Loading…

Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives

Barbiturates form strong, specific hydrogen bonds with derivatives of adenine. This highly specific interaction which is more extensive than the hydrogen bonding between thymine (or uracil) derivatives and adenine derivatives may help to explain the different biological effects of barbiturates.

Saved in:
Bibliographic Details
Published in:Nature (London) 1968-04, Vol.218 (5136), p.69-72
Main Authors: KYOGOKU, YOSHIMASA, LORD, R. C., RICH, ALEXANDER
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c312t-8fa0498a1140ec79fdba37a99abf0622c07d1fc57b879ee67018c3916316f3c13
cites cdi_FETCH-LOGICAL-c312t-8fa0498a1140ec79fdba37a99abf0622c07d1fc57b879ee67018c3916316f3c13
container_end_page 72
container_issue 5136
container_start_page 69
container_title Nature (London)
container_volume 218
creator KYOGOKU, YOSHIMASA
LORD, R. C.
RICH, ALEXANDER
description Barbiturates form strong, specific hydrogen bonds with derivatives of adenine. This highly specific interaction which is more extensive than the hydrogen bonding between thymine (or uracil) derivatives and adenine derivatives may help to explain the different biological effects of barbiturates.
doi_str_mv 10.1038/218069a0
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_84834648</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>84834648</sourcerecordid><originalsourceid>FETCH-LOGICAL-c312t-8fa0498a1140ec79fdba37a99abf0622c07d1fc57b879ee67018c3916316f3c13</originalsourceid><addsrcrecordid>eNplkE1LAzEURYMotVbBPyDMSnQx-jLJJJmdbf2oUHChrodM5qWktJmazBT67x1pdePm3cW9HHiHkEsKdxSYus-oAlFoOCJDyqVIuVDymAwBMpWCYuKUnMW4BICcSj4gg1xwlnM2JA_vGzTOOpPMdnVoFuiTSeNr5xdJY5OJDpVru6BbjEnbJOMavfOYPGJwW926LcZzcmL1KuLFIUfk8_npYzpL528vr9PxPDWMZm2qrAZeKE0pBzSysHWlmdRFoSsLIssMyJpak8tKyQJRSKDKsIIKRoVlhrIRud5zN6H56jC25dpFg6uV9th0sVRcMS76MyI3-6EJTYwBbbkJbq3DrqRQ_sgqf2X106sDs6vWWP8ND3b6_nbfx77xCwzlsumC79_8z_oGn6VwKQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>84834648</pqid></control><display><type>article</type><title>Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives</title><source>Springer Nature - Connect here FIRST to enable access</source><creator>KYOGOKU, YOSHIMASA ; LORD, R. C. ; RICH, ALEXANDER</creator><creatorcontrib>KYOGOKU, YOSHIMASA ; LORD, R. C. ; RICH, ALEXANDER</creatorcontrib><description>Barbiturates form strong, specific hydrogen bonds with derivatives of adenine. This highly specific interaction which is more extensive than the hydrogen bonding between thymine (or uracil) derivatives and adenine derivatives may help to explain the different biological effects of barbiturates.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/218069a0</identifier><identifier>PMID: 5643543</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Adenine ; Barbiturates ; Chemical Phenomena ; Chemistry ; Humanities and Social Sciences ; Infrared Rays ; Models, Theoretical ; multidisciplinary ; Protein Binding ; Science ; Science (multidisciplinary) ; Spectrum Analysis ; Thymine ; Uracil</subject><ispartof>Nature (London), 1968-04, Vol.218 (5136), p.69-72</ispartof><rights>Springer Nature Limited 1968</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c312t-8fa0498a1140ec79fdba37a99abf0622c07d1fc57b879ee67018c3916316f3c13</citedby><cites>FETCH-LOGICAL-c312t-8fa0498a1140ec79fdba37a99abf0622c07d1fc57b879ee67018c3916316f3c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5643543$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KYOGOKU, YOSHIMASA</creatorcontrib><creatorcontrib>LORD, R. C.</creatorcontrib><creatorcontrib>RICH, ALEXANDER</creatorcontrib><title>Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>Barbiturates form strong, specific hydrogen bonds with derivatives of adenine. This highly specific interaction which is more extensive than the hydrogen bonding between thymine (or uracil) derivatives and adenine derivatives may help to explain the different biological effects of barbiturates.</description><subject>Adenine</subject><subject>Barbiturates</subject><subject>Chemical Phenomena</subject><subject>Chemistry</subject><subject>Humanities and Social Sciences</subject><subject>Infrared Rays</subject><subject>Models, Theoretical</subject><subject>multidisciplinary</subject><subject>Protein Binding</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Spectrum Analysis</subject><subject>Thymine</subject><subject>Uracil</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1968</creationdate><recordtype>article</recordtype><recordid>eNplkE1LAzEURYMotVbBPyDMSnQx-jLJJJmdbf2oUHChrodM5qWktJmazBT67x1pdePm3cW9HHiHkEsKdxSYus-oAlFoOCJDyqVIuVDymAwBMpWCYuKUnMW4BICcSj4gg1xwlnM2JA_vGzTOOpPMdnVoFuiTSeNr5xdJY5OJDpVru6BbjEnbJOMavfOYPGJwW926LcZzcmL1KuLFIUfk8_npYzpL528vr9PxPDWMZm2qrAZeKE0pBzSysHWlmdRFoSsLIssMyJpak8tKyQJRSKDKsIIKRoVlhrIRud5zN6H56jC25dpFg6uV9th0sVRcMS76MyI3-6EJTYwBbbkJbq3DrqRQ_sgqf2X106sDs6vWWP8ND3b6_nbfx77xCwzlsumC79_8z_oGn6VwKQ</recordid><startdate>19680406</startdate><enddate>19680406</enddate><creator>KYOGOKU, YOSHIMASA</creator><creator>LORD, R. C.</creator><creator>RICH, ALEXANDER</creator><general>Nature Publishing Group UK</general><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>19680406</creationdate><title>Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives</title><author>KYOGOKU, YOSHIMASA ; LORD, R. C. ; RICH, ALEXANDER</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c312t-8fa0498a1140ec79fdba37a99abf0622c07d1fc57b879ee67018c3916316f3c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1968</creationdate><topic>Adenine</topic><topic>Barbiturates</topic><topic>Chemical Phenomena</topic><topic>Chemistry</topic><topic>Humanities and Social Sciences</topic><topic>Infrared Rays</topic><topic>Models, Theoretical</topic><topic>multidisciplinary</topic><topic>Protein Binding</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Spectrum Analysis</topic><topic>Thymine</topic><topic>Uracil</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KYOGOKU, YOSHIMASA</creatorcontrib><creatorcontrib>LORD, R. C.</creatorcontrib><creatorcontrib>RICH, ALEXANDER</creatorcontrib><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>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KYOGOKU, YOSHIMASA</au><au>LORD, R. C.</au><au>RICH, ALEXANDER</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>1968-04-06</date><risdate>1968</risdate><volume>218</volume><issue>5136</issue><spage>69</spage><epage>72</epage><pages>69-72</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>Barbiturates form strong, specific hydrogen bonds with derivatives of adenine. This highly specific interaction which is more extensive than the hydrogen bonding between thymine (or uracil) derivatives and adenine derivatives may help to explain the different biological effects of barbiturates.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>5643543</pmid><doi>10.1038/218069a0</doi><tpages>4</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0028-0836
ispartof Nature (London), 1968-04, Vol.218 (5136), p.69-72
issn 0028-0836
1476-4687
language eng
recordid cdi_proquest_miscellaneous_84834648
source Springer Nature - Connect here FIRST to enable access
subjects Adenine
Barbiturates
Chemical Phenomena
Chemistry
Humanities and Social Sciences
Infrared Rays
Models, Theoretical
multidisciplinary
Protein Binding
Science
Science (multidisciplinary)
Spectrum Analysis
Thymine
Uracil
title Specific Hydrogen Bonding of Barbiturates to Adenine Derivatives
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T20%3A42%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Specific%20Hydrogen%20Bonding%20of%20Barbiturates%20to%20Adenine%20Derivatives&rft.jtitle=Nature%20(London)&rft.au=KYOGOKU,%20YOSHIMASA&rft.date=1968-04-06&rft.volume=218&rft.issue=5136&rft.spage=69&rft.epage=72&rft.pages=69-72&rft.issn=0028-0836&rft.eissn=1476-4687&rft_id=info:doi/10.1038/218069a0&rft_dat=%3Cproquest_cross%3E84834648%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c312t-8fa0498a1140ec79fdba37a99abf0622c07d1fc57b879ee67018c3916316f3c13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=84834648&rft_id=info:pmid/5643543&rfr_iscdi=true