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Cysteamine HCl Antioxidant chemical

Cat.No.S4206

Cysteamine HCl(Mercaptamine) is an autophagy-stimulatory proteostasis regulator. This compound can be used for the treatment of nephropathic cystinosis and an antioxidant.It can be used to induce animal models of Duodenal Ulcer.
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Quality Control

Batch: S420601 DMSO]23 mg/mL]false]Water]23 mg/mL]false]Ethanol]23 mg/mL]false Purity: 100.0%
100.0

Solubility

In vitro
Batch:

DMSO : 23 mg/mL (202.44 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 23 mg/mL

Ethanol : 23 mg/mL

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In vivo
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Chemical Information, Storage & Stability

Molecular Weight 113.61 Formula

C2H7NS.HCl

Storage (From the date of receipt) 3 years -20°C powder (seal)
CAS No. 156-57-0 Download SDF Storage of Stock Solutions Solutions are unstable. Prepare fresh or purchase small, pre-packaged sizes. Repackage upon receipt.
Synonyms Mercaptamine SMILES C(CS)N.Cl

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Mechanism of Action

In vitro

Cysteamine HCl has been shown to increase intracellular glutathione levels in cystinotic cells, thus restoring the altered redox state of the cells. Also increased rates of apoptosis in cystinotic cells, which are thought to be the result of increased caspase 3 and protein kinase Cε activity, is counteracted by this compound administration. It has antioxidant properties as a result of increasing glutathione production. This chemical is an excellent scavenger of OH and HOCl; it also reacts with H2O2. This agent increases the production of several heat shock proteins (HSP), including the murine Hsp40. It exerts a dose-dependent effect on the doxorubicin-induced death of cancer cells, measured in both HeLa cells and B16 cells, whereas this compound treatment alone had no influence on cell survival. In addition, in a doxorubicin-resistant breast cancer cell line, the addition of this chemical to doxorubicin results in a dramatic increase in cell death. This compound (100 μM) significantly is able to increase the intracellular GSH levels and the percentage of embryos that developed to the blastocyst stage of culture matured oocytes.

In vivo

Cysteamine is introduced as a treatment for cystinosis by depleting lysosomal cystine. This compound can inhibit transglutaminase activity by binding to the cysteine in its active center. It increases brain levels of brain-derived neurotrophic factor (BDNF), which is caused by the increased expression of the heat shock DNAJ-containing protein 1 (HSJ1). This chemical inhibits the formation of gastric and mammary tumors that are induced chemically or after irradiation, respectively. The administration of this compound is also able to inhibit the metastasis of pancreatic cancer in a mouse model by decreasing the expression and activity of metalloproteinases.

References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2026-07-24)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT06990984 NOT_YET_RECRUITING
Leigh Syndrome
Thiogenesis Therapeutics, Inc.
2026-10 PHASE2
NCT05994534 ACTIVE_NOT_RECRUITING
Cystinosis
Nacuity Pharmaceuticals, Inc.
2023-10-29 PHASE1; PHASE2
NCT02735707 RECRUITING
Community-acquired Pneumonia, Influenza, COVID-19
UMC Utrecht
2016-04-11 PHASE3
NCT07477288 COMPLETED
Skin Aging
Hasanuddin University
2025-03-12 PHASE2
NCT06278948 UNKNOWN
Melasma
Cosmetique Active International
2023-10-06
NCT05656833 UNKNOWN
Melasma
UnionDerm
2022-10-28

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