New C-Glycoside derivatives and uses thereof
C-beta -glycosides (I) containing a hydroxy-substituted hydrocarbyl group and their pharmaceutically acceptable salts are new. Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. C-beta -glycosides of formula (I) containing a h...
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description | C-beta -glycosides (I) containing a hydroxy-substituted hydrocarbyl group and their pharmaceutically acceptable salts are new. Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. C-beta -glycosides of formula (I) containing a hydroxy-substituted hydrocarbyl group and their pharmaceutically acceptable salts are new. Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. S : mono- or poly-saccharide of up to 20 sugar units as D series pyranose and/or furanose, including at least one free hydroxy and optionally one or more amino, optionally protected; R : 1-18C (perfluoro)alkyl or hydrofluoroalkyl, linear or branched, saturated or unsaturated, 3-11C cyclo(perfluoro)alkyl or cyclohydrofluoroalkyl, phenyl or benzyl, and the chain or rings may be interrupted by one or more of O, S, N or Si, and optionally substituted by one or more of OR 1, SR 1, N(R 1) 2, COOR 1, CONHR 1, cyano, halo, 1-18C (per)fluoroalkyl and/or 3-11C cycloalkyl, aryl or heterocyclic, optionally substituted; each R 1hydrogen, 1-30C (per)fluoroalkyl, hydroxy and/or hydrofluoroalkyl, linear or branched, saturated or unsaturated. An independent claim is also included for a method of preparing (I) by reducing the corresponding ketone S-CO-R (II). [Image] ACTIVITY : Dermatological; Vulnerary. MECHANISM OF ACTION : (I) stimulate synthesis of glycosaminoglycans (GAG) that contain D-glucosamine and/or N-acetylglucosamine residues, especially hyaluronic acid (HA), and/or of proteoglycans by fibroblasts and keratinocytes. It also modulates the activity of growth factors and cytokines. HA synthesis in a culture of human fibroblasts was detected by incorporation of radiolabeled glucosamine. The mean number of counts per minute (cpm) after 72 hours was 5010; compare 40770 (814 % of control) for a culture containing 3 mM C-beta -D-xylopyranoside-2(S)-hydroxypropane. |
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Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. C-beta -glycosides of formula (I) containing a hydroxy-substituted hydrocarbyl group and their pharmaceutically acceptable salts are new. Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. S : mono- or poly-saccharide of up to 20 sugar units as D series pyranose and/or furanose, including at least one free hydroxy and optionally one or more amino, optionally protected; R : 1-18C (perfluoro)alkyl or hydrofluoroalkyl, linear or branched, saturated or unsaturated, 3-11C cyclo(perfluoro)alkyl or cyclohydrofluoroalkyl, phenyl or benzyl, and the chain or rings may be interrupted by one or more of O, S, N or Si, and optionally substituted by one or more of OR 1, SR 1, N(R 1) 2, COOR 1, CONHR 1, cyano, halo, 1-18C (per)fluoroalkyl and/or 3-11C cycloalkyl, aryl or heterocyclic, optionally substituted; each R 1hydrogen, 1-30C (per)fluoroalkyl, hydroxy and/or hydrofluoroalkyl, linear or branched, saturated or unsaturated. An independent claim is also included for a method of preparing (I) by reducing the corresponding ketone S-CO-R (II). [Image] ACTIVITY : Dermatological; Vulnerary. MECHANISM OF ACTION : (I) stimulate synthesis of glycosaminoglycans (GAG) that contain D-glucosamine and/or N-acetylglucosamine residues, especially hyaluronic acid (HA), and/or of proteoglycans by fibroblasts and keratinocytes. It also modulates the activity of growth factors and cytokines. HA synthesis in a culture of human fibroblasts was detected by incorporation of radiolabeled glucosamine. The mean number of counts per minute (cpm) after 72 hours was 5010; compare 40770 (814 % of control) for a culture containing 3 mM C-beta -D-xylopyranoside-2(S)-hydroxypropane.</description><language>eng ; fre ; ger</language><subject>CHEMISTRY ; DERIVATIVES THEREOF ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; NUCLEIC ACIDS ; NUCLEOSIDES ; NUCLEOTIDES ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC USE OF COSMETICS OR SIMILAR TOILETPREPARATIONS ; SUGARS</subject><creationdate>2008</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=20080611&DB=EPODOC&CC=EP&NR=1589010B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,778,883,25551,76302</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20080611&DB=EPODOC&CC=EP&NR=1589010B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>CAVEZZA, ALEXANDRE</creatorcontrib><creatorcontrib>TROUILLE, SIMON</creatorcontrib><creatorcontrib>PICHAUD, PATRICK</creatorcontrib><title>New C-Glycoside derivatives and uses thereof</title><description>C-beta -glycosides (I) containing a hydroxy-substituted hydrocarbyl group and their pharmaceutically acceptable salts are new. Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. C-beta -glycosides of formula (I) containing a hydroxy-substituted hydrocarbyl group and their pharmaceutically acceptable salts are new. Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. S : mono- or poly-saccharide of up to 20 sugar units as D series pyranose and/or furanose, including at least one free hydroxy and optionally one or more amino, optionally protected; R : 1-18C (perfluoro)alkyl or hydrofluoroalkyl, linear or branched, saturated or unsaturated, 3-11C cyclo(perfluoro)alkyl or cyclohydrofluoroalkyl, phenyl or benzyl, and the chain or rings may be interrupted by one or more of O, S, N or Si, and optionally substituted by one or more of OR 1, SR 1, N(R 1) 2, COOR 1, CONHR 1, cyano, halo, 1-18C (per)fluoroalkyl and/or 3-11C cycloalkyl, aryl or heterocyclic, optionally substituted; each R 1hydrogen, 1-30C (per)fluoroalkyl, hydroxy and/or hydrofluoroalkyl, linear or branched, saturated or unsaturated. An independent claim is also included for a method of preparing (I) by reducing the corresponding ketone S-CO-R (II). [Image] ACTIVITY : Dermatological; Vulnerary. MECHANISM OF ACTION : (I) stimulate synthesis of glycosaminoglycans (GAG) that contain D-glucosamine and/or N-acetylglucosamine residues, especially hyaluronic acid (HA), and/or of proteoglycans by fibroblasts and keratinocytes. It also modulates the activity of growth factors and cytokines. HA synthesis in a culture of human fibroblasts was detected by incorporation of radiolabeled glucosamine. 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Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. C-beta -glycosides of formula (I) containing a hydroxy-substituted hydrocarbyl group and their pharmaceutically acceptable salts are new. Excluded are C-beta -glycopyranoside-2(S),3-dihydroxypropane and C-beta -D-(2-deoxyglycopyranoside)-2(S),3-dihydroxypropane. S : mono- or poly-saccharide of up to 20 sugar units as D series pyranose and/or furanose, including at least one free hydroxy and optionally one or more amino, optionally protected; R : 1-18C (perfluoro)alkyl or hydrofluoroalkyl, linear or branched, saturated or unsaturated, 3-11C cyclo(perfluoro)alkyl or cyclohydrofluoroalkyl, phenyl or benzyl, and the chain or rings may be interrupted by one or more of O, S, N or Si, and optionally substituted by one or more of OR 1, SR 1, N(R 1) 2, COOR 1, CONHR 1, cyano, halo, 1-18C (per)fluoroalkyl and/or 3-11C cycloalkyl, aryl or heterocyclic, optionally substituted; each R 1hydrogen, 1-30C (per)fluoroalkyl, hydroxy and/or hydrofluoroalkyl, linear or branched, saturated or unsaturated. An independent claim is also included for a method of preparing (I) by reducing the corresponding ketone S-CO-R (II). [Image] ACTIVITY : Dermatological; Vulnerary. MECHANISM OF ACTION : (I) stimulate synthesis of glycosaminoglycans (GAG) that contain D-glucosamine and/or N-acetylglucosamine residues, especially hyaluronic acid (HA), and/or of proteoglycans by fibroblasts and keratinocytes. It also modulates the activity of growth factors and cytokines. HA synthesis in a culture of human fibroblasts was detected by incorporation of radiolabeled glucosamine. The mean number of counts per minute (cpm) after 72 hours was 5010; compare 40770 (814 % of control) for a culture containing 3 mM C-beta -D-xylopyranoside-2(S)-hydroxypropane.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY DERIVATIVES THEREOF HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HYGIENE MEDICAL OR VETERINARY SCIENCE METALLURGY NUCLEIC ACIDS NUCLEOSIDES NUCLEOTIDES ORGANIC CHEMISTRY PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES SPECIFIC USE OF COSMETICS OR SIMILAR TOILETPREPARATIONS SUGARS |
title | New C-Glycoside derivatives and uses thereof |
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