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N-Isobutyryl-D-cysteine (CAS 124529-07-3)

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Alternate Names:
N-(2-Methylpropionyl)-D-cysteine;
CAS Number:
124529-07-3
Purity:
≥97%
Molecular Weight:
191.25
Molecular Formula:
C7H13NO3S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-Isobutyryl-D-cysteine plays a role in molecular biology by modulating cellular processes and pathways. It interacts with specific enzymes and proteins, influencing their activity and function within the cell. N-Isobutyryl-D-cysteine regulates redox signaling pathways, affecting the balance of reactive oxygen species and antioxidant defenses. N-Isobutyryl-D-cysteine modulates the expression of genes involved in cell proliferation, differentiation, and apoptosis. Its interaction with key signaling molecules also impacts various cellular processes, including cell cycle progression, DNA repair, and protein synthesis. N-Isobutyryl-D-cysteine regulates the activity of transcription factors, influencing the expression of genes involved in immune response and inflammation. N-Isobutyryl-D-cysteine exerts a significant influence on molecular biology by modulating cellular processes and pathways for cell function and homeostasis.


N-Isobutyryl-D-cysteine (CAS 124529-07-3) References

  1. Determination of amino acid enantiomers in human urine and blood serum by gas chromatography-mass spectrometry.  |  Brückner, H. and Schieber, A. 2001. Biomed Chromatogr. 15: 166-72. PMID: 11391672
  2. Chromatographic determination of L- and D-amino acids in plants.  |  Brückner, H. and Westhauser, T. 2003. Amino Acids. 24: 43-55. PMID: 12624734
  3. Chiral N-isobutyryl-cysteine protected gold nanoparticles: preparation, size selection, and optical activity in the UV-vis and infrared.  |  Gautier, C. and Bürgi, T. 2006. J Am Chem Soc. 128: 11079-87. PMID: 16925425
  4. Application of chiral derivatizing agents in the high-performance liquid chromatographic separation of amino acid enantiomers: a review.  |  Ilisz, I., et al. 2008. J Pharm Biomed Anal. 47: 1-15. PMID: 18242036
  5. Discovery of amide (peptide) bond synthetic activity in Acyl-CoA synthetase.  |  Abe, T., et al. 2008. J Biol Chem. 283: 11312-21. PMID: 18305111
  6. Stereoselective analysis of tiopronin enantiomers in rat plasma using high-performance liquid chromatography-electrospray ionization mass spectrometry after chiral derivatization.  |  Wang, H., et al. 2009. Chirality. 21: 531-8. PMID: 18655161
  7. Inhibitory effects of cysteine and cysteine derivatives on germination of sporangiospores and hyphal growth of different Zygomycetes.  |  Galgóczy, L., et al. 2009. Mycopathologia. 168: 125-34. PMID: 19381868
  8. Greater enhancement of Bacillus subtilis spore yields in submerged cultures by optimization of medium composition through statistical experimental designs.  |  Chen, ZM., et al. 2010. Appl Microbiol Biotechnol. 85: 1353-60. PMID: 19697022
  9. Stereochemical effects of chiral monolayers on enhancing the resistance to mammalian cell adhesion.  |  Bandyopadhyay, D., et al. 2011. Chem Commun (Camb). 47: 6165-7. PMID: 21523309
  10. Liquid chromatographic determination of D- and L-amino acids by derivatization with o-phthaldialdehyde and N-isobutyryl-L-cysteine. Applications with reference to the analysis of peptidic antibiotics, toxins, drugs and pharmaceutically used amino acids.  |  Brückner, H., et al. 1995. J Chromatogr A. 711: 201-15. PMID: 7496491

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Isobutyryl-D-cysteine, 250 mg

sc-236051
250 mg
$295.00