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Chemical structure of CAS 4430-35-7

6-Methylsulfinylhexyl isothiocyanate

In Stock•Starting at $214 for 5 mg
CAS No.4430-35-7
MDL No.N/A
MFC8H15NOS2
MW205.30
InChI KeyXQZVZULJKVALRI-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
5 mgTo Be Confirmed$214In Stock
10 mgTo Be Confirmed$403In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

1-Isothiocyanato-6-(methylsulfinyl)hexane is a sulfoxide-containing compound.

CAS No.4430-35-7
Product Name6-Methylsulfinylhexyl isothiocyanate
Heavy Atom Count12Rotatable Bond Count7
Atom Stereo Count1Bond Stereo Count0
HBA3HBD0
TPSA29.430 ŲCharge0
Exact Mass205.05951Complexity169.90
pKa6.620XLogP2.028

Related Articles

Studies related to this compound and its mechanism of action

Effects of 6-(methylsulfinyl)hexyl isothiocyanate on cyclooxygenase-2 expression induced by lipopolysaccharide, interferon-gamma and 12-O-tetradecanoylphorbol-13-acetate.

Oncology reports • Vol. 17, Issue 1 • 2007
PMID: 17143503

Preventive effect of oral administration of 6-(methylsulfinyl)hexyl isothiocyanate derived from wasabi (Wasabia japonica Matsum) against pulmonary metastasis of B16-BL6 mouse melanoma cells.

Cancer detection and prevention • Vol. 30, Issue 2 • 2006
PMID: 16647224DOI: 10.1016/j.cdp.2005.10.005

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 • Vol. 70, Issue 12 • 2005
PMID: 16256955DOI: 10.1016/j.bcp.2005.09.023

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 • Vol. 70, Issue 8 • 2005
PMID: 16139249DOI: 10.1016/j.bcp.2005.07.011

Documentation

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