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By Target- ADC Linker
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Results for "
dbco-peg1-acid
" in TargetMol Product Catalog- Inhibitor Products191
- Natural Products23
- PROTAC Products18
- Peptides Products16
- Dye Reagents4
- Isotope products2
DBCO-PEG1-acid
T177762228857-38-1
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 within cells.
- $82
Size
QTY
JQ-1 (carboxylic acid)
Cited
T5443202592-23-2
JQ-1 (carboxylic acid) is a cell-permeable BRD4 inhibitor with IC50s of 77 nM for BRD4(1) and 33 nM for BRD4(2)
- $64
Size
QTY
CitedDBCO-NHCO-PEG4-acid
T150611870899-46-9
DBCO-Amide-PEG5-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
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DBCO-PEG4-acid
T395562110448-99-0
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 within cells.
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DBCO-(PEG)3-VC-PAB-MMAE
T17817
DBCO-(PEG)3-VC-PAB-MMAE is a chemical compound where monomethyl auristatin E (MMAE), a potent tubulin inhibitor acting as a toxin payload in antibody-drug conjugates, is conjugated to a DBCO-(PEG)3-vc-PAB linker.
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DBCO-C3-Acid
T92821207355-31-4
DBCO acid 2 is a Click Chemistry intermidate used for antibody-drug conjugates.
- $30
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QTY
N-DBCO-N-bis(PEG2-C2-acid)
T184092110449-00-6
N-DBCO-N-bis(PEG2-C2-acid) is a polyethylene glycol (PEG) linker commonly employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
- $55
Size
QTY
DBCO-PEG4-C2-acid
T150701537170-85-6
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 within cells.
- $39
Size
QTY
DBCO-acid
T150571353016-70-2
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].
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DBCO-PEG8-acid
T17806
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 within cells.
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DBCO-NHCO-PEG3-acid
T17768
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 system within cells.
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DBCO-PEG2-acid
T177852304558-25-4
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 within cells.
- $42
Size
QTY
DBCO-PEG12-acid
T17782
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 within cells.
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1-Boc-azetidine-3-carboxylic acid
T67359142253-55-2
1-Boc-azetidine-3-carboxylic acid is a useful organic compound for research related to life sciences. The catalog number is T67359 and the CAS number is 142253-55-2.
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DBCO-NHCO-PEG13-acid
T17761
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 system within cells.
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DBCO-C6-acid
T150591425485-72-8
DBCO-C6-acid is a non-cleavable linker utilized for the synthesis of antibody-drug conjugates (ADCs) and carmaphycin analogues[1].
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1-Cbz-azetidine-3-carboxylic acid
T6660997628-92-7
1-Cbz-azetidine-3-carboxylic acid is a useful organic compound for research related to life sciences. The catalog number is T66609 and the CAS number is 97628-92-7.
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DBCO-NHCO-PEG7-acid
T17773
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 system within cells.
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