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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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N3-PEG3-CH2CH2-Boc is a Boc-protected, azide-terminated PEG3 linker used in conjugation chemistry for synthesizing PROTACs and antibody-drug conjugates. It contains a three-unit polyethylene glycol spacer with an azide functional group that enables click chemistry reactions such as copper-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC).
Boc-protected azide terminus for selective conjugation.
Three-unit PEG spacer provides flexibility and improves solubility.
Compatible with CuAAC and SPAAC click reaction methodologies.
High purity suitable for synthetic applications (≥98.0%).
Available in multiple pack sizes, including 250 MG.
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Azido-PEG5-acid is an azide-functional, five-unit polyethylene glycol (PEG5) linker used for conjugation chemistry, including PROTAC and antibody-drug conjugate synthesis, and for click-chemistry applications. Supplied for research use only.
Peg5 linker with azide functionality for click chemistry.
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BM-PEG3 is a polyethylene glycol (PEG)-based PROTAC linker designed for the synthesis of PROTACs. PROTACs (Proteolysis Targeting Chimeras) are compounds that utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins. They function by connecting two different ligands, one for an E3 ubiquitin ligase and another for the target protein, enabling targeted degradation.
PEG-based PROTAC linker
For research use only
Purity: 98.0%
Molecular weight: 352.34
Molecular formula: C16H20N2O7
Appearance: White to light yellow solid
Storage as powder: -20°C for 3 years, 4°C for 2 years
Storage in solvent: -80°C for 6 months, -20°C for 1 month
Solubility in DMSO: 100 mg/mL (in vitro)
Solubility in 10% DMSO, 90% corn oil: ≥ 2.5 mg/mL (in vivo)
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Bis-PEG5-acid is a polyethylene glycol (PEG) linker bearing two terminal carboxylic acid groups, used as a hydrophilic spacer in PROTAC construction and bioconjugation chemistry. It facilitates coupling reactions and improves aqueous solubility for assembled molecules.
Two terminal carboxylic acid groups enable standard amide coupling reactions.
PEG5 spacer provides hydrophilicity and conformational flexibility.
Molecular weight 338.35 g/mol and formula C14H26O9 for precise stoichiometry.
Suitable for PROTAC synthesis and general linker applications in medicinal chemistry.
Offered in research quantities including 1 g for small-scale synthesis.
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Azido-PEG3-DYKDDDDK (azide-PEG3-FLAG) TFA is a multifunctional fusion tag used for the purification of recombinant proteins. This click chemistry reagent contains an azide group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with molecules containing alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
Multifunctional fusion tag for the purification of recombinant proteins
Contains an azide group
Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with molecules containing alkyne groups
Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups
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Aminooxy-PEG3-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
PEG-based PROTAC linker
Used in the synthesis of PROTACs
Exploits intracellular ubiquitin-proteasome system
Selectively degrades target proteins
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N-(Boc-PEG3)-N-bis(PEG2-alcohol) is a PEG-based PROTAC linker used in the synthesis of Proteolysis Targeting Chimeras (PROTACs). PROTACs are designed to leverage the intracellular ubiquitin-proteasome system for the selective degradation of target proteins. This product is intended for research use only.
PEG-based PROTAC linker
Used in the synthesis of PROTACs
Enables targeted protein degradation via the ubiquitin-proteasome system
Facilitates connection between an E3 ubiquitin ligase ligand and a target protein ligand
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Bromoacetamido-PEG3-C2-Boc is a PEG-based PROTAC linker that is utilized in the synthesis of PROTACs. PROTACs themselves are small molecules composed of two different ligands connected by a linker; one ligand targets an E3 ubiquitin ligase, and the other targets a protein of interest. This mechanism allows PROTACs to leverage the intracellular ubiquitin-proteasome system for the selective degradation of target proteins.
Application: used in the synthesis of PROTACs.
Mechanism: facilitates the degradation of target proteins via the ubiquitin-proteasome system when incorporated into PROTACs.
Research use: for research purposes only; not intended for sale to patients.
Form: liquid (density: 1.252 g/cm3), colorless to light yellow.
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Ms-PEG5-t-butyl ester is a PEG-based PROTAC linker designed for use in the synthesis of PROTACs. PROTACs are molecules that contain two different ligands connected by a linker, one for an E3 ubiquitin ligase and the other for a target protein. They leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
PROTAC linker
PEG-based structure
Target PROTACs
Pathway PROTAC
Used in the synthesis of PROTACs
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N-(Azido-PEG3)-N-bis(PEG4-acid) is a PEG-based PROTAC linker designed for use in the synthesis of PROTACs. This compound acts as a click chemistry reagent, featuring an Azide group. It can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions when combined with Alkyne groups. Additionally, it is capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
PEG-based PROTAC linker
Used in the synthesis of PROTACs
Functions as a click chemistry reagent
Contains an Azide group
Undergoes copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with Alkyne groups
Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups
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Tos-PEG3 is a PEG-based PROTAC linker that can be utilized in the synthesis of PROTACs. It can also be used for the synthesis of 3'-aminooxy oligonucleotides solid supports.
Can be used in the synthesis of PROTACs
Can be utilized for the synthesis of 3'-aminooxy oligonucleotides solid supports
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DBCO-NHCO-PEG3-Fmoc is a DBCO-functionalized PEG3 linker with an Fmoc-protected amine designed for use as a click-chemistry reagent in PROTAC synthesis and bioconjugation. It participates in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing partners, offering modular attachment and improved handling for linker assembly.
Click-reactive DBCO group enables strain-promoted alkyne-azide cycloaddition (SPAAC).
Peg3 spacer improves solubility and reduces steric hindrance.
Fmoc-protected amine allows compatibility with solid-phase and solution-phase synthesis workflows.
High purity suitable for research applications.
Stable as powder at -20°C for extended storage and recommended cold storage in solution.
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N-(acid-PEG3)-N-bis(PEG3-azide) is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, containing an Azide group. This allows it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules that contain Alkyne groups, or in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
Composed of two different ligands connected by a linker
One ligand targets an E3 ubiquitin ligase
The other targets the protein of interest
Operates by harnessing the intracellular ubiquitin-proteasome system
Facilitates the selective degradation of target proteins
Intended for research use only
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Bromoacetamido-PEG3-NH-Boc is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs are designed to selectively degrade target proteins by utilizing the ubiquitin-proteasome system, connecting ligands for an E3 ubiquitin ligase and the target protein via a linker.
Suitable for PROTAC synthesis
Utilizes PEG-based linker technology
Facilitates targeted protein degradation
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