| Weight | 143.255 g/mol |
|---|---|
| Formula | C7H13NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
Hexyl isothiocyanate (4404-45-9)
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- 6-(Methylsulfinyl)hexyl isothiocyanate suppresses inducible nitric oxide synthase expression through the inhibition of Janus kinase 2-mediated JNK pathway in lipopolysaccharide-activated murine macrophages. (Biochemical Pharmacology, 2005)
- Glutathione Biosynthesis via Activation of the Nuclear Factor E2Related Factor 2 (Nrf2) Antioxidant-Response Element (ARE) Pathway Is Essential for Neuroprotective Effects of Sulforaphane and 6-(Methylsulfinyl) Hexyl Isothiocyanate (Journal of Pharmacological Sciences, 2011)
- Inhibition of lipopolysaccharide-induced cyclooxygenase-2 transcription by 6-(methylsulfinyl) hexyl isothiocyanate, a chemopreventive compound from Wasabia japonica (Miq.) Matsumura, in mouse macrophages (Biochemical Pharmacology, 2005)
- Transcriptional regulation of nicotinamide adenine dinucleotide phosphate: quinone oxidoreductase in murine hepatoma cells by 6-(methylsufinyl)hexyl isothiocyanate, an active principle of wasabi (Eutrema wasabi Maxim) (Cancer Letters, 2000)
- Stage and organ dependent effects of 1 Ohexyl2,3,5trimethylhydroquinone, ascorbic acid derivatives, Nheptadecane8,10dione and phenylethyl isothiocyanate in a rat multiorgan carcinogenesis model (International Journal of Cancer, 1998)
- Selective sensitivity to wasabi-derived 6-(methylsulfinyl)hexyl isothiocyanate of human breast cancer and melanoma cell lines studied in vitro (Cancer Detection and Prevention, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCCCN=C=S
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InChIKeyWXYAXKKXIGHXDS-UHFFFAOYSA-N
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Similar Compounds
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icosan-1-amine
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27421-70-1
(27421-70-1)
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(2016-56-0)
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(108-91-8)
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Dinonylamine
(2044-21-5)
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Hexyl isothiocyanate
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