Description
N-Acetyl-S-(N-methylsulfinylbutylthiocarbamoyl)-L-cysteine is a conjugate of N-acetyl-cysteine and sulforaphane. Like other isothiocyanates (ITCs), this compound likely displays antioxidative activity.
N-Acetyl-S-(N-methylsulfinylbutylthiocarbamoyl)-L-cysteine
Product ID A0822
Cas No. 334829-66-2
Purity ≥98%
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Product Info
| Cas No. | 334829-66-2 |
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| Purity | ≥98% |
| Formula | C11H20N2O4S3 |
| Formula Wt. | 340.48 |
| Chemical Name | N-Acetyl-S-(N-methylsulfinylbutylthiocarbamoyl)-L-cysteine |
| IUPAC Name | N-Acetyl-S-{[4-(methylsulfinyl)butyl]carbamothioyl}-L-cysteine |
| Synonym | N-Acetyl cysteine sulforaphane; sulforaphane N-acetyl cysteine conjugate; SFNAC; SFN-NAC |
| Solubility | Ethanol (5 mg/ml), DMSO (10 mg/ml ), DMF (10 mg/ml) |
| Appearance | White to off white powder |
Shipping and Storage
| Store Temp | -20°C |
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| Ship Temp | Ambient |
Downloads
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References
Zimmermann M, Kolmar H, Zimmer A. S-Sulfocysteine - Investigation of cellular uptake in CHO cells. J Biotechnol. 2021 Jul 20;335:27-38. PMID: 34090949.
Son ES, Park JW, Kim YJ, et al. Effects of antioxidants on oxidative stress and inflammatory responses of human bronchial epithelial cells exposed to particulate matter and cigarette smoke extract. Toxicol In Vitro. 2020 Sep;67:104883. PMID: 32387680.
Langston-Cox A, Anderson D, Creek D, et al. Measuring sulforaphane and its metabolites in human plasma: a high throughput method. Molecules. 2020 Feb 13;25(4):829. PMID: 32070059.
Liu HJ, Wang L, Kang L, et al. Sulforaphane-N-acetyl-cysteine induces autophagy through activation of ERK1/2 in U87MG and U373MG cells. Cell Physiol Biochem. 2018;51(2):528-542. PMID: 30458452.