| Weight | 177.294 g/mol |
|---|---|
| Formula | C6H11NOS2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
sulforaphane (4478-93-7)
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#874 in Neuroscience
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#1734 in Biochemistry
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#3831 in Biology
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#4824 in Chemistry
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- Identification of Nrf2-regulated Genes Induced by the Chemopreventive Agent Sulforaphane by Oligonucleotide Microarray (Cancer Research, 2002)
- Anticarcinogenic activities of sulforaphane and structurally related synthetic norbornyl isothiocyanates. (Proceedings of the National Academy of Sciences of the United States of America, 1994)
- Sulforaphane inhibits extracellular, intracellular, and antibiotic-resistant strains of Helicobacter pylori and prevents benzo[a]pyrene-induced stomach tumors (Proceedings of the National Academy of Sciences of the United States of America, 2002)
- Sulforaphane, a Naturally Occurring Isothiocyanate, Induces Cell Cycle Arrest and Apoptosis in HT29 Human Colon Cancer Cells (Cancer Research, 2000)
- Molecular basis for chemoprevention by sulforaphane: a comprehensive review (Cellular and Molecular Life Sciences, 2007)
- Nuclear Factor B Is a Molecular Target for Sulforaphane-mediated Anti-inflammatory Mechanisms (Journal of Biological Chemistry, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCS(=O)CCCCN=C=S
-
InChIKeySUVMJBTUFCVSAD-UHFFFAOYSA-N
- Pubchem - sulforaphane
- Wikipedia - (+/-)-sulforaphane
Sulforaphane (sulphoraphane in British English) is a compound within the isothiocyanate group of organosulfur compounds. It is obtained from cruciferous vegetables such as broccoli, Brussels sprouts, and cabbages. It is produced when the enzyme myrosinase transforms glucoraphanin, a glucosinolate, into sulforaphane upon damage to the plant (such as from chewing), which allows the two compounds to mix and react.
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sulforaphane
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