4430-36-8
4430-36-8
Chemical Structure
Erucin
- CAS No.: 4430-36-8
- Formula:C6H11NS2
- Molecular Weight:161.29
IUPAC Name: (4-isothiocyanatobutyl)(methyl)sulfane
InChIKey: IHQDGXUYTSZGOG-UHFFFAOYSA-N
SMILES: CSCCCCN=C=S
Biological Activity: Erucin (ERU) is an isothiocyanate particularly abundant in arugula. Erucin shows anticancer, neuroprotective, and anti-inflammatory activities[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Erucin | 98.15% | Erucin (ERU) is an isothiocyanate particularly abundant in arugula. Erucin shows anticancer, neuroprotective, and anti-inflammatory activities. | ||||||||||||||||||||
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Erucin (Standard) | ≥98% | Acarbose (Standard) is the analytical standard of Acarbose. This product is intended for research and analytical applications. Acarbose (BAY g 5421), antihyperglycemic agent, is an orally active alpha-glucosidase inhibitor (IC50=11 nM). Acarbose can potentiate the hypoglycemic effects of sulfonylureas or insulin. | ||||||||||||||||||||
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References
- [1]. Valentina Citi, et al. Anticancer properties of erucin, an H2 S-releasing isothiocyanate, on human pancreatic adenocarcinoma cells (AsPC-1). Phytother Res. 2019 Mar;33(3):845-855. [Content Brief]
- [2]. A. Melchini, et al. Erucin, a new promising cancer chemopreventive agent from rocket salads, shows anti-proliferative activity on human lung carcinoma A549 cells. Food Chem Toxicol. 2009 Jul;47(7):1430-6. [Content Brief]
- [3]. Han Jin Cho, et al. Erucin exerts anti-inflammatory properties in murine macrophages and mouse skin: possible mediation through the inhibition of NFκB signaling. Int J Mol Sci. 2013 Oct 15;14(10):20564-77. [Content Brief]
- [4]. Fabiana Morroni, et al. Comparison of Adaptive Neuroprotective Mechanisms of Sulforaphane and its Interconversion Product Erucin in in Vitro and in Vivo Models of Parkinson's Disease. J Agric Food Chem. 2018 Jan 31;66(4):856-865. [Content Brief]
