Diethylene glycol 1, 2-bis (succinimidyl 3-oxypropionate) is a PEGn linker for antibody-drug-conjugation (ADC).

N-Boc-PEG4-bromide is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

(S)-5-Tert-butoxy-4-(3-((S)-1, 5-di-tert-butoxy-1, 5-dioxopentan-2-yl)ureido)-5-oxopentanoic acid is a PEGn linker for antibody-drug-conjugation (ADC).

N-Butanoyl-DL-homoserine lactone ((Rac)-C4-HSL) is a racemic mixture of N-Butanoyl-D-homoserine lactone and N-Butanoyl-L-homoserine lactone. N-Butanoyl-L-homoserine lactone is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). N-Butanoyl-L-homoserine lactone has antibacterial activity and is used in antibacterial biofilm. N-Butanoyl-L-homoserine lactone aptamers blocks qurom sensing and inhibits biofilm formation in Pseudomonas aeruginosa.

(S)-Di-tert-butyl 2-(3-((S)-6-amino-1-tert-butoxy-1-oxohexan-2-yl)ureido)pentanedioate is a PEGn linker for antibody-drug-conjugation (ADC).

DM1（Mertansine）是一种微管抑制剂和抗体可结合的美坦新类物质，旨在克服美坦新的全身毒性并增强肿瘤特异性递送。美坦新可以通过连接子附着到单克隆抗体上，以形成抗体-药物结合物（ADC）。

6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.

Propargyl-PEG3-acid is a non-cleavable (3 unit PEG) ADC linker and also a PEG-based PROTAC linker that can be used to synthesis 6-OHDA-PEG3-yne. 6-OHDA-PEG3-yne contains 6-OHDA (HY-B1081, HY-B1081A) and Propargyl-PEG3-acid.

Mal-PEG3-PFP is a PEGn linker for antibody-drug-conjugation (ADC).

NHS-PEG4-azide is a PEGn linker for antibody-drug-conjugation (ADC).

Boc-NH-PEG6-CH2CH2COOH is a cleavable ADC linker used as a linker for antibody-drug conjugates (ADC).

Fmoc-Gly-Gly-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Boc-Dap-NE is an antibody drug conjugate.

Fmoc-Val-Cit-PAB-OH is a linker for ADC through cleaveage by catepsin B only present in lysosome at Val-Cit site, thus making ACD payload be released only in the cell.

Val-Cit-PAB-OH is a linker for ADC through cleaveage by catepsin B only present in lysosome at Val-Cit site, thus making ACD payload be released only in the cell.

15-(2-Pyridyldithio)-4, 7, 10, 13-tetraoxapentadecanoic acid N-hydroxysuccinimide Ester is a bis-sulfone-PEGn linker for antibody-drug-conjugation (ADC).

Boc-Val-Ala-PAB-PNP is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

Perfluorophenyl 3-(2-(2-(2-(1, 3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)ethoxy)propanoate is a PEGn linker for antibody-drug-conjugation (ADC).

2, 5-Dioxopyrrolidin-1-yl 3-(2-(2-(1, 3-dioxoisoindolin-2-yloxy)ethoxy)ethoxy)propanoate is a PEGn linker for antibody-drug-conjugation (ADC).

Bis(2, 5-dioxopyrrolidin-1-yl)3, 3'-((2-((3-((2, 5-dioxopyrrolidin-1-yl)oxy)-3-oxopropoxy)methyl)-2-methylpropane-1, 3-diyl)bis (oxy))dipropanoate is a PEGn linker for antibody-drug-conjugation (ADC).