AFFINITY ADSOBENTS FOR FIBRINOGEN
For the separation, removal, isolation, purification, characterisation, identification or quantification of fibrinogen or a protein that is a fibrinogen analogue, an affinity adsorbent is used that is a compound of formula II wherein one X is N and the other is N, C-Cl or C-CN; Y is O, S or NR2; 0 Z...
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description | For the separation, removal, isolation, purification, characterisation, identification or quantification of fibrinogen or a protein that is a fibrinogen analogue, an affinity adsorbent is used that is a compound of formula II wherein one X is N and the other is N, C-Cl or C-CN; Y is O, S or NR2; 0 Z is O, S or NR3; R2 and R3 are each H, alkyl, hydroxyalkyl, benzyl or ß-phenylethyl; n is 0 to 6; A is a support matrix, optionally linked to the triazine ring by a spacer; R7 is a group bearing a positive charge at neutral pH; W is an optional linker; V is an aromatic group; and R8 and R9 are each H, OH, alkyl, alkoxy, amino, NH2, acyloxy, acylamino, CO2H, sulphonic acid, carbamoyl, sulphamoyl, alkylsulphonyl or halogen or a cyclic structure such as a morpholino group, or R8 and R9 are linked to form such a cyclic structure.
La présente invention concerne la séparation, l'élimination, l'isolation, la purification, la caractérisation, l'identification ou la quantification du fibrinogène ou d'une protéine qui est un analogue du fibrinogène. L'invention utilise dans ce but un adsorbant d'affinité qui est un composé de formule II dans laquelle un X est N et l'autre est N, C-Cl ou C-CN ; Y est O, S ou NR2 ; 0 Z est O, S ou NR3 ; R2 et R3 sont chacun H, alkyle, hydroxyalkyle, benzyle ou ß-phényléthyle ; n est de 0 à 6 ; A est une matrice de soutien, facultativement liée au cycle triazine par un espaceur ; R7 est un groupe portant une charge positive à pH neutre ; W est un lieur facultatif ; V est un groupe aromatique ; et R8 et R9 sont chacun H, OH, alkyle, alcoxy, amino, NH2, acyloxy, acylamino, CO2H, acide sulfonique, carbamyle, sulfamyle, alkylsulfonyle ou halogène ou une structure cyclique telle qu'un groupe morpholino, ou R8 et R9 sont liés pour former une telle structure cyclique. |
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La présente invention concerne la séparation, l'élimination, l'isolation, la purification, la caractérisation, l'identification ou la quantification du fibrinogène ou d'une protéine qui est un analogue du fibrinogène. L'invention utilise dans ce but un adsorbant d'affinité qui est un composé de formule II dans laquelle un X est N et l'autre est N, C-Cl ou C-CN ; Y est O, S ou NR2 ; 0 Z est O, S ou NR3 ; R2 et R3 sont chacun H, alkyle, hydroxyalkyle, benzyle ou ß-phényléthyle ; n est de 0 à 6 ; A est une matrice de soutien, facultativement liée au cycle triazine par un espaceur ; R7 est un groupe portant une charge positive à pH neutre ; W est un lieur facultatif ; V est un groupe aromatique ; et R8 et R9 sont chacun H, OH, alkyle, alcoxy, amino, NH2, acyloxy, acylamino, CO2H, acide sulfonique, carbamyle, sulfamyle, alkylsulfonyle ou halogène ou une structure cyclique telle qu'un groupe morpholino, ou R8 et R9 sont liés pour former une telle structure cyclique.</description><language>eng ; fre</language><subject>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY ; CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES ; MEASURING ; METALLURGY ; ORGANIC CHEMISTRY ; PEPTIDES ; PERFORMING OPERATIONS ; PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL ; PHYSICS ; TESTING ; THEIR RELEVANT APPARATUS ; TRANSPORTING</subject><creationdate>2006</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=20061116&DB=EPODOC&CC=WO&NR=2006120429A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,778,883,25551,76302</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20061116&DB=EPODOC&CC=WO&NR=2006120429A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>PEARSON, JAMES, CHRISTOPHER</creatorcontrib><creatorcontrib>BEACOM, BEN, MARTIN</creatorcontrib><creatorcontrib>BETLEY, JASON, RICHARD</creatorcontrib><creatorcontrib>PODGORSKI, TADEUSZ, ANTONI</creatorcontrib><creatorcontrib>PANNELL, ROBERT, WILLIAM</creatorcontrib><title>AFFINITY ADSOBENTS FOR FIBRINOGEN</title><description>For the separation, removal, isolation, purification, characterisation, identification or quantification of fibrinogen or a protein that is a fibrinogen analogue, an affinity adsorbent is used that is a compound of formula II wherein one X is N and the other is N, C-Cl or C-CN; Y is O, S or NR2; 0 Z is O, S or NR3; R2 and R3 are each H, alkyl, hydroxyalkyl, benzyl or ß-phenylethyl; n is 0 to 6; A is a support matrix, optionally linked to the triazine ring by a spacer; R7 is a group bearing a positive charge at neutral pH; W is an optional linker; V is an aromatic group; and R8 and R9 are each H, OH, alkyl, alkoxy, amino, NH2, acyloxy, acylamino, CO2H, sulphonic acid, carbamoyl, sulphamoyl, alkylsulphonyl or halogen or a cyclic structure such as a morpholino group, or R8 and R9 are linked to form such a cyclic structure.
La présente invention concerne la séparation, l'élimination, l'isolation, la purification, la caractérisation, l'identification ou la quantification du fibrinogène ou d'une protéine qui est un analogue du fibrinogène. L'invention utilise dans ce but un adsorbant d'affinité qui est un composé de formule II dans laquelle un X est N et l'autre est N, C-Cl ou C-CN ; Y est O, S ou NR2 ; 0 Z est O, S ou NR3 ; R2 et R3 sont chacun H, alkyle, hydroxyalkyle, benzyle ou ß-phényléthyle ; n est de 0 à 6 ; A est une matrice de soutien, facultativement liée au cycle triazine par un espaceur ; R7 est un groupe portant une charge positive à pH neutre ; W est un lieur facultatif ; V est un groupe aromatique ; et R8 et R9 sont chacun H, OH, alkyle, alcoxy, amino, NH2, acyloxy, acylamino, CO2H, acide sulfonique, carbamyle, sulfamyle, alkylsulfonyle ou halogène ou une structure cyclique telle qu'un groupe morpholino, ou R8 et R9 sont liés pour former une telle structure cyclique.</description><subject>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</subject><subject>MEASURING</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PEPTIDES</subject><subject>PERFORMING OPERATIONS</subject><subject>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</subject><subject>PHYSICS</subject><subject>TESTING</subject><subject>THEIR RELEVANT APPARATUS</subject><subject>TRANSPORTING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2006</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFB0dHPz9PMMiVRwdAn2d3L1CwlWcPMPUnDzdAry9PN3d_XjYWBNS8wpTuWF0twMym6uIc4euqkF-fGpxQWJyal5qSXx4f5GBgZmhkYGJkaWjobGxKkCAKCYIxM</recordid><startdate>20061116</startdate><enddate>20061116</enddate><creator>PEARSON, JAMES, CHRISTOPHER</creator><creator>BEACOM, BEN, MARTIN</creator><creator>BETLEY, JASON, RICHARD</creator><creator>PODGORSKI, TADEUSZ, ANTONI</creator><creator>PANNELL, ROBERT, WILLIAM</creator><scope>EVB</scope></search><sort><creationdate>20061116</creationdate><title>AFFINITY ADSOBENTS FOR FIBRINOGEN</title><author>PEARSON, JAMES, CHRISTOPHER ; BEACOM, BEN, MARTIN ; BETLEY, JASON, RICHARD ; PODGORSKI, TADEUSZ, ANTONI ; PANNELL, ROBERT, WILLIAM</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_WO2006120429A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>2006</creationdate><topic>CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES</topic><topic>MEASURING</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEPTIDES</topic><topic>PERFORMING OPERATIONS</topic><topic>PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL</topic><topic>PHYSICS</topic><topic>TESTING</topic><topic>THEIR RELEVANT APPARATUS</topic><topic>TRANSPORTING</topic><toplevel>online_resources</toplevel><creatorcontrib>PEARSON, JAMES, CHRISTOPHER</creatorcontrib><creatorcontrib>BEACOM, BEN, MARTIN</creatorcontrib><creatorcontrib>BETLEY, JASON, RICHARD</creatorcontrib><creatorcontrib>PODGORSKI, TADEUSZ, ANTONI</creatorcontrib><creatorcontrib>PANNELL, ROBERT, WILLIAM</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>PEARSON, JAMES, CHRISTOPHER</au><au>BEACOM, BEN, MARTIN</au><au>BETLEY, JASON, RICHARD</au><au>PODGORSKI, TADEUSZ, ANTONI</au><au>PANNELL, ROBERT, WILLIAM</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>AFFINITY ADSOBENTS FOR FIBRINOGEN</title><date>2006-11-16</date><risdate>2006</risdate><abstract>For the separation, removal, isolation, purification, characterisation, identification or quantification of fibrinogen or a protein that is a fibrinogen analogue, an affinity adsorbent is used that is a compound of formula II wherein one X is N and the other is N, C-Cl or C-CN; Y is O, S or NR2; 0 Z is O, S or NR3; R2 and R3 are each H, alkyl, hydroxyalkyl, benzyl or ß-phenylethyl; n is 0 to 6; A is a support matrix, optionally linked to the triazine ring by a spacer; R7 is a group bearing a positive charge at neutral pH; W is an optional linker; V is an aromatic group; and R8 and R9 are each H, OH, alkyl, alkoxy, amino, NH2, acyloxy, acylamino, CO2H, sulphonic acid, carbamoyl, sulphamoyl, alkylsulphonyl or halogen or a cyclic structure such as a morpholino group, or R8 and R9 are linked to form such a cyclic structure.
La présente invention concerne la séparation, l'élimination, l'isolation, la purification, la caractérisation, l'identification ou la quantification du fibrinogène ou d'une protéine qui est un analogue du fibrinogène. L'invention utilise dans ce but un adsorbant d'affinité qui est un composé de formule II dans laquelle un X est N et l'autre est N, C-Cl ou C-CN ; Y est O, S ou NR2 ; 0 Z est O, S ou NR3 ; R2 et R3 sont chacun H, alkyle, hydroxyalkyle, benzyle ou ß-phényléthyle ; n est de 0 à 6 ; A est une matrice de soutien, facultativement liée au cycle triazine par un espaceur ; R7 est un groupe portant une charge positive à pH neutre ; W est un lieur facultatif ; V est un groupe aromatique ; et R8 et R9 sont chacun H, OH, alkyle, alcoxy, amino, NH2, acyloxy, acylamino, CO2H, acide sulfonique, carbamyle, sulfamyle, alkylsulfonyle ou halogène ou une structure cyclique telle qu'un groupe morpholino, ou R8 et R9 sont liés pour former une telle structure cyclique.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOIDCHEMISTRY CHEMISTRY HETEROCYCLIC COMPOUNDS INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIRCHEMICAL OR PHYSICAL PROPERTIES MEASURING METALLURGY ORGANIC CHEMISTRY PEPTIDES PERFORMING OPERATIONS PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL PHYSICS TESTING THEIR RELEVANT APPARATUS TRANSPORTING |
title | AFFINITY ADSOBENTS FOR FIBRINOGEN |
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