Inquiry Basket
| Catalog | Product Name | CAS Number |
|---|---|---|
| BADC-02015 | (21S,24S)-tert-Butyl 1-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-24-((4-(hydroxymethyl)phenyl)carbamoyl)-21-isopropyl-3,19,22-trioxo-7,10,13,16-tetraoxa-4,20,23-triazaheptacosan-27-oate | |
| It is an ADC linker used in antibody-conjugated drugs. | Inquiry | |
| BADC-02016 | t-Boc-aminooxy-PEG3-propargyl | 1951439-46-5 |
| t-Boc-aminooxy-PEG3-propargyl is a crosslinker containing a propargyl group and t-Boc-aminooxy group. t-Boc-aminooxy-PEG3-propargyl can be used as an ADC linker. | Inquiry | |
| BADC-02017 | Azidoethyl-SS-ethylamine hydrochloride | 2712401-25-5 |
| Azidoethyl-SS-ethylamine hydrochloride is a cleavable ADC linker that can be used in the synthesis of antibody-drug conjugates (ADCs). | Inquiry | |
| BADC-02018 | Poc-AEEA DCHA | |
| Poc-AEEA DCHA is a derivative with a propargyloxycarbonyl (Poc) group and an AEEA (2-(2-aminoethoxy)ethoxy acetic acid) linker, existing as a dicyclohexylammonium (DCHA) salt. It is used in bioconjugation and peptide synthesis for introducing alkyne-functionalized residues that can participate in click chemistry reactions, enabling site-specific modifications and functionalization. | Inquiry | |
| BADC-02019 | Poc-AEEA | 2988660-57-5 |
| Poc-AEEA is a derivative with a propargyloxycarbonyl (Poc) group and an AEEA (2-(2-aminoethoxy)ethoxy acetic acid) linker. It is used in bioconjugation and peptide synthesis for introducing alkyne-functionalized residues that can participate in click chemistry reactions, enabling site-specific modifications and functionalization. | Inquiry | |
| BADC-02021 | N1-Azido-spermine | 1190203-77-0 |
| N1-Azido-spermine is a derivative of spermine with an azide (N3) group attached to the N1 position. It is used in chemical and biological research for its ability to participate in click chemistry reactions, enabling site-specific modifications and functionalization. | Inquiry | |
| BADC-02022 | N3-DABu-Suc-OH | 2226183-50-0 |
| N3-DABu-Suc-OH can be used as an ADC (Antibody-Drug Conjugate) linker. It features an azide (N3) group attached to a butylenediamine (DABu) moiety and a succinoyl (Suc) group at the end. This compound is used in click chemistry and other conjugation reactions, particularly for labeling and functionalizing biomolecules through copper-catalyzed or copper-free click reactions. This structure allows for the attachment of a cytotoxic payload to an antibody through the succinoyl group, while the azide group can be used for further functionalization or conjugation reactions. | Inquiry | |
| BADC-02023 | N3-DAPr-Suc-OH | 929894-58-6 |
| N3-DAPr-Suc-OH can be used as an ADC (Antibody-Drug Conjugate) linker. It features an azide (N3) group attached to a propylenediamine (DAPr) moiety and a succinoyl (Suc) group at the end. This structure allows for the attachment of a cytotoxic payload to an antibody through the succinoyl group, while the azide group can be used for further functionalization or conjugation reactions. | Inquiry | |
| BADC-02024 | Boc-Cystamine-Suc-OH | 946849-79-2 |
| Boc-Cystamine-Suc-OH is a cleavable linker used in the synthesis of antibody-drug conjugates (ADCs). It features a Boc (tert-butyloxycarbonyl) protecting group and a succinyl (Suc) linker, making it suitable for attaching cytotoxic drugs to antibodies. This linker is designed to be stable in circulation but can be cleaved in the tumor microenvironment, allowing for controlled drug release and enhancing the effectiveness of ADCs. | Inquiry | |
| BADC-02025 | Fmoc-Cystamine-Suc | 946849-80-5 |
| Fmoc-Cystamine-Suc-OH is a compound used in solid-phase peptide synthesis (SPPS) and bioconjugation applications. It features an Fmoc (9-fluorenylmethyloxycarbonyl) protecting group and a succinyl (Suc) linker, making it suitable for constructing peptide sequences with specific functional groups. | Inquiry | |
| BADC-02026 | Mal(Br2)-Aca-OSu | 2389064-41-7 |
| Mal(Br2)-Aca-OSu is a bioconjugation reagent used in antibody-drug conjugate (ADC) synthesis. It features a dibromo maleimide group and an aminocaproic acid (Aca) linker, terminated with an N-hydroxysuccinimide (OSu) ester. This compound is designed for conjugating antibodies to cytotoxic drugs, with the dibromo maleimide group facilitating selective attachment to thiol groups in the antibody. | Inquiry | |
| BADC-02027 | Fmoc-Cystamine hydrochloride | 2893917-85-4 |
| Fmoc-Cystamine hydrochloride can be used as an ADC linker. It is a cleavable linker that can be reduced under reducing conditions to release the payload. This type of linker is useful for creating ADCs that can selectively release their cytotoxic payload in the reducing environment of cells, thereby minimizing off-target effects. | Inquiry | |
| BADC-02028 | Fmoc-Cystamine | 2576471-32-2 |
| Fmoc-Cystamine can be used as an ADC linker. It is a cleavable linker that can be reduced under reducing conditions to release the payload. This type of linker is useful for creating ADCs that can selectively release their cytotoxic payload in the reducing environment of cells, thereby minimizing off-target effects. | Inquiry |
