PPAR-AKTIVIERENDE VERBINDUNG UND DIESE ENTHALTENDE PHARMAZEUTISCHE ZUSAMMENSETZUNG
A COMPOUND REPRESENTED BY THE FOLLOWING FORMULA (I): (WHEREIN EACH OF R₁ AND R₂, WHICH MAY BE IDENTICAL TO OR DIFFERENT FROM EACH OTHER, REPRESENTS A HYDROGEN ATOM, A METHYL GROUP, OR AN ETHYL GROUP; EACH OF R3a, R3b, R4a AND R4b, WHICH MAY BE IDENTICAL TO OR DIFFERNT FROM EACH OTEHR, REPRESENTS A H...
Gespeichert in:
Hauptverfasser: | , , , , , , , |
---|---|
Format: | Patent |
Sprache: | ger |
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 | ARAKI, TAKAAKI OKUDA, AYUMU TOMA, TSUTOMU ABE, KAZUTOYO NISHIKAWA, MASAHIRO OZAWA, HIDEFUMI YAMAZAKI, YUKIYOSHI ODA, SOICHI |
description | A COMPOUND REPRESENTED BY THE FOLLOWING FORMULA (I): (WHEREIN EACH OF R₁ AND R₂, WHICH MAY BE IDENTICAL TO OR DIFFERENT FROM EACH OTHER, REPRESENTS A HYDROGEN ATOM, A METHYL GROUP, OR AN ETHYL GROUP; EACH OF R3a, R3b, R4a AND R4b, WHICH MAY BE IDENTICAL TO OR DIFFERNT FROM EACH OTEHR, REPRESENTS A HYDROGEN ATOM, A HALOGEN ATOM, A NITRO GROUP, A HYDROXYL GROUP, A C₁-₄ ALKYL GROUP, A TRIFLUOROMETHYL GROUP, A C₁-₄ ALKOXY GROUP, A C₁-₄ ALKYLCARBONYLOXY GROUP, A di-C₁-₄ ALKYLAMINO GROUP, A C₁-₄ ALKYSULFONYLOXY GROUP, A C₁-₄ ALKYSULFONYL GROUP, A C₁-₄ ALKYSULFINYL GROUP, OR A C₁-₄ ALKYLTHIO GROUP, OR R3a AND R3b, OR R4a AND R4b MAY BE LINKED TOGETHER TO FORM AN ALKYLENEDIOXY GROUP; X REPRESENTS AN OXYGEN ATOM, A SULFUR ATOM, OR N-R5 (R5 REPRESENTS A HYDROGEN ATOM, A C₁-₄ ALKYL GROUP, A C₁-₄ ALKYLSULFONYL GROUP, OR A C₁-₄ ALKYLOXYCARBONYL GROUP); Y REPRESENTS AN OXYGEN ATOM, S (O)₁ (1 IS A NUMBER OF 0 TO 2), A CARBONYL GROUP, A CARBONYLAMINO GROUP, AN AMINOCARBONYL GROUP, A SULFONYLAMINO GROUP, OR AN AMINOSULFONYL GROUP; Z REPRESENTS CH OR N; n IS A NUMBER OF 1 TO 6; AND m IS A NUMBER OF 2 TO 6) OR A SALT THEREOF; AND THERAPEUTIC DRUGS CONTAINING ANY OF SUCH A COMPOUND OR SALT. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_ATE494281TT1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ATE494281TT1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_ATE494281TT13</originalsourceid><addsrcrecordid>eNqNy7EOwiAURmEWB6O-Az5Ah2oHHa_lV4hCCFw6sDSNwclok_r-0RgfwOks35mL4D2Fis5sOoMApyA7hINxKrmTTE5JZRAh4VjThb_AawqWMhKb2GrInCJZCxfB-XMtxew23Key-nUh1kdwq6syPvsyjcO1PMqrJ0azbza7mrne_mPeMhww7A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>PPAR-AKTIVIERENDE VERBINDUNG UND DIESE ENTHALTENDE PHARMAZEUTISCHE ZUSAMMENSETZUNG</title><source>esp@cenet</source><creator>ARAKI, TAKAAKI ; OKUDA, AYUMU ; TOMA, TSUTOMU ; ABE, KAZUTOYO ; NISHIKAWA, MASAHIRO ; OZAWA, HIDEFUMI ; YAMAZAKI, YUKIYOSHI ; ODA, SOICHI</creator><creatorcontrib>ARAKI, TAKAAKI ; OKUDA, AYUMU ; TOMA, TSUTOMU ; ABE, KAZUTOYO ; NISHIKAWA, MASAHIRO ; OZAWA, HIDEFUMI ; YAMAZAKI, YUKIYOSHI ; ODA, SOICHI</creatorcontrib><description>A COMPOUND REPRESENTED BY THE FOLLOWING FORMULA (I): (WHEREIN EACH OF R₁ AND R₂, WHICH MAY BE IDENTICAL TO OR DIFFERENT FROM EACH OTHER, REPRESENTS A HYDROGEN ATOM, A METHYL GROUP, OR AN ETHYL GROUP; EACH OF R3a, R3b, R4a AND R4b, WHICH MAY BE IDENTICAL TO OR DIFFERNT FROM EACH OTEHR, REPRESENTS A HYDROGEN ATOM, A HALOGEN ATOM, A NITRO GROUP, A HYDROXYL GROUP, A C₁-₄ ALKYL GROUP, A TRIFLUOROMETHYL GROUP, A C₁-₄ ALKOXY GROUP, A C₁-₄ ALKYLCARBONYLOXY GROUP, A di-C₁-₄ ALKYLAMINO GROUP, A C₁-₄ ALKYSULFONYLOXY GROUP, A C₁-₄ ALKYSULFONYL GROUP, A C₁-₄ ALKYSULFINYL GROUP, OR A C₁-₄ ALKYLTHIO GROUP, OR R3a AND R3b, OR R4a AND R4b MAY BE LINKED TOGETHER TO FORM AN ALKYLENEDIOXY GROUP; X REPRESENTS AN OXYGEN ATOM, A SULFUR ATOM, OR N-R5 (R5 REPRESENTS A HYDROGEN ATOM, A C₁-₄ ALKYL GROUP, A C₁-₄ ALKYLSULFONYL GROUP, OR A C₁-₄ ALKYLOXYCARBONYL GROUP); Y REPRESENTS AN OXYGEN ATOM, S (O)₁ (1 IS A NUMBER OF 0 TO 2), A CARBONYL GROUP, A CARBONYLAMINO GROUP, AN AMINOCARBONYL GROUP, A SULFONYLAMINO GROUP, OR AN AMINOSULFONYL GROUP; Z REPRESENTS CH OR N; n IS A NUMBER OF 1 TO 6; AND m IS A NUMBER OF 2 TO 6) OR A SALT THEREOF; AND THERAPEUTIC DRUGS CONTAINING ANY OF SUCH A COMPOUND OR SALT.</description><language>ger</language><creationdate>2011</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&date=20110115&DB=EPODOC&CC=AT&NR=E494281T1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,309,781,886,25566,76549</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20110115&DB=EPODOC&CC=AT&NR=E494281T1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>ARAKI, TAKAAKI</creatorcontrib><creatorcontrib>OKUDA, AYUMU</creatorcontrib><creatorcontrib>TOMA, TSUTOMU</creatorcontrib><creatorcontrib>ABE, KAZUTOYO</creatorcontrib><creatorcontrib>NISHIKAWA, MASAHIRO</creatorcontrib><creatorcontrib>OZAWA, HIDEFUMI</creatorcontrib><creatorcontrib>YAMAZAKI, YUKIYOSHI</creatorcontrib><creatorcontrib>ODA, SOICHI</creatorcontrib><title>PPAR-AKTIVIERENDE VERBINDUNG UND DIESE ENTHALTENDE PHARMAZEUTISCHE ZUSAMMENSETZUNG</title><description>A COMPOUND REPRESENTED BY THE FOLLOWING FORMULA (I): (WHEREIN EACH OF R₁ AND R₂, WHICH MAY BE IDENTICAL TO OR DIFFERENT FROM EACH OTHER, REPRESENTS A HYDROGEN ATOM, A METHYL GROUP, OR AN ETHYL GROUP; EACH OF R3a, R3b, R4a AND R4b, WHICH MAY BE IDENTICAL TO OR DIFFERNT FROM EACH OTEHR, REPRESENTS A HYDROGEN ATOM, A HALOGEN ATOM, A NITRO GROUP, A HYDROXYL GROUP, A C₁-₄ ALKYL GROUP, A TRIFLUOROMETHYL GROUP, A C₁-₄ ALKOXY GROUP, A C₁-₄ ALKYLCARBONYLOXY GROUP, A di-C₁-₄ ALKYLAMINO GROUP, A C₁-₄ ALKYSULFONYLOXY GROUP, A C₁-₄ ALKYSULFONYL GROUP, A C₁-₄ ALKYSULFINYL GROUP, OR A C₁-₄ ALKYLTHIO GROUP, OR R3a AND R3b, OR R4a AND R4b MAY BE LINKED TOGETHER TO FORM AN ALKYLENEDIOXY GROUP; X REPRESENTS AN OXYGEN ATOM, A SULFUR ATOM, OR N-R5 (R5 REPRESENTS A HYDROGEN ATOM, A C₁-₄ ALKYL GROUP, A C₁-₄ ALKYLSULFONYL GROUP, OR A C₁-₄ ALKYLOXYCARBONYL GROUP); Y REPRESENTS AN OXYGEN ATOM, S (O)₁ (1 IS A NUMBER OF 0 TO 2), A CARBONYL GROUP, A CARBONYLAMINO GROUP, AN AMINOCARBONYL GROUP, A SULFONYLAMINO GROUP, OR AN AMINOSULFONYL GROUP; Z REPRESENTS CH OR N; n IS A NUMBER OF 1 TO 6; AND m IS A NUMBER OF 2 TO 6) OR A SALT THEREOF; AND THERAPEUTIC DRUGS CONTAINING ANY OF SUCH A COMPOUND OR SALT.</description><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2011</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNy7EOwiAURmEWB6O-Az5Ah2oHHa_lV4hCCFw6sDSNwclok_r-0RgfwOks35mL4D2Fis5sOoMApyA7hINxKrmTTE5JZRAh4VjThb_AawqWMhKb2GrInCJZCxfB-XMtxew23Key-nUh1kdwq6syPvsyjcO1PMqrJ0azbza7mrne_mPeMhww7A</recordid><startdate>20110115</startdate><enddate>20110115</enddate><creator>ARAKI, TAKAAKI</creator><creator>OKUDA, AYUMU</creator><creator>TOMA, TSUTOMU</creator><creator>ABE, KAZUTOYO</creator><creator>NISHIKAWA, MASAHIRO</creator><creator>OZAWA, HIDEFUMI</creator><creator>YAMAZAKI, YUKIYOSHI</creator><creator>ODA, SOICHI</creator><scope>EVB</scope></search><sort><creationdate>20110115</creationdate><title>PPAR-AKTIVIERENDE VERBINDUNG UND DIESE ENTHALTENDE PHARMAZEUTISCHE ZUSAMMENSETZUNG</title><author>ARAKI, TAKAAKI ; OKUDA, AYUMU ; TOMA, TSUTOMU ; ABE, KAZUTOYO ; NISHIKAWA, MASAHIRO ; OZAWA, HIDEFUMI ; YAMAZAKI, YUKIYOSHI ; ODA, SOICHI</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ATE494281TT13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>2011</creationdate><toplevel>online_resources</toplevel><creatorcontrib>ARAKI, TAKAAKI</creatorcontrib><creatorcontrib>OKUDA, AYUMU</creatorcontrib><creatorcontrib>TOMA, TSUTOMU</creatorcontrib><creatorcontrib>ABE, KAZUTOYO</creatorcontrib><creatorcontrib>NISHIKAWA, MASAHIRO</creatorcontrib><creatorcontrib>OZAWA, HIDEFUMI</creatorcontrib><creatorcontrib>YAMAZAKI, YUKIYOSHI</creatorcontrib><creatorcontrib>ODA, SOICHI</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>ARAKI, TAKAAKI</au><au>OKUDA, AYUMU</au><au>TOMA, TSUTOMU</au><au>ABE, KAZUTOYO</au><au>NISHIKAWA, MASAHIRO</au><au>OZAWA, HIDEFUMI</au><au>YAMAZAKI, YUKIYOSHI</au><au>ODA, SOICHI</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PPAR-AKTIVIERENDE VERBINDUNG UND DIESE ENTHALTENDE PHARMAZEUTISCHE ZUSAMMENSETZUNG</title><date>2011-01-15</date><risdate>2011</risdate><abstract>A COMPOUND REPRESENTED BY THE FOLLOWING FORMULA (I): (WHEREIN EACH OF R₁ AND R₂, WHICH MAY BE IDENTICAL TO OR DIFFERENT FROM EACH OTHER, REPRESENTS A HYDROGEN ATOM, A METHYL GROUP, OR AN ETHYL GROUP; EACH OF R3a, R3b, R4a AND R4b, WHICH MAY BE IDENTICAL TO OR DIFFERNT FROM EACH OTEHR, REPRESENTS A HYDROGEN ATOM, A HALOGEN ATOM, A NITRO GROUP, A HYDROXYL GROUP, A C₁-₄ ALKYL GROUP, A TRIFLUOROMETHYL GROUP, A C₁-₄ ALKOXY GROUP, A C₁-₄ ALKYLCARBONYLOXY GROUP, A di-C₁-₄ ALKYLAMINO GROUP, A C₁-₄ ALKYSULFONYLOXY GROUP, A C₁-₄ ALKYSULFONYL GROUP, A C₁-₄ ALKYSULFINYL GROUP, OR A C₁-₄ ALKYLTHIO GROUP, OR R3a AND R3b, OR R4a AND R4b MAY BE LINKED TOGETHER TO FORM AN ALKYLENEDIOXY GROUP; X REPRESENTS AN OXYGEN ATOM, A SULFUR ATOM, OR N-R5 (R5 REPRESENTS A HYDROGEN ATOM, A C₁-₄ ALKYL GROUP, A C₁-₄ ALKYLSULFONYL GROUP, OR A C₁-₄ ALKYLOXYCARBONYL GROUP); Y REPRESENTS AN OXYGEN ATOM, S (O)₁ (1 IS A NUMBER OF 0 TO 2), A CARBONYL GROUP, A CARBONYLAMINO GROUP, AN AMINOCARBONYL GROUP, A SULFONYLAMINO GROUP, OR AN AMINOSULFONYL GROUP; Z REPRESENTS CH OR N; n IS A NUMBER OF 1 TO 6; AND m IS A NUMBER OF 2 TO 6) OR A SALT THEREOF; AND THERAPEUTIC DRUGS CONTAINING ANY OF SUCH A COMPOUND OR SALT.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | ger |
recordid | cdi_epo_espacenet_ATE494281TT1 |
source | esp@cenet |
title | PPAR-AKTIVIERENDE VERBINDUNG UND DIESE ENTHALTENDE PHARMAZEUTISCHE ZUSAMMENSETZUNG |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T23%3A19%3A19IST&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=ARAKI,%20TAKAAKI&rft.date=2011-01-15&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EATE494281TT1%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 |