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 |
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| 50MG | 65 | In Stock |
|
| 100MG | 110 | In Stock |
|
| 200MG | 160 | In Stock |
|
| 500MG | 267 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameN-Acetyl-D-cysteine
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NoteResearch use only, not for human use.
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Brief DescriptionN-Acetyl-D-cysteine has antioxidant activities and scavenges ROS through the reaction with its thiol group.
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DescriptionN-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).
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In VitroN-Acetyl-D-cysteine (20 mM; 1 hour pretreatment; 12 hours) does not increase intracellular GSH levels, but GSH monoester does. D-NAC can not enhance hypoxic apoptosis. This demonstrate that GSH rather thanD-NAC or NAC is responsible for enhancing hypoxic apoptosis.
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In Vivo——
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Synonyms(S)-2-Acetamido-3-mercaptopropanoic acid
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PathwayImmunology/Inflammation
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TargetROS
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RecptorTopo I|Topo II|Apoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number26117-28-2
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Formula Weight163.19
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Molecular FormulaC5H9NO3S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?H2O : 250 mg/mL (1531.96 mM)
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SMILESCC(=O)N[C@H](CS)C(O)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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