N-Acetyl-D-cysteine

CAS No. 26117-28-2

N-Acetyl-D-cysteine ( (S)-2-Acetamido-3-mercaptopropanoic acid )

Catalog No. M28158 CAS No. 26117-28-2

N-Acetyl-D-cysteine has antioxidant activities and scavenges ROS through the reaction with its thiol group.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 53 In Stock
50MG 65 In Stock
100MG 110 In Stock
200MG 160 In Stock
500MG 267 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    N-Acetyl-D-cysteine
  • Note
    Research use only, not for human use.
  • Brief Description
    N-Acetyl-D-cysteine has antioxidant activities and scavenges ROS through the reaction with its thiol group.
  • Description
    N-Acetyl-D-cysteine has antioxidant activities and scavenges ROS through the reaction with its thiol group.(In Vitro):Consistent with the known stereoselectivity of many biological processes, the unnatural D isomer of N-acetylcysteine failed to increase hepatic glutathione. Liver concentrations remained similar to control suggesting that the D isomer was unable to increase the rate of glutathione synthesis. The D isomer further differed from its L enantiomer in failing to increase the plasma concentration and the urinary excretion of inorganic sulfate. Congruent with these observations, much more N-acetyl-D-cysteine (47% of dose) was recovered unchanged in 24 hr urine than N-acetyl-L-cysteine (6.1% of dose).
  • Synonyms
    (S)-2-Acetamido-3-mercaptopropanoic acid
  • Pathway
    Immunology/Inflammation
  • Target
    ROS
  • Recptor
    Topo I;Topo II;Apoptosis
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    26117-28-2
  • Formula Weight
    163.2
  • Molecular Formula
    C5H9NO3S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC(=O)N[C@H](CS)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Chen DS, et al. Combinatorial synthesis of pyrazoloquinoline and pyrazoloacridine derivatives with high regioselectivity. Comb Chem High Throughput Screen. 2013 Jun 28;16(7):550-61.
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