Date published: 2025-12-1

1-800-457-3801

SCBT Portrait Logo
Seach Input

L-Sulforaphane (CAS 142825-10-3)

0.0(0)
Write a reviewAsk a question

See product citations (3)

Alternate Names:
L-Sulforaphane is also known as R-Sulforaphane.
Application:
L-Sulforaphane is an inducer of apoptosis, phase II detoxification enzymes, and xenobiotic enzymes.
CAS Number:
142825-10-3
Purity:
≥93%
Molecular Weight:
177.29
Molecular Formula:
C6H11NOS2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

L-Sulforaphane, a compound found at high levels in broccoli, has been reported to prevent NFκB binding which results in downregulation of apoptosis inhibitors, therefore inducing apoptosis. Research has demonstrated L-Sulforaphane to be a potent inducer of phase II detoxification enzymes and displays chemoprotective properties. Other experiments have shown L-Sulforaphane to induce enzymes of xenobiotic metabolism and therefore accelerate the metabolic disposal of xenobiotics. L-Sulforaphane also displays a capacity to inhibit intracellular, extracellular, and antibiotic-resistant strains of Helicobacter pylori. Additionally, it has been found to prevent clonogenicity.


L-Sulforaphane (CAS 142825-10-3) References

  1. Sulforaphane inhibits extracellular, intracellular, and antibiotic-resistant strains of Helicobacter pylori and prevents benzo[a]pyrene-induced stomach tumors.  |  Fahey, JW., et al. 2002. Proc Natl Acad Sci U S A. 99: 7610-5. PMID: 12032331
  2. A novel mechanism of chemoprotection by sulforaphane: inhibition of histone deacetylase.  |  Myzak, MC., et al. 2004. Cancer Res. 64: 5767-74. PMID: 15313918
  3. A major inducer of anticarcinogenic protective enzymes from broccoli: isolation and elucidation of structure.  |  Zhang, Y., et al. 1992. Proc Natl Acad Sci U S A. 89: 2399-403. PMID: 1549603
  4. D,L-Sulforaphane-induced cell death in human prostate cancer cells is regulated by inhibitor of apoptosis family proteins and Apaf-1.  |  Choi, S., et al. 2007. Carcinogenesis. 28: 151-62. PMID: 16920735
  5. Reprogramming of keratin biosynthesis by sulforaphane restores skin integrity in epidermolysis bullosa simplex.  |  Kerns, ML., et al. 2007. Proc Natl Acad Sci U S A. 104: 14460-5. PMID: 17724334
  6. Sulforaphane targets pancreatic tumour-initiating cells by NF-kappaB-induced antiapoptotic signalling.  |  Kallifatidis, G., et al. 2009. Gut. 58: 949-63. PMID: 18829980
  7. Sulforaphane inhibits mitotic clonal expansion during adipogenesis through cell cycle arrest.  |  Choi, KM., et al. 2012. Obesity (Silver Spring). 20: 1365-71. PMID: 22282047
  8. Antiplatelet activity of L-sulforaphane by regulation of platelet activation factors, glycoprotein IIb/IIIa and thromboxane A2.  |  Oh, CH., et al. 2013. Blood Coagul Fibrinolysis. 24: 498-504. PMID: 23412354
  9. Cell cycle effects of L-sulforaphane, a major antioxidant from cruciferous vegetables: The role of the anaphase promoting complex.  |  Shelley, Z., et al. 2014. Hell J Nucl Med. 17 Suppl 1: 11-6. PMID: 24392461
  10. Modulating potential of L-sulforaphane in the expression of cytochrome p450 to identify potential targets for breast cancer chemoprevention and therapy using breast cell lines.  |  Licznerska, B., et al. 2015. Phytother Res. 29: 93-9. PMID: 25234182
  11. L-Sulforaphane Confers Protection Against Oxidative Stress in an In Vitro Model of Age-Related Macular Degeneration.  |  Dulull, NK., et al. 2018. Curr Mol Pharmacol. 11: 237-253. PMID: 29376497
  12. Investigation of potential anti-pneumococcal effects of l-sulforaphane and metabolites: Insights from synchrotron-FTIR microspectroscopy and molecular docking studies.  |  Liang, J., et al. 2020. J Mol Graph Model. 97: 107568. PMID: 32097886
  13. Examination of Novel Immunomodulatory Effects of L-Sulforaphane.  |  Mazarakis, N., et al. 2021. Nutrients. 13: PMID: 33673203
  14. The effects of the dietary compound L-sulforaphane against respiratory pathogens.  |  Mazarakis, N., et al. 2021. Int J Antimicrob Agents. 58: 106460. PMID: 34695564
  15. Anticarcinogenic activities of sulforaphane and structurally related synthetic norbornyl isothiocyanates.  |  Zhang, Y., et al. 1994. Proc Natl Acad Sci U S A. 91: 3147-50. PMID: 8159717

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

L-Sulforaphane, 1 mg

sc-203099D
1 mg
$143.00

L-Sulforaphane, 5 mg

sc-203099E
5 mg
$234.00

L-Sulforaphane, 10 mg

sc-203099
10 mg
$418.00

L-Sulforaphane, 25 mg

sc-203099F
25 mg
$819.00

L-Sulforaphane, 50 mg

sc-203099A
50 mg
$1592.00

L-Sulforaphane, 100 mg

sc-203099B
100 mg
$2560.00

L-Sulforaphane, 1 g

sc-203099C
1 g
$20410.00