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Results for "

sulfo dbco amine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
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Sulfo DBCO-amine
T169562028284-70-8
Sulfo DBCO-amine, an alkyl chain-derived PROTAC linker, is utilized for synthesizing PROTACs [1].
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Sulfo DBCO-PEG4-amine
T169572055198-05-3
Sulfo DBCO-PEG4-amine is a PEG-based linker for PROTACs, connecting two essential ligands crucial for forming PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.
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3-Azidopropionic Acid Sulfo-NHS Ester
T293892055198-09-7
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 NHS ester can be used to label the p
  • $259
3-6 months
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Sulfo DBCO-TFP Ester
T878112268816-76-6
Sulfo DBCO-TFP Ester, a water-soluble, sulfo-containing click chemistry reagent, facilitates the efficient and straightforward incorporation of sulfo-DBCO moieties onto amine-containing molecules [1].
  • $1,690
4-6 weeks
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Sulfo DBCO-PEG3-acid
T896862566404-75-7
Sulfo DBCO-PEG3-acid is a click chemistry reagent featuring an azide group. This compound is an analog of DBCO-acid, equipped with a PEG linker and a DBCO moiety. The DBCO group, known for its strain-promoted high-energy state, is commonly utilized in copper-free click reactions. The hydrophilic polyethylene glycol chain and the sulfonyl group enhance its water solubility. The terminal carboxylic acid can react with primary amine groups in the presence of activators (such as EDC or HATU) to form stable amide bonds. This reagent is for research use only and is of reagent grade.
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10-14 weeks
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Sulfo DBCO-PEG3-NHS ester
TYD-02678
Sulfo DBCO-PEG3-NHS ester is a click chemistry reagent featuring an azide group. It serves as an analog of DBCO-acid, incorporating a PEG linker and a DBCO group. The DBCO group is often utilized in copper-free click reactions due to its high-energy strain. The hydrophilic polyethylene glycol chain and sulfo group enhance its water solubility. The terminal carboxylic acid can react with primary amine groups to form stable amide bonds in the presence of activators such as EDC or HATU. This is a reagent-grade compound intended solely for research purposes.
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