S6317

L-Sulforaphan

≥95% (HPLC), oil

• Synonym(e): (R)-1-Isothiocyanato-4-(methylsulfinyl)-butan, 4-Methylsulfinylbutyl-isothiocyanat
• Empirische Formel (Hill-System): C₆H₁₁NOS₂
• CAS-Nummer: 142825-10-3
• Molekulargewicht: 177.29
• MDL-Nummer: MFCD09039283
• UNSPSC-Code: 12352200
• PubChem Substanz-ID: 24724618
• NACRES: NA.77

Eigenschaften

• Assay: ≥95% (HPLC)
• Form: oil
• Optische Aktivität: [α]/D -70 to -90°, c = 1.0 in chloroform-d
• Farbe: light yellow
• Löslichkeit: DMSO: >5 mg/mL
• Lagertemp.: −20°C
• SMILES String: CS(=O)CCCCN=C=S
• InChI: 1S/C6H11NOS2/c1-10(8)5-3-2-4-7-6-9/h2-5H2,1H3/t10-/m1/s1
• InChIKey: SUVMJBTUFCVSAD-SNVBAGLBSA-N

Beschreibung

Anwendung

L-Sulforaphane was used to study Nrf2-mediated signaling in mouse primary preadipocytes⁶ and murine macrophage RAW 264.7 cell line.⁷

Biochem./physiol. Wirkung

L-Sulforaphane is a potent, 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.^3,4 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.^3,5

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves