ANALOGIFOERFARANDE FOER FRAMSTAELLNING AV FARMACEUTISKT ANVAENDBARA 2-DEOXI-2-NIKOTINAMIDO-1-0-NIKOTINOYL-GLUKOPYRANOS-DERIVAT
1451181 2 - Nicotinamides - 1 - nicotinoyloxy- 0-glycopyranoses F HOFFMAN-LA ROCHE AG 24 Jan 1975 [25 Jan 1974] 3180/75 Heading C2C Novel compounds I in which R is C 1-6 alkanoyl, C 1-6 alkoxy C 1-6 alkanoyl or aryl are prepared by replacing X in a compound II where X is halogen or optionally protec...
Gespeichert in:
Hauptverfasser: | , , , , |
---|---|
Format: | Patent |
Sprache: | fin |
Schlagworte: | |
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 | LENGSFELD HANS WYSS PIERREARLES GEY KARL FRIEDRICH SCHUEEP WILLY KISS JOSEPH |
description | 1451181 2 - Nicotinamides - 1 - nicotinoyloxy- 0-glycopyranoses F HOFFMAN-LA ROCHE AG 24 Jan 1975 [25 Jan 1974] 3180/75 Heading C2C Novel compounds I in which R is C 1-6 alkanoyl, C 1-6 alkoxy C 1-6 alkanoyl or aryl are prepared by replacing X in a compound II where X is halogen or optionally protected hydroxy, by a nicotinoyloxy group in known manner. Compounds I (R=acetyl, propionyl, benzoyl) are prepared. Compound II (X=Cl, R=acetyl) is prepared by reacting N-nicotinoyl-D-glucosamine with acetyl chloride. Compound II (X=acetoxy, R=acetyl) is prepared by reacting 1,3,4,6- tetra - O - acetyl - D - glucosamine with nicotinic acid. Compounds I have plasma lipid-lowering activity and form with a carrier a pharmaceutical composition which may be administered orally, parenterally or rectally. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_FI61193CC</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>FI61193CC</sourcerecordid><originalsourceid>FETCH-epo_espacenet_FI61193CC3</originalsourceid><addsrcrecordid>eNqFjb0KwkAQhNNYiPoKci9wYCIIluv9xCWXXUkuwVQhyFmJBmLts3uC1lYzzMzHzJMXEDjO0bKpLFRA2oiPF7aCsvZgnCOkXEArYl2CMo3HuvACqAVD-hAZkUlt-Iwyk4QFeyQoUbNM5eYXcOdk7pqCT1384DoCFbbgl8nsOtymsPrqIllb49VRhvHRh2kcLuEenr3FXZrut0pt_w7exIc63g</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>ANALOGIFOERFARANDE FOER FRAMSTAELLNING AV FARMACEUTISKT ANVAENDBARA 2-DEOXI-2-NIKOTINAMIDO-1-0-NIKOTINOYL-GLUKOPYRANOS-DERIVAT</title><source>esp@cenet</source><creator>LENGSFELD HANS ; WYSS PIERREARLES ; GEY KARL FRIEDRICH ; SCHUEEP WILLY ; KISS JOSEPH</creator><creatorcontrib>LENGSFELD HANS ; WYSS PIERREARLES ; GEY KARL FRIEDRICH ; SCHUEEP WILLY ; KISS JOSEPH</creatorcontrib><description>1451181 2 - Nicotinamides - 1 - nicotinoyloxy- 0-glycopyranoses F HOFFMAN-LA ROCHE AG 24 Jan 1975 [25 Jan 1974] 3180/75 Heading C2C Novel compounds I in which R is C 1-6 alkanoyl, C 1-6 alkoxy C 1-6 alkanoyl or aryl are prepared by replacing X in a compound II where X is halogen or optionally protected hydroxy, by a nicotinoyloxy group in known manner. Compounds I (R=acetyl, propionyl, benzoyl) are prepared. Compound II (X=Cl, R=acetyl) is prepared by reacting N-nicotinoyl-D-glucosamine with acetyl chloride. Compound II (X=acetoxy, R=acetyl) is prepared by reacting 1,3,4,6- tetra - O - acetyl - D - glucosamine with nicotinic acid. Compounds I have plasma lipid-lowering activity and form with a carrier a pharmaceutical composition which may be administered orally, parenterally or rectally.</description><edition>3</edition><language>fin</language><subject>CHEMISTRY ; DERIVATIVES THEREOF ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; NUCLEIC ACIDS ; NUCLEOSIDES ; NUCLEOTIDES ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SUGARS</subject><creationdate>1982</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=19820610&DB=EPODOC&CC=FI&NR=61193C$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19820610&DB=EPODOC&CC=FI&NR=61193C$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>LENGSFELD HANS</creatorcontrib><creatorcontrib>WYSS PIERREARLES</creatorcontrib><creatorcontrib>GEY KARL FRIEDRICH</creatorcontrib><creatorcontrib>SCHUEEP WILLY</creatorcontrib><creatorcontrib>KISS JOSEPH</creatorcontrib><title>ANALOGIFOERFARANDE FOER FRAMSTAELLNING AV FARMACEUTISKT ANVAENDBARA 2-DEOXI-2-NIKOTINAMIDO-1-0-NIKOTINOYL-GLUKOPYRANOS-DERIVAT</title><description>1451181 2 - Nicotinamides - 1 - nicotinoyloxy- 0-glycopyranoses F HOFFMAN-LA ROCHE AG 24 Jan 1975 [25 Jan 1974] 3180/75 Heading C2C Novel compounds I in which R is C 1-6 alkanoyl, C 1-6 alkoxy C 1-6 alkanoyl or aryl are prepared by replacing X in a compound II where X is halogen or optionally protected hydroxy, by a nicotinoyloxy group in known manner. Compounds I (R=acetyl, propionyl, benzoyl) are prepared. Compound II (X=Cl, R=acetyl) is prepared by reacting N-nicotinoyl-D-glucosamine with acetyl chloride. Compound II (X=acetoxy, R=acetyl) is prepared by reacting 1,3,4,6- tetra - O - acetyl - D - glucosamine with nicotinic acid. Compounds I have plasma lipid-lowering activity and form with a carrier a pharmaceutical composition which may be administered orally, parenterally or rectally.</description><subject>CHEMISTRY</subject><subject>DERIVATIVES THEREOF</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>NUCLEIC ACIDS</subject><subject>NUCLEOSIDES</subject><subject>NUCLEOTIDES</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>SUGARS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1982</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFjb0KwkAQhNNYiPoKci9wYCIIluv9xCWXXUkuwVQhyFmJBmLts3uC1lYzzMzHzJMXEDjO0bKpLFRA2oiPF7aCsvZgnCOkXEArYl2CMo3HuvACqAVD-hAZkUlt-Iwyk4QFeyQoUbNM5eYXcOdk7pqCT1384DoCFbbgl8nsOtymsPrqIllb49VRhvHRh2kcLuEenr3FXZrut0pt_w7exIc63g</recordid><startdate>19820610</startdate><enddate>19820610</enddate><creator>LENGSFELD HANS</creator><creator>WYSS PIERREARLES</creator><creator>GEY KARL FRIEDRICH</creator><creator>SCHUEEP WILLY</creator><creator>KISS JOSEPH</creator><scope>EVB</scope></search><sort><creationdate>19820610</creationdate><title>ANALOGIFOERFARANDE FOER FRAMSTAELLNING AV FARMACEUTISKT ANVAENDBARA 2-DEOXI-2-NIKOTINAMIDO-1-0-NIKOTINOYL-GLUKOPYRANOS-DERIVAT</title><author>LENGSFELD HANS ; WYSS PIERREARLES ; GEY KARL FRIEDRICH ; SCHUEEP WILLY ; KISS JOSEPH</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_FI61193CC3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>fin</language><creationdate>1982</creationdate><topic>CHEMISTRY</topic><topic>DERIVATIVES THEREOF</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>NUCLEIC ACIDS</topic><topic>NUCLEOSIDES</topic><topic>NUCLEOTIDES</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>SUGARS</topic><toplevel>online_resources</toplevel><creatorcontrib>LENGSFELD HANS</creatorcontrib><creatorcontrib>WYSS PIERREARLES</creatorcontrib><creatorcontrib>GEY KARL FRIEDRICH</creatorcontrib><creatorcontrib>SCHUEEP WILLY</creatorcontrib><creatorcontrib>KISS JOSEPH</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LENGSFELD HANS</au><au>WYSS PIERREARLES</au><au>GEY KARL FRIEDRICH</au><au>SCHUEEP WILLY</au><au>KISS JOSEPH</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>ANALOGIFOERFARANDE FOER FRAMSTAELLNING AV FARMACEUTISKT ANVAENDBARA 2-DEOXI-2-NIKOTINAMIDO-1-0-NIKOTINOYL-GLUKOPYRANOS-DERIVAT</title><date>1982-06-10</date><risdate>1982</risdate><abstract>1451181 2 - Nicotinamides - 1 - nicotinoyloxy- 0-glycopyranoses F HOFFMAN-LA ROCHE AG 24 Jan 1975 [25 Jan 1974] 3180/75 Heading C2C Novel compounds I in which R is C 1-6 alkanoyl, C 1-6 alkoxy C 1-6 alkanoyl or aryl are prepared by replacing X in a compound II where X is halogen or optionally protected hydroxy, by a nicotinoyloxy group in known manner. Compounds I (R=acetyl, propionyl, benzoyl) are prepared. Compound II (X=Cl, R=acetyl) is prepared by reacting N-nicotinoyl-D-glucosamine with acetyl chloride. Compound II (X=acetoxy, R=acetyl) is prepared by reacting 1,3,4,6- tetra - O - acetyl - D - glucosamine with nicotinic acid. Compounds I have plasma lipid-lowering activity and form with a carrier a pharmaceutical composition which may be administered orally, parenterally or rectally.</abstract><edition>3</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | fin |
recordid | cdi_epo_espacenet_FI61193CC |
source | esp@cenet |
subjects | CHEMISTRY DERIVATIVES THEREOF HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY NUCLEIC ACIDS NUCLEOSIDES NUCLEOTIDES ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SUGARS |
title | ANALOGIFOERFARANDE FOER FRAMSTAELLNING AV FARMACEUTISKT ANVAENDBARA 2-DEOXI-2-NIKOTINAMIDO-1-0-NIKOTINOYL-GLUKOPYRANOS-DERIVAT |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T17%3A57%3A49IST&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=LENGSFELD%20HANS&rft.date=1982-06-10&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EFI61193CC%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 |