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Metabolic Fate of N6‐Benzyladenosine and N6-Benzyladenosine-5′-phosphate in Rats
The radiolabeled antitumor nucleoside (14C‐8)‐N6‐benzyladenosine and its (14C‐8)‐5′‐phosphate were administered to rats intravenously, and their metabolic fate was studied. Twenty‐nine percent of the radioactivity was recovered in the 48‐hr urine collection after (14C‐8)‐N6‐benzyladenosine administr...
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Published in: | Journal of pharmaceutical sciences 1979-08, Vol.68 (8), p.1054-1056 |
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creator | Chheda, G.B. Mittelman, A. Hong, C.I. Gurwara, S.K. |
description | The radiolabeled antitumor nucleoside (14C‐8)‐N6‐benzyladenosine and its (14C‐8)‐5′‐phosphate were administered to rats intravenously, and their metabolic fate was studied. Twenty‐nine percent of the radioactivity was recovered in the 48‐hr urine collection after (14C‐8)‐N6‐benzyladenosine administration. The following metabolites were isolated: unchangedN6‐benzyladenosine (20%), adenine (12%), uric acid (5%), andN6‐benzyladenine (0.3%). In the case of (14C‐8)‐N6‐benzyladenosine‐5′‐phosphate, a total of 28% of the radioactivity was recovered in the 48‐hr urine collection and the following metabolites were isolated:N6‐benzyladenosine (40%), uric acid (12%), adenine (trace), and unidentified urea derivatives (30%). Metabolism ofN6‐benzyladenosine appears to involveN‐debenzylation to some extent, followed by conversion to adenine and uric acid.N6‐Benzyladenosine and its 5′‐phosphate differ from other adenosine analogs in being retained in significant amounts by the animals. |
doi_str_mv | 10.1002/jps.2600680836 |
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Twenty‐nine percent of the radioactivity was recovered in the 48‐hr urine collection after (14C‐8)‐N6‐benzyladenosine administration. The following metabolites were isolated: unchangedN6‐benzyladenosine (20%), adenine (12%), uric acid (5%), andN6‐benzyladenine (0.3%). In the case of (14C‐8)‐N6‐benzyladenosine‐5′‐phosphate, a total of 28% of the radioactivity was recovered in the 48‐hr urine collection and the following metabolites were isolated:N6‐benzyladenosine (40%), uric acid (12%), adenine (trace), and unidentified urea derivatives (30%). Metabolism ofN6‐benzyladenosine appears to involveN‐debenzylation to some extent, followed by conversion to adenine and uric acid.N6‐Benzyladenosine and its 5′‐phosphate differ from other adenosine analogs in being retained in significant amounts by the animals.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600680836</identifier><identifier>PMID: 480162</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Adenosine - analogs & derivatives ; Adenosine - metabolism ; Adenosine - urine ; Adenosine Monophosphate - analogs & derivatives ; Adenosine Monophosphate - metabolism ; Adenosine Monophosphate - urine ; Animals ; Antineoplastic agents-benzyladenosine ; Antineoplastic agents—benzyladenosine, metabolism, rats ; Benzyl Compounds - metabolism ; Benzyl Compounds - urine ; Benzyladenosine phosphate-metabolism ; Benzyladenosine phosphate—metabolism, rats ; Benzyladenosine-metabolism ; Benzyladenosine—metabolism, rats ; Carbon Radioisotopes ; Chromatography, Paper ; Feces - analysis ; Male ; metabolism ; Rats ; Tissue Distribution</subject><ispartof>Journal of pharmaceutical sciences, 1979-08, Vol.68 (8), p.1054-1056</ispartof><rights>1979 Wiley-Liss, Inc., A Wiley Company</rights><rights>Copyright © 1979 Wiley‐Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.2600680836$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.2600680836$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/480162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chheda, G.B.</creatorcontrib><creatorcontrib>Mittelman, A.</creatorcontrib><creatorcontrib>Hong, C.I.</creatorcontrib><creatorcontrib>Gurwara, S.K.</creatorcontrib><title>Metabolic Fate of N6‐Benzyladenosine and N6-Benzyladenosine-5′-phosphate in Rats</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>The radiolabeled antitumor nucleoside (14C‐8)‐N6‐benzyladenosine and its (14C‐8)‐5′‐phosphate were administered to rats intravenously, and their metabolic fate was studied. Twenty‐nine percent of the radioactivity was recovered in the 48‐hr urine collection after (14C‐8)‐N6‐benzyladenosine administration. The following metabolites were isolated: unchangedN6‐benzyladenosine (20%), adenine (12%), uric acid (5%), andN6‐benzyladenine (0.3%). In the case of (14C‐8)‐N6‐benzyladenosine‐5′‐phosphate, a total of 28% of the radioactivity was recovered in the 48‐hr urine collection and the following metabolites were isolated:N6‐benzyladenosine (40%), uric acid (12%), adenine (trace), and unidentified urea derivatives (30%). Metabolism ofN6‐benzyladenosine appears to involveN‐debenzylation to some extent, followed by conversion to adenine and uric acid.N6‐Benzyladenosine and its 5′‐phosphate differ from other adenosine analogs in being retained in significant amounts by the animals.</description><subject>Adenosine - analogs & derivatives</subject><subject>Adenosine - metabolism</subject><subject>Adenosine - urine</subject><subject>Adenosine Monophosphate - analogs & derivatives</subject><subject>Adenosine Monophosphate - metabolism</subject><subject>Adenosine Monophosphate - urine</subject><subject>Animals</subject><subject>Antineoplastic agents-benzyladenosine</subject><subject>Antineoplastic agents—benzyladenosine, metabolism, rats</subject><subject>Benzyl Compounds - metabolism</subject><subject>Benzyl Compounds - urine</subject><subject>Benzyladenosine phosphate-metabolism</subject><subject>Benzyladenosine phosphate—metabolism, rats</subject><subject>Benzyladenosine-metabolism</subject><subject>Benzyladenosine—metabolism, rats</subject><subject>Carbon Radioisotopes</subject><subject>Chromatography, Paper</subject><subject>Feces - analysis</subject><subject>Male</subject><subject>metabolism</subject><subject>Rats</subject><subject>Tissue Distribution</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1979</creationdate><recordtype>article</recordtype><recordid>eNp1kM1O3DAURq2qLR1ot6y6yKo7D9c_sZ0ljAptRWnVjtSl5Tg3wjSThDgDDKt5hD5LH4knqVEQSEhdWdff-e6VDiH7DOYMgB9c9HHOFYAyYIR6QWYs50AVMP2SzBLAqchl8YbsxngBCYM83yGvpQGm-Iwsv-Loyq4JPjt2I2ZdnZ2pu-2fI2xvN42rsO1iaDFzbZUC-uyb5nfbv7Q_72J_ft8ObfbDjfEteVW7JuK7h3ePLI8_Lhef6Om3k8-Lw1OKXEtFSyZ8YTgzRtUMa6nr2msh6wK4Z16iMlgUhdPSQ6mgrrwQYLQGV8lSoBR75MO0th-6yzXG0a5C9Ng0rsVuHa2WGkwueALfP4DrcoWV7YewcsPGThJSXEzxdWhw85gysPeCbRJsnwTbL99_Pk2pS6duiCPePHbd8NsqLXRuf52dWH5kGDOisCbxZuIxebkKONjoA7YeqzCgH23Vhf8cFv8AXoWRaA</recordid><startdate>197908</startdate><enddate>197908</enddate><creator>Chheda, G.B.</creator><creator>Mittelman, A.</creator><creator>Hong, C.I.</creator><creator>Gurwara, S.K.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>197908</creationdate><title>Metabolic Fate of N6‐Benzyladenosine and N6-Benzyladenosine-5′-phosphate in Rats</title><author>Chheda, G.B. ; Mittelman, A. ; Hong, C.I. ; Gurwara, S.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e2746-b13c9821886f1ef47ffc734f902c1c4e68e999a74c0b60fdc3308770ad4b3e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1979</creationdate><topic>Adenosine - analogs & derivatives</topic><topic>Adenosine - metabolism</topic><topic>Adenosine - urine</topic><topic>Adenosine Monophosphate - analogs & derivatives</topic><topic>Adenosine Monophosphate - metabolism</topic><topic>Adenosine Monophosphate - urine</topic><topic>Animals</topic><topic>Antineoplastic agents-benzyladenosine</topic><topic>Antineoplastic agents—benzyladenosine, metabolism, rats</topic><topic>Benzyl Compounds - metabolism</topic><topic>Benzyl Compounds - urine</topic><topic>Benzyladenosine phosphate-metabolism</topic><topic>Benzyladenosine phosphate—metabolism, rats</topic><topic>Benzyladenosine-metabolism</topic><topic>Benzyladenosine—metabolism, rats</topic><topic>Carbon Radioisotopes</topic><topic>Chromatography, Paper</topic><topic>Feces - analysis</topic><topic>Male</topic><topic>metabolism</topic><topic>Rats</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chheda, G.B.</creatorcontrib><creatorcontrib>Mittelman, A.</creatorcontrib><creatorcontrib>Hong, C.I.</creatorcontrib><creatorcontrib>Gurwara, S.K.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chheda, G.B.</au><au>Mittelman, A.</au><au>Hong, C.I.</au><au>Gurwara, S.K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic Fate of N6‐Benzyladenosine and N6-Benzyladenosine-5′-phosphate in Rats</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1979-08</date><risdate>1979</risdate><volume>68</volume><issue>8</issue><spage>1054</spage><epage>1056</epage><pages>1054-1056</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><abstract>The radiolabeled antitumor nucleoside (14C‐8)‐N6‐benzyladenosine and its (14C‐8)‐5′‐phosphate were administered to rats intravenously, and their metabolic fate was studied. Twenty‐nine percent of the radioactivity was recovered in the 48‐hr urine collection after (14C‐8)‐N6‐benzyladenosine administration. The following metabolites were isolated: unchangedN6‐benzyladenosine (20%), adenine (12%), uric acid (5%), andN6‐benzyladenine (0.3%). In the case of (14C‐8)‐N6‐benzyladenosine‐5′‐phosphate, a total of 28% of the radioactivity was recovered in the 48‐hr urine collection and the following metabolites were isolated:N6‐benzyladenosine (40%), uric acid (12%), adenine (trace), and unidentified urea derivatives (30%). Metabolism ofN6‐benzyladenosine appears to involveN‐debenzylation to some extent, followed by conversion to adenine and uric acid.N6‐Benzyladenosine and its 5′‐phosphate differ from other adenosine analogs in being retained in significant amounts by the animals.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>480162</pmid><doi>10.1002/jps.2600680836</doi><tpages>3</tpages></addata></record> |
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subjects | Adenosine - analogs & derivatives Adenosine - metabolism Adenosine - urine Adenosine Monophosphate - analogs & derivatives Adenosine Monophosphate - metabolism Adenosine Monophosphate - urine Animals Antineoplastic agents-benzyladenosine Antineoplastic agents—benzyladenosine, metabolism, rats Benzyl Compounds - metabolism Benzyl Compounds - urine Benzyladenosine phosphate-metabolism Benzyladenosine phosphate—metabolism, rats Benzyladenosine-metabolism Benzyladenosine—metabolism, rats Carbon Radioisotopes Chromatography, Paper Feces - analysis Male metabolism Rats Tissue Distribution |
title | Metabolic Fate of N6‐Benzyladenosine and N6-Benzyladenosine-5′-phosphate in Rats |
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