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Organometallic compounds contain direct bonds between carbon atoms and metal atoms/ions and play roles as homogeneous catalysts and stoichiometric reagents in reactions; available in various chemical compositions, quantities, purities, and reagent grades.
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Azido-PEG3-SSPy is a cleavable three-unit polyethylene glycol (PEG3) linker used for assembling antibody-drug conjugates (ADCs) and general bioconjugation. It contains an azide functional group enabling copper-catalyzed azide-alkyne cycloaddition (CuAAC) and is compatible with strain-promoted azide-alkyne cycloaddition (SPAAC) with DBCO or BCN partners.
Cleavable disulfide linker for controlled release.
Azide-functionalized for CuAAC click chemistry.
Compatible with SPAAC (DBCO and BCN) reactions.
High purity suitable for conjugation workflows.
Multiple pack sizes available for research use.
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Azide-PEG5-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is a click chemistry reagent containing an Azide group, capable of undergoing copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Also available in 100 mg and bulk. Please contact Fisher for quotes. Brimonidine Tartrate (AGN190342 tartrate) is a quinoxaline derivative and adrenergic (alpha)-2 receptor agonist (EC50 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension. purity: 99%
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Azido-PEG5-CH2CO2-NHS is a PEG-based PROTAC linker designed for synthesizing PROTACs. It features an Azide group, enabling click chemistry reactions like copper-catalyzed azide-alkyne cycloaddition (CuAAc) with Alkyne-containing molecules, and strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups.
Can be used in the synthesis of PROTACs
Contains an Azide group for click chemistry reactions
Undergoes copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups
Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups
Exploits the intracellular ubiquitin-proteasome system to selectively degrade target proteins
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Azido-PEG3-C3-OH is a PEG-based PROTAC linker designed for use in the synthesis of PROTACs. This click chemistry reagent features an Azide group, facilitating copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. It also supports strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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N-(Azido-PEG3)-N-Biotin-PEG4-methyl ester is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, enabling specific reactions with other molecules. This product is intended for research use only.
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N-Boc-PEG5-bromide is a Boc-protected polyethylene glycol (PEG) linker bearing a terminal bromide functional group. It is used as a reactive building block in the synthesis of antibody-drug conjugates (ADCs) and PROTACs to introduce a five-unit PEG spacer that improves solubility and provides a reactive handle for conjugation chemistry.
Boc-protected amine allows selective deprotection under acidic conditions.
Terminal bromide enables alkylation and nucleophilic substitution reactions.
Five-unit PEG spacer improves aqueous solubility and linker flexibility.
High purity suitable for research applications (98.0%).
Supplied as a solid and available in small-scale pack sizes including 100 MG.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More