| Weight | 143.255 g/mol |
|---|---|
| Formula | C7H13NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
2-Hexyl isothiocyanate (5334-87-2)
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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)
- 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)
- Inhibition of DMBA-initiated rat mammary tumour development by 1-O-hexyl-2,3,5-trimethylhydroquinone, phenylethyl isothiocyanate, and novel synthetic ascorbic acid derivatives (European Journal of Cancer Prevention, 1998)
- Effects of 6-(methylsulfinyl)hexyl isothiocyanate on cyclooxygenase-2 expression induced by lipopolysaccharide, interferon- and 12-O-tetradecanoylphorbol-13-acetate (Oncology Reports, 2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCCC(C)N=C=S
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InChIKeyGCZWLZBNDSJSQF-UHFFFAOYSA-N
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