A broad spectrum anticancer nucleoside with selective toxicity against human colon cells in vitro |
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Authors: | Shelton Jadd R Burt Scott R Peterson Matt A |
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Affiliation: | Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, United States |
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Abstract: | 2′,3′-Bis-O-tert-butyldimethylsilyl-5′-deoxy-5′-[N-(methylcarbamoyl)amino]-N6-(N-phenylcarbamoyl)adenosine, a new member of the N6,5′-bis-ureidoadenosine class of anticancer nucleosides, is found to exhibit broad spectrum antiproliferative activity. A majority of the cell lines in the NCI-60 are inhibited with an average GI50 = 3.13 μM. Selective toxicity against human colon cancer cell lines (COLO 205, HCC-2998, HCT-116, HT29, KM12) was also exhibited (LC50’s = 6-10 μM). |
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Keywords: | Purine nucleosides Bio-active adenosine derivatives Antiproliferative nucleosides |
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