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Synthesis of the L-Enantiomer of 4'-C-Ethynyl-2'-deoxycytidine
The L-enantiomer of 4'-C-ethynyl-2'-deoxycytidine (2) was synthesized, but did not show any activity against HIV-1 up to 100 μM.
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Published in: | Bioscience, biotechnology, and biochemistry biotechnology, and biochemistry, 2001-08, Vol.65 (8), p.1879-1882 |
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cites | cdi_FETCH-LOGICAL-c582t-57aaed875a0c51d7b75ce8062daa263a6d9d3acffe469731d40d2822be6f68373 |
container_end_page | 1882 |
container_issue | 8 |
container_start_page | 1879 |
container_title | Bioscience, biotechnology, and biochemistry |
container_volume | 65 |
creator | KOHGO, Satoru MITSUYA, Hiroaki OHRUI, Hiroshi |
description | The L-enantiomer of 4'-C-ethynyl-2'-deoxycytidine (2) was synthesized, but did not show any activity against HIV-1 up to 100 μM. |
doi_str_mv | 10.1271/bbb.65.1879 |
format | article |
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Nucleosides and nucleotides ; Cell Line ; Chemistry ; Coloring Agents ; Deoxycytidine - analogs & derivatives ; Deoxycytidine - chemical synthesis ; Deoxycytidine - pharmacology ; Exact sciences and technology ; HIV-1 - drug effects ; Hydrogen-Ion Concentration ; Indicators and Reagents ; L-configuration nucleosides ; Magnetic Resonance Spectroscopy ; Nucleosides, nucleotides and oligonucleotides ; Organic chemistry ; Preparations and properties ; Spectrometry, Mass, Fast Atom Bombardment ; Stereoisomerism ; Tetrazolium Salts ; Thiazoles</subject><ispartof>Bioscience, biotechnology, and biochemistry, 2001-08, Vol.65 (8), p.1879-1882</ispartof><rights>2001 by Japan Society for Bioscience, Biotechnology, and Agrochemistry 2001</rights><rights>2002 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c582t-57aaed875a0c51d7b75ce8062daa263a6d9d3acffe469731d40d2822be6f68373</citedby><cites>FETCH-LOGICAL-c582t-57aaed875a0c51d7b75ce8062daa263a6d9d3acffe469731d40d2822be6f68373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14147782$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11577734$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KOHGO, Satoru</creatorcontrib><creatorcontrib>MITSUYA, Hiroaki</creatorcontrib><creatorcontrib>OHRUI, Hiroshi</creatorcontrib><title>Synthesis of the L-Enantiomer of 4'-C-Ethynyl-2'-deoxycytidine</title><title>Bioscience, biotechnology, and biochemistry</title><addtitle>Biosci Biotechnol Biochem</addtitle><description>The L-enantiomer of 4'-C-ethynyl-2'-deoxycytidine (2) was synthesized, but did not show any activity against HIV-1 up to 100 μM.</description><subject>4'-C-ethynyl-2'-deoxycytidine</subject><subject>anti-HIV activity</subject><subject>Anti-HIV Agents - chemical synthesis</subject><subject>Anti-HIV Agents - pharmacology</subject><subject>Carbohydrates. Nucleosides and nucleotides</subject><subject>Cell Line</subject><subject>Chemistry</subject><subject>Coloring Agents</subject><subject>Deoxycytidine - analogs & derivatives</subject><subject>Deoxycytidine - chemical synthesis</subject><subject>Deoxycytidine - pharmacology</subject><subject>Exact sciences and technology</subject><subject>HIV-1 - drug effects</subject><subject>Hydrogen-Ion Concentration</subject><subject>Indicators and Reagents</subject><subject>L-configuration nucleosides</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Nucleosides, nucleotides and oligonucleotides</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><subject>Spectrometry, Mass, Fast Atom Bombardment</subject><subject>Stereoisomerism</subject><subject>Tetrazolium Salts</subject><subject>Thiazoles</subject><issn>0916-8451</issn><issn>1347-6947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpt0FFrFDEQB_AgFXtWn3wvB6J9kJyZbJLZfSnIcVXhwAf1OWSTLLfHbtIme-h-e3PclYL0aYbhN8PwJ-QdsBVwhM9t266UXEGNzQuygEogVY3AC7JgDShaCwmX5HXOe8bKQMIrcgkgEbESC3L7cw7Tzuc-L2O3LN1ySzfBhKmPo0_Hmbiha7qZdnOYB8pvqPPx72znqXd98G_Iy84M2b891yvy-27za_2Nbn98_b7-sqVW1nyiEo3xrkZpmJXgsEVpfc0Ud8ZwVRnlGlcZ23VeqAYrcII5XnPeetWpusLqinw83b1P8eHg86THPls_DCb4eMgagXNsOBT4_j-4j4cUym8ahGiEEChZUZ9OyqaYc_Kdvk_9aNKsgeljqLqEqpXUx1CLvj7fPLSjd0_2nGIBH87AZGuGLplg-_zkBAjEmhenTq4PXUyj-RPT4PRk5iGmx6XquQ_-AUg_j1g</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>KOHGO, Satoru</creator><creator>MITSUYA, Hiroaki</creator><creator>OHRUI, Hiroshi</creator><general>Japan Society for Bioscience, Biotechnology, and Agrochemistry</general><general>Japan Society for Bioscience Biotechnology and Agrochemistry</general><general>Oxford University Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20010801</creationdate><title>Synthesis of the L-Enantiomer of 4'-C-Ethynyl-2'-deoxycytidine</title><author>KOHGO, Satoru ; MITSUYA, Hiroaki ; OHRUI, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c582t-57aaed875a0c51d7b75ce8062daa263a6d9d3acffe469731d40d2822be6f68373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>4'-C-ethynyl-2'-deoxycytidine</topic><topic>anti-HIV activity</topic><topic>Anti-HIV Agents - chemical synthesis</topic><topic>Anti-HIV Agents - pharmacology</topic><topic>Carbohydrates. Nucleosides and nucleotides</topic><topic>Cell Line</topic><topic>Chemistry</topic><topic>Coloring Agents</topic><topic>Deoxycytidine - analogs & derivatives</topic><topic>Deoxycytidine - chemical synthesis</topic><topic>Deoxycytidine - pharmacology</topic><topic>Exact sciences and technology</topic><topic>HIV-1 - drug effects</topic><topic>Hydrogen-Ion Concentration</topic><topic>Indicators and Reagents</topic><topic>L-configuration nucleosides</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Nucleosides, nucleotides and oligonucleotides</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><topic>Spectrometry, Mass, Fast Atom Bombardment</topic><topic>Stereoisomerism</topic><topic>Tetrazolium Salts</topic><topic>Thiazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KOHGO, Satoru</creatorcontrib><creatorcontrib>MITSUYA, Hiroaki</creatorcontrib><creatorcontrib>OHRUI, Hiroshi</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioscience, biotechnology, and biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KOHGO, Satoru</au><au>MITSUYA, Hiroaki</au><au>OHRUI, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of the L-Enantiomer of 4'-C-Ethynyl-2'-deoxycytidine</atitle><jtitle>Bioscience, biotechnology, and biochemistry</jtitle><addtitle>Biosci Biotechnol Biochem</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>65</volume><issue>8</issue><spage>1879</spage><epage>1882</epage><pages>1879-1882</pages><issn>0916-8451</issn><eissn>1347-6947</eissn><abstract>The L-enantiomer of 4'-C-ethynyl-2'-deoxycytidine (2) was synthesized, but did not show any activity against HIV-1 up to 100 μM.</abstract><cop>Tokyo</cop><pub>Japan Society for Bioscience, Biotechnology, and Agrochemistry</pub><pmid>11577734</pmid><doi>10.1271/bbb.65.1879</doi><tpages>4</tpages></addata></record> |
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identifier | ISSN: 0916-8451 |
ispartof | Bioscience, biotechnology, and biochemistry, 2001-08, Vol.65 (8), p.1879-1882 |
issn | 0916-8451 1347-6947 |
language | eng |
recordid | cdi_crossref_primary_10_1271_bbb_65_1879 |
source | Oxford Journals Online; EZB Electronic Journals Library |
subjects | 4'-C-ethynyl-2'-deoxycytidine anti-HIV activity Anti-HIV Agents - chemical synthesis Anti-HIV Agents - pharmacology Carbohydrates. Nucleosides and nucleotides Cell Line Chemistry Coloring Agents Deoxycytidine - analogs & derivatives Deoxycytidine - chemical synthesis Deoxycytidine - pharmacology Exact sciences and technology HIV-1 - drug effects Hydrogen-Ion Concentration Indicators and Reagents L-configuration nucleosides Magnetic Resonance Spectroscopy Nucleosides, nucleotides and oligonucleotides Organic chemistry Preparations and properties Spectrometry, Mass, Fast Atom Bombardment Stereoisomerism Tetrazolium Salts Thiazoles |
title | Synthesis of the L-Enantiomer of 4'-C-Ethynyl-2'-deoxycytidine |
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