aeide c1 nhs ester

Aeide-C1-NHS ester, an alkyl ether-based PROTAC linker, finds utility in the synthesis of PROTACs[1].

N3-PEG4-C2-NHS ester is a noncleavable, four-unit polyethylene glycol (PEG) linker essential for the synthesis of antibody-drug conjugates (ADCs).

N3-C4-NHS ester, a non-cleavable ADC linker, is utilized in the synthesis of antibody-drug conjugates (ADCs).

Azido-PEG12-NHS ester, a PEG-based PROTAC linker, is utilized in PROTAC synthesis.

DBCO-PEG3-NHS ester is a degradable ADC linker that can be used to synthesize antibody-coupled active molecules.

DBCO-PEG4-NHS ester is a PEG-based PROTAC linker utilized in PROTAC synthesis[1].

N3-Ph-NHS ester is a noncleavable ADC linker that can be utilized in the synthesis of antibody-drug conjugates (ADCs).

Fmoc-NH-PEG8-NHS ester is a PEG-based PROTAC linker employed in PROTAC synthesis [1].

Mal-PEG1-NHS ester is a cleavable, PEG-based linker utilized in the synthesis of antibody-drug conjugates (ADCs) and PROTACs, serving as both an ADC linker and a PROTAC linker. [Mal-PEG1-NHS ester]

Fmoc-PEG12-NHS ester, a PEG-based linker for PROTACs, facilitates the joining of two essential ligands, crucial for the formation of PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Boc-NH-PEG3-NHS ester is a PEG-based linker utilized in the synthesis of PROTACs.

Propargyl-C1-NHS ester (4-Pentynoic Acid Succinimidyl Ester) is a nonclaevable linker used for antibody-drug-conjugation (ADC).

Tetrazine-Ph-NHCO-C3-NHS ester is a PEG-derived linker used for PROTAC synthesis.

Ald-Ph-NHS ester is a non-cleavable linker utilized in antibody-drug conjugation (ADC).

Boc-NH-O-C1-NHS ester, an alkyl ether-based PROTAC linker, is utilized in PROTAC synthesis.

Tri-GalNAc-NHS ester, a LYsosome TArgeting Chimera (LYTAC) and ligand for the asialoglycoprotein receptor (ASGPR), facilitates the degradation of extracellular proteins, including membrane proteins, via the lysosomal targeting receptor expressed on liver cells. This compound is utilized as a protein degrader in LYTAC research [1].

Mal-PEG8-NHS ester is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.

DBCO-PEG4-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

TCO-PEG2-Sulfo-NHS ester is a Polyethylene glycol (PEG)-based linker for PROTAC synthesis[1].

Fmoc-PEG3-CH2CH2-NHS ester is a PEG-based linker derived from fluorenylmethoxycarbonyl (Fmoc) used for the efficient synthesis of PROTACs (proteolysis-targeting chimeras)[1], offering a practical solution for connecting desired molecules and targeting specific proteins for degradation.

Tetrazine-Ph-NHS ester is an alkyl ether-based PROTAC linker commonly used for synthesizing PROTACs[1].

Bromoacetamido-PEG4-NHS ester is a PEGylated N-hydroxysuccinimide ester linker designed for PROTAC synthesis, facilitating the creation of protein-targeted chimeras (PROTACs)[1].

Azido-PEG8-C1-NHS ester is a polyethylene glycol (PEG)-based linker designed for synthesizing proteolysis targeting chimeras (PROTACs)[1].

Fluorescein-PEG6-bis-NHS ester, a polyethylene glycol (PEG)-based linker, is utilized in the synthesis of proteolysis targeting chimeras (PROTACs)[1].

Boc-N-PEG5-C2-NHS ester is a PEG-based linker used in PROTACs to join two essential ligands, facilitating selective protein degradation by harnessing the ubiquitin-proteasome system within cells.

Benzyloxy carbonyl-PEG3-NHS ester is a polyethylene glycol (PEG) derivative compound utilized as a PROTAC linker in the synthesis of PROTACs [1].

NHS-PEG4-(m-PEG4)3-ester is a PEG-based PROTAC linker used for synthesizing PROTACs [1].

Methyltetrazine-PEG8-NHS ester is a polyethylene glycol (PEG) derivative specifically designed as a PROTAC linker for synthesizing Proteolysis Targeting Chimeras (PROTACs)[1].

Azido-PEG6-NHS ester is a cleavable 6-unit polyethylene glycol (PEG) linker, commonly employed in the synthesis of antibody-drug conjugates (ADCs)[1], and serves as a PEG- and alkyl ether-based linker for the synthesis of proteolysis targeting chimeras (PROTACs)[2].

Biotin-PEG2-NHS ester is a biotinylated polyethylene glycol (PEG)-based linker used in PROTAC synthesis for biotin attachment[1].

Methyltetrazine-PEG13-NHS ester, a polyethylene glycol (PEG)-derived linker, is designed specifically for the synthesis of proteolysis targeting chimeras (PROTACs)[1].

m-PEG37-NHS ester is a PEG-based linker for PROTACs, which connects two essential ligands crucial for PROTAC molecule formation. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.

DBCO-NHCO-PEG5-NHS ester is a polyethylene glycol (PEG)-based linker used in the synthesis of PROTACs [1].

m-PEG4-NHS ester is a PEG-based linker for PROTACs that connects two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Azido-PEG3-O-NHS ester, a PEG-based linker for PROTACs, connects two essential ligands crucial for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Azido-PEG4-NHS-ester is a PEG-based linker for PROTACs, joining two essential ligands and facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

SPDP-C6-NHS ester is an alkyl ether-based linker used in the synthesis of PROTACs [1].

Mal-amido-PEG1-C2-NHS ester is a noncleavable antibody-drug conjugate (ADC) linker that incorporates a maleimide functional group and an N-hydroxysuccinimide (NHS) ester. The NHS ester offers a means to specifically modify primary amines (-NH2) present in proteins, amine-modified oligonucleotides, and other amine-containing molecules[1][2].

Bromo-PEG2-NHS ester, a PEG-based linker for PROTACs, connects two essential ligands necessary for PROTAC molecule formation and enables selective protein degradation through the ubiquitin-proteasome system within cells.

DBCO-NHCO-PEG13-NHS ester is a pegylated PROteolysis-TArgeting Chimera (PROTAC) linker, serving as a valuable tool for PROTAC synthesis [1].

DBCO-NHS ester 3 (Compound 12) is a cleavable linker utilized in the synthesis of antibody-drug conjugate (ADC). It is a derivative of Dibenzylcyclooctyne (DBCO) resulting from the activation of N-hydroxysuccinimide by the carboxylic acid moiety of both methyl-oxanorbornadiene (MeOND) and dibenzoazacyclooctyne (DIBAC)[1][2].

Propargyl-O-C1-amido-PEG4-C2-NHS ester is a non-cleavable 4-unit PEG linker used in antibody-drug conjugation (ADC) to link antibodies with drugs.

Mal-PEG36-NHS ester is a PEG-based linker used in PROTAC development, joining two essential ligands to form PROTAC molecules. This linker facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Iodoacetyl-PEG4-NHS ester is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

2-(Azido-PEG3-amido)-1,3-bis(NHS ester) is a polyethylene glycol (PEG)-based linker used for PROTAC synthesis [1].

Maleimide-C10-NHS ester is an alkyl ether-based linker utilized in PROTAC synthesis.

N3-C5-NHS ester, a noncleavable ADC linker, can be used in the synthesis of antibody-drug conjugates (ADCs).

DBCO-CONH-S-S-NHS ester is a disulfide-linked ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Methyltetrazine-PEG24-NHS ester is a polyethylene glycol (PEG) linker utilized in the synthesis of proteolysis targeting chimeras (PROTACs)[1].

TCO-PEG3-NHS ester is a PEG-based linker for PROTACs that joins two essential ligands, crucial for PROTAC molecule formation, enabling selective protein degradation via the ubiquitin-proteasome system [in cells].