Therapeutic azide compounds
Pharmaceutical prodrug compositions are provided comprising azide derivatives of drugs which are capable of being converted to the drug in vivo. Azide derivatives of drugs having amine, ketone and hydroxy substituents are converted in vivo to the corresponding drugs, increasing the half-life of the...
Gespeichert in:
Hauptverfasser: | , , , , |
---|---|
Format: | Patent |
Sprache: | eng |
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 | Chu, Chung K Kotra, Lakshmi P Manouilov, Konstantine Du, Jinfa Schinazi, Raymond |
description | Pharmaceutical prodrug compositions are provided comprising azide derivatives of drugs which are capable of being converted to the drug in vivo. Azide derivatives of drugs having amine, ketone and hydroxy substituents are converted in vivo to the corresponding drugs, increasing the half-life of the drugs. In addition azide prodrugs are often better able to penetrate the blood-brain barrier than the corresponding drugs. Especially useful are azide derivatives of cordycepin, 2′-F-ara-ddI, AraA, acyclovir, penciclovir and related drugs. Useful azide prodrugs are azide derivatives of therapeutic alicyclic amines, ketones, and hydroxy-substituted compounds, including aralkyl, heterocyclic aralkyl, and cyclic aliphatic compounds, where the amine or oxygen moiety is on the ring, or where the amine or oxygen moiety is on an aliphatic side chain, as well as therapeutic purines and pyrimidines, nucleoside analogs and phosphorylated nucleoside analogs. |
format | Patent |
fullrecord | <record><control><sourceid>uspatents_EFH</sourceid><recordid>TN_cdi_uspatents_grants_06949521</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>06949521</sourcerecordid><originalsourceid>FETCH-uspatents_grants_069495213</originalsourceid><addsrcrecordid>eNrjZJAOyUgtSixILS3JTFZIrMpMSVVIzs8tyC_NSynmYWBNS8wpTuWF0twMCm6uIc4euqXFBYklqXklxfHpRYkgysDM0sTS1MjQmAglAHdqJJs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Therapeutic azide compounds</title><source>USPTO Issued Patents</source><creator>Chu, Chung K ; Kotra, Lakshmi P ; Manouilov, Konstantine ; Du, Jinfa ; Schinazi, Raymond</creator><creatorcontrib>Chu, Chung K ; Kotra, Lakshmi P ; Manouilov, Konstantine ; Du, Jinfa ; Schinazi, Raymond ; Emory University ; The University of Georgia Research Foundation, Inc</creatorcontrib><description>Pharmaceutical prodrug compositions are provided comprising azide derivatives of drugs which are capable of being converted to the drug in vivo. Azide derivatives of drugs having amine, ketone and hydroxy substituents are converted in vivo to the corresponding drugs, increasing the half-life of the drugs. In addition azide prodrugs are often better able to penetrate the blood-brain barrier than the corresponding drugs. Especially useful are azide derivatives of cordycepin, 2′-F-ara-ddI, AraA, acyclovir, penciclovir and related drugs. Useful azide prodrugs are azide derivatives of therapeutic alicyclic amines, ketones, and hydroxy-substituted compounds, including aralkyl, heterocyclic aralkyl, and cyclic aliphatic compounds, where the amine or oxygen moiety is on the ring, or where the amine or oxygen moiety is on an aliphatic side chain, as well as therapeutic purines and pyrimidines, nucleoside analogs and phosphorylated nucleoside analogs.</description><language>eng</language><creationdate>2005</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://image-ppubs.uspto.gov/dirsearch-public/print/downloadPdf/6949521$$EPDF$$P50$$Guspatents$$Hfree_for_read</linktopdf><link.rule.ids>230,308,780,802,885,64039</link.rule.ids><linktorsrc>$$Uhttps://image-ppubs.uspto.gov/dirsearch-public/print/downloadPdf/6949521$$EView_record_in_USPTO$$FView_record_in_$$GUSPTO$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Chu, Chung K</creatorcontrib><creatorcontrib>Kotra, Lakshmi P</creatorcontrib><creatorcontrib>Manouilov, Konstantine</creatorcontrib><creatorcontrib>Du, Jinfa</creatorcontrib><creatorcontrib>Schinazi, Raymond</creatorcontrib><creatorcontrib>Emory University</creatorcontrib><creatorcontrib>The University of Georgia Research Foundation, Inc</creatorcontrib><title>Therapeutic azide compounds</title><description>Pharmaceutical prodrug compositions are provided comprising azide derivatives of drugs which are capable of being converted to the drug in vivo. Azide derivatives of drugs having amine, ketone and hydroxy substituents are converted in vivo to the corresponding drugs, increasing the half-life of the drugs. In addition azide prodrugs are often better able to penetrate the blood-brain barrier than the corresponding drugs. Especially useful are azide derivatives of cordycepin, 2′-F-ara-ddI, AraA, acyclovir, penciclovir and related drugs. Useful azide prodrugs are azide derivatives of therapeutic alicyclic amines, ketones, and hydroxy-substituted compounds, including aralkyl, heterocyclic aralkyl, and cyclic aliphatic compounds, where the amine or oxygen moiety is on the ring, or where the amine or oxygen moiety is on an aliphatic side chain, as well as therapeutic purines and pyrimidines, nucleoside analogs and phosphorylated nucleoside analogs.</description><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2005</creationdate><recordtype>patent</recordtype><sourceid>EFH</sourceid><recordid>eNrjZJAOyUgtSixILS3JTFZIrMpMSVVIzs8tyC_NSynmYWBNS8wpTuWF0twMCm6uIc4euqXFBYklqXklxfHpRYkgysDM0sTS1MjQmAglAHdqJJs</recordid><startdate>20050927</startdate><enddate>20050927</enddate><creator>Chu, Chung K</creator><creator>Kotra, Lakshmi P</creator><creator>Manouilov, Konstantine</creator><creator>Du, Jinfa</creator><creator>Schinazi, Raymond</creator><scope>EFH</scope></search><sort><creationdate>20050927</creationdate><title>Therapeutic azide compounds</title><author>Chu, Chung K ; Kotra, Lakshmi P ; Manouilov, Konstantine ; Du, Jinfa ; Schinazi, Raymond</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-uspatents_grants_069495213</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2005</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Chu, Chung K</creatorcontrib><creatorcontrib>Kotra, Lakshmi P</creatorcontrib><creatorcontrib>Manouilov, Konstantine</creatorcontrib><creatorcontrib>Du, Jinfa</creatorcontrib><creatorcontrib>Schinazi, Raymond</creatorcontrib><creatorcontrib>Emory University</creatorcontrib><creatorcontrib>The University of Georgia Research Foundation, Inc</creatorcontrib><collection>USPTO Issued Patents</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Chu, Chung K</au><au>Kotra, Lakshmi P</au><au>Manouilov, Konstantine</au><au>Du, Jinfa</au><au>Schinazi, Raymond</au><aucorp>Emory University</aucorp><aucorp>The University of Georgia Research Foundation, Inc</aucorp><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Therapeutic azide compounds</title><date>2005-09-27</date><risdate>2005</risdate><abstract>Pharmaceutical prodrug compositions are provided comprising azide derivatives of drugs which are capable of being converted to the drug in vivo. Azide derivatives of drugs having amine, ketone and hydroxy substituents are converted in vivo to the corresponding drugs, increasing the half-life of the drugs. In addition azide prodrugs are often better able to penetrate the blood-brain barrier than the corresponding drugs. Especially useful are azide derivatives of cordycepin, 2′-F-ara-ddI, AraA, acyclovir, penciclovir and related drugs. Useful azide prodrugs are azide derivatives of therapeutic alicyclic amines, ketones, and hydroxy-substituted compounds, including aralkyl, heterocyclic aralkyl, and cyclic aliphatic compounds, where the amine or oxygen moiety is on the ring, or where the amine or oxygen moiety is on an aliphatic side chain, as well as therapeutic purines and pyrimidines, nucleoside analogs and phosphorylated nucleoside analogs.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | eng |
recordid | cdi_uspatents_grants_06949521 |
source | USPTO Issued Patents |
title | Therapeutic azide compounds |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T13%3A43%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-uspatents_EFH&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=Chu,%20Chung%20K&rft.aucorp=Emory%20University&rft.date=2005-09-27&rft_id=info:doi/&rft_dat=%3Cuspatents_EFH%3E06949521%3C/uspatents_EFH%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 |