| Identification | More | [Name]
DL-SULFORAPHANE | [CAS]
4478-93-7 | [Synonyms]
(+)-1-ISOTHIOCYANATE-4R(METHYLSULFINYL)-BUTANE
1-ISOTHIOCYANATO-4-(METHYLSULFINYL)-BUTANE
1-ISOTHIOCYANATO-4-(METHYLSULFIYL)-BUTANE
((-)1-ISOTHIOCYANATO-4R-METHYLSULFINYL)BUTANE
(-)1-ISOTHIOCYANATO-4S-(METHYLSULFINYL)-BUTANE
(+)1-ISOTHIOCYANATO-4S-(METHYLSULFINYL)-BUTANE
1-ISOTHISCYANATO-4-(METHYLSULFINYL)-BUTANE
4-METHYLSULFINYLBUTYL ISOTHIOCYANATE
(-)-(4R)-SULFORAPHANE
DL-SULFORAPHANE
DL-SULPHORAPHANE
D-SULFORAPHANE
(-)-ISOTHIOCYANATO-(4R)-(METHYLSULFINYL)BUTANE
L-SULFORAPHANE
(R)-1-ISOTHIOCYANATO-4-(METHYLSULFINYL)BUTANE
R,S-SULFORAPHANE
R-SULFORAPHANE
S-SULFORAPHANE
SULFORAPHANE, D-
SULFORAPHANE, DL- | [EINECS(EC#)]
200-001-8 | [Molecular Formula]
C6H11NOS2 | [MDL Number]
MFCD00198068 | [Molecular Weight]
177.29 | [MOL File]
4478-93-7.mol |
| Chemical Properties | Back Directory | [Appearance]
Light Yellow Liquid | [Boiling point ]
125-135°C | [density ]
1.17±0.1 g/cm3(Predicted) | [storage temp. ]
−20°C
| [solubility ]
DMSO: 40 mg/mL, soluble
| [form ]
liquid
| [color ]
slightly yellow
| [biological source]
synthetic | [Usage]
Potent, selective inducer of phase II detoxification enzymes with anticarcinogenic properties. Occurs naturally in broccoli. It was found to inhibit chemically induced mammary tumor formation in rats. Antitumor agent | [Stability:]
Light Sensitive | [Cosmetics Ingredients Functions]
BLEACHING
SKIN PROTECTING | [InChI]
InChI=1S/C6H11NOS2/c1-10(8)5-3-2-4-7-6-9/h2-5H2,1H3 | [InChIKey]
SUVMJBTUFCVSAD-UHFFFAOYSA-N | [SMILES]
C(N=C=S)CCCS(C)=O | [LogP]
0.407 (est) | [CAS DataBase Reference]
4478-93-7(CAS DataBase Reference) |
| Questions And Answer | Back Directory | [Preparation]
Currently, there are three main methods for the artificial synthesis of DL-Sulforaphane: 1. Chemical synthesis; 2. Enzymatic method; 3. A combination of chemical and enzymatic methods.
1. Chemical synthesis: In 2003, a research group led by Desai et al. synthesized DL-Sulforaphane in five steps using isotope labeling, with a yield of ~10%.
2. Enzymatic method: The DL-Sulforaphane precursor, glucoraphane glycoside, is extracted from cruciferous vegetables and then hydrolyzed to prepare DL-Sulforaphane.
3. Combination of chemical and enzymatic methods: A method combining chemical synthesis and enzymatic extraction involves extracting glucosyltriernate from arugula seeds, using glucosyltriernate as a raw material, and then selectively oxidizing it to prepare glucoraphane glycoside, followed by hydrolysis to obtain DL-Sulforaphane. This process holds promise for industrialization.
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| Hazard Information | Back Directory | [Description]
Sulforaphane is a compound within the isothiocyanate group of organosulfur compounds and mainly found in cruciferous vegetables. It is produced when the enzyme myrosinase transforms glucoraphanin,a prodrug or storage form of SFN, into SFN upon damage to the plant (such as from chewing),which allows the two compounds to mix and react. Glucoraphanin is one of a few molecules known as isothiocyanates, existing alongside Sinigrin (metabolized into allylisothiocyanate). | [Chemical Properties]
DL-Sulforaphane (SFN) is a slightly yellow liquid. soluble in DMSO, methanol, or water-like solvents. SFN exists in food in its food-bound form known as Glucoraphanin. It is present in a wide range of vegetables such as cabbage, cauliflower, bok choy, kale, chinese broccoli, mustard, turnip, radish, and watercress. | [Uses]
Potent, selective inducer of phase II detoxification enzymes with anticarcinogenic properties. Occurs naturally in broccoli. It was found to inhibit chemically induced mammary tumor formation in rats. Antitumor agent
LNCaP prostate cancer cells were treated with DL-Sulforaphane to study the effect on androgen receptor. Effects on malathion toxicity was studied in rats by treating them with DL-Sulforaphane.
Nrf2 activation of the antioxidant response element (ARE) is central to cytoprotective gene expression against oxidative and/or electrophilic stress.
Unless activated by inflammatory, environmental, or oxidative stressors, Nrf2 is sequestered in the cytoplasm by its repressor, Keap1.
Because of its protective capabilities, small molecules that activate Nrf2 signaling are being examined as potential anti-cancer or anti-inflammatory agents.
Sulforaphane is an isothiocyanate derived from cruciferous vegetables, including broccoli, that potently induces chemopreventative enzymes via Keap1-Nrf2 signaling and ARE-driven gene expression.
At 15 μM, sulforaphane inhibits class I and II HDAC activity and suppresses tumor growth by inducing cell cycle arrest and apoptosis selectively in various cancerous prostate epithelial cells without affecting normal cells.
Differential effects of sulforaphane on histone deacetylases, cell cycle arrest and apoptosis in normal prostate cells versus hyperplastic and cancerous prostate cells | [Definition]
ChEBI: Sulforaphane is an isothiocyanate having a 4-(methylsulfinyl)butyl group attached to the nitrogen. It has a role as an antineoplastic agent, a plant metabolite, an antioxidant and an EC 3.5.1.98 (histone deacetylase) inhibitor. It is a sulfoxide and an isothiocyanate. | [benefits]
Sulforaphane(SFN) promotes detoxification,prevents and combats
cancer,lowers cholesterol,improves diabetes, can boost the immune
system, is antiviral, antibacterial, and antifungal, combats
inflammation,protect skin,eyes,kidneys, and brain, and restores its
cognitive function. Deep insight in several studies has reported that
dietary intake of cruciferous vegetables has a direct association in the
decline in the incidence of various tumors such as prostate, cervical,
ovarian, and lung cancer. It improves the liver function, attenuates
pain, improves hair growth,promotes bone formation, and prevents muscle
damage.SFN treatment reducesDNA damage and mutation rate when
cancer-causing chemicals bind DNA.Although an ideal dosage is not known,
the dietary addition of 0.1-0.5mg/kg SFN to rats has been noted to be
bioactive. This is an estimated human dose of 7-34mg for a 1501b person;
9-45mg for a 2001b person; 11-57mg for a 250lb person. | [General Description]
An isothiocyanate isolated from broccoli that acts as a potent inducer of phase II detoxifying enzymes in mouse tissues and murine hepatoma cells in culture. It has been shown to be an effective agent in prevention of chemically-induced mammary tumors in rats. It also inhibits the phase I cytochrome P450 isoenzymes 2E1 and IA2 which have been associated with the activation of carcinogens. The induction of phase II enzymes is mediated by mitogen-activated protein kinase (MAPK) pathway. | [Biological Activity]
Selective inducer of phase II detoxification enzymes with anticarcinogenic properties. Organosulfur compound found in cruciferous vegetables, including broccoli.
Sulforaphane is an anti-cancer, anti-microbial and anti-diabetic compound found in cruciferous vegetables. It induces the production of detoxifying enzymes such as quinone reductase and glutathione S-transferase that cause xenobiotic transformation. Sulforaphane also increases the transcription of tumor suppressor proteins and inhibits histone deacetylases. It modulates inflammatory responses by suppressing the LPS-mediated expression of iNOS, COX-2, IL-1β and TNF-α. | [Anticancer Research]
Sulforaphane is an isothiocyanate compound found in cruciferous vegetables like broccoli,Brussels sprouts, and cabbages. It induces phase II drug metabolism enzymes ofxenobiotic transformation and enhances the transcription of tumor suppressionproteins. It promotes cytotoxicity in p53-deleted colon cancer cells by mitochondriaandlysosome-dependent cell death. Due to the effect of sulforaphane, Bax is alsobeing increased in the presence of inhibition of JNK-induced Bcl-2 followed bymitochondrial cytochrome-C release and activation of apoptosis. Self-renewal Wnt/β-catenin signaling pathway is downregulated by sulforaphane in breast cancer stemcells. It has been reported to inhibit the activity of histone deacetylase (HDAC) andto reduce the number of polyps in Apcmin/+ mouse by inhibiting AKT and ERKsignaling and protein expression of COX-2 and cyclin-D1. Sulforaphane alsoinhibits the growth of SW620 cells by inducing apoptosis (Clarke et al. 2008). Inhuman colon cancer cells (HT-29), sulforaphane showed increased dose-dependentluciferase activity of AP-1, induced JAK activity, and inhibited NF-κB luciferaseactivation induced by LPS. It is also reported to inhibit cellular proliferation and toinduce apoptosis. In HepG2 human hepatoma cells, sulforaphane significantlyinduces the expression of the Nrf-2 protein and activation of ARE-mediatedtranscription, delays Nrf-2 degradation by inhibition of Keap1, and activates theexpression of transcription of the antioxidant HO-1 enzyme. This activation of thetranscription is partially modulated by the signaling pathway of p38 MAPK, whilep38 MAPK phosphorylates Nrf-2 and improves the binding between the proteinsNrf-2 and Keap1. In the PC-3 cells of human prostate cancer, sulforaphanesuppresses the expression regulated by NF-κB and NF-κB signaling pathway by theIκBα and IKK pathways (Wang et al. 2012). | [target]
Akt | ERK | TNF-α | p65 | NF-kB | IkB | COX | Nrf2 | HO-1 | Bcl-2/Bax | Caspase | AChR | IKK | [References]
[1] gamet-payrastre l, li p, lumeau s, et al. sulforaphane, a naturally occurring isothiocyanate, induces cell cycle arrest and apoptosis in ht29 human colon cancer cells[j]. cancer research, 2000, 60(5): 1426-1433.
[2] kansanen e, kuosmanen s m, leinonen h, et al. the keap1-nrf2 pathway: mechanisms of activation and dysregulation in cancer[j]. redox biology, 2013, 1(1): 45-49. |
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Spectrum Chemical Manufacturing Corp.
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