ss-a

Propargyl-PEG1-SS-alcohol is a cleavable, 1-unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

THP-SS-alcohol is a cleavable linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Amino-PEG3-SS-acid is a cleavable, three-unit polyethylene glycol (PEG) linker frequently used in the synthesis of antibody-drug conjugates (ADCs)[1].

BCN-SS-amine is a cleavable linker essential in the synthesis of antibody-drug conjugates (ADC). It connects cytotoxic drugs to antibodies, allowing for precise delivery to targeted cells or proteins. The cleavable nature ensures controlled drug release, thereby optimizing the effectiveness of ADCs.

Biotin-PEG3-SS-azide (Biotin-PEG3-amido-SS-amido-azide) is a cleavable ADC linker containing 3-unit PEG and can be used to synthesize antibody-drug conjugates (ADCs).

Boc-amino-PEG3-SS-acid is a cleavable, three-unit polyethylene glycol (PEG) linker frequently used in the synthesis of antibody-drug conjugates (ADCs) [1].

DBCO-SS-amine is a cleavable linker essential in ADC synthesis, facilitating the attachment of cytotoxic drugs to antibodies for targeted delivery to cells or proteins. Its cleavable nature allows for controlled drug release, enhancing the effectiveness of ADCs (antibody-drug conjugates).

TCO-SS-amine, a cleavable linker crucial in ADC synthesis, joins cytotoxic drugs to antibodies for precise delivery to target cells or proteins. Its cleavable nature ensures controlled drug release, optimizing the effectiveness of ADCs.

Tetrazine-PEG5-SS-amine, a cleavable 5-unit polyethylene glycol (PEG) linker, is utilized in the synthesis of antibody-drug conjugates (ADCs)[1].

Biotin-PEG4-SS-azide, a biotin-labeled ADC linker, is primarily utilized in the synthesis of antibody-drug conjugates (ADCs). This compound serves as a click chemistry reagent featuring an Azide group, enabling it to partake in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-bearing molecules. Additionally, it can engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.

Tetrazine-Ph-SS-amine, a cleavable ADC linker, facilitates the synthesis of antibody-drug conjugates (ADCs) [1]. This click chemistry reagent features a Tetrazine group capable of engaging in an inverse electron demand Diels-Alder reaction (iEDDA) with TCO group-containing molecules.

Biotin-PEG(4)-SS-Azide, a click chemistry reagent featuring an azide group, is utilized in various biochemical research applications.

Biotin-PEG(4)-SS-Alkyne is an alkyne-containing click chemistry reagent suitable for a wide range of biochemical studies.

DBCO-SS-aldehyde is an ADC linker employed for ADC synthesis[1]. This cleavable linker is designed to facilitate the conjugation of antibodies and drugs, resulting in antibody-drug conjugates (ADCs).

SS-208 is a selective inhibitor of HDAC6 (IC50 = 12 nM) with anti-tumor activity. SS-208 shows selectivity over other HDAC subtypes.

NHS-PEG1-SS-PEG1-NHS is a reversible linker used for interacting biomolecules with active small molecules and is effective for linking protein liposomes or nanoparticles (NHS-PEG1-SS-PEG1-NHS).

Acid-PEG2-SS-PEG2-acid, a 4-unit PEG ADC linker with cleavable bonds, is used in the synthesis of antibody-drug conjugates (ADCs)[1].

Acid-PEG3-SS-PEG3-acid is a cleavable six-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs) [1].

Amino-ethyl-SS-PEG3-NHBoc is a cleavable 3-unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs) [1].

Aminoethyl-SS-ethylalcohol (Compound 3) is an Alkyl-Chain-based PROTAC linker can be used in the synthesis of PROTACs[1]. Aminoethyl-SS-ethylalcohol is also a glutathione cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[2].

Aminoethyl-SS-propionic acid is an ADC linker compound employed in ADC synthesis [1]. It functions as a cleavable linker in the conjugation of antibodies with drugs, allowing for targeted drug delivery.

Azide-C2-SS-C2-biotin is a cleavable linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Azido-C2-SS-PEG2-C2-acid is a cleavable PEG linker with two units used in the synthesis of antibody-drug conjugates (ADCs) [1].

Azido-PEG3-SS-PEG3-azide, a polyethylene glycol (PEG) based linker, is commonly used in the synthesis of proteolysis targeting chimeras (PROTACs)[1].