Catalog No.
Product Name
Application
Product Information
Citations
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S-IIP inhibitor/KRASG12C Probe
ARS-1323-Alkyne is a novel KRASG12C occupancy probe. -
BET inhibitor
JQ1-TCO (JQ1-trans-cyclooctene) is a derivative of JQ1, a BET inhibitor, modified for click chemistry applications. It serves as a molecular probe for in vitro and in vivo studies. -
NAT10 Inhibitor
CPTH2-Alkyne is a selective inhibitor of N-acetyltransferase 10 (NAT10), which plays a crucial role in cellular processes. This compound exhibits distinctive localization, accumulating in nucleoli and associating with the nuclear periphery and cytoplasm. CPTH2-Alkyne is utilized in research focused on nuclear architecture and has potential applications in the study of laminopathies, aiding the understanding of cellular structural dynamics. -
ADC Linker
DBCO-NHS ester is a non-cleavable linker utilized in the synthesis of antibody-drug conjugates (ADCs). It serves as a click chemistry reagent, featuring a DBCO moiety that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This compound is essential for bioconjugation applications, allowing for the stable attachment of therapeutics to antibodies, thereby enhancing the efficacy and specificity of targeted drug delivery in cancer research. -
ADC Linker
DBCO-PEG4-Maleimide is a non-cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs). This compound features a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, enabling efficient conjugation. It is essential for applications in targeted drug delivery, enhancing the therapeutic efficacy of ADCs while minimizing off-target effects. -
ADC/PROTAC Linker
DBCO-PEG5-NHS ester is a cleavable linker designed for use in antibody-drug conjugates (ADCs) and PROTAC synthesis. This PEG/alkyl/ether-based reagent facilitates the formation of stable covalent bonds through strain-promoted alkyne-azide cycloaddition (SPAAC), targeting azide-functionalized molecules. Its defined structure enhances the efficacy and specificity of therapeutic compounds, making it a valuable tool for researchers in the development of targeted therapies. -
ADC Linker
Gly-Gly-Gly-PEG4-DBCO is a polyethylene glycol (PEG) linker designed for use in antibody-drug conjugates (ADCs). Featuring a dibenzocyclooctyne (DBCO) functional group, this compound facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with azide-bearing compounds. Its high stability and efficiency make it an essential tool in the development of targeted therapeutics for improved delivery of cytotoxic drugs. -
ADC Linker
DBCO-Maleimide is a non-cleavable linker specifically designed for the synthesis of antibody-drug conjugates (ADCs). As a click chemistry reagent, it features a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This property enables seamless conjugation and enhances the therapeutic efficacy of ADCs, making DBCO-Maleimide an essential tool in bioconjugation and targeted drug delivery research. -
Click Chemical Agent
DBCO-PEG24-NHS ester is a click chemistry reagent designed for selective conjugation through the reaction with primary amines, such as lysine side chains or aminosilane-coated surfaces, under neutral to slightly basic conditions. The NHS ester facilitates the formation of a stable covalent bond, while the hydrophilic PEG spacer enhances water solubility and offers a flexible linkage that reduces steric hindrance during ligation. This compound is particularly suited for applications in bioconjugation and the development of targeted delivery systems. -
ADC Linker
DBCO-Sulfo-NHS ester sodium is an efficient ADC linker designed for the synthesis of antibody-drug conjugates (ADCs), facilitating targeted drug delivery. This reagent features a DBCO group that enables strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its versatile coupling capabilities make it an essential tool for researchers developing novel therapeutics in cancer and other diseases. -
ADC Linker
Fluorescein-DBCO is a non-cleavable linker designed for use in the formation of antibody-drug conjugates (ADCs). This compound features a dibenzocyclooctyne (DBCO) group, enabling it to participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with azide-containing molecules. Its unique properties make Fluorescein-DBCO an essential tool for researchers focusing on targeted drug delivery and cancer therapy applications through ADC development. -
ADC Linker
DBCO-Val-Cit-PABC-PNP is a cleavable linker designed for the construction of antibody-drug conjugates (ADCs). This compound features a DBCO moiety that participates in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing substrates. Its unique structure enables precise conjugation and controlled release of cytotoxic agents, making it essential for advancing ADC research and therapeutic development. -
Azide Compound
DBCO-PEG2-NHS ester is a click chemistry reagent with an azide group, designed to facilitate bioconjugation through reactions with primary amines, such as lysine side chains or aminosilane-coated surfaces. This PEG-based compound features an NHS ester, which enables the formation of stable covalent bonds under neutral to slightly basic conditions. The hydrophilic polyethylene glycol (PEG) spacer enhances solubility and adds flexibility, reducing steric hindrance during ligation. DBCO-PEG2-NHS ester is ideal for applications in copper-free Click Chemistry and other bioconjugation studies. -
ADC Linker
DBCO-CONH-S-S-NHS ester is a cleavable linker specifically designed for the synthesis of antibody-drug conjugates (ADCs). Its primary mechanism involves the DBCO group, facilitating strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This reagent plays a crucial role in the development of ADCs, allowing for targeted delivery of cytotoxic agents and enhancing therapeutic efficacy. Suitable for various applications in chemical biology and bioconjugation research. -
ADC Linker
Tetrazine-biotin is a cleavable linker designed for use in the synthesis of antibody-drug conjugates (ADCs). This compound features a tetrazine moiety that participates in the inverse electron demand Diels-Alder (iEDDA) reaction with TCO-containing molecules, facilitating efficient click chemistry. Tetrazine-biotin is a valuable tool for researchers exploring targeted drug delivery and the development of novel ADC therapies. -
ADC Linker
BCN-PEG3-Biotin is a non-cleavable three-unit polyethylene glycol (PEG) linker specifically designed for use in antibody-drug conjugates (ADCs). This reagent features a bicyclo[6.1.0]nonyne (BCN) group that facilitates strain-promoted azide-alkyne cycloaddition (SPAAC) with azide-containing molecules. It serves as a valuable tool in the synthesis of ADCs, enhancing stability while providing biotin functionality for further bioconjugation applications in research and development. -
ADC/PROTAC Linker
DBCO-PEG4-DBCO is a PEG-based linker primarily designed for use in antibody-drug conjugates (ADCs) and PROTAC synthesis. This compound features a dibenzocyclooctyne (DBCO) group, facilitating strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its versatile reactivity enables the development of targeted therapeutics, enhancing specificity and efficacy in research applications focused on protein degradation and targeted delivery systems. -
Click Chemistry Reagent
TCO-PEG3-maleimide is a click chemistry reagent that facilitates the efficient conjugation of trans-cyclooctene (TCO) moieties to thiol-containing molecules, including antibodies and cysteine-containing peptides. Through a rapid and selective reaction with thiol groups, this compound is valuable for a variety of bioconjugation applications. Its unique properties enable researchers to explore novel therapeutic strategies and enhance the development of bioconjugates in chemical biology. -
ADC Linker
DBCO-PEG3-oxyamine is a non-cleavable linker specifically designed for antibody-drug conjugate (ADC) synthesis. Featuring a DBCO moiety, this reagent facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with azide-containing molecules. Its application in conjugating antibodies to therapeutic agents enhances targeted delivery and efficacy in cancer research and drug development. -
ADC Linker
BCN-endo-PEG2-maleimide is a bifunctional ADC linker featuring two polyethylene glycol (PEG) units and a maleimide group. It acts as a bioconjugation reagent, facilitating stable linkages to azide-containing molecules through a copper-free click chemistry reaction, yielding stable triazoles. The maleimide moiety allows for selective conjugation to thiol groups, making it suitable for drug delivery applications. This compound is primarily utilized in the development of antibody-drug conjugates (ADCs) and other bioconjugation strategies. -
ADC Linker
DBCO-Sulfo-Link-biotin is a cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs). It features a DBCO moiety that enables efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing compounds. This reagent is valuable in the development of targeted therapies, facilitating precise delivery of cytotoxic agents to tumor cells while minimizing off-target effects. Its application enhances the effectiveness of therapeutic strategies in oncology and related fields. -
ADC Linker
endo-BCN-PEG4-acid is a versatile cleavable linker designed for antibody-drug conjugates (ADCs), facilitating targeted drug delivery. Featuring a bicyclo[6.1.0]nonyne (BCN) moiety, this compound enables efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. It is particularly useful in bioconjugation and drug development applications, allowing for the precise attachment of therapeutic agents to antibodies. -
PROTAC Linkers
BCN-PEG4-NHS ester is a PEG-based linker specifically designed for the synthesis of PROTACs (Proteolysis Targeting Chimeras). Its primary mechanism involves the BCN group, which facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This reagent is essential for enabling targeted protein degradation and enhancing the therapeutic potential of PROTACs in chemical biology research. Additionally, it serves as an effective tool for bioconjugation applications, expanding the versatility of synthetic approaches in drug discovery. -
ADC Linker
DBCO-NHCO-S-S-NHS ester is a cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs). This compound contains a DBCO group, facilitating strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Its application is crucial in the construction of targeted therapies, enabling the selective delivery of cytotoxic agents to specific cells. -
ADC Linker
DBCO-C6-acid is a non-cleavable ADC linker that facilitates the formation of antibody-drug conjugates (ADCs). Its unique DBCO moiety allows for efficient strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing compounds. This reagent is particularly useful in the synthesis of carmaphycin analogues, enabling targeted delivery of therapeutic agents for enhanced efficacy in research applications related to targeted cancer therapies. -
ADC/PROTAC Linker
TCO-PEG12-NHS ester is a PEG-based linker designed for use in the synthesis of PROTACs (Proteolysis Targeting Chimeras) and antibody-drug conjugates (ADCs). This cleavable linker facilitates the conjugation of therapeutics, enabling targeted degradation of specific proteins via the ubiquitin-proteasome pathway. Its unique properties make it suitable for advancing research in targeted therapies and optimizing drug delivery systems. -
ADC Linker
Azido-methyltetrazine di-arm linker is a novel linker specifically designed for the synthesis of antibody-drug conjugates (ADCs). This multivalent linker facilitates the conjugation of therapeutic agents to antibodies, enhancing the efficacy and targeting capabilities of ADCs. It is an essential reagent for researchers exploring the development of targeted cancer therapies and improving the selectivity of drug delivery systems. -
ADC/PROTAC Linker
DBCO-PEG4-amine is a PEG-based linker designed for use in the synthesis of PROTACs and antibody-drug conjugates (ADCs). This versatile cleavable linker allows for efficient conjugation through its DBCO group, enabling strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with azide-containing molecules. Its applications extend to the creation of homobifunctional cross-linkers, such as FPM-PEG4-DBCO, facilitating advanced drug delivery and targeted degradation strategies in chemical biology research. -
ADC Linker
BCN-exo-PEG7-maleimide is an ADC linker featuring a polyethylene glycol (PEG) spacer of seven units, facilitating improved solubility and stability. This compound incorporates the bidentate macrocyclic ligand BCN, enabling efficient synthesis of macrocyclic complexes. In click chemistry applications, BCN selectively reacts with azide-containing molecules to yield stable triazoles without the need for catalysts. Additionally, the maleimide functional group undergoes hydrolytic degradation, making it suitable for drug delivery research. -
Cycloalkynes Compound
Cy5.5 DBCO is a cycloalkyne-based click chemistry reagent featuring a cyanine 5.5 fluorophore. The presence of the DBCO moiety facilitates copper-free, biocompatible click reactions characterized by rapid kinetics and enhanced stability. This reagent is widely utilized in bioconjugation applications, enabling efficient labeling of biomolecules for imaging and detection in various biological studies. -
ADC linker
Tetrazine-SS-Biotin is a cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs). Featuring a Tetrazine moiety, it facilitates the inverse electron demand Diels-Alder reaction with trans-cyclooctene (TCO) derivatives. This unique reactivity enables precise targeting and controlled release of therapeutic agents, making it valuable in cancer research and the development of targeted therapies. -
ADC Linker
DBCO-PEG2-DBCO is a versatile click chemistry reagent featuring two terminal dibenzocyclooctyne (DBCO) groups connected by a polyethylene glycol (PEG) linker. This compound is engineered for efficient, copper-free click reactions, making it particularly valuable in the development of antibody-drug conjugates (ADCs). Its unique chemical properties promote strong and selective labeling, enabling researchers to explore novel therapeutic applications and enhance drug delivery systems in biomedical research. This reagent is intended for research use only. -
ADC Linker
BCN-PEG3-OH is a non-cleavable linker specifically designed for antibody-drug conjugate (ADC) synthesis. As a click chemistry reagent, it features a bicyclo[6.1.0]nonyne (BCN) moiety that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This compound supports robust conjugation strategies, enhancing the delivery of cytotoxic agents in targeted cancer therapies. Its efficiency makes it an invaluable tool in the development of ADCs for various research applications. -
ADC Linker
Tetrazine-PEG4-amine hydrochloride functions as a cleavable linker in the synthesis of antibody-drug conjugates (ADCs). This compound features a tetrazine group, enabling it to participate in inverse electron demand Diels-Alder (iEDDA) reactions with trans-cyclooctene (TCO) functionalized molecules. It is essential for the development of targeted therapies, facilitating the selective delivery of cytotoxic agents to cancer cells while minimizing off-target effects. -
Click Chemistry Reagent
TCO-NHS Ester (axial) is a versatile click chemistry reagent primarily used for site-specific labeling in amine reactions. The compound features TCO groups that participate in inverse electron demand Diels-Alder (iEDDA) reactions with tetrazine-containing molecules. It is valuable in bioconjugation and molecular imaging applications, enabling researchers to construct complex biomolecular structures. -
ADC Linker
Gly-Gly-Gly-PEG3-TCO is a polyethylene glycol (PEG) linker featuring a TCO moiety, primarily utilized in the synthesis of antibody-drug conjugates (ADCs). This compound facilitates click chemistry through its ability to participate in inverse electron demand Diels-Alder (iEDDA) reactions with tetrazine-containing molecules. Its application in ADC development enhances targeted delivery and therapeutic efficacy in the treatment of various diseases. -
ADC Linker
BCN-SS-NHS is a cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs). This reagent features a BCN group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, enabling efficient conjugation. Its unique properties enhance the targeting and delivery of therapeutic agents, making it a valuable tool in the development of ADCs for various cancer research applications. -
ADC Linker
DBCO-PEG2-Val-Cit-PAB-MMAE is an antibody-drug conjugate (ADC) linker that employs a DBCO group for efficient click chemistry with azide moieties. This reagent incorporates a Val-Cit dipeptide, which is cleavable by proteases, facilitating the targeted release of the MMAE warhead within cells through an elimination mechanism. Its design is optimized for applications in targeted cancer therapy, enhancing the specificity and efficacy of drug delivery systems. -
ADC Linker
DBCO-PEG4-Val-Cit-PAB-PNP is a cleavable ADC linker that facilitates targeted drug delivery. The Val-Cit moiety is specifically cleaved by Cathepsin B, enabling the release of an amine-containing payload when substituted. The DBCO group allows for efficient click chemistry with azide-bearing compounds, making this linker suitable for various antibody-drug conjugate applications in therapeutic research. -
ADC Linker
DBCO-PEG3-acid is a non-cleavable ADC linker featuring a 3-unit polyethylene glycol (PEG) chain. Its primary mechanism involves the strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, enabling effective conjugation in the synthesis of antibody-drug conjugates (ADCs). This reagent is particularly valuable in therapeutic research applications, facilitating targeted drug delivery and enhancing the pharmacological properties of antibody-based treatments. -
ADC Linker
DBCO-PEG24-Maleimide is a versatile linker featuring a maleimide group and a DBCO (dibenzocyclooctyne) moiety. This compound is ideal for conjugating thiol-containing biomolecules and facilitates efficient click chemistry reactions with azide-bearing substrates. Its unique structure enables stable linkages, making it suitable for applications in antibody-drug conjugates (ADCs) and other bioconjugation frameworks in chemical biology research. -
ADC Linker
DBCO-PEG4-Val-Ala-PAB-PNP is a cleavable antibody-drug conjugate (ADC) linker designed for targeted delivery applications. The Val-Ala sequence enables selective cleavage by Cathepsin B, facilitating the release of the therapeutic payload. The incorporation of a PEG spacer enhances aqueous solubility, while the DBCO group is suitable for Click Chemistry reactions due to its reactivity. Additionally, the PNP moiety serves as an efficient leaving group, making this compound valuable in bioconjugation and therapeutic development. -
ADC Linker
Methyltetrazine-DBCO is a non-cleavable linker designed for the synthesis of antibody-drug conjugates (ADCs). This compound features a DBCO group that enables strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. Additionally, the inclusion of a tetrazine moiety allows for inverse electron demand Diels-Alder reactions (iEDDA) with trans-cyclooctene (TCO) compounds. Methyltetrazine-DBCO is an essential reagent for researchers developing targeted therapies through click chemistry methodologies. -
Fluorescent Dye
Sulfo-cyanine7 alkyne is a water-soluble near-infrared fluorescent dye designed for use in copper-catalyzed click chemistry. This compound features a sulfonated terminal alkyne, enabling efficient conjugation with azides in aqueous conditions. Sulfo-cyanine7 alkyne is ideal for biological imaging applications and can enhance the visualization of biomolecules in various research settings. -
Fluorescent Dye
Sulfo-cyanine7 alkyne potassium is a water-soluble near-infrared fluorescent dye designed for applications in copper-catalyzed click chemistry. Its sulfonated terminal alkyne enables efficient conjugation with azides under aqueous conditions. This compound is ideal for use in biological imaging and labeling studies, providing enhanced detection of biomolecules in various research applications. -
Fluorescent Dye
Bodipy TR alkyne is a boron dipyrromethene-based fluorescent dye designed for applications in the ROX (Texas Red) channel. This versatile fluorophore exhibits strong fluorescence, making it suitable for use in microscopy and fluorescence polarization assays. The terminal alkyne moiety facilitates efficient incorporation into biomolecular probes via copper-catalyzed click chemistry, enabling a wide range of research applications including cellular imaging and labeling studies. -
Fluorescent Dye
5-ROX-alkyne is a rhodamine-based fluorescent dye designed for the labeling of DNA fragments. It exhibits strong fluorescence, facilitating the visualization of results in capillary electrophoresis genotyping and gel shift assays. This reagent is essential for applications in nucleic acid analysis and characterization, enabling researchers to obtain precise and reliable data in molecular biology experiments. -
Click Chemistry Reagent
Trisulfo-Cy3-Alkyne is a water-soluble click chemistry reagent containing an alkyne functional group, facilitating the attachment of trisulfated Cy3 to azide-bearing molecules via copper-catalyzed azide-alkyne cycloaddition (CuAAc). This reagent exhibits significant biological activity as a fluorescent probe, characterized by its bright fluorescence and photostability, making it suitable for a variety of imaging techniques, including gel detection and microscopy. It is designed for use in research applications requiring precise labeling and tracking of biomolecules. -
Fluorescent Dye
Cy5-DBCO is a near-infrared fluorescent dye that features an absorption maximum at 646 nm and emission maximum at 670 nm. This compound functions as a click chemistry reagent, containing a DBCO group that readily participates in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. It is particularly useful in bioconjugation applications, facilitating the labeling of proteins and other biomolecules for imaging and tracking studies, although it is not recommended for staining intracellular components in permeabilized cells due to potential high background. -
Orange Fluorescent Dye
DBCO-Cy3 is an orange fluorescent dye derived from the Cyanine3 fluorophore, exhibiting stable fluorescence across a pH range of 4-10. It has an excitation maximum at 555 nm and an emission maximum at 580 nm, making it suitable for various fluorescence applications. DBCO-Cy3 features rapid reaction kinetics and is compatible with standard fluorescence instruments. As a click chemistry reagent, it contains a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules, enabling targeted labeling and imaging in biochemical research.
