ss

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

SS28 inhibits tubulin polymerization to cause cell cycle arrest at G2/M phase.

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].

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

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

Azidoethyl-SS-PEG2-Boc is a PEG-based linker for PROTACs that joins two essential ligands, facilitating selective protein degradation by the ubiquitin-proteasome system within cells.

Biotin-bis-amido-SS-NHS is an alkyl/ether-based PROTAC linker used in the synthesis of PROTACs.

Boc-aminooxy-ethyl-SS-propanol is a cleavable linker used in the synthesis of antibody-drug conjugates (ADCs) [1].

Boc-NH-ethyl-SS-propionic acid, an ADC linker compound, is utilized for the synthesis of antibody-drug conjugates (ADCs)[1].

Fmoc-NH-ethyl-SS-propionic acid is a cleavable linker compound used in the synthesis of antibody-drug conjugates (ADCs)[1].

Fmoc-NH-ethyl-SS-propionic NHS ester is a cleavable linker for antibody-drug conjugates (ADCs)[1], used in the synthesis of ADCs to facilitate the covalent attachment of drugs to antibodies through stable amide bond formation.

Hydroxy-PEG3-SS-PEG3-alcohol, a 6-unit polyethylene glycol (PEG) linker that can be cleaved, is commonly used in the synthesis of antibody-drug conjugates (ADCs) [1].

Mal-NH-ethyl-SS-propionic acid, a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs)[1], plays a crucial role in the modulation of drug release from the conjugate.

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

Propargyl-PEG1-SS-PEG1-acid is a cleavable two-unit polyethylene glycol (PEG) linker frequently utilized in the synthesis of antibody-drug conjugates (ADCs) [1].

Propargyl-PEG1-SS-PEG1-C2-Boc is a cleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs)[1].

Propargyl-PEG1-SS-PEG1-PFP ester is a cleavable linker containing a 1-unit polyethylene glycol (PEG) backbone, designed for the synthesis of antibody-drug conjugates (ADCs)[1].