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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T15057 | DBCO-acid | Others | |
DBCO-acid is a cleavable ADC linker used in the synthesis of ADC linker DBCO-NHS ester, and drug-linker conjugates DBCO-PEG-MMAE[1]. | |||
T9282 | DBCO-C3-Acid | DBCO-ACID | Others |
DBCO acid 2 is a Click Chemistry intermidate used for antibody-drug conjugates. | |||
T39556 | DBCO-PEG4-acid | DBCO-PEG4-acid | |
DBCO-PEG4-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T15059 | DBCO-C6-acid | Others | |
DBCO-C6-acid is a non-cleavable linker utilized for the synthesis of antibody-drug conjugates (ADCs) and carmaphycin analogues[1]. | |||
T17785 | DBCO-PEG2-acid | Others | |
DBCO-PEG2-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T17782 | DBCO-PEG12-acid | Others | |
DBCO-PEG12-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system w... | |||
T17776 | DBCO-PEG1-acid | Others | |
DBCO-PEG1-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T17806 | DBCO-PEG8-acid | Others | |
DBCO-PEG8-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system wi... | |||
T17761 | DBCO-NHCO-PEG13-acid | Others | |
DBCO-NHCO-PEG13-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome sys... | |||
T15061 | DBCO-NHCO-PEG4-acid | Others | |
DBCO-Amide-PEG5-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T17768 | DBCO-NHCO-PEG3-acid | Others | |
DBCO-NHCO-PEG3-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome syst... | |||
T17773 | DBCO-NHCO-PEG7-acid | Others | |
DBCO-NHCO-PEG7-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome syst... | |||
T15070 | DBCO-PEG4-C2-acid | Others | |
DBCO-PEG4-C2-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system... | |||
T18409 | N-DBCO-N-bis(PEG2-C2-acid) | Others | |
N-DBCO-N-bis(PEG2-C2-acid) is a polyethylene glycol (PEG) linker commonly employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1]. | |||
T17775 | DBCO-NHS ester 3 | Others | |
DBCO-NHS ester 3 (Compound 12) is a cleavable linker utilized in the synthesis of antibody-drug conjugate (ADC). It is a derivative of Dibenzylcyclooctyne (DBCO) resulting from the activation of N-hydroxysuccinimide by t... | |||
T77827 | DBCO-PEG4-acetic-Val-Cit-PAB | ||
DBCO-PEG4-acetic-Val-Cit-PAB is a cleavable tetraethylene glycol-based linker for antibody-drug conjugate (ADC) synthesis, consisting of a dibenzocyclooctyne group, an acetic acid moiety, a valine-citrulline dipeptide, a... | |||
T29389 | 3-Azidopropionic Acid Sulfo-NHS Ester | ||
3-Azidopropionic Acid Sulfo-NHS Ester is a water-soluble compound containing an azide group and an NHS ester. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The N... |