Date published: 2026-4-26

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S-(3-Carboxypropyl)-L-cysteine (CAS 30845-11-5)

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Alternate Names:
(R)-4-[(2-Amino-2-carboxyethyl)thio]butanoic Acid; L-4-[(2-Amino-2-carboxyethyl)thio]butyric Acid; 3-(3-Carboxypropylthio)alanine
CAS Number:
30845-11-5
Molecular Weight:
207.25
Molecular Formula:
C7H13NO4S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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S-(3-Carboxypropyl)-L-cysteine is a compound that functions as a chelating agent in experimental applications. It acts by forming stable complexes with metal ions, particularly heavy metals such as lead and cadmium. This chelation process involves the formation of coordinate covalent bonds between the sulfur atom of the cysteine moiety and the metal ion, leading to the formation of a stable, water-soluble complex. S-(3-Carboxypropyl)-L-cysteine′s mode of action involves sequestering metal ions. S-(3-Carboxypropyl)-L-cysteine may exhibit antioxidant properties, which may further contribute to its role in experimental applications. Its ability to chelate metal ions and scavenge free radicals.


S-(3-Carboxypropyl)-L-cysteine (CAS 30845-11-5) References

  1. The ceramide moiety of disialoganglioside (GD3) is essential for GD3 recognition by the sialic acid-binding lectin SIGLEC7 on the cell surface.  |  Hashimoto, N., et al. 2019. J Biol Chem. 294: 10833-10845. PMID: 31138648
  2. S-3-Carboxypropyl-l-cysteine specifically inhibits cystathionine γ-lyase-dependent hydrogen sulfide synthesis.  |  Yadav, PK., et al. 2019. J Biol Chem. 294: 11011-11022. PMID: 31160338
  3. Thioredoxin regulates human mercaptopyruvate sulfurtransferase at physiologically-relevant concentrations.  |  Yadav, PK., et al. 2020. J Biol Chem. 295: 6299-6311. PMID: 32179647
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  5. H2S-mediated blockage of protein acetylation and oxidative stress attenuates lipid overload-induced cardiac senescence.  |  Yu, R., et al. 2021. Arch Physiol Biochem. 1-14. PMID: 34511001
  6. Structural and Functional Studies of S-(2-Carboxyethyl)-L-Cysteine and S-(2-Carboxyethyl)-l-Cysteine Sulfoxide.  |  Waters, JK., et al. 2022. Molecules. 27: PMID: 36014554
  7. Estimation of exposure to alkylating carcinogens by the GC-MS determination of adducts to hemoglobin and nucleic acid bases in urine.  |  Bailey, E., et al. 1987. Arch Toxicol. 60: 187-91. PMID: 3619640
  8. Structural basis of the inhibition of cystathionine γ-lyase from Toxoplasma gondii by propargylglycine and cysteine.  |  Fernández-Rodríguez, C., et al. 2023. Protein Sci. 32: e4619. PMID: 36883335
  9. Mechanism-based and computational modeling of hydrogen sulfide biogenesis inhibition: interfacial inhibition.  |  Le Corre, L. and Padovani, D. 2023. Sci Rep. 13: 7287. PMID: 37142727

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

S-(3-Carboxypropyl)-L-cysteine, 100 mg

sc-504679
100 mg
$337.00