Catalog No.
Product Name
Application
Product Information
Citations
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Azide Reaction Probe
Cyanine5 DBCO hexafluorophosphate is an azide-reactive probe designed for copper-free "click" reactions, enabling the selective imaging of azide-labeled biomolecules. This near-infrared fluorescent dye exhibits low toxicity to cells, making it suitable for both in vitro and in vivo applications without compromising the physiological functions of non-target cells. Its optimal excitation and emission wavelengths (Ex=635 nm, Em=650-700 nm) facilitate efficient cellular labeling and tracking, providing valuable insights in biological research. -
ADC Linker
DBCO-PEG3-TCO is a non-cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs), featuring a 3-unit polyethylene glycol (PEG) spacer. This reagent facilitates click chemistry through its dibenzocyclooctyne (DBCO) moiety, enabling strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-functionalized compounds. Additionally, the TCO group supports inverse electron demand Diels-Alder (iEDDA) reactions with tetrazine-containing molecules, making DBCO-PEG3-TCO a versatile tool for advancing ADC development in therapeutic research. -
ADC/PROTAC Linker
DBCO-NHCO-PEG4-NH-Boc is a versatile PROTAC linker featuring a cleavable structure designed for the synthesis of PROTACs and antibody-drug conjugates (ADCs). This compound utilizes a DBCO moiety, enabling efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its PEG4 spacer enhances solubility and stability, making it suitable for various biological applications in drug development and therapeutic research. -
ADC/PROTAC Linker
DBCO-NHCO-PEG4-amine is a PEG-based linker designed for use in antibody-drug conjugates (ADCs) and PROTACs. This cleavable linker facilitates the conjugation of payloads such as MMAE to antibodies, enhancing targeted delivery to cancer cells. It has demonstrated compelling biological activities, with EC50 values of 280 nM and 22 nM for DBCO-VCpAB MMAE and DBCO-TRX MMAE, respectively, in SKBR3 cells, making it a valuable tool for researchers investigating targeted therapies. -
PROTAC Linkers
DBCO-N-bis(PEG4-NHS ester) is a bifunctional polyethylene glycol (PEG) linker featuring two NHS ester groups and a dibenzocyclooctyne (DBCO) moiety. This reagent facilitates protein modification and labeling, enhancing bioconjugation applications. As a click chemistry tool, DBCO-N-bis(PEG4-NHS ester) enables efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, making it valuable for constructing PROTAC molecules and other bioorthogonal conjugates in various biochemical research settings. -
Click Chemical Agent
DBCO-PEG24-acid is a click chemistry reagent that incorporates a dibenzocyclooctyne (DBCO) group linked to a hydrophilic polyethylene glycol (PEG) chain. This compound facilitates copper-free click reactions, leveraging the high energy associated with the DBCO moiety for efficient bioconjugation. The terminal carboxylic acid allows for the formation of stable amide bonds with primary amines in the presence of coupling agents such as EDC or HATU. It is a valuable tool in bioconjugation studies and the development of drug delivery systems. -
ADC linker
DBCO-NHS Ester 3 is a cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs). This compound features a dibenzocyclooctyne (DBCO) moiety that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, enabling efficient conjugation. DBCO-NHS Ester 3 is utilized in various applications involving targeted drug delivery and bioconjugation strategies in chemical biology and therapeutic development. -
Click Chemistry Intermediate
DBCO-C3-Acid is a versatile Click Chemistry intermediate that serves as a key component in the development of antibody-drug conjugate (ADC) linkers. Its chemical structure facilitates efficient conjugation processes, enabling precise attachment of cytotoxic agents to antibodies. This reagent is essential for advancing research in targeted cancer therapeutics and improving drug delivery systems. -
ADC Linker
Mal-bis-PEG3-DBCO is a cleavable linker designed for antibody-drug conjugate (ADC) synthesis, functioning through the efficient coupling of DBCO and azide moieties. This reagent incorporates a 3-unit polyethylene glycol (PEG) chain, enhancing solubility and biocompatibility. Its mechanism relies on strain-promoted alkyne-azide cycloaddition (SPAAC), making it ideal for precise conjugation applications in targeted drug delivery and cancer therapeutics research. -
PROTAC Linker
TCO-PEG4-DBCO is a versatile PROTAC linker known for its ability to facilitate the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features a DBCO moiety that enables strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing compounds, while the TCO component allows for inverse electron demand Diels-Alder (iEDDA) reactions with tetrazine derivatives. TCO-PEG4-DBCO finds applications in the development of antibody-drug conjugates (ADCs), enhancing the precision and efficacy of targeted therapeutics. Its unique chemical properties make it a valuable tool for researchers in chemical biology and drug development. -
ADC Linker
Mal-Sulfo-DBCO is a cleavable linker designed for use in antibody-drug conjugate (ADC) synthesis. Featuring a DBCO moiety, it facilitates the efficient strain-promoted alkyne-azide cycloaddition (SPAAC) reaction with azide-containing compounds. This property makes Mal-Sulfo-DBCO valuable for precise conjugation in targeted drug delivery applications, enhancing therapeutic efficacy while minimizing off-target effects. -
Azide Compound
Hydroxy-PEG3-DBCO is a versatile click chemistry reagent featuring a DBCO moiety and a terminal hydroxyl group. This PEG-based linker enhances solubility for labeled molecules while enabling efficient reactions with various functional groups. DBCO facilitates copper-free click chemistry, making it suitable for a wide range of bioconjugation applications in chemical and biochemical research. Designed for use in laboratory research, this reagent provides a reliable tool for developing complex biological systems and materials. -
ADC/PROTAC Linker
DBCO-NHCO-PEG4-NHS ester is a versatile linker designed for use in the synthesis of PROTACs and antibody-drug conjugates (ADCs). This PEG/alkyl/ether-based compound features a DBCO moiety that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its cleavable nature enhances the functionality and targeting capabilities of therapeutic agents, making it essential for researchers involved in drug development and bioconjugation applications. -
ADC Linker
DBCO-PEG1-OH is an ADC linker designed for effective conjugation in antibody-drug conjugate (ADC) applications. This compound facilitates the synthesis of ADCs by providing a stable and efficient link between monoclonal antibodies and therapeutic agents. Its utility in ADC development supports research in targeted cancer therapies and drug delivery systems. -
ADC Linker
DBCO-PEG3-C1-acid is an efficient ADC linker designed to facilitate strain-promoted azide-alkyne click reactions. This reagent serves as a powerful tool in the development of antibody-drug conjugates, enhancing target specificity and therapeutic efficacy. Its biocompatible PEG spacer provides solubility and flexibility, making it ideal for conjugating various cytotoxic agents for targeted cancer therapy applications. -
ADC Linker
DBCO-PEG4-Val-Ala-PAB is a cleavable ADC linker that effectively targets Cathepsin B for linker cleavage. The incorporation of Val-Ala linkers facilitates the controlled release of therapeutic agents, enhancing the efficacy of antibody-drug conjugates (ADCs). The DBCO moiety enables efficient Click Chemistry reactions, while the PEG spacer enhances the aqueous solubility of the compound, making it suitable for various biochemical applications. -
ADC Linker
Mal-PEG4-bis-PEG3-DBCO is a cleavable linker designed for use in antibody-drug conjugates (ADCs), facilitating targeted delivery of therapeutics. This reagent features a DBCO group that enables strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, allowing for efficient conjugation. Its PEGylated structure enhances solubility and provides stability in biological applications, making it suitable for ADC development and related research endeavors. -
ADC Linker
DBCO-PEG3 acetic-EVCit-PAB is a cleavable ADC linker that features a three-unit polyethylene glycol (PEG) chain. This compound facilitates the construction of antibody-drug conjugates (ADCs) by employing click chemistry through its dibenzocyclooctyne (DBCO) moiety, which engages in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. DBCO-PEG3 acetic-EVCit-PAB is integral in enhancing the specificity and efficacy of therapeutic agents in targeted cancer treatments, making it a valuable tool for bioconjugation research. -
ADC Linker
DBCO-PEG4-alkyne is a non-cleavable linker designed for antibody-drug conjugates (ADCs), featuring a 4-unit polyethylene glycol (PEG) chain. This compound serves as a versatile click chemistry reagent, incorporating an alkyne functional group that enables the efficient copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. Its application in ADC synthesis facilitates the stable conjugation of therapeutic agents, enhancing the efficacy and selectivity of targeted cancer treatments. -
ADC Linker
Bromoacetamide-PEG4-DBCO is an efficient ADC linker that facilitates the synthesis of antibody-drug conjugates. This compound features a bromoacetamide moiety for selective labeling and a DBCO group for click chemistry applications. It is ideal for enhancing the therapeutic efficacy of targeted cancer treatments by enabling stable conjugation to antibodies. This linker is suitable for a variety of research applications focused on drug delivery systems and cancer therapeutics. -
ADC Linker
DBCO-PEG2-C2-acid is an efficient ADC linker that facilitates the synthesis of Antibody-Drug Conjugates (ADCs). This compound utilizes the DBCO (dibenzocyclooctyne) chemistry for site-specific conjugation, enhancing the stability and efficacy of the resulting ADCs. It is essential for researchers focused on developing targeted therapies in oncology and other therapeutic areas, allowing for improved drug delivery and minimized off-target effects. -
ADC Linker
DBCO-S-S-acid is a cleavable linker designed for the construction of antibody-drug conjugates (ADCs). It features a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, allowing for selective and efficient conjugation. This reagent is essential in bioconjugation strategies aimed at enhancing targeted therapeutic delivery in cancer research and other therapeutic applications. -
ADC/PROTAC Linker
DBCO-NHCO-PEG4-acid is a PEG-based linker designed for application in antibody-drug conjugates (ADCs) and PROTAC synthesis. This linker features a DBCO group that participates in strain-promoted alkyne-azide cycloaddition (SPAAC), facilitating selective conjugation with azide-containing molecules. Its chemical properties make it ideal for developing targeted therapeutics that can modulate protein levels in biological research, enhancing experimental outcomes in drug discovery and development. -
Azide Compound
Sulfo DBCO-PEG3-acid is a click chemistry reagent featuring an azide group that facilitates copper-free Click Chemistry reactions through its DBCO moiety. The compound's hydrophilic PEG linker and sulfonate group enhance solubility in aqueous environments, making it suitable for biological applications. The terminal carboxylic acid reacts with primary amine groups in the presence of coupling agents such as EDC or HATU, generating stable amide bonds for bioconjugation studies. This reagent is intended for research purposes only. -
Click Chemistry Reagent
Sulfo DBCO-TFP Ester is a water-soluble click chemistry reagent that features a sulfo group. This compound facilitates the efficient and straightforward conjugation of sulfo-DBCO moieties to amine-containing biomolecules. Its applications include labeling, drug delivery, and the development of bioconjugates in various biochemical and biomedical research fields. -
Azide-Labelled Probe
Cy5 DBCO chloride is a DBCO-based probe designed for applications involving azide-labeled biomolecules. It facilitates copper-free "Click Chemistry" through strain-promoted alkyne-azide cycloaddition (SPAAC), enabling efficient imaging of azide-modified targets. This reagent is particularly valuable for studies involving bioorthogonal labeling and tracking of biomolecules in various research applications, including cellular visualization and bioimaging. -
PROTAC Linkers
DBCO-NHCO-PEG12-biotin is a PEG-based PROTAC linker that facilitates the synthesis of PROTACs through its reactive DBCO moiety. This compound engages in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-bearing molecules, allowing for precise conjugation in chemical biology applications. Its utility in targeted protein degradation research makes it a valuable tool for biochemists developing innovative therapeutic strategies. -
Fluorescent Dye
TAMRA DBCO, 5-isomer is a fluorescent dye derivative of tetramethylrhodamine (TMR) featuring a dibenzocyclooctyne (DBCO) moiety. It enables rapid and efficient labeling of azide-containing biomolecules through a sterically promoted azide-alkyne cycloaddition (SPAAC) reaction, eliminating the need for copper catalysts. This compound is suitable for a wide range of applications, including the labeling of proteins, peptides, and nucleic acids, facilitating advanced studies in biochemistry and cellular imaging. -
TARMA Dye
DBCO-PEG4-TAMRA is a PEG-conjugated TAMRA dye featuring a dibenzocyclooctyne (DBCO) moiety, facilitating efficient Click Chemistry through strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This reagent is crucial for oligonucleotide labeling and is widely utilized in automated DNA sequencing applications. Its bioconjugation capabilities enhance the specificity and sensitivity of various research techniques, making it a valuable tool in molecular biology and biochemical studies. -
AOC Linker
Bis-Mal-Lysine-PEG4-DBCO is a dibenzocyclooctyne (DBCO) linker designed for use in alkyne-azide cycloaddition (AOC) applications. This compound facilitates the synthesis of AOC drugs, enabling the targeted inhibition of DMPK gene expression. Its efficient coupling properties make it a valuable tool for research in gene regulation and therapeutic development. -
STING Agonist
diABZI-V/C-DBCO is a potent STING agonist with an EC50 of 1.47 nM. It activates the STING pathway to promote the production of type I interferons, particularly IFN-β, enhancing immune responses. This compound acts as a substrate for cathepsin B, leading to the release of active diABZI-amine through cathepsin B-mediated cleavage. In preclinical studies using an orthotopic mouse model of breast cancer, diABZI-V/C-DBCO has been shown to elevate serum levels of IFN-β and increase the frequency of granzyme B+ CD8+ T cells, making it valuable for research in triple-negative breast cancer. -
Lipid
DMG-PEG(2k)-DBCO is a clickable PEG lipid featuring a DBCO moiety. This compound is primarily utilized in the formulation of lipid nanoparticles, facilitating effective drug delivery applications. Its biochemical properties enable efficient conjugation processes, making it valuable for various bioconjugation strategies in lipid-based formulations. -
PROTAC Linker
DBCO-PEG3-NHS is a PROTAC linker featuring an alkynyl (DBCO) and N-hydroxysuccinimide (NHS) ester group, facilitating the chemical modification of proteins and antibodies. This reagent is instrumental in the synthesis of PROTACs, enhancing targeted protein degradation applications, as well as contributing to drug delivery systems and the development of biosensors and diagnostic assays. It allows for precise conjugation chemistry, enabling innovative research in therapeutic development and biomolecular interactions. -
PROTAC Linker
Sulfo DBCO-PEG4-amine is a polyethylene glycol (PEG)-based linker designed for use in proteolysis-targeting chimera (PROTAC) synthesis. This compound facilitates targeted degradation of proteins by connecting E3 ubiquitin ligases to specific proteins of interest. Its application in PROTAC development enhances selectivity and efficacy in degradation pathways, supporting research in targeted protein modulation and therapeutic interventions. -
PROTAC Linker
DBCO-PEG4-C2-acid is a PEG-based linker designed for use in the synthesis of PROTACs. It features a dibenzocyclooctyne (DBCO) moiety, enabling reaction via strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing compounds. This reagent is essential for the development of targeted protein degradation strategies, facilitating precise modular assembly in therapeutic research applications. -
PROTAC Linker
DBCO-PEG4-Desthiobiotin is a PEG-based linker designed for use in the synthesis of PROTACs (Proteolysis Targeting Chimeras). It features a DBCO moiety that facilitates efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing compounds. This reagent is essential for developing targeted protein degradation tools, enabling researchers to investigate protein function and cellular pathways through controlled protein turnover. -
PROTAC Linkers
Oleic-DBCO is a versatile PROTAC linker featuring an alkyl chain structure. It serves as a click chemistry reagent, incorporating a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This property makes Oleic-DBCO valuable for the synthesis of targeted protein degradation compounds in chemical biology research, enabling the study of protein function and drug development. -
PROTAC Linkers
DBCO-PEG1-NHS ester is a PEG-based PROTAC linker designed for the synthesis of PROTACs. This compound features a DBCO group, enabling strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. It facilitates the development of targeted protein degradation strategies, making it valuable in research applications focused on therapeutic interventions targeting specific proteins. -
PROTAC Linker
Dde Biotin-PEG4-DBCO is a PEG-based PROTAC linker designed for the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, enabling efficient conjugation. Its unique properties make it suitable for applications in cellular proteomic studies and drug discovery, highlighting its utility in targeted protein degradation research. -
PROTAC Linkers
N-(DBCO-PEG4)-N-Biotin-PEG4-NHS is a PEG-based linker designed for the synthesis of PROTACs. This reagent features a DBCO group that allows for efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its biotin component enhances labeling and purification processes, making it valuable in target protein degradation studies and other biochemical applications. -
PROTAC Linker
DBCO-PEG5-GGG-NH2 is a versatile PROTAC linker that facilitates the creation of proteolysis-targeting chimeras (PROTACs). This compound efficiently connects target proteins with E3 ligases, enabling the modulation of protein degradation pathways. Its application in synthetic biology allows researchers to explore targeted protein degradation strategies for therapeutic interventions. -
PROTAC Linkers
DBCO-PEG5-DBCO is a PEG-based linker specifically designed for synthesizing PROTACs. Featuring a dibenzocyclooctyne (DBCO) moiety, this reagent enables efficient strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with azide-containing molecules. Its versatility makes it an invaluable tool in the development of targeted protein degradation strategies, facilitating research into novel therapeutic approaches in various biological systems. -
PROTAC Linker
Sulfo DBCO-amine is a versatile PROTAC linker designed to facilitate the synthesis of PROTACs. This compound features a DBCO moiety that enables strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, allowing for efficient and selective conjugation. Its application in chemical biology is crucial for developing targeted protein degraders, thereby advancing research in protein modulation and therapeutic intervention. -
PROTAC linker
N-DBCO-N-bis(PEG2-C2-acid) is a PEG-based linker designed for PROTAC synthesis, functioning primarily through click chemistry. Featuring a DBCO moiety, it facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing compounds. This reagent enhances the development of targeted protein degradation strategies, proving valuable in various biochemical applications and studies aimed at modulating protein levels within cellular systems. -
PROTAC Linker
DBCO-PEG4-alcohol is a PEG-based linker specifically designed for PROTAC (Proteolysis Targeting Chimera) synthesis. Featuring a DBCO group, this compound facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its application in the development of targeted protein degradation strategies underscores its significance in chemical biology and therapeutic research. -
PROTAC Linkers
DBCO-PEG12-Maleimide is a PEG-based linker designed for use in the synthesis of PROTACs (proteolysis-targeting chimeras). It features a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with azide-containing molecules, enabling efficient and selective conjugation. This chemical reagent is valuable in targeted protein degradation studies and the development of novel therapeutic strategies. -
PROTAC linker
DSPE-PEG4-DBCO is a polyethylene glycol (PEG)-based linker designed for use in the synthesis of PROTACs. This compound features a dibenzocyclooctyne (DBCO) moiety, enabling efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. As a versatile click chemistry reagent, DSPE-PEG4-DBCO facilitates the construction of bifunctional probes for targeted protein degradation studies and other applications in chemical biology. -
PROTAC Linkers
DBCO-NHCO-PEG6-Biotin is a PEG-based linker designed for use in the synthesis of PROTACs (proteolysis-targeting chimeras). It features a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, enabling the conjugation of biotin for enhanced target protein degradation. This reagent is ideal for applications in chemical biology and drug discovery, particularly in the development of advanced therapeutic modalities. -
PROTAC Linker
PC DBCO-PEG4-NHS ester is a PEG-based linker designed for use in the synthesis of PROTACs, functioning as a critical component in targeted protein degradation. This compound features a DBCO moiety that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-functionalized molecules. It serves as a valuable tool in chemical biology for developing novel therapeutic strategies by enabling the creation of bifunctional compounds that can modulate protein interactions. -
PROTAC Linkers
DBCO-NHCO-PEG2-maleimide is a PEG-based linker designed for use in the synthesis of PROTACs (proteolysis-targeting chimeras). This compound features a DBCO (dibenzocyclooctyne) moiety, enabling efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its application in PROTAC development facilitates targeted degradation of specific proteins, enhancing research in pharmacology and therapeutic discovery.
