| Catalog | name | Description | price |
|---|---|---|---|
| R-M2-9892 | Inulin-NH2 | Inulin-NH2 can efficiently couple target molecules through the click reaction between DBCO and azides (or NHS esters and primary amines) Inulin-NH2 can be used for drug delivery and biomaterials. Drug delivery: As a carrier material, used for the sustained release of targeted intestinal or immunomodulatory drugs. Biomaterials: Used for constructing functional foods or medical materials, such as enhancing intestinal barriers or resisting oxidative stress. | price> |
| R-M2-9898 | DBCO-TK-mPEG2000 | DBCO-TK-mPEG2000/Dibenzocyclooctyne-TK-mPEG2000 is a ROS-responsive PEG derivative consisting of dibenzocyclooctyne (DBCO), a thioketal (TK) linker, and methoxy polyethylene glycol (mPEG, MW 2000 Da). This conjugate is typically used for ROS-responsive nanoparticle or liposome modification, targeted drug delivery, and bioorthogonal surface functionalization in redox-sensitive therapeutic systems. | price> |
| R-M2-9916 | Tri-L-Tyrosine-DBCO | Tri-L-Tyrosine-DBCO/Tri-L-Tyrosine-Dibenzocyclooctyne is a bioorthogonal coupling reagent designed for site-specific labeling or surface modification of azide-bearing biomolecules.The trityrosine unit provides biocompatibility and potential antioxidant or aromatic interaction properties, while DBCO allows for fast, metal-free click reactions. Applications: Click chemistry bioconjugation with azide-modified proteins, peptides, or polymers. Surface functionalization of nanoparticles, liposomes, or hydrogels. Fluorescent or functional probe construction via DBCO–azide coupling. Peptide–nanomaterial interface or enzyme labeling studies. | price> |
| R-M2-9917 | Tri-L-Phenylalanine-DBCO | Tri-L-Phenylalanine-DBCO is a bioorthogonal click-functionalized tripeptide designed for azide-reactive conjugation. Applications: Copper-free click conjugation with azide-modified biomolecules (e.g., proteins, lipids, polysaccharides). Peptide-based self-assembly into nanofibers or hydrogels for drug delivery or imaging. Surface modification of nanoparticles or liposomes with aromatic or bioactive coatings. Bioorthogonal labeling in chemical biology and nanomedicine. | price> |
| R-M1-8312 | DBCO-trisulfo-Cyanine5.5 | DBCO trisulfo Cyanine 5.5 is a fluorescent point reaction compound. | price> |
| R-M1-8419 | DBCO-SS-DBCO | DBCO-SS-DBCO is a versatile tool in bioconjugation, with potential applications in drug delivery, protein labeling, and the creation of antibody-drug conjugates. | price> |
| R-M1-8452 | Methyltetrazine-DBCO | Methyltetrazine-DBCO compound is particularly useful in bioconjugation, labeling, and imaging applications. It enables the selective and bioorthogonal labeling of biomolecules or surfaces, allowing for the visualization and tracking of specific targets or structures. This compound is often used in combination with other imaging agents or labels to facilitate the detection and study of biological processes in cells or living organisms. | price> |
| R-M1-8523 | DBCO-Hemin-DBCO | DBCO-Hemin-DBCO is a compound that includes two DBCO reactive groups and a Hemin molecule. This compound enables the conjugation of Hemin to other molecules or surfaces through the use of click chemistry. The DBCO groups provide a simple and efficient way to attach Hemin to azide-containing molecules for various applications in biology and biomedicine. | price> |
| R-M1-8527 | DBCO-C6-Br | DBCO-C6-Br can be used as a building block or intermediate in bioconjugation strategies, where the DBCO moiety selectively reacts with azide-containing molecules or surfaces via SPAAC reaction. | price> |
| R-M1-8528 | DBCO-ß-Cyclodextrin | DBCO-ß-Cyclodextrin can be utilized in various fields such as pharmaceuticals, chemistry, and biomedical research where efficient solubilization and targeted delivery of hydrophobic compounds are required. | price> |

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