ANTIVIRAL NUCLEOSIDE ANALOGUES

Antiviral nucleoside analogues contain a substituted benzimidazole base attached to a carbocyclic ring in place of the conventional sugar residue. Particularly preferred compounds include those in which the 2-, 5- and 6- positions of the benzimidazole base are substituted by halogen. The compounds h...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: LEROY B TOWNSEND, JOHN CHARLES DRACH, SUSAN MARY DALUGE, MICHAEL TOLAR MARTIN, STEVEN SPENCER GOOD
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator LEROY B TOWNSEND
JOHN CHARLES DRACH
SUSAN MARY DALUGE
MICHAEL TOLAR MARTIN
STEVEN SPENCER GOOD
description Antiviral nucleoside analogues contain a substituted benzimidazole base attached to a carbocyclic ring in place of the conventional sugar residue. Particularly preferred compounds include those in which the 2-, 5- and 6- positions of the benzimidazole base are substituted by halogen. The compounds have activity against herpes virus especially cytomegalovirus and also hepatitis B virus infections.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_AU3643293A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>AU3643293A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_AU3643293A3</originalsourceid><addsrcrecordid>eNrjZJBz9AvxDPMMcvRR8At19nH1D_Z0cVVw9HP08XcPdQ3mYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxjqHGZibGRpbGjsaEVQAARCsguw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>ANTIVIRAL NUCLEOSIDE ANALOGUES</title><source>esp@cenet</source><creator>LEROY B TOWNSEND ; JOHN CHARLES DRACH ; SUSAN MARY DALUGE ; MICHAEL TOLAR MARTIN ; STEVEN SPENCER GOOD</creator><creatorcontrib>LEROY B TOWNSEND ; JOHN CHARLES DRACH ; SUSAN MARY DALUGE ; MICHAEL TOLAR MARTIN ; STEVEN SPENCER GOOD</creatorcontrib><description>Antiviral nucleoside analogues contain a substituted benzimidazole base attached to a carbocyclic ring in place of the conventional sugar residue. Particularly preferred compounds include those in which the 2-, 5- and 6- positions of the benzimidazole base are substituted by halogen. The compounds have activity against herpes virus especially cytomegalovirus and also hepatitis B virus infections.</description><edition>5</edition><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1993</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19931005&amp;DB=EPODOC&amp;CC=AU&amp;NR=3643293A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76294</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19931005&amp;DB=EPODOC&amp;CC=AU&amp;NR=3643293A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>LEROY B TOWNSEND</creatorcontrib><creatorcontrib>JOHN CHARLES DRACH</creatorcontrib><creatorcontrib>SUSAN MARY DALUGE</creatorcontrib><creatorcontrib>MICHAEL TOLAR MARTIN</creatorcontrib><creatorcontrib>STEVEN SPENCER GOOD</creatorcontrib><title>ANTIVIRAL NUCLEOSIDE ANALOGUES</title><description>Antiviral nucleoside analogues contain a substituted benzimidazole base attached to a carbocyclic ring in place of the conventional sugar residue. Particularly preferred compounds include those in which the 2-, 5- and 6- positions of the benzimidazole base are substituted by halogen. The compounds have activity against herpes virus especially cytomegalovirus and also hepatitis B virus infections.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1993</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJBz9AvxDPMMcvRR8At19nH1D_Z0cVVw9HP08XcPdQ3mYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxjqHGZibGRpbGjsaEVQAARCsguw</recordid><startdate>19931005</startdate><enddate>19931005</enddate><creator>LEROY B TOWNSEND</creator><creator>JOHN CHARLES DRACH</creator><creator>SUSAN MARY DALUGE</creator><creator>MICHAEL TOLAR MARTIN</creator><creator>STEVEN SPENCER GOOD</creator><scope>EVB</scope></search><sort><creationdate>19931005</creationdate><title>ANTIVIRAL NUCLEOSIDE ANALOGUES</title><author>LEROY B TOWNSEND ; JOHN CHARLES DRACH ; SUSAN MARY DALUGE ; MICHAEL TOLAR MARTIN ; STEVEN SPENCER GOOD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_AU3643293A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1993</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>LEROY B TOWNSEND</creatorcontrib><creatorcontrib>JOHN CHARLES DRACH</creatorcontrib><creatorcontrib>SUSAN MARY DALUGE</creatorcontrib><creatorcontrib>MICHAEL TOLAR MARTIN</creatorcontrib><creatorcontrib>STEVEN SPENCER GOOD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LEROY B TOWNSEND</au><au>JOHN CHARLES DRACH</au><au>SUSAN MARY DALUGE</au><au>MICHAEL TOLAR MARTIN</au><au>STEVEN SPENCER GOOD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>ANTIVIRAL NUCLEOSIDE ANALOGUES</title><date>1993-10-05</date><risdate>1993</risdate><abstract>Antiviral nucleoside analogues contain a substituted benzimidazole base attached to a carbocyclic ring in place of the conventional sugar residue. Particularly preferred compounds include those in which the 2-, 5- and 6- positions of the benzimidazole base are substituted by halogen. The compounds have activity against herpes virus especially cytomegalovirus and also hepatitis B virus infections.</abstract><edition>5</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_AU3643293A
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title ANTIVIRAL NUCLEOSIDE ANALOGUES
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T22%3A08%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=LEROY%20B%20TOWNSEND&rft.date=1993-10-05&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EAU3643293A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true