Inhibitors of memapsin 2 and use thereof

−9 Methods for the production of purified, catalytically active, recombinant memapsin 2 have been developed. The substrate and subsite specificity of the catalytically active enzyme have been determined and were used to design substrate analogs of the natural -2 substrate that can inhibit the functi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Tang, Jordan J. N, Ghosh, Arun K
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 Tang, Jordan J. N
Ghosh, Arun K
description −9 Methods for the production of purified, catalytically active, recombinant memapsin 2 have been developed. The substrate and subsite specificity of the catalytically active enzyme have been determined and were used to design substrate analogs of the natural -2 substrate that can inhibit the function of memapsin 2. Processes for the synthesis of two substrate analogues including isosteres at the sites of the critical amino acid residues were developed and the substrate analogues, OMR99-1 and OM99-2, were synthesized. The inhibition constant of OM99-2 is 1.6×10M against recombinant pro-memapsin 2. Crystallography of memapsin 2 bound to this inhibitor was used to determine the three dimensional structure of the protein, and the importance of the various residues in binding. This information is useful for designing new inhibitors to memapsin 2, for diagnosing and treating and/or preventing Alzheimer's disease.
format Patent
fullrecord <record><control><sourceid>uspatents_EFH</sourceid><recordid>TN_cdi_uspatents_grants_07244708</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>07244708</sourcerecordid><originalsourceid>FETCH-uspatents_grants_072447083</originalsourceid><addsrcrecordid>eNrjZNDwzMvITMosyS8qVshPU8hNzU0sKM7MUzBSSMxLUSgtTlUoyUgtSs1P42FgTUvMKU7lhdLcDApuriHOHrqlxQWJJal5JcXx6UWJIMrA3MjExNzAwpgIJQB0SCim</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Inhibitors of memapsin 2 and use thereof</title><source>USPTO Issued Patents</source><creator>Tang, Jordan J. N ; Ghosh, Arun K</creator><creatorcontrib>Tang, Jordan J. N ; Ghosh, Arun K ; The Board of Trustees of the University of Illinois ; Oklahoma Medical Research Foundation</creatorcontrib><description>−9 Methods for the production of purified, catalytically active, recombinant memapsin 2 have been developed. The substrate and subsite specificity of the catalytically active enzyme have been determined and were used to design substrate analogs of the natural -2 substrate that can inhibit the function of memapsin 2. Processes for the synthesis of two substrate analogues including isosteres at the sites of the critical amino acid residues were developed and the substrate analogues, OMR99-1 and OM99-2, were synthesized. The inhibition constant of OM99-2 is 1.6×10M against recombinant pro-memapsin 2. Crystallography of memapsin 2 bound to this inhibitor was used to determine the three dimensional structure of the protein, and the importance of the various residues in binding. This information is useful for designing new inhibitors to memapsin 2, for diagnosing and treating and/or preventing Alzheimer's disease.</description><language>eng</language><creationdate>2007</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/7244708$$EPDF$$P50$$Guspatents$$Hfree_for_read</linktopdf><link.rule.ids>230,308,776,798,881,64012</link.rule.ids><linktorsrc>$$Uhttps://image-ppubs.uspto.gov/dirsearch-public/print/downloadPdf/7244708$$EView_record_in_USPTO$$FView_record_in_$$GUSPTO$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Tang, Jordan J. N</creatorcontrib><creatorcontrib>Ghosh, Arun K</creatorcontrib><creatorcontrib>The Board of Trustees of the University of Illinois</creatorcontrib><creatorcontrib>Oklahoma Medical Research Foundation</creatorcontrib><title>Inhibitors of memapsin 2 and use thereof</title><description>−9 Methods for the production of purified, catalytically active, recombinant memapsin 2 have been developed. The substrate and subsite specificity of the catalytically active enzyme have been determined and were used to design substrate analogs of the natural -2 substrate that can inhibit the function of memapsin 2. Processes for the synthesis of two substrate analogues including isosteres at the sites of the critical amino acid residues were developed and the substrate analogues, OMR99-1 and OM99-2, were synthesized. The inhibition constant of OM99-2 is 1.6×10M against recombinant pro-memapsin 2. Crystallography of memapsin 2 bound to this inhibitor was used to determine the three dimensional structure of the protein, and the importance of the various residues in binding. This information is useful for designing new inhibitors to memapsin 2, for diagnosing and treating and/or preventing Alzheimer's disease.</description><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2007</creationdate><recordtype>patent</recordtype><sourceid>EFH</sourceid><recordid>eNrjZNDwzMvITMosyS8qVshPU8hNzU0sKM7MUzBSSMxLUSgtTlUoyUgtSs1P42FgTUvMKU7lhdLcDApuriHOHrqlxQWJJal5JcXx6UWJIMrA3MjExNzAwpgIJQB0SCim</recordid><startdate>20070717</startdate><enddate>20070717</enddate><creator>Tang, Jordan J. N</creator><creator>Ghosh, Arun K</creator><scope>EFH</scope></search><sort><creationdate>20070717</creationdate><title>Inhibitors of memapsin 2 and use thereof</title><author>Tang, Jordan J. N ; Ghosh, Arun K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-uspatents_grants_072447083</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2007</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Tang, Jordan J. N</creatorcontrib><creatorcontrib>Ghosh, Arun K</creatorcontrib><creatorcontrib>The Board of Trustees of the University of Illinois</creatorcontrib><creatorcontrib>Oklahoma Medical Research Foundation</creatorcontrib><collection>USPTO Issued Patents</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Tang, Jordan J. N</au><au>Ghosh, Arun K</au><aucorp>The Board of Trustees of the University of Illinois</aucorp><aucorp>Oklahoma Medical Research Foundation</aucorp><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Inhibitors of memapsin 2 and use thereof</title><date>2007-07-17</date><risdate>2007</risdate><abstract>−9 Methods for the production of purified, catalytically active, recombinant memapsin 2 have been developed. The substrate and subsite specificity of the catalytically active enzyme have been determined and were used to design substrate analogs of the natural -2 substrate that can inhibit the function of memapsin 2. Processes for the synthesis of two substrate analogues including isosteres at the sites of the critical amino acid residues were developed and the substrate analogues, OMR99-1 and OM99-2, were synthesized. The inhibition constant of OM99-2 is 1.6×10M against recombinant pro-memapsin 2. Crystallography of memapsin 2 bound to this inhibitor was used to determine the three dimensional structure of the protein, and the importance of the various residues in binding. This information is useful for designing new inhibitors to memapsin 2, for diagnosing and treating and/or preventing Alzheimer's disease.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_uspatents_grants_07244708
source USPTO Issued Patents
title Inhibitors of memapsin 2 and use thereof
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T18%3A33%3A12IST&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=Tang,%20Jordan%20J.%20N&rft.aucorp=The%20Board%20of%20Trustees%20of%20the%20University%20of%20Illinois&rft.date=2007-07-17&rft_id=info:doi/&rft_dat=%3Cuspatents_EFH%3E07244708%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