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N-Nitrosophenacetin: Its Synthesis, Characterization, Mutagenicity, and Teratogenicity
Reaction of phenacetin (CAS: 62-44-2; p-aceto-phenetidide) with nitrous fumes (N2O3) in glacial acetic acid at 0–5°C yields N-nitrosophenacetin (NP), 2-nitrophenacetin, N-nitroso-2-nitrophenacetin (NNP), and other compounds. Both NP and NNP are fairly stable at low temperature (−30° C) but extremely...
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Published in: | JNCI : Journal of the National Cancer Institute 1984-04, Vol.72 (4), p.863-869 |
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description | Reaction of phenacetin (CAS: 62-44-2; p-aceto-phenetidide) with nitrous fumes (N2O3) in glacial acetic acid at 0–5°C yields N-nitrosophenacetin (NP), 2-nitrophenacetin, N-nitroso-2-nitrophenacetin (NNP), and other compounds. Both NP and NNP are fairly stable at low temperature (−30° C) but extremely labile at ambient temperature. NP (median lethal dose to Sprague-Dawley rat: 21 mg/kg body wt) is 80 times more toxic than its parent compound phenacetin and is directly mutagenic to bacterial cells including Salmonella typhimurium and Sarcina lutea. The mutagenicity of NP is comparable to that of N-methyl-N′-nitro-N-nitrosoguanidine [(MNNG) CAS: 70-25-7; 1-methyl-3-nitro-1-nitrosoguanidine] and requires no microsomal metabolic activation. The teratogenic potential of NP was studied in White Leghorn chick embryos given a single dose of 5–15 μg/egg on day 6 of incubation. A low incidence of exencephaly and eyelid defect and a high incidence of feather and claw malformations were found in the treated group; no such malformed embryos were found in the control group. The teratogenicity of NP was found to be weaker than that of MNNG, but stronger than that of N-methyl-N-nitrosourea (CAS: 684-93-5), dimethylnitrosamine (CAS: 62-75-9; N-nitrosodimethylamine), and diethylnitrosamine (CAS: 15-18-5; N-nitrosodiethylamine). |
doi_str_mv | 10.1093/jnci/72.4.863 |
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Both NP and NNP are fairly stable at low temperature (−30° C) but extremely labile at ambient temperature. NP (median lethal dose to Sprague-Dawley rat: 21 mg/kg body wt) is 80 times more toxic than its parent compound phenacetin and is directly mutagenic to bacterial cells including Salmonella typhimurium and Sarcina lutea. The mutagenicity of NP is comparable to that of N-methyl-N′-nitro-N-nitrosoguanidine [(MNNG) CAS: 70-25-7; 1-methyl-3-nitro-1-nitrosoguanidine] and requires no microsomal metabolic activation. The teratogenic potential of NP was studied in White Leghorn chick embryos given a single dose of 5–15 μg/egg on day 6 of incubation. A low incidence of exencephaly and eyelid defect and a high incidence of feather and claw malformations were found in the treated group; no such malformed embryos were found in the control group. The teratogenicity of NP was found to be weaker than that of MNNG, but stronger than that of N-methyl-N-nitrosourea (CAS: 684-93-5), dimethylnitrosamine (CAS: 62-75-9; N-nitrosodimethylamine), and diethylnitrosamine (CAS: 15-18-5; N-nitrosodiethylamine).</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/72.4.863</identifier><identifier>PMID: 6584662</identifier><language>eng</language><publisher>Cary, NC: Oxford University Press</publisher><subject>Abnormalities, Drug-Induced - embryology ; Animals ; Biological and medical sciences ; Chemical mutagenesis ; Chemical Phenomena ; Chemistry ; Chick Embryo ; Diethylnitrosamine - toxicity ; Dimethylnitrosamine - toxicity ; Lethal Dose 50 ; Medical sciences ; Methylnitronitrosoguanidine - toxicity ; Methylnitrosourea - toxicity ; Mutagenicity Tests ; Mutagens - toxicity ; Nitrosamines - analysis ; Nitrosamines - chemical synthesis ; Nitrosamines - toxicity ; Rats ; Rats, Inbred Strains ; Spectrophotometry ; Teratogens - toxicity ; Toxicology</subject><ispartof>JNCI : Journal of the National Cancer Institute, 1984-04, Vol.72 (4), p.863-869</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8873127$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6584662$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Jen-Kun</creatorcontrib><creatorcontrib>Yen, Jong-Young</creatorcontrib><creatorcontrib>Chang, Han-Wei</creatorcontrib><creatorcontrib>Lin-Shiau, Shoei-Yn</creatorcontrib><title>N-Nitrosophenacetin: Its Synthesis, Characterization, Mutagenicity, and Teratogenicity</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>Journal of the National Cancer Institute</addtitle><description>Reaction of phenacetin (CAS: 62-44-2; p-aceto-phenetidide) with nitrous fumes (N2O3) in glacial acetic acid at 0–5°C yields N-nitrosophenacetin (NP), 2-nitrophenacetin, N-nitroso-2-nitrophenacetin (NNP), and other compounds. Both NP and NNP are fairly stable at low temperature (−30° C) but extremely labile at ambient temperature. NP (median lethal dose to Sprague-Dawley rat: 21 mg/kg body wt) is 80 times more toxic than its parent compound phenacetin and is directly mutagenic to bacterial cells including Salmonella typhimurium and Sarcina lutea. The mutagenicity of NP is comparable to that of N-methyl-N′-nitro-N-nitrosoguanidine [(MNNG) CAS: 70-25-7; 1-methyl-3-nitro-1-nitrosoguanidine] and requires no microsomal metabolic activation. The teratogenic potential of NP was studied in White Leghorn chick embryos given a single dose of 5–15 μg/egg on day 6 of incubation. A low incidence of exencephaly and eyelid defect and a high incidence of feather and claw malformations were found in the treated group; no such malformed embryos were found in the control group. The teratogenicity of NP was found to be weaker than that of MNNG, but stronger than that of N-methyl-N-nitrosourea (CAS: 684-93-5), dimethylnitrosamine (CAS: 62-75-9; N-nitrosodimethylamine), and diethylnitrosamine (CAS: 15-18-5; N-nitrosodiethylamine).</description><subject>Abnormalities, Drug-Induced - embryology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chemical mutagenesis</subject><subject>Chemical Phenomena</subject><subject>Chemistry</subject><subject>Chick Embryo</subject><subject>Diethylnitrosamine - toxicity</subject><subject>Dimethylnitrosamine - toxicity</subject><subject>Lethal Dose 50</subject><subject>Medical sciences</subject><subject>Methylnitronitrosoguanidine - toxicity</subject><subject>Methylnitrosourea - toxicity</subject><subject>Mutagenicity Tests</subject><subject>Mutagens - toxicity</subject><subject>Nitrosamines - analysis</subject><subject>Nitrosamines - chemical synthesis</subject><subject>Nitrosamines - toxicity</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Spectrophotometry</subject><subject>Teratogens - toxicity</subject><subject>Toxicology</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><recordid>eNo9kMFPwjAUxhujQUSPHk128Mig7bp282YWBQziQTTGy9J1r1KEjbQlEf96m4C8y0u-35eX930IXRM8IDhPhstGmaGgAzbIeHKCuoRxHFOC01PUxZiKOMsEO0cXzi1xmJyyDurwNGOc0y56n8Uz423r2s0CGqnAm-YumngXve4avwBnXD8qFtJK5cGaX-lN2_Sj562XX9AYZfyuH8mmjuZgpW__tUt0puXKwdVh99Db48O8GMfTl9GkuJ_GhorEx5zleaqx5irFtNKM1iqFOtNEAGDIJNFBy2pFQWEdAFSiUlxUDKqKEIGTHrrZ391sqzXU5caatbS78pAv8NsDl07JlbYytOWOtlBNQsInPRTvbcZ5-Dliab9LLhKRluOPz1LM89GTmLJylvwBviZwGg</recordid><startdate>198404</startdate><enddate>198404</enddate><creator>Lin, Jen-Kun</creator><creator>Yen, Jong-Young</creator><creator>Chang, Han-Wei</creator><creator>Lin-Shiau, Shoei-Yn</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>198404</creationdate><title>N-Nitrosophenacetin: Its Synthesis, Characterization, Mutagenicity, and Teratogenicity</title><author>Lin, Jen-Kun ; Yen, Jong-Young ; Chang, Han-Wei ; Lin-Shiau, Shoei-Yn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i273t-64995f0f6c502bf42dc5ed8f17ee0e8a1ff428dc2ec0fed8eb7bc67b4ebb11703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Abnormalities, Drug-Induced - embryology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chemical mutagenesis</topic><topic>Chemical Phenomena</topic><topic>Chemistry</topic><topic>Chick Embryo</topic><topic>Diethylnitrosamine - toxicity</topic><topic>Dimethylnitrosamine - toxicity</topic><topic>Lethal Dose 50</topic><topic>Medical sciences</topic><topic>Methylnitronitrosoguanidine - toxicity</topic><topic>Methylnitrosourea - toxicity</topic><topic>Mutagenicity Tests</topic><topic>Mutagens - toxicity</topic><topic>Nitrosamines - analysis</topic><topic>Nitrosamines - chemical synthesis</topic><topic>Nitrosamines - toxicity</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Spectrophotometry</topic><topic>Teratogens - toxicity</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Jen-Kun</creatorcontrib><creatorcontrib>Yen, Jong-Young</creatorcontrib><creatorcontrib>Chang, Han-Wei</creatorcontrib><creatorcontrib>Lin-Shiau, Shoei-Yn</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Jen-Kun</au><au>Yen, Jong-Young</au><au>Chang, Han-Wei</au><au>Lin-Shiau, Shoei-Yn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-Nitrosophenacetin: Its Synthesis, Characterization, Mutagenicity, and Teratogenicity</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>Journal of the National Cancer Institute</addtitle><date>1984-04</date><risdate>1984</risdate><volume>72</volume><issue>4</issue><spage>863</spage><epage>869</epage><pages>863-869</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><abstract>Reaction of phenacetin (CAS: 62-44-2; p-aceto-phenetidide) with nitrous fumes (N2O3) in glacial acetic acid at 0–5°C yields N-nitrosophenacetin (NP), 2-nitrophenacetin, N-nitroso-2-nitrophenacetin (NNP), and other compounds. Both NP and NNP are fairly stable at low temperature (−30° C) but extremely labile at ambient temperature. NP (median lethal dose to Sprague-Dawley rat: 21 mg/kg body wt) is 80 times more toxic than its parent compound phenacetin and is directly mutagenic to bacterial cells including Salmonella typhimurium and Sarcina lutea. The mutagenicity of NP is comparable to that of N-methyl-N′-nitro-N-nitrosoguanidine [(MNNG) CAS: 70-25-7; 1-methyl-3-nitro-1-nitrosoguanidine] and requires no microsomal metabolic activation. The teratogenic potential of NP was studied in White Leghorn chick embryos given a single dose of 5–15 μg/egg on day 6 of incubation. A low incidence of exencephaly and eyelid defect and a high incidence of feather and claw malformations were found in the treated group; no such malformed embryos were found in the control group. The teratogenicity of NP was found to be weaker than that of MNNG, but stronger than that of N-methyl-N-nitrosourea (CAS: 684-93-5), dimethylnitrosamine (CAS: 62-75-9; N-nitrosodimethylamine), and diethylnitrosamine (CAS: 15-18-5; N-nitrosodiethylamine).</abstract><cop>Cary, NC</cop><pub>Oxford University Press</pub><pmid>6584662</pmid><doi>10.1093/jnci/72.4.863</doi><tpages>7</tpages></addata></record> |
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subjects | Abnormalities, Drug-Induced - embryology Animals Biological and medical sciences Chemical mutagenesis Chemical Phenomena Chemistry Chick Embryo Diethylnitrosamine - toxicity Dimethylnitrosamine - toxicity Lethal Dose 50 Medical sciences Methylnitronitrosoguanidine - toxicity Methylnitrosourea - toxicity Mutagenicity Tests Mutagens - toxicity Nitrosamines - analysis Nitrosamines - chemical synthesis Nitrosamines - toxicity Rats Rats, Inbred Strains Spectrophotometry Teratogens - toxicity Toxicology |
title | N-Nitrosophenacetin: Its Synthesis, Characterization, Mutagenicity, and Teratogenicity |
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