Inquiry Basket
| Catalog | Product Name | CAS Number |
|---|---|---|
| BADC-01208 | Amino-bis-PEG3-TCO | |
| Amino-bis-PEG3-TCO is a bifunctional ADC linker with TCO moieties enabling dual site-specific click conjugations, improving payload loading and pharmacokinetics in antibody-drug conjugates. | Inquiry | |
| BADC-01209 | Aminooxy-PEG2-bis-PEG3-DBCO | |
| Aminooxy-PEG2-bis-PEG3-DBCO is a cleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-01210 | Amino-PEG3-SS-acid | |
| Amino-PEG3-SS-acid is a cleavable ADC linker featuring PEG spacer and disulfide bond for controlled drug release. It enables efficient antibody conjugation and enhances solubility, widely used in antibody-drug conjugate (ADC) synthesis for targeted cancer therapy. | Inquiry | |
| BADC-01211 | Amino-PEG4-bis-PEG3-methyltetrazine | |
| Amino-PEG4-bis-PEG3-methyltetrazine is a cleavable 7 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-01212 | Amino-PEG4-bis-PEG3-N3 | |
| Amino-PEG4-bis-PEG3-N3 is a bifunctional ADC linker combining amine and azide functionalities with PEG spacers. It facilitates efficient bioorthogonal conjugation and improves antibody-drug conjugate solubility and targeting. | Inquiry | |
| BADC-01213 | Amino-PEG4-bis-PEG3-propargyl | |
| Amino-PEG4-bis-PEG3-propargyl is a cleavable 6 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-01214 | Amino-PEG6-amido-bis-PEG5-N3 | |
| Amino-PEG6-amido-bis-PEG5-N3 is a cleavable 11 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-01215 | Amino-SS-PEG12-acid | |
| Amino-SS-PEG12-acid offers a long PEG12 cleavable ADC linker with disulfide bond and terminal amino/acid groups. This linker improves biocompatibility and facilitates precise payload release in ADC applications targeting tumor cells. | Inquiry | |
| BADC-01216 | APN-PEG4-Amine hydrochloride | |
| APN-PEG4-Amine (hydrochloride) is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-01217 | APN-PEG4-BCN | |
| APN-PEG4-BCN is a bioorthogonal ADC linker combining PEG4 spacer and BCN for click chemistry. It enhances antibody conjugation efficiency and payload stability in ADCs for targeted drug delivery in oncology research. | Inquiry | |
| BADC-01218 | APN-PEG4-DBCO | |
| APN-PEG4-DBCO is a cleavable ADC linker featuring PEG4 and DBCO for efficient strain-promoted click conjugation. It supports stable payload attachment and controlled release in antibody-drug conjugates for cancer therapeutics. | Inquiry | |
| BADC-01219 | APN-PEG4-tetrazine | |
| APN-PEG4-tetrazine is a bioorthogonal ADC linker featuring tetrazine and PEG spacers, enabling rapid inverse-electron-demand Diels–Alder (IEDDA) click chemistry for site-specific antibody conjugation and enhanced payload delivery. | Inquiry | |
| BADC-01220 | Azido-PEG1-Val-Cit-OH | |
| Azido-PEG1-Val-Cit-OH is a versatile ADC linker with azide functionality and Val-Cit dipeptide for enzymatic cleavage. Ideal for bioorthogonal conjugation and selective payload release in antibody-drug conjugate development. | Inquiry | |
| BADC-01221 | Azido-PEG1-Val-Cit-PABC-PNP | |
| Azido-PEG1-Val-Cit-PABC-PNP is a reactive ADC linker featuring azide, valine-citrulline, and PABC for efficient enzymatic drug release. Supports click chemistry conjugation in precise ADC synthesis targeting tumor cells. | Inquiry | |
| BADC-01222 | Azido-PEG3-SS-NHS | |
| Azido-PEG3-SS-NHS is a cleavable ADC linker with azide for click chemistry and NHS ester for amine coupling. It enables stable antibody conjugation and controlled payload release in ADCs for targeted therapies. | Inquiry | |
| BADC-01223 | Azido-PEG3-SSPy | |
| Azido-PEG3-SSPy combines azide and pyridyl disulfide in a PEG3 linker for cleavable ADCs. Facilitates bioorthogonal conjugation and controlled drug release in antibody-drug conjugates targeting cancer. | Inquiry | |
| BADC-01224 | BCN-PEG1-Val-Cit-OH | |
| BCN-PEG1-Val-Cit-OH is a cleavable ADC linker featuring BCN for strain-promoted azide-alkyne cycloaddition and Val-Cit dipeptide for enzymatic cleavage. Optimized for efficient payload delivery in ADCs. | Inquiry | |
| BADC-01225 | BCN-PEG1-Val-Cit-PABC-OH | |
| BCN-PEG1-Val-Cit-PABC-OH integrates BCN click chemistry and PABC self-immolative spacer with Val-Cit peptide, enhancing enzymatic payload release and stability in antibody-drug conjugates. | Inquiry | |
| BADC-01228 | BCN-PEG3-Val-Cit | |
| BCN-PEG3-Val-Cit is a click chemistry-compatible ADC linker integrating a cleavable Val-Cit dipeptide for intracellular drug release. The BCN group enables SPAAC with azides, making it ideal for tumor-specific antibody-drug conjugation applications. | Inquiry | |
| BADC-01231 | BCN-SS-NHS | |
| BCN-SS-NHS is a strained alkyne ADC linker with cleavable disulfide bond and NHS ester, enabling bioorthogonal click chemistry and controlled payload release in antibody-drug conjugate synthesis. | Inquiry |
