sulfo-smpb sodium

Sulfo-SMPB sodium is a non-cleavable heterobifunctional chemical cross-linking reagent that combines N-hydroxysuccinimide ester and maleimide groups. This compound enables the covalent conjugation of molecules possessing amine and sulfhydryl functionalities.

S-Sulfo-L-cysteine sodium salt 在高浓度下对 mGluR1α 和 mGluR5a 显示出较弱的亲和力且具有潜在的抗氧化活性。

Sulfo-SIAB sodium is a non-cleavable monovalent bifunctional linker.

Sulfo-SPP sodium is a heterobifunctional, thiol-cleavable, and membrane-impermeable crosslinker.

Sulfo-NHS-LC-Biotin sodium 是一种胺反应性生物素化试剂，可用于抗体标记[1]。

DBCO-Sulfo-NHS ester sodium is a cleavable linker predominantly employed in the synthesis of antibody-drug conjugates (ADCs)[1].

6-O-Sulfo-β-cyclodextrin is a sulfated cyclodextrin.1It has been used for the chiral separation of nadolol racemates by capillary electrophoresis. 1.Wang, F., Dowling, T., Bicker, G., et al.Electrophoretic chiral separation of pharmaceutical compounds with multiple stereogenic centers in charged cyclodextrin mediaJ. Sep. Sci.24(5)378-384(2001)

Sulfo-SMCC sodium 是一种异双功能、不可裂解的 ADC 交联剂，带有 N-羟基琥珀酰亚胺酯和马来酰亚胺基团，分别与伯胺和巯基反应。

Methyltetrazine-Sulfo-NHS ester (sodium) is an alkyl ether-based PROTAC linker utilized for PROTAC synthesis[1].

Sulfo-SPDP-C6-NHS sodium is a sodium salt form of a cleavable ADC linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].

ICG-Sulfo-OSu sodium 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.

Sulfo-DGN462 sodium undergoes degradation to DGN462 when subjected to culture medium and plasma. DGN462, a highly effective DNA-alkylating agent, exhibits anti-tumor properties that are particularly active against acute myeloid leukemia (AML).