cystamine

Cystamine (2,2'-Disulfanediyldiethanamine) is an inhibitor of transglutaminase and inhibits caspase-3 with an IC50 value of 23.6 μM. Cystamine can be used in studies about Huntington's diseases.

Cystamine dihydrochloride is a radiation-protective agent. It also protects against carbon tetrachloride liver damage.

Boc-Cystamine is a cleavable linker vital in ADC synthesis. Boc-Cystamine joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.

Poc-Cystamine is a click chemistry reagent consisting of a cystamine structural unit derived from a propargyl group.

N3-Cystamine-Suc-OSu is a click chemistry reagent containing an azido group. It is useful for a variety of biochemical studies.

Boc-Cystamine-Poc is a click chemistry reagent featuring a cystamine structural unit.

Cystamine-D8 dihydrochloride is the deuterated form of Cystamine (dihydrochloride), which represents the disulfide form of the free thiol cysteamine. Cystamine functions as an orally active transglutaminase (Tgase) inhibitor and also inhibits caspase-3 with an IC50 value of 23.6 μM. It is utilized in research on various diseases, including Huntington's disease (HD).

Cystamine-D8 Dihydrochloride (Standard) is a reference standard of Cystamine-D8 Dihydrochloride intended for quantitative analysis, quality control, and related biochemical research applications. Cystamine-d8 (dihydrochloride) is the deuterated form of Cystamine (dihydrochloride), which represents the disulfide form of the free thiol cysteamine. Cystamine functions as an orally active transglutaminase (Tgase) inhibitor and also inhibits caspase-3 with an IC50 value of 23.6 μM. It is utilized in research on various diseases, including Huntington's disease (HD).

Poc-Cystamine hydrochloride is a click chemistry reagent that consists of a cystamine structure unit derived from propargyl.