OLIGOMER BONDED TO NUCLEIC ACID
PROBLEM TO BE SOLVED: To obtain the subject new compound having new C-branches and N-branches, suitable for suppressing the expression of genes, exhibiting an antiviral property and useful for treating virus-infected diseases or cancers. SOLUTION: A compound of formula I [A is CO, etc.; B is thymine...
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creator | SCHWEMLER CHRISTOPH DR STROPP UDO DR KOSCH WINFRIED DR JORDAN STEPHAN DR KRETSCHMER AXEL DR |
description | PROBLEM TO BE SOLVED: To obtain the subject new compound having new C-branches and N-branches, suitable for suppressing the expression of genes, exhibiting an antiviral property and useful for treating virus-infected diseases or cancers. SOLUTION: A compound of formula I [A is CO, etc.; B is thymine, acetyl, etc.; C is CH, etc.; D is NH, etc.; E is NRR' (R, R' are each OH, methyl, etc., F is CH2 , etc.; G is NH, etc.; H is CR R (R is H, methyl; R is H, a 1-4C alkyl, etc.), etc.; L is (CH2 )p ((p) is 0-2), etc.; M is CH2 , etc.; Q is OH, O, etc.; T is hydroxyl group, etc.; (r) is 0, 1; (s) is 1-30], e.g. δ-N-Boc-α-N-L-ornithine methyl ester. The compound of formula I is produced e.g. by subjecting δ-N-Boc- protected L-ornithine methyl ester to a reductive amination reaction to introduce a benzyl protecting group, subjecting the obtained compound of formula II to an α-N-methylation reaction, introducing a nucleic acid base to the obtained compound of formula II, and subsequently hydrolyzing the compound of formula IV. The produced compound of formula I is suitable for oligomerization. |
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SOLUTION: A compound of formula I [A is CO, etc.; B is thymine, acetyl, etc.; C is CH, etc.; D is NH, etc.; E is NRR' (R, R' are each OH, methyl, etc., F is CH2 , etc.; G is NH, etc.; H is CR R (R is H, methyl; R is H, a 1-4C alkyl, etc.), etc.; L is (CH2 )p ((p) is 0-2), etc.; M is CH2 , etc.; Q is OH, O, etc.; T is hydroxyl group, etc.; (r) is 0, 1; (s) is 1-30], e.g. δ-N-Boc-α-N-L-ornithine methyl ester. The compound of formula I is produced e.g. by subjecting δ-N-Boc- protected L-ornithine methyl ester to a reductive amination reaction to introduce a benzyl protecting group, subjecting the obtained compound of formula II to an α-N-methylation reaction, introducing a nucleic acid base to the obtained compound of formula II, and subsequently hydrolyzing the compound of formula IV. The produced compound of formula I is suitable for oligomerization.</description><edition>6</edition><language>eng</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS THEREOF ; CULTURE MEDIA ; ENZYMOLOGY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; ORGANIC CHEMISTRY ; PEPTIDES ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>1998</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=19980407&DB=EPODOC&CC=JP&NR=H1087634A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19980407&DB=EPODOC&CC=JP&NR=H1087634A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SCHWEMLER CHRISTOPH DR</creatorcontrib><creatorcontrib>STROPP UDO DR</creatorcontrib><creatorcontrib>KOSCH WINFRIED DR</creatorcontrib><creatorcontrib>JORDAN STEPHAN DR</creatorcontrib><creatorcontrib>KRETSCHMER AXEL DR</creatorcontrib><title>OLIGOMER BONDED TO NUCLEIC ACID</title><description>PROBLEM TO BE SOLVED: To obtain the subject new compound having new C-branches and N-branches, suitable for suppressing the expression of genes, exhibiting an antiviral property and useful for treating virus-infected diseases or cancers. SOLUTION: A compound of formula I [A is CO, etc.; B is thymine, acetyl, etc.; C is CH, etc.; D is NH, etc.; E is NRR' (R, R' are each OH, methyl, etc., F is CH2 , etc.; G is NH, etc.; H is CR R (R is H, methyl; R is H, a 1-4C alkyl, etc.), etc.; L is (CH2 )p ((p) is 0-2), etc.; M is CH2 , etc.; Q is OH, O, etc.; T is hydroxyl group, etc.; (r) is 0, 1; (s) is 1-30], e.g. δ-N-Boc-α-N-L-ornithine methyl ester. The compound of formula I is produced e.g. by subjecting δ-N-Boc- protected L-ornithine methyl ester to a reductive amination reaction to introduce a benzyl protecting group, subjecting the obtained compound of formula II to an α-N-methylation reaction, introducing a nucleic acid base to the obtained compound of formula II, and subsequently hydrolyzing the compound of formula IV. The produced compound of formula I is suitable for oligomerization.</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS THEREOF</subject><subject>CULTURE MEDIA</subject><subject>ENZYMOLOGY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>ORGANIC CHEMISTRY</subject><subject>PEPTIDES</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1998</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJD39_F09_d1DVJw8vdzcXVRCPFX8At19nH1dFZwdPZ04WFgTUvMKU7lhdLcDApuriHOHrqpBfnxqcUFicmpeakl8V4BHoYGFuZmxiaOxkQoAQB7nCEh</recordid><startdate>19980407</startdate><enddate>19980407</enddate><creator>SCHWEMLER CHRISTOPH DR</creator><creator>STROPP UDO DR</creator><creator>KOSCH WINFRIED DR</creator><creator>JORDAN STEPHAN DR</creator><creator>KRETSCHMER AXEL DR</creator><scope>EVB</scope></search><sort><creationdate>19980407</creationdate><title>OLIGOMER BONDED TO NUCLEIC ACID</title><author>SCHWEMLER CHRISTOPH DR ; STROPP UDO DR ; KOSCH WINFRIED DR ; JORDAN STEPHAN DR ; KRETSCHMER AXEL DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPH1087634A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1998</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS THEREOF</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEPTIDES</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>SCHWEMLER CHRISTOPH DR</creatorcontrib><creatorcontrib>STROPP UDO DR</creatorcontrib><creatorcontrib>KOSCH WINFRIED DR</creatorcontrib><creatorcontrib>JORDAN STEPHAN DR</creatorcontrib><creatorcontrib>KRETSCHMER AXEL DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SCHWEMLER CHRISTOPH DR</au><au>STROPP UDO DR</au><au>KOSCH WINFRIED DR</au><au>JORDAN STEPHAN DR</au><au>KRETSCHMER AXEL DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>OLIGOMER BONDED TO NUCLEIC ACID</title><date>1998-04-07</date><risdate>1998</risdate><abstract>PROBLEM TO BE SOLVED: To obtain the subject new compound having new C-branches and N-branches, suitable for suppressing the expression of genes, exhibiting an antiviral property and useful for treating virus-infected diseases or cancers. SOLUTION: A compound of formula I [A is CO, etc.; B is thymine, acetyl, etc.; C is CH, etc.; D is NH, etc.; E is NRR' (R, R' are each OH, methyl, etc., F is CH2 , etc.; G is NH, etc.; H is CR R (R is H, methyl; R is H, a 1-4C alkyl, etc.), etc.; L is (CH2 )p ((p) is 0-2), etc.; M is CH2 , etc.; Q is OH, O, etc.; T is hydroxyl group, etc.; (r) is 0, 1; (s) is 1-30], e.g. δ-N-Boc-α-N-L-ornithine methyl ester. The compound of formula I is produced e.g. by subjecting δ-N-Boc- protected L-ornithine methyl ester to a reductive amination reaction to introduce a benzyl protecting group, subjecting the obtained compound of formula II to an α-N-methylation reaction, introducing a nucleic acid base to the obtained compound of formula II, and subsequently hydrolyzing the compound of formula IV. The produced compound of formula I is suitable for oligomerization.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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subjects | BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS THEREOF CULTURE MEDIA ENZYMOLOGY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING ORGANIC CHEMISTRY PEPTIDES PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS SPIRITS VINEGAR WINE |
title | OLIGOMER BONDED TO NUCLEIC ACID |
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