cysteamine

Cysteamine hydrochloride is an orally administered small-molecule drug commonly used for the treatment of nephropathic cystinosis. It also functions as an antioxidant and is used in experimental studies to induce gastrointestinal disorders, duodenal ulcers, and kidney injury models in mice.

2-Aminoethanethiol (Cysteamine) is a Cystine Depleting Agent. The mechanism of action of cysteamine is as a Cystine Disulfide Reduction.

2-(Pyridyldithio)ethylamine hydrochloride ((S)-2-Pyridylthio Cysteamine Hydrochloride) is a disulfide intercalating cross-linking reagent.

Pep-1-Cysteamine, a chimeric cell-penetrating peptide (CPP), exhibits primary amphipathicity and facilitates the translocation of active proteins across biological membranes into cells [1].

Pep-1-Cysteamine TFA is a chimeric cell-penetrating peptide (CPP) with primary amphipathic properties. It possesses the capability to traverse biological membranes and facilitate the intracellular delivery of active proteins.

Cysteamine bitartrate is a useful organic compound for research related to life sciences. The catalog number is T35383 and the CAS number is 27761-19-9.

Cysteamine-d4 (hydrochloride) is the deuterated form of cysteamine hydrochloride. Cysteamine hydrochloride (2-Aminoethanethiol hydrochloride) is an orally administrable small molecule active compound used to treat nephropathic cystinosis and also serves as an antioxidant.

KB 5492 is an agent of anti-ulcer. It preventing cysteamine-induced duodenal ulcers by stimulating duodenal HCO3- secretion.

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).