomes. The PEG4 spacer improves solubility and biocompatibility, while the cleavable VC-PAB linker ensures the controlled release of the active drug within the target cells. This enhances the efficacy and safety profile of nanoparticle-based therapeutics.

Cancer Therapeutics Research: DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA) is widely used in preclinical research to explore new cancer therapeutic strategies. By studying the pharmacodynamics and pharmacokinetics of this compound, researchers can optimize its design for better targeting and reduced toxicity. This accelerates the development of next-generation cancer therapies.

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: DBCO-PEG4-vc-PAB-(PEG2)-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 | MPB-MMAF | Mylotarg-linker | OSu-PEG4-vc-PAB-DMEA-Duocarmycin DM | DBCO-PEG4-vc-PAB-(PEG2)-Duocarmycin TM | DBCO-PEG4-vc-PAB-Duocarmycin SA | DBCO-PEG4-VC-PAB-DMEA-((S)-Seco-Duocarmycin SA)
Send Inquiry
Verification code
Inquiry Basket