Catalog No.
Product Name
Application
Product Information
Citations
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PROTAC Linker
Azide-PEG12-Tos is a PEG-based linker designed for use in PROTAC synthesis. This compound features an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN functionalized compounds. Azide-PEG12-Tos is valuable for researchers working on targeted protein degradation and other bioconjugation applications. -
PROTAC Linker
m-PEG5-Hydrazide is a polyethylene glycol (PEG)-based linker designed for use in the synthesis of Proteolysis Targeting Chimeras (PROTACs). This compound facilitates the conjugation of protein ligands to E3 ligases, enhancing the targeted degradation of specific proteins within the cell. m-PEG5-Hydrazide is essential for researchers aiming to develop novel therapeutic strategies through targeted protein modulation and degradation. -
PROTAC Linker
1-Isothiocyanato-PEG3-azide is a versatile PEG-based PROTAC linker that facilitates the synthesis of proteolysis targeting chimeras (PROTACs). This compound features an azide group that enables copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules. Additionally, it is capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) with entities possessing DBCO or BCN groups. Its utility in conjugation chemistry supports various applications in chemical biology and drug development. -
PROTAC Linker
(S,R,S)-Ahpc-PEG6-azide is a click chemistry PROTAC linker that integrates an E3 ligase ligand and a PEG6 arm, facilitating the advancement of PROTAC research and discovery. The hydrophilic PEG spacer enhances solubility in aqueous environments, making it suitable for various biological applications. The presence of the azide functionality allows for efficient click chemistry reactions with alkyne, DBCO, or BCN molecules, thereby enabling versatile conjugation strategies in drug development. -
PROTAC Linker
m-PEG6-Hydrazide is a polyethylene glycol (PEG)-based linker designed for use in the synthesis of PROTACs (proteolysis-targeting chimeras). This compound facilitates the conjugation of E3 ligase ligands to target proteins by providing a flexible and hydrophilic spacer. Its unique structure enhances the solubility and stability of PROTACs, making it an essential tool for studies focused on targeted protein degradation and drug discovery applications. -
PROTAC Linker
H2N-PEG4-Hydrazide is a PEG-based linker designed for use in the synthesis of Proteolysis Targeting Chimeras (PROTACs). This compound facilitates the conjugation of target proteins to E3 ligases, enhancing target degradation through the ubiquitin-proteasome system. H2N-PEG4-Hydrazide is essential for researchers exploring targeted protein degradation approaches in drug discovery and development. -
PROTAC Linkers
t-Boc-Aminooxy-PEG5-azide is a PEG-based linker designed for PROTAC (Proteolysis Targeting Chimera) synthesis. It features an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing compounds. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN derivatives. This linker is valuable for researchers developing targeted protein degradation strategies in chemical biology and therapeutic applications. -
PROTAC Linker
Bromo-PEG7-azide is a polyethylene glycol (PEG)-based linker for PROTAC (Proteolysis Targeting Chimeras) synthesis, facilitating targeted protein degradation. This compound features an azide functional group, enabling its use in click chemistry, specifically copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it a versatile tool for researchers in chemical biology and drug development applications. -
PROTAC Linker
Azide-PEG2-MS is a PEG-based linker designed for use in the synthesis of PROTACs, targeting protein degradation pathways. Featuring an azide group, it is a versatile click chemistry reagent that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing compounds. Additionally, Azide-PEG2-MS can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN-containing molecules, facilitating the development of innovative protein-targeting therapies. This linker is ideal for researchers investigating protein degradation and its therapeutic potential. -
PROTAC Linker
1,1,1-Trifluoroethyl-PEG2-azide is a PEG-based PROTAC linker designed for the synthesis of targeted protein degraders. This compound features an azide moiety that allows for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkynyl-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzoazacyclooctyne (DBCO) or bicyclononyne (BCN) groups, facilitating the development of versatile bioconjugates in chemical biology research. -
PROTAC Linker
Azido-PEG11-azide is a PEG-based PROTAC linker designed to facilitate the synthesis of protein degradation therapeutics. Featuring azide functional groups, it is a versatile click chemistry reagent capable of participating in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN derivatives, enabling effective modular assembly in drug development and chemical biology applications. -
PROTAC Linkers
N-(Acid-PEG2)-N-bis(PEG3-azide) serves as a PEG-based linker for the synthesis of PROTACs, facilitating targeted protein degradation. This compound features an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it is capable of undergoing strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it a versatile tool in chemical biology and drug development. -
PROTAC Linker
Mal-C2-cyclohexylcarboxyl-hydrazide hydrochloride is a versatile PROTAC linker designed for targeted protein degradation applications. This hydrazide compound facilitates the formation of bifunctional molecules, promoting the effective assembly of E3 ligases and target proteins. It serves as a key building block in the development of novel PROTACs for studying protein dynamics and therapeutic interventions in various diseases. -
PROTAC Linker
Benzyl-PEG2-azide is a PEG-based linker specifically designed for the synthesis of PROTACs (Proteolysis Targeting Chimeras). It features an azide functional group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with compounds possessing DBCO or BCN groups. This reagent is instrumental in the development of targeted protein degradation strategies in chemical biology research. -
PROTAC Linker
Methylamino-PEG3-azide serves as a versatile PROTAC linker, facilitating the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing substrates. In addition, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it a valuable tool for chemical biology applications, particularly in targeted protein degradation studies. -
PROTAC Linkers
APN-C3-PEG4-azide is a PEG-based PROTAC linker featuring an azide functional group, designed for the synthesis of PROTACs. It facilitates the copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN moieties. This versatile linker is essential for drug development studies involving targeted protein degradation and can enhance the efficiency of modular PROTAC assembly. -
PROTAC Linker
Lipoamido-PEG4-azide is a PEG-based linker designed for use in PROTAC synthesis. This compound features an azide group capable of participating in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN-containing compounds, making it a versatile tool in chemical research for targeted protein degradation studies. -
PROTAC linker
Aminooxy-PEG1-azide is a PEG-based PROTAC linker designed for the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) functionalized compounds, enhancing its versatility in chemical biology applications. -
PROTAC linker
Aminooxy-PEG4-azide is a PEG-based linker designed for use in PROTAC (Proteolysis Targeting Chimera) synthesis. With its azide functional group, it effectively participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules, as well as DBCO or BCN derivatives. This reagent is essential for enhancing the specificity and efficacy of targeted protein degradation approaches in chemical biology research. -
PROTAC Linkers
Azido-PEG7-azide is a PEG-based linker designed for the synthesis of PROTACs, functioning through click chemistry. This compound features an azide group, allowing it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) groups. Its versatile reactivity makes it a valuable tool for researchers in chemical biology and drug development. -
PROTAC linker
NH-bis(C2-PEG1-azide) is a versatile PEG-based PROTAC linker designed for the synthesis of PROTACs. It features an azide functional group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN moieties. This compound is essential for developing targeted protein degradation strategies and is widely applicable in chemical biology and drug discovery research. -
PROTAC Linker
Azido-PEG9-azide is a PEG-based PROTAC linker that facilitates the synthesis of proteolysis-targeting chimeras (PROTACs). Featuring an azide group, it participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-bearing compounds. This reagent is instrumental in the development of targeted protein degradation strategies, promoting innovative research in drug discovery and protein regulation. -
PROTAC Linkers
Benzyl-PEG7-azide is a PEG-based PROTAC linker designed for the synthesis of proteolysis-targeting chimeras (PROTACs). Featuring an azide functional group, it facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing compounds. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups. This compound plays a crucial role in drug discovery and development by enabling the selective degradation of target proteins. -
PROTAC Linker
Azide-PEG3-L-alanine-Fmoc is a PEG-based PROTAC linker that facilitates the synthesis of PROTACs through its azide functionality. This compound is capable of participating in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules and can also engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN-modified compounds. Its unique properties make it a valuable tool for researchers working on targeted protein degradation and related applications in chemical biology. -
PROTAC Linker
Azido-PEG4-hydrazide-Boc is a PEG-based linker designed for use in the synthesis of PROTACs, functioning primarily as a tool for targeted protein degradation. This compound features an azide group that facilitates click chemistry reactions, specifically copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it suitable for various bioconjugation applications in chemical biology and drug discovery research. -
PROTAC Linker
Ald-Ph-amido-C2-PEG3-azide is a PEG-based PROTAC linker designed for the synthesis of Proteolysis Targeting Chimeras (PROTACs). This compound features an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkynyl compounds, as well as strain-promoted azide-alkyne cycloaddition (SPAAC) reactions with DBCO or BCN-modified molecules. Its versatile reactivity makes it a valuable tool for researchers in the development of targeted protein degradation strategies. -
PROTAC Linkers
Trityl-PEG10-azide is a PEG-based linker specifically designed for the synthesis of PROTACs, facilitating targeted protein degradation. This compound features an azide functional group that allows for efficient copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, Trityl-PEG10-azide can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN-modified compounds, making it a versatile tool for chemical biology applications in PROTAC development. -
PROTAC Linker
Phthalamide-PEG3-azide is a PEG-based linker designed for PROTAC synthesis. This compound features an azide moiety, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Its utility in these chemical reactions makes it a valuable tool for researchers developing targeted protein degradation strategies. -
PROTAC Linker
AZD-CO-C2-Ph-amido-Ph-azide is a versatile PROTAC linker designed for the synthesis of proteolysis-targeting chimeras (PROTACs). It features an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN moieties. This compound is essential for facilitating targeted protein degradation and advancing research in therapeutic development. -
ADC/PROTAC Linker
Propargyl-PEG5-azide is a PEG-based linker designed for antibody-drug conjugate (ADC) and PROTAC applications. This compound features an azide functional group, facilitating copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, Propargyl-PEG5-azide can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it a versatile and effective tool for chemical biologists developing targeted therapeutics. -
PROTAC linker
N-(Ac-PEG3)-N'-(azide-PEG3)-Cy7 chloride functions as a PEG-based PROTAC linker, facilitating the synthesis of PROTACs. This compound features an azide functional group, enabling efficient copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN moieties, making it a versatile tool for chemical biology applications in targeted protein degradation studies. -
PROTAC linker
N-(m-PEG4)-N'-(azide-PEG3)-Cy5 serves as a PEG-based linker for PROTAC technology, facilitating the synthesis of targeted protein degraders. This compound features an azide functional group, enabling it to engage in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing partners. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN derivatives, making it a versatile tool for researchers in the field of chemical biology and drug development. -
PROTAC Linkers
PC-PEG11-Azide is a PEG-based linker designed for use in PROTAC synthesis, facilitating targeted protein degradation. It features an Azide group that enables copper-catalyzed azide-alkyne cycloaddition reactions with alkyne-containing compounds. Additionally, PC-PEG11-Azide can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) derivatives. This versatility makes it a valuable tool for chemical biology and drug discovery applications. -
PROTAC Linker
Boc-NH-PEG7-azide is a PEG-based PROTAC linker that facilitates the synthesis of PROTACs by leveraging its azide group. It enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-functionalized compounds and can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN functionalized molecules. This linker is essential for the development of targeted protein degradation strategies in chemical biology research. -
PROTAC linker
N-(azide-PEG3)-N'-(m-PEG4)-Benzothiazole Cy5 is a PEG-based PROTAC linker designed for the synthesis of proteolysis-targeting chimeras (PROTACs). This compound features an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it can participate in strain-promoted azide-alkyne cycloaddition (SPAAC) reactions with DBCO or BCN moieties, facilitating efficient conjugation in chemical biology research applications. -
PROTAC Linkers
Mal-C2-cyclohexylcarboxyl-hydrazide TFA is a versatile linker designed for the synthesis of PROTACs (Proteolysis Targeting Chimeras). This compound features an alkyl chain structure that facilitates the conjugation of target proteins and E3 ligases, enabling selective degradation of specific proteins within biological systems. It is a valuable tool for researchers exploring targeted protein degradation as a therapeutic strategy. -
PROTAC Linkers
Benzyl-PEG5-azide is a polyethylene glycol (PEG)-based linker designed for use in the synthesis of PROTACs (proteolysis-targeting chimeras). This compound features an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with entities bearing DBCO or BCN groups. The versatility and efficiency of Benzyl-PEG5-azide make it a valuable tool in the development of targeted protein degradation strategies and related chemical biology applications. -
PROTAC Linkers
N-PEG3-N'-(azide-PEG3)-Cy5 is a PEG-based PROTAC linker designed for the synthesis of PROTACs. It features an azide functional group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, this linker can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups, making it a versatile tool in chemical biology and drug development research. Its application in PROTAC technology supports studies targeting protein degradation pathways for therapeutic discovery. -
PROTAC Linker
Fluorescein-thiourea-PEG4-azide is a PROTAC linker designed for the synthesis of proteolysis-targeting chimera (PROTAC) molecules. It features an azide group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing partners, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN moieties. This reagent is critical for studies focused on targeted protein degradation and can facilitate the development of innovative therapeutic strategies in chemical biology and pharmacology. -
PROTAC Linker
Boc-Aminooxy-PEG3-azide is a versatile PEG-based linker utilized in the synthesis of PROTACs (proteolysis targeting chimeras). This compound features an azide functional group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-bearing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) derivatives. Its application in PROTAC development enables efficient targeting and degradation of specific proteins, making it valuable for research in targeted protein degradation and related fields. -
PROTAC Linker
Pyrene-amido-PEG4-azide is a PEG-based PROTAC linker designed for the synthesis of Proteolysis Targeting Chimeras (PROTACs). It features an azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing compounds. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules that have DBCO or BCN functionalities, making it a versatile tool for targeted protein degradation studies. -
PROTAC Linkers
Ald-CH2-PEG8-azide is a PEG-based linker designed for the synthesis of PROTACs (proteolysis-targeting chimeras). It features an azide functional group, enabling it to engage in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing compounds. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN moieties. This versatility makes Ald-CH2-PEG8-azide ideal for applications in targeted protein degradation and medicinal chemistry research. -
PROTAC Linker
Carboxyrhodamine 110-PEG3-Azide is a PEG-based linker designed for the synthesis of PROTACs, facilitating targeted protein degradation. This compound features an azide functional group that permits efficient copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-modified partners. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN derivatives, making it versatile for various click chemistry applications in chemical biology research. -
PROTAC Linker
Azido-PEG8-azide is a PEG-based PROTAC linker that facilitates the synthesis of PROTACs. It features an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, this compound can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN-functionalized partners, making it a versatile tool for applications in targeted protein degradation research. -
PROTAC Linker
Dde Biotin-PEG4-Picolyl azide is a PEG-based PROTAC linker designed for the synthesis of targeted protein degradation agents. This compound functions through click chemistry, featuring an azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups. Its unique structure and reactivity make it a valuable tool for advancing research in targeted protein degradation and other applications in chemical biology. -
PROTAC Linker
N-Boc-N-bis(PEG4-azide) is a PEG-based linker designed for the synthesis of PROTACs, facilitating targeted protein degradation. This compound features an azide group enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules. Additionally, it is compatible with strain-promoted alkyne-azide cycloaddition (SPAAC) reactions involving DBCO or BCN groups, making it a versatile tool for chemical biology applications, including drug discovery and development. -
PROTAC Linkers
Boc-NH-PEG5-azide is a polyethylene glycol (PEG)-based linker designed for PROTAC synthesis. Featuring an azide functional group, it is compatible with copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) using alkyne-containing substrates or compounds with DBCO or BCN groups. This reagent is essential for the development of bifunctional molecules in targeted protein degradation research applications and facilitates the efficient assembly of PROTACs. -
PROTAC linker
Boc-NH-PEG9-azide is a PEG-based linker designed for usage in the synthesis of PROTACs (Proteolysis Targeting Chimeras). This compound features an azide group, facilitating copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it is capable of participating in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN functionalized compounds, making it a versatile tool for protein degradation studies and drug development applications. -
PROTAC Linker
S-Acetyl-PEG3-azide is a PEG-based linker designed for use in the synthesis of PROTACs, targeting protein degradation pathways via targeted ubiquitination. This compound contains an azide functional group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-bearing partners. Additionally, S-Acetyl-PEG3-azide can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-reactive molecules such as DBCO or BCN. Its applications in chemical biology are crucial for the development of innovative therapeutic strategies. -
PROTAC Linkers
(+) -Biotin-PEG6-hydrazide is a PEG-based linker designed for use in the synthesis of PROTACs (Proteolysis Targeting Chimeras). This compound facilitates the recruitment of E3 ligases and targets specific proteins for degradation, thereby enabling the study of protein function and regulation in various biological contexts. Its hydrazide moiety allows for selective conjugation, enhancing the versatility of PROTAC development in chemical biology research.
