Synthesis and excretion profile of 1,4-[14C]phenylenebis(methylene)selenocyanate in the rat.

Abstract

1,4-Phenylenebis(methylene)selenocyanate (p-XSC) inhibits chemically induced tumors in several laboratory animal models. To understand its mode of action, we synthesized p-[14C]XSC, examined its excretion pattern in female CD rats and also the nature of its metabolites. p-[14C]XSC was synthesized from alpha,alpha-dibromo-p-[ring-14C]xylene in 80% yield. The excretion profile of p-[14C]XSC (15.8 mg/kg body wt, 200 microCi/rat, oral administration, in 1 ml corn oil) in vivo was monitored by measuring radioactivity and selenium content. On the basis of radioactivity, approximately 20% of the dose was excreted in the urine and 68% in the feces over 3 days. The cumulative percentages of the dose excreted over 7 days were 24% in urine and 75% in feces, similar to excretion rates of selenium. According to selenium measurement, <1% of the dose was detected in exhaled air; radioactivity was not detected. Only 15% of the dose was extractable from the feces with EtOAc and was identified as tetraselenocyclophane (TSC). Most of the radioactivity remained tightly bound to the feces. Approximately 10% of this bound material converted to TSC on reduction with NaBH4. Organic soluble metabolites in urine did not exceed 2% of the dose; sulfate (9 % of urinary metabolites) and glucuronic acid (19.5% of urinary metabolites) conjugates were observed but their structural identification is still underway. Co-chromatography with a synthetic standard led to the detection of terephthalic acid (1,4-benzenedicarboxylic acid) as a minor metabolite. The major urinary conjugates contained selenium. Despite the low levels of selenium in the exhaled air, the reductive metabolism of p-XSC to H2Se cannot be ruled out. Identification of TSC in vivo indicates that a selenol may be a key intermediate responsible for the chemopreventive action of p-XSC.

• Authors: K El-Bayoumy, P Upadhyaya, O S Sohn, J G Rosa, E S Fiala
• Journal: Carcinogenesis (Carcinogenesis) Vol. 19 Issue 9 Pg. 1603-7 (Sep 1998) ISSN: 0143-3334 [Print] England
• PMID: 9771931 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Antineoplastic Agents
• Carbon Radioisotopes
• Organoselenium Compounds
• 1,4-phenylenebis(methylene)selenocyanate
• Selenium

Topics

• Animals
• Antineoplastic Agents (pharmacokinetics)
• Carbon Radioisotopes
• Female
• Organoselenium Compounds (chemical synthesis, pharmacokinetics)
• Rats
• Selenium (pharmacokinetics)