Description
S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine is a conjugate of L-cysteine and sulforaphane. Like other isothiocyanates (ITCs), this compound likely displays antioxidative activity.
S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine
Product ID M1873
Cas No. 364083-21-6
Purity ≥98%
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Product Info
| Cas No. | 364083-21-6 |
|---|---|
| Purity | ≥98% |
| Formula | C9H18N2O3S3 |
| Formula Wt. | 298.45 |
| Chemical Name | S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine |
| IUPAC Name | S-{[4-(Methylsulfinyl)butyl]carbamothioyl}cysteine |
| Synonym | L-cysteine sulforaphane; sulforaphane L-cysteine conjugate; sulforaphane-cysteine; SFN-Cys |
| Solubility | Methanol, Water |
| Appearance | Yellow Powder |
Shipping and Storage
| Store Temp | -20°C |
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| Ship Temp | Ambient |
Downloads
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References
Zhou Y, Wang Y, Wu S, et al. Sulforaphane-cysteine inhibited migration and invasion via enhancing mitophagosome fusion to lysosome in human glioblastoma cells. Cell Death Dis. 2020 Oct 1;11(9):819. PMID: 33004792.
Li J, Zhou Y, Yan Y, et al. Sulforaphane-cysteine downregulates CDK4/CDK6 and inhibits tubulin polymerization contributing to cell cycle arrest and apoptosis in human glioblastoma cells. Aging (Albany NY). 2020 Aug 29;12(17):16837-16851. PMID: 32860670.
Sun J, Charron CS, Novotny JA, et al. Profiling glucosinolate metabolites in human urine and plasma after broccoli consumption using non-targeted and targeted metabolomic analyses. Food Chem. 2020 Mar 30;309:125660. PMID: 31670121.
Zheng Z, Lin K, Hu Y, et al. Sulforaphane metabolites inhibit migration and invasion via microtubule-mediated Claudins dysfunction or inhibition of autolysosome formation in human non-small cell lung cancer cells. Dell Death Dis. 2019 Mar 15;10(4):259. PMID: 30874545.