Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T18799 | Tetrazine-Ph-OPSS | Others | Others |
Tetrazine-Ph-OPSS is an ADC linker employed for synthesizing ADCs, or antibody-drug conjugates [1]. | |||
T18510 |
OPSS-PEG36-acid
|
Others | Others |
OPSS-PEG36-acid is a 36-unit PEG linker amenable to cleavage, specifically designed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T16400 |
OPSS-PEG8-COOH
|
Others | Others |
OPSS-PEG8-COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17369 |
Ald-Ph-amido-PEG23-OPSS
|
Others | Others |
Ald-Ph-amido-PEG23-OPSS is a cleavable 23-unit polyethylene glycol linker commonly employed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T19780 |
2,2′-Dipyridyl disulfide
2,2'-Dipyridyl disulfide,OPSS,2,2'-二硫二吡啶,Aldrithiol 2,Orthopyridyl disulfide |
Others | Others |
2,2′-Dipyridyl disulfide (Aldrithiol 2) 是肽化学中的常用试剂,是测定巯基的有用试剂,常用于氧化还原缩合以形成肽键或用于偶联反应以形成二硫键连接的异二聚体。 | |||
T18512 |
OPSS-Val-Cit-PAB-PNP
|
Others | Others |
OPSS-Val-Cit-PAB-PNP is a cleavable linker employed in ADC (antibody-drug conjugates) synthesis [1]. | |||
T18511 |
OPSS-Val-Cit-PAB-OH
|
Others | Others |
OPSS-Val-Cit-PAB-OH is an ADC linker utilized for the synthesis of antibody-drug conjugates (ADCs) [1]. | |||
T30477 |
Bis-PEG5-thiol
|
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Bis-PEG5-thiol is a PEG derivative containing two thiol groups. The thiol groups react with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc. The hydrophilic PEG spacer increases solubility in aqueous media. | |||
T71953 |
Thiol-PEG2-acid
|
||
Thiol-PEG2-acid is a PEG derivative containing a thiol group and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The thiol group reacts with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. |