Solunum sistemi sinsitiyal virüsünün replikasyonunu inhibe edici maddeler

Bu bulus, formül (I)e sahip bilesiklerin, virütik enfeksiyonlari, özellikle RSV enfeksiyonlarini tedavi etmeye mahsus bir ilaç üretiminde kullanimi ile ilgili olup; burada -a1=a2-a3=a4, -CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH- veya -CH=CH-CH=N- formüle sahip bir radikaldir ve buradaki...

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Hauptverfasser: JER ME EMILE GEORGES GUILLEMONT, KOENRAAD JOZEF LODEWIJK MARCEL ANDRIES, JEAN FERNEND ARMAND LACRAMPE, FRANS EDUARD JANSSENS, FRANCOIS MARIA SOMMEN, KATHLEEN PETRUS MARIE-JOS MEERSMAN
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creator JER ME EMILE GEORGES GUILLEMONT
KOENRAAD JOZEF LODEWIJK MARCEL ANDRIES
JEAN FERNEND ARMAND LACRAMPE
FRANS EDUARD JANSSENS
FRANCOIS MARIA SOMMEN
KATHLEEN PETRUS MARIE-JOS MEERSMAN
description Bu bulus, formül (I)e sahip bilesiklerin, virütik enfeksiyonlari, özellikle RSV enfeksiyonlarini tedavi etmeye mahsus bir ilaç üretiminde kullanimi ile ilgili olup; burada -a1=a2-a3=a4, -CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH- veya -CH=CH-CH=N- formüle sahip bir radikaldir ve buradaki her bir hidrojen atomu, istege bagli olarak subsititüe edilebilir;Q,(b-1), (b-2), (b-3), (b-4), (b-5), (b-6), (b-7) ve (b-8) formülüne sahip bir radikaldir, G,bir dogrudan bag veya C1-10 alkandiildir;R1, istege bagli olarak sübstitüe edilmis bir monosiklik bir heterohalkadir.Formül (I)e sahip bazi bilesikler yenidir. This invention concerns compounds of formula prodrugs, N-oxides, addition salts, quaternary amines, metal complexes or stereochemically isomeric forms thereof wherein -a =a -a =a - is a radical of formula - CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH-, -CH=CH-CH=N- wherein each hydrogen atom may optionally be substituted; Q is a radical of formula wherein Alk is C1-6alkanediyl; Y is a bivalent radical of formula -NR - or -CH(NR R )-; X is NR , S, S(=O), S(=O)2, O, CH2, C(=O), CH(=CH2), CH(OH), CH(CH3), CH(OCH3), CH(SCH3), CH(NR R ), CH2-NR or NR -CH2; X is a direct bond, CH2, C(=O), NR , C1-4alkyl-NR , NR -C1-4alkyl; t is 2 to 5; u is 1 to 5; v is 2 or 3; and whereby each hydrogen in Alk and in (b-3), (b-4), (b-5), (b-6), (b-7) and (b-8), may optionally be replaced by R ; provided that when R is hydroxy or C1-6alkyloxy, then R can not replace a hydrogen atom in the alpha position relative to a nitrogen atom; G is a direct bond or C1-10alkanediyl; R is an optionally substituted monocyclic heterocycle; R is hydrogen, formyl, pyrrolidinyl, piperidinyl, homoiperidinyl, C3- 7cycloalkyl or C1-10alkyl substituted with N(R )2 and optionally with another substituent; R is hydrogen, hydroxy, C1-6alkyl, C1-6alkyloxy, arylC1-6alkyl or arylC1- 6alkyloxy; R is hydrogen, C1-6alkyl or arylC1-6alkyl; R , R , R and R each independently are hydrogen or C1-6alkyl; or R and R , or R and R taken together from a bivalent radical of formula -(CH2)s- wherein s is 4 or 5; R is hydrogen, C1- 4alkyl, formyl, hydroxyC1-6alkyl, C1-6alkylcarbonyl or C1-alkyloxyarbonyl; aryl is optionally substituted phenyl; and their use for the manufacture of a medicament for the treatment of viral infections, in particular RSV infections.
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This invention concerns compounds of formula prodrugs, N-oxides, addition salts, quaternary amines, metal complexes or stereochemically isomeric forms thereof wherein -a =a -a =a - is a radical of formula - CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH-, -CH=CH-CH=N- wherein each hydrogen atom may optionally be substituted; Q is a radical of formula wherein Alk is C1-6alkanediyl; Y is a bivalent radical of formula -NR - or -CH(NR R )-; X is NR , S, S(=O), S(=O)2, O, CH2, C(=O), CH(=CH2), CH(OH), CH(CH3), CH(OCH3), CH(SCH3), CH(NR R ), CH2-NR or NR -CH2; X is a direct bond, CH2, C(=O), NR , C1-4alkyl-NR , NR -C1-4alkyl; t is 2 to 5; u is 1 to 5; v is 2 or 3; and whereby each hydrogen in Alk and in (b-3), (b-4), (b-5), (b-6), (b-7) and (b-8), may optionally be replaced by R ; provided that when R is hydroxy or C1-6alkyloxy, then R can not replace a hydrogen atom in the alpha position relative to a nitrogen atom; G is a direct bond or C1-10alkanediyl; R is an optionally substituted monocyclic heterocycle; R is hydrogen, formyl, pyrrolidinyl, piperidinyl, homoiperidinyl, C3- 7cycloalkyl or C1-10alkyl substituted with N(R )2 and optionally with another substituent; R is hydrogen, hydroxy, C1-6alkyl, C1-6alkyloxy, arylC1-6alkyl or arylC1- 6alkyloxy; R is hydrogen, C1-6alkyl or arylC1-6alkyl; R , R , R and R each independently are hydrogen or C1-6alkyl; or R and R , or R and R taken together from a bivalent radical of formula -(CH2)s- wherein s is 4 or 5; R is hydrogen, C1- 4alkyl, formyl, hydroxyC1-6alkyl, C1-6alkylcarbonyl or C1-alkyloxyarbonyl; aryl is optionally substituted phenyl; and their use for the manufacture of a medicament for the treatment of viral infections, in particular RSV infections.</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&amp;date=20020521&amp;DB=EPODOC&amp;CC=TR&amp;NR=200103804T2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20020521&amp;DB=EPODOC&amp;CC=TR&amp;NR=200103804T2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JER ME EMILE GEORGES GUILLEMONT</creatorcontrib><creatorcontrib>KOENRAAD JOZEF LODEWIJK MARCEL ANDRIES</creatorcontrib><creatorcontrib>JEAN FERNEND ARMAND LACRAMPE</creatorcontrib><creatorcontrib>FRANS EDUARD JANSSENS</creatorcontrib><creatorcontrib>FRANCOIS MARIA SOMMEN</creatorcontrib><creatorcontrib>KATHLEEN PETRUS MARIE-JOS MEERSMAN</creatorcontrib><title>Solunum sistemi sinsitiyal virüsünün replikasyonunu inhibe edici maddeler</title><description>Bu bulus, formül (I)e sahip bilesiklerin, virütik enfeksiyonlari, özellikle RSV enfeksiyonlarini tedavi etmeye mahsus bir ilaç üretiminde kullanimi ile ilgili olup; burada -a1=a2-a3=a4, -CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH- veya -CH=CH-CH=N- formüle sahip bir radikaldir ve buradaki her bir hidrojen atomu, istege bagli olarak subsititüe edilebilir;Q,(b-1), (b-2), (b-3), (b-4), (b-5), (b-6), (b-7) ve (b-8) formülüne sahip bir radikaldir, G,bir dogrudan bag veya C1-10 alkandiildir;R1, istege bagli olarak sübstitüe edilmis bir monosiklik bir heterohalkadir.Formül (I)e sahip bazi bilesikler yenidir. This invention concerns compounds of formula prodrugs, N-oxides, addition salts, quaternary amines, metal complexes or stereochemically isomeric forms thereof wherein -a =a -a =a - is a radical of formula - CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH-, -CH=CH-CH=N- wherein each hydrogen atom may optionally be substituted; Q is a radical of formula wherein Alk is C1-6alkanediyl; Y is a bivalent radical of formula -NR - or -CH(NR R )-; X is NR , S, S(=O), S(=O)2, O, CH2, C(=O), CH(=CH2), CH(OH), CH(CH3), CH(OCH3), CH(SCH3), CH(NR R ), CH2-NR or NR -CH2; X is a direct bond, CH2, C(=O), NR , C1-4alkyl-NR , NR -C1-4alkyl; t is 2 to 5; u is 1 to 5; v is 2 or 3; and whereby each hydrogen in Alk and in (b-3), (b-4), (b-5), (b-6), (b-7) and (b-8), may optionally be replaced by R ; provided that when R is hydroxy or C1-6alkyloxy, then R can not replace a hydrogen atom in the alpha position relative to a nitrogen atom; G is a direct bond or C1-10alkanediyl; R is an optionally substituted monocyclic heterocycle; R is hydrogen, formyl, pyrrolidinyl, piperidinyl, homoiperidinyl, C3- 7cycloalkyl or C1-10alkyl substituted with N(R )2 and optionally with another substituent; R is hydrogen, hydroxy, C1-6alkyl, C1-6alkyloxy, arylC1-6alkyl or arylC1- 6alkyloxy; R is hydrogen, C1-6alkyl or arylC1-6alkyl; R , R , R and R each independently are hydrogen or C1-6alkyl; or R and R , or R and R taken together from a bivalent radical of formula -(CH2)s- wherein s is 4 or 5; R is hydrogen, C1- 4alkyl, formyl, hydroxyC1-6alkyl, C1-6alkylcarbonyl or C1-alkyloxyarbonyl; aryl is optionally substituted phenyl; and their use for the manufacture of a medicament for the treatment of viral infections, in particular RSV infections.</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>eNrjZPAJzs8pzSvNVSjOLC5Jzc0E0nnFmSWZlYk5CmWZRYf3FB_ekwdECkWpBTmZ2YnFlfl5QPUKmXkZmUmpCqkpmcmZCrmJKSmpOalFPAysaYk5xam8UJqbQdnNNcTZQze1ID8-tbggMTk1L7UkPiTIyMDA0MDYwsAkJMTImDhVAEHDOmI</recordid><startdate>20020521</startdate><enddate>20020521</enddate><creator>JER ME EMILE GEORGES GUILLEMONT</creator><creator>KOENRAAD JOZEF LODEWIJK MARCEL ANDRIES</creator><creator>JEAN FERNEND ARMAND LACRAMPE</creator><creator>FRANS EDUARD JANSSENS</creator><creator>FRANCOIS MARIA SOMMEN</creator><creator>KATHLEEN PETRUS MARIE-JOS MEERSMAN</creator><scope>EVB</scope></search><sort><creationdate>20020521</creationdate><title>Solunum sistemi sinsitiyal virüsünün replikasyonunu inhibe edici maddeler</title><author>JER ME EMILE GEORGES GUILLEMONT ; KOENRAAD JOZEF LODEWIJK MARCEL ANDRIES ; JEAN FERNEND ARMAND LACRAMPE ; FRANS EDUARD JANSSENS ; FRANCOIS MARIA SOMMEN ; KATHLEEN PETRUS MARIE-JOS MEERSMAN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_TR200103804TT23</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>JER ME EMILE GEORGES GUILLEMONT</creatorcontrib><creatorcontrib>KOENRAAD JOZEF LODEWIJK MARCEL ANDRIES</creatorcontrib><creatorcontrib>JEAN FERNEND ARMAND LACRAMPE</creatorcontrib><creatorcontrib>FRANS EDUARD JANSSENS</creatorcontrib><creatorcontrib>FRANCOIS MARIA SOMMEN</creatorcontrib><creatorcontrib>KATHLEEN PETRUS MARIE-JOS MEERSMAN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JER ME EMILE GEORGES GUILLEMONT</au><au>KOENRAAD JOZEF LODEWIJK MARCEL ANDRIES</au><au>JEAN FERNEND ARMAND LACRAMPE</au><au>FRANS EDUARD JANSSENS</au><au>FRANCOIS MARIA SOMMEN</au><au>KATHLEEN PETRUS MARIE-JOS MEERSMAN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Solunum sistemi sinsitiyal virüsünün replikasyonunu inhibe edici maddeler</title><date>2002-05-21</date><risdate>2002</risdate><abstract>Bu bulus, formül (I)e sahip bilesiklerin, virütik enfeksiyonlari, özellikle RSV enfeksiyonlarini tedavi etmeye mahsus bir ilaç üretiminde kullanimi ile ilgili olup; burada -a1=a2-a3=a4, -CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH- veya -CH=CH-CH=N- formüle sahip bir radikaldir ve buradaki her bir hidrojen atomu, istege bagli olarak subsititüe edilebilir;Q,(b-1), (b-2), (b-3), (b-4), (b-5), (b-6), (b-7) ve (b-8) formülüne sahip bir radikaldir, G,bir dogrudan bag veya C1-10 alkandiildir;R1, istege bagli olarak sübstitüe edilmis bir monosiklik bir heterohalkadir.Formül (I)e sahip bazi bilesikler yenidir. This invention concerns compounds of formula prodrugs, N-oxides, addition salts, quaternary amines, metal complexes or stereochemically isomeric forms thereof wherein -a =a -a =a - is a radical of formula - CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH-, -CH=CH-CH=N- wherein each hydrogen atom may optionally be substituted; Q is a radical of formula wherein Alk is C1-6alkanediyl; Y is a bivalent radical of formula -NR - or -CH(NR R )-; X is NR , S, S(=O), S(=O)2, O, CH2, C(=O), CH(=CH2), CH(OH), CH(CH3), CH(OCH3), CH(SCH3), CH(NR R ), CH2-NR or NR -CH2; X is a direct bond, CH2, C(=O), NR , C1-4alkyl-NR , NR -C1-4alkyl; t is 2 to 5; u is 1 to 5; v is 2 or 3; and whereby each hydrogen in Alk and in (b-3), (b-4), (b-5), (b-6), (b-7) and (b-8), may optionally be replaced by R ; provided that when R is hydroxy or C1-6alkyloxy, then R can not replace a hydrogen atom in the alpha position relative to a nitrogen atom; G is a direct bond or C1-10alkanediyl; R is an optionally substituted monocyclic heterocycle; R is hydrogen, formyl, pyrrolidinyl, piperidinyl, homoiperidinyl, C3- 7cycloalkyl or C1-10alkyl substituted with N(R )2 and optionally with another substituent; R is hydrogen, hydroxy, C1-6alkyl, C1-6alkyloxy, arylC1-6alkyl or arylC1- 6alkyloxy; R is hydrogen, C1-6alkyl or arylC1-6alkyl; R , R , R and R each independently are hydrogen or C1-6alkyl; or R and R , or R and R taken together from a bivalent radical of formula -(CH2)s- wherein s is 4 or 5; R is hydrogen, C1- 4alkyl, formyl, hydroxyC1-6alkyl, C1-6alkylcarbonyl or C1-alkyloxyarbonyl; aryl is optionally substituted phenyl; and their use for the manufacture of a medicament for the treatment of viral infections, in particular RSV infections.</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 Solunum sistemi sinsitiyal virüsünün replikasyonunu inhibe edici maddeler
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