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Structural Analogues of Homoeriodictyol as Flavor Modifiers. Part III: Short Chain Gingerdione Derivatives
In order to find new flavor modifiers, various short chain gingerdione derivatives were synthesized as structural analogues of the known bitter masker homoeriodictyol and evaluated by a sensory panel for masking and sweetness enhancing activities. 1-(4-Hydroxy-3-methoxyphenyl)hexa-3,5-dione ([2]-gin...
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Published in: | Journal of agricultural and food chemistry 2008-08, Vol.56 (15), p.6656-6664 |
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container_title | Journal of agricultural and food chemistry |
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creator | Ley, Jakob P. Paetz, Susanne Blings, Maria Hoffmann-Lücke, Petra Bertram, Heinz-Jürgen Krammer, Gerhard E. |
description | In order to find new flavor modifiers, various short chain gingerdione derivatives were synthesized as structural analogues of the known bitter masker homoeriodictyol and evaluated by a sensory panel for masking and sweetness enhancing activities. 1-(4-Hydroxy-3-methoxyphenyl)hexa-3,5-dione ([2]-gingerdione) and the homologue 1-(4-hydroxy-3-methoxyphenyl)hepta-3,5-dione ([3]-gingerdione) at concentration ranges 50−500 mg kg−1 showed the most promising masking activity of 20−30% against bitterness of a 500 mg kg−1 aqueous caffeine solution. Additionally, both compounds were able to reduce the bitterness of a 5 mg kg−1 quinine solution by about 20%; however, the bitter tastes of salicine, the model peptide H-Leu-Trp-OH, and KCl solutions were not reduced. Whereas for bitter masking activity a vanillyl moiety seems to be important, some of the tested isovanillyl isomers showed an interesting sweet enhancing effect without exhibiting a significant intrinsic sweetness. The isomer 1-(3-hydroxy-4-methoxyphenyl)hexa-3,5-dione ([2]-isogingerdione) at 100 mg kg−1 caused a significant and synergistic increase of 27% of sweet taste of a 5% sucrose solution. |
doi_str_mv | 10.1021/jf8006536 |
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Part III: Short Chain Gingerdione Derivatives</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Ley, Jakob P. ; Paetz, Susanne ; Blings, Maria ; Hoffmann-Lücke, Petra ; Bertram, Heinz-Jürgen ; Krammer, Gerhard E.</creator><creatorcontrib>Ley, Jakob P. ; Paetz, Susanne ; Blings, Maria ; Hoffmann-Lücke, Petra ; Bertram, Heinz-Jürgen ; Krammer, Gerhard E.</creatorcontrib><description>In order to find new flavor modifiers, various short chain gingerdione derivatives were synthesized as structural analogues of the known bitter masker homoeriodictyol and evaluated by a sensory panel for masking and sweetness enhancing activities. 1-(4-Hydroxy-3-methoxyphenyl)hexa-3,5-dione ([2]-gingerdione) and the homologue 1-(4-hydroxy-3-methoxyphenyl)hepta-3,5-dione ([3]-gingerdione) at concentration ranges 50−500 mg kg−1 showed the most promising masking activity of 20−30% against bitterness of a 500 mg kg−1 aqueous caffeine solution. Additionally, both compounds were able to reduce the bitterness of a 5 mg kg−1 quinine solution by about 20%; however, the bitter tastes of salicine, the model peptide H-Leu-Trp-OH, and KCl solutions were not reduced. Whereas for bitter masking activity a vanillyl moiety seems to be important, some of the tested isovanillyl isomers showed an interesting sweet enhancing effect without exhibiting a significant intrinsic sweetness. The isomer 1-(3-hydroxy-4-methoxyphenyl)hexa-3,5-dione ([2]-isogingerdione) at 100 mg kg−1 caused a significant and synergistic increase of 27% of sweet taste of a 5% sucrose solution.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf8006536</identifier><identifier>PMID: 18598048</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Benzyl Alcohols ; Biological and medical sciences ; bitter masking ; Caffeine ; Carbohydrates ; Confectionery products and chocolate industries, honey ; Flavones - chemistry ; Flavoring Agents - chemistry ; Flavoring Agents - pharmacology ; Flavors and Aromas/Chemosensory Perception ; Food industries ; Fundamental and applied biological sciences. Psychology ; gingerdiones ; Glucosides ; Guaiacol - analogs & derivatives ; Guaiacol - chemistry ; Guaiacol - pharmacology ; Quinine ; Structure-Activity Relationship ; sweet enhancing ; Taste - drug effects ; Taste modifying</subject><ispartof>Journal of agricultural and food chemistry, 2008-08, Vol.56 (15), p.6656-6664</ispartof><rights>Copyright © 2008 American Chemical Society</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-8fb1892abb6e34034ad614177713d18c17870cfe855eb2fb5d4e15feee87d8d63</citedby><cites>FETCH-LOGICAL-a381t-8fb1892abb6e34034ad614177713d18c17870cfe855eb2fb5d4e15feee87d8d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20577238$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18598048$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ley, Jakob P.</creatorcontrib><creatorcontrib>Paetz, Susanne</creatorcontrib><creatorcontrib>Blings, Maria</creatorcontrib><creatorcontrib>Hoffmann-Lücke, Petra</creatorcontrib><creatorcontrib>Bertram, Heinz-Jürgen</creatorcontrib><creatorcontrib>Krammer, Gerhard E.</creatorcontrib><title>Structural Analogues of Homoeriodictyol as Flavor Modifiers. Part III: Short Chain Gingerdione Derivatives</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>In order to find new flavor modifiers, various short chain gingerdione derivatives were synthesized as structural analogues of the known bitter masker homoeriodictyol and evaluated by a sensory panel for masking and sweetness enhancing activities. 1-(4-Hydroxy-3-methoxyphenyl)hexa-3,5-dione ([2]-gingerdione) and the homologue 1-(4-hydroxy-3-methoxyphenyl)hepta-3,5-dione ([3]-gingerdione) at concentration ranges 50−500 mg kg−1 showed the most promising masking activity of 20−30% against bitterness of a 500 mg kg−1 aqueous caffeine solution. Additionally, both compounds were able to reduce the bitterness of a 5 mg kg−1 quinine solution by about 20%; however, the bitter tastes of salicine, the model peptide H-Leu-Trp-OH, and KCl solutions were not reduced. Whereas for bitter masking activity a vanillyl moiety seems to be important, some of the tested isovanillyl isomers showed an interesting sweet enhancing effect without exhibiting a significant intrinsic sweetness. The isomer 1-(3-hydroxy-4-methoxyphenyl)hexa-3,5-dione ([2]-isogingerdione) at 100 mg kg−1 caused a significant and synergistic increase of 27% of sweet taste of a 5% sucrose solution.</description><subject>Benzyl Alcohols</subject><subject>Biological and medical sciences</subject><subject>bitter masking</subject><subject>Caffeine</subject><subject>Carbohydrates</subject><subject>Confectionery products and chocolate industries, honey</subject><subject>Flavones - chemistry</subject><subject>Flavoring Agents - chemistry</subject><subject>Flavoring Agents - pharmacology</subject><subject>Flavors and Aromas/Chemosensory Perception</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gingerdiones</subject><subject>Glucosides</subject><subject>Guaiacol - analogs & derivatives</subject><subject>Guaiacol - chemistry</subject><subject>Guaiacol - pharmacology</subject><subject>Quinine</subject><subject>Structure-Activity Relationship</subject><subject>sweet enhancing</subject><subject>Taste - drug effects</subject><subject>Taste modifying</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNpt0UFv0zAYBmALgVgZHPgDyBeQOGTYcRw73KbC2kpDVOq4cLG-OJ83lzTe7KRi_x5PrQoHTrb8PXplvybkLWcXnJX809Zpxmop6mdkxmXJCsm5fk5mLA8LLWt-Rl6ltGWMaanYS3LGtWw0q_SMbDdjnOw4Rejp5QB9uJ0w0eDoMuwCRh86b8fH0FNI9KqHfYj0Wz5zHmO6oGuII12tVp_p5i7k7fwO_EAXfrjF2PkwIP2SM_Yw-j2m1-SFgz7hm-N6Tn5cfb2ZL4vr74vV_PK6AKH5WGjXct2U0LY1ioqJCrqaV1wpxUXHteVKK2YdaimxLV0ruwq5dIioVae7WpyTD4fc-xge8mtGs_PJYt_DgGFKpm5EoxumM_x4gDaGlCI6cx_9DuKj4cw8FWtOxWb77hg6tTvs_spjkxm8PwJIFnoXYbA-nVzJpFKleHLFwfk04u_THOIvUyuhpLlZb8xaLcXi57Ix_-SCTWYbppg_Kf3ngn8AyoabHA</recordid><startdate>20080813</startdate><enddate>20080813</enddate><creator>Ley, Jakob P.</creator><creator>Paetz, Susanne</creator><creator>Blings, Maria</creator><creator>Hoffmann-Lücke, Petra</creator><creator>Bertram, Heinz-Jürgen</creator><creator>Krammer, Gerhard E.</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080813</creationdate><title>Structural Analogues of Homoeriodictyol as Flavor Modifiers. Part III: Short Chain Gingerdione Derivatives</title><author>Ley, Jakob P. ; Paetz, Susanne ; Blings, Maria ; Hoffmann-Lücke, Petra ; Bertram, Heinz-Jürgen ; Krammer, Gerhard E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-8fb1892abb6e34034ad614177713d18c17870cfe855eb2fb5d4e15feee87d8d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Benzyl Alcohols</topic><topic>Biological and medical sciences</topic><topic>bitter masking</topic><topic>Caffeine</topic><topic>Carbohydrates</topic><topic>Confectionery products and chocolate industries, honey</topic><topic>Flavones - chemistry</topic><topic>Flavoring Agents - chemistry</topic><topic>Flavoring Agents - pharmacology</topic><topic>Flavors and Aromas/Chemosensory Perception</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gingerdiones</topic><topic>Glucosides</topic><topic>Guaiacol - analogs & derivatives</topic><topic>Guaiacol - chemistry</topic><topic>Guaiacol - pharmacology</topic><topic>Quinine</topic><topic>Structure-Activity Relationship</topic><topic>sweet enhancing</topic><topic>Taste - drug effects</topic><topic>Taste modifying</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ley, Jakob P.</creatorcontrib><creatorcontrib>Paetz, Susanne</creatorcontrib><creatorcontrib>Blings, Maria</creatorcontrib><creatorcontrib>Hoffmann-Lücke, Petra</creatorcontrib><creatorcontrib>Bertram, Heinz-Jürgen</creatorcontrib><creatorcontrib>Krammer, Gerhard E.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ley, Jakob P.</au><au>Paetz, Susanne</au><au>Blings, Maria</au><au>Hoffmann-Lücke, Petra</au><au>Bertram, Heinz-Jürgen</au><au>Krammer, Gerhard E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural Analogues of Homoeriodictyol as Flavor Modifiers. Part III: Short Chain Gingerdione Derivatives</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2008-08-13</date><risdate>2008</risdate><volume>56</volume><issue>15</issue><spage>6656</spage><epage>6664</epage><pages>6656-6664</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>In order to find new flavor modifiers, various short chain gingerdione derivatives were synthesized as structural analogues of the known bitter masker homoeriodictyol and evaluated by a sensory panel for masking and sweetness enhancing activities. 1-(4-Hydroxy-3-methoxyphenyl)hexa-3,5-dione ([2]-gingerdione) and the homologue 1-(4-hydroxy-3-methoxyphenyl)hepta-3,5-dione ([3]-gingerdione) at concentration ranges 50−500 mg kg−1 showed the most promising masking activity of 20−30% against bitterness of a 500 mg kg−1 aqueous caffeine solution. Additionally, both compounds were able to reduce the bitterness of a 5 mg kg−1 quinine solution by about 20%; however, the bitter tastes of salicine, the model peptide H-Leu-Trp-OH, and KCl solutions were not reduced. Whereas for bitter masking activity a vanillyl moiety seems to be important, some of the tested isovanillyl isomers showed an interesting sweet enhancing effect without exhibiting a significant intrinsic sweetness. The isomer 1-(3-hydroxy-4-methoxyphenyl)hexa-3,5-dione ([2]-isogingerdione) at 100 mg kg−1 caused a significant and synergistic increase of 27% of sweet taste of a 5% sucrose solution.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>18598048</pmid><doi>10.1021/jf8006536</doi><tpages>9</tpages></addata></record> |
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subjects | Benzyl Alcohols Biological and medical sciences bitter masking Caffeine Carbohydrates Confectionery products and chocolate industries, honey Flavones - chemistry Flavoring Agents - chemistry Flavoring Agents - pharmacology Flavors and Aromas/Chemosensory Perception Food industries Fundamental and applied biological sciences. Psychology gingerdiones Glucosides Guaiacol - analogs & derivatives Guaiacol - chemistry Guaiacol - pharmacology Quinine Structure-Activity Relationship sweet enhancing Taste - drug effects Taste modifying |
title | Structural Analogues of Homoeriodictyol as Flavor Modifiers. Part III: Short Chain Gingerdione Derivatives |
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