Antibakteriyel aktif maddeler
Formül (II)'deki bilesikler Q'nun -N(OH)CH(=O) veya -C(=O)NH(OH) formüllerinin radikalini temsil ettigi antibakteriyel maddelerdir. R1 hidrojen, C1-C6 alkil veya bir veya daha fazla halojen tarafindan ikame edilen C1-C6 alkil veya Q'nun -N(OH)CH(=O) formülünün radikali olmasi haricind...
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creator | KENNETH NOEL KEAVEY LAURENT FRANCK MOUNIER GILLES DENIS PAIN LISA MARIE PRATT |
description | Formül (II)'deki bilesikler Q'nun -N(OH)CH(=O) veya -C(=O)NH(OH) formüllerinin radikalini temsil ettigi antibakteriyel maddelerdir. R1 hidrojen, C1-C6 alkil veya bir veya daha fazla halojen tarafindan ikame edilen C1-C6 alkil veya Q'nun -N(OH)CH(=O) formülünün radikali olmasi haricinde; hidroksi, C1-C6 alkoksi, C1-C6 alkeniloksi, amino, C1-C6 alkilamino veya di-(C1-C6 alkil) amino grubu temsil eder. R2, ikame edilmis veya edilmemis C1-C6 alkil, sikloalkil(C1-C6 alkil)- veya aril(C1-C6 alkil)- grubu temsil eder ve A, R4'ün dogal veya dogal olmayan alfa amino asitin yan zincirini temsil ettigi ve R5 ve R6'in bagli olduklari nitrojen atomu ile birlikte alindiginda tarifde belirtildigi gibi bir doyurulmus heterosiklik 5 ila 7 atomlu birinci halka olusturdugu (IIA) veya (IIB) formüllerindeki bir grubu temsil eder.
Compounds of formula (II) are antibacterial agents wherein Q represents a radical of the formula: -N(OH)CH( O) or the formula: -C( O)NH(OH); R1 represents hydrogen, C1-C6 alkyl or C1-C6 alkyl substituted by one or more halogen atoms, or, except when Q is a radical of the formula: -N(OH)CH( O), a hydroxy, C1-C6 alkoxy, C1-C6 alkenyloxy, amino, C1-C6 alkylamino, or di-(C1-C6 alkylamino group; R2 represents a substituted or unsubstituted C1-C6 alkyl, cycloalkyl(C1-C6 alkyl)- or aryl(C1-C6 alkyl)-group; and A represents a group of formula (IIA), or (IIB) wherein R4 represents the side chain of a natural or non-natural alpha amino acid, and R5 and R6 when taken together with the nitrogen atom to which they are attached form a saturated heterocyclic first ring of 5 to 7 atoms as specified in the description. |
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Compounds of formula (II) are antibacterial agents wherein Q represents a radical of the formula: -N(OH)CH( O) or the formula: -C( O)NH(OH); R1 represents hydrogen, C1-C6 alkyl or C1-C6 alkyl substituted by one or more halogen atoms, or, except when Q is a radical of the formula: -N(OH)CH( O), a hydroxy, C1-C6 alkoxy, C1-C6 alkenyloxy, amino, C1-C6 alkylamino, or di-(C1-C6 alkylamino group; R2 represents a substituted or unsubstituted C1-C6 alkyl, cycloalkyl(C1-C6 alkyl)- or aryl(C1-C6 alkyl)-group; and A represents a group of formula (IIA), or (IIB) wherein R4 represents the side chain of a natural or non-natural alpha amino acid, and R5 and R6 when taken together with the nitrogen atom to which they are attached form a saturated heterocyclic first ring of 5 to 7 atoms as specified in the description.</description><edition>7</edition><language>tur</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>2002</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=20020621&DB=EPODOC&CC=TR&NR=200200360T2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20020621&DB=EPODOC&CC=TR&NR=200200360T2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KENNETH NOEL KEAVEY</creatorcontrib><creatorcontrib>LAURENT FRANCK MOUNIER</creatorcontrib><creatorcontrib>GILLES DENIS PAIN</creatorcontrib><creatorcontrib>LISA MARIE PRATT</creatorcontrib><title>Antibakteriyel aktif maddeler</title><description>Formül (II)'deki bilesikler Q'nun -N(OH)CH(=O) veya -C(=O)NH(OH) formüllerinin radikalini temsil ettigi antibakteriyel maddelerdir. R1 hidrojen, C1-C6 alkil veya bir veya daha fazla halojen tarafindan ikame edilen C1-C6 alkil veya Q'nun -N(OH)CH(=O) formülünün radikali olmasi haricinde; hidroksi, C1-C6 alkoksi, C1-C6 alkeniloksi, amino, C1-C6 alkilamino veya di-(C1-C6 alkil) amino grubu temsil eder. R2, ikame edilmis veya edilmemis C1-C6 alkil, sikloalkil(C1-C6 alkil)- veya aril(C1-C6 alkil)- grubu temsil eder ve A, R4'ün dogal veya dogal olmayan alfa amino asitin yan zincirini temsil ettigi ve R5 ve R6'in bagli olduklari nitrojen atomu ile birlikte alindiginda tarifde belirtildigi gibi bir doyurulmus heterosiklik 5 ila 7 atomlu birinci halka olusturdugu (IIA) veya (IIB) formüllerindeki bir grubu temsil eder.
Compounds of formula (II) are antibacterial agents wherein Q represents a radical of the formula: -N(OH)CH( O) or the formula: -C( O)NH(OH); R1 represents hydrogen, C1-C6 alkyl or C1-C6 alkyl substituted by one or more halogen atoms, or, except when Q is a radical of the formula: -N(OH)CH( O), a hydroxy, C1-C6 alkoxy, C1-C6 alkenyloxy, amino, C1-C6 alkylamino, or di-(C1-C6 alkylamino group; R2 represents a substituted or unsubstituted C1-C6 alkyl, cycloalkyl(C1-C6 alkyl)- or aryl(C1-C6 alkyl)-group; and A represents a group of formula (IIA), or (IIB) wherein R4 represents the side chain of a natural or non-natural alpha amino acid, and R5 and R6 when taken together with the nitrogen atom to which they are attached form a saturated heterocyclic first ring of 5 to 7 atoms as specified in the description.</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>2002</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJB1zCvJTErMLkktyqxMzVEAsjLTFHITU1JSc1KLeBhY0xJzilN5oTQ3g7Kba4izh25qQX58anFBYnJqXmpJfEiQkYEBEBmbGYSEGBkTpwoAdsElgw</recordid><startdate>20020621</startdate><enddate>20020621</enddate><creator>KENNETH NOEL KEAVEY</creator><creator>LAURENT FRANCK MOUNIER</creator><creator>GILLES DENIS PAIN</creator><creator>LISA MARIE PRATT</creator><scope>EVB</scope></search><sort><creationdate>20020621</creationdate><title>Antibakteriyel aktif maddeler</title><author>KENNETH NOEL KEAVEY ; LAURENT FRANCK MOUNIER ; GILLES DENIS PAIN ; LISA MARIE PRATT</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_TR200200360TT23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>tur</language><creationdate>2002</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>KENNETH NOEL KEAVEY</creatorcontrib><creatorcontrib>LAURENT FRANCK MOUNIER</creatorcontrib><creatorcontrib>GILLES DENIS PAIN</creatorcontrib><creatorcontrib>LISA MARIE PRATT</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KENNETH NOEL KEAVEY</au><au>LAURENT FRANCK MOUNIER</au><au>GILLES DENIS PAIN</au><au>LISA MARIE PRATT</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Antibakteriyel aktif maddeler</title><date>2002-06-21</date><risdate>2002</risdate><abstract>Formül (II)'deki bilesikler Q'nun -N(OH)CH(=O) veya -C(=O)NH(OH) formüllerinin radikalini temsil ettigi antibakteriyel maddelerdir. R1 hidrojen, C1-C6 alkil veya bir veya daha fazla halojen tarafindan ikame edilen C1-C6 alkil veya Q'nun -N(OH)CH(=O) formülünün radikali olmasi haricinde; hidroksi, C1-C6 alkoksi, C1-C6 alkeniloksi, amino, C1-C6 alkilamino veya di-(C1-C6 alkil) amino grubu temsil eder. R2, ikame edilmis veya edilmemis C1-C6 alkil, sikloalkil(C1-C6 alkil)- veya aril(C1-C6 alkil)- grubu temsil eder ve A, R4'ün dogal veya dogal olmayan alfa amino asitin yan zincirini temsil ettigi ve R5 ve R6'in bagli olduklari nitrojen atomu ile birlikte alindiginda tarifde belirtildigi gibi bir doyurulmus heterosiklik 5 ila 7 atomlu birinci halka olusturdugu (IIA) veya (IIB) formüllerindeki bir grubu temsil eder.
Compounds of formula (II) are antibacterial agents wherein Q represents a radical of the formula: -N(OH)CH( O) or the formula: -C( O)NH(OH); R1 represents hydrogen, C1-C6 alkyl or C1-C6 alkyl substituted by one or more halogen atoms, or, except when Q is a radical of the formula: -N(OH)CH( O), a hydroxy, C1-C6 alkoxy, C1-C6 alkenyloxy, amino, C1-C6 alkylamino, or di-(C1-C6 alkylamino group; R2 represents a substituted or unsubstituted C1-C6 alkyl, cycloalkyl(C1-C6 alkyl)- or aryl(C1-C6 alkyl)-group; and A represents a group of formula (IIA), or (IIB) wherein R4 represents the side chain of a natural or non-natural alpha amino acid, and R5 and R6 when taken together with the nitrogen atom to which they are attached form a saturated heterocyclic first ring of 5 to 7 atoms as specified in the description.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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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 | Antibakteriyel aktif maddeler |
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