Description
p-Xyleneselenocyanate is a synthetic derivative of selenocyanate. Derivatives of selenocyanate exhibit antioxidative, anticancer, and anti-parasitic activities.
Product Unit Size | Cost | Quantity | Stock |
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p-Xyleneselenocyanate is a synthetic derivative of selenocyanate. Derivatives of selenocyanate exhibit antioxidative, anticancer, and anti-parasitic activities.
Cas No. | 85539-83-9 |
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Purity | ≥99% |
Formula | C10H8N2Se2 |
Formula Wt. | 314.10 |
Chemical Name | 1,4-Phenylenebis(methylene)selenocyanate |
IUPAC Name | 2-methylsulfanylethylurea |
Synonym | p-XSC |
Melting Point | 156°C |
Solubility | Soluble in DMSO (>10 mg/mL). Insoluble in water. |
Appearance | White Crystalline Powder |
Store Temp | 4°C |
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Ship Temp | Ambient |
MSDS | |
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Info Sheet |
Das JK, Sarkar S, Hossain SU, et al. Diphenylmethyl selenocyanate attenuates malachite green induced oxidative injury through antioxidation & inhibition of DNA damage in mice. Indian J Med Res. 2013 Jun;137(6):1163-73. PMID: 23852297.
Facompre ND, Sinha I, El-Bayoumy K, et al. Remarkable inhibition of mTOR signaling by the combination of rapamycin and 1,4-phenylenebis(methylene)selenocyanate in human prostate cancer cells. Int J Cancer. 2012 Nov 1;131(9):2134-42. PMID: 22307455.
Plano D, Baquedano Y, Moreno-Mateos D, et al. Selenocyanates and diselenides: a new class of potent antileishmanial agents. Eur J Med Chem. 2011 Aug;46(8):3315-23. PMID: 21571403.
Poerschke RL, Moos PJ. Thioredoxin reductase 1 knockdown enhances selenazolidine cytotoxicity in human lung cancer cells via mitochondrial dysfunction. Biochem Pharmacol. 2011 Jan 15;81(2):211-221. PMID: 20920480.
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