JP2010522700A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2010522700A5 JP2010522700A5 JP2010500048A JP2010500048A JP2010522700A5 JP 2010522700 A5 JP2010522700 A5 JP 2010522700A5 JP 2010500048 A JP2010500048 A JP 2010500048A JP 2010500048 A JP2010500048 A JP 2010500048A JP 2010522700 A5 JP2010522700 A5 JP 2010522700A5
- Authority
- JP
- Japan
- Prior art keywords
- acid
- methyl
- methylspiro
- cyclopropyl
- heptane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 2,2,6-trimethylcyclohexyl Chemical group 0.000 claims 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 6
- 230000000903 blocking Effects 0.000 claims 4
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butanoic acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- VTCRWXGVGZLALO-UHFFFAOYSA-N 1-methyl-2-[(1,2,2-trimethyl-3-bicyclo[3.1.0]hexanyl)methyl]cyclopropane-1-carboxylic acid Chemical compound OC(=O)C1(C)CC1CC1C(C)(C)C2(C)CC2C1 VTCRWXGVGZLALO-UHFFFAOYSA-N 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- RERQSUBOVZBXHE-VOTSOKGWSA-N (E)-3-[1-(2,2,3-trimethylcyclopent-3-en-1-yl)cyclopropyl]prop-2-enoic acid Chemical compound CC1(C)C(C)=CCC1C1(\C=C\C(O)=O)CC1 RERQSUBOVZBXHE-VOTSOKGWSA-N 0.000 claims 1
- VCCJRCPLNWXPON-NSCUHMNNSA-N (E)-4-(1-methyl-2-bicyclo[3.1.0]hexanyl)but-3-enoic acid Chemical compound C1CC(\C=C\CC(O)=O)C2(C)C1C2 VCCJRCPLNWXPON-NSCUHMNNSA-N 0.000 claims 1
- JDSGMYDTHXDPSJ-GQCTYLIASA-N (E)-4-(2,2,3-trimethylcyclopentyl)but-2-enoic acid Chemical compound CC1CCC(C\C=C\C(O)=O)C1(C)C JDSGMYDTHXDPSJ-GQCTYLIASA-N 0.000 claims 1
- UBOAGQFOYPWMRQ-SNAWJCMRSA-N (E)-4-(2,2,3-trimethylcyclopentyl)but-3-enoic acid Chemical compound CC1CCC(\C=C\CC(O)=O)C1(C)C UBOAGQFOYPWMRQ-SNAWJCMRSA-N 0.000 claims 1
- FSYYIWKNWSLCDN-DUXPYHPUSA-N (E)-4-(4-methylspiro[2.4]heptan-7-yl)but-2-enoic acid Chemical compound CC1CCC(C\C=C\C(O)=O)C11CC1 FSYYIWKNWSLCDN-DUXPYHPUSA-N 0.000 claims 1
- RNTNQSXSWNVYGY-NSCUHMNNSA-N (E)-4-(4-methylspiro[2.4]heptan-7-yl)but-3-enoic acid Chemical compound CC1CCC(\C=C\CC(O)=O)C11CC1 RNTNQSXSWNVYGY-NSCUHMNNSA-N 0.000 claims 1
- SPCQQNDKLJFBNA-DUXPYHPUSA-N (E)-4-(7-methylspiro[2.4]hept-6-en-4-yl)but-2-enoic acid Chemical compound CC1=CCC(C\C=C\C(O)=O)C11CC1 SPCQQNDKLJFBNA-DUXPYHPUSA-N 0.000 claims 1
- DXSRHFVZAUTTBE-XVNBXDOJSA-N (E)-4-(8-methylspiro[2.5]oct-7-en-4-yl)but-2-enoic acid Chemical compound CC1=CCCC(C\C=C\C(O)=O)C11CC1 DXSRHFVZAUTTBE-XVNBXDOJSA-N 0.000 claims 1
- HZLWXBYPIARCGW-SNAWJCMRSA-N 1-[(E)-2-(1-methyl-2-bicyclo[3.1.0]hexanyl)ethenyl]cyclopropane-1-carboxylic acid Chemical compound CC12CC1CCC2\C=C\C1(C(O)=O)CC1 HZLWXBYPIARCGW-SNAWJCMRSA-N 0.000 claims 1
- JKSQXNOUOSUVNZ-SNAWJCMRSA-N 1-[(E)-2-(4-methylspiro[2.4]heptan-7-yl)ethenyl]cyclopropane-1-carboxylic acid Chemical compound C1CC11C(C)CCC1\C=C\C1(C(O)=O)CC1 JKSQXNOUOSUVNZ-SNAWJCMRSA-N 0.000 claims 1
- MMEKRTLZYPFBNP-UHFFFAOYSA-N 1-[2-(4-methylspiro[2.4]heptan-7-yl)ethyl]cyclopropane-1-carboxylic acid Chemical compound C1CC11C(C)CCC1CCC1(C(O)=O)CC1 MMEKRTLZYPFBNP-UHFFFAOYSA-N 0.000 claims 1
- VQBSGHGICMYQGM-UHFFFAOYSA-N 2,2-dimethyl-4-(2,2,3-trimethylcyclopentyl)butanoic acid Chemical compound CC1CCC(CCC(C)(C)C(O)=O)C1(C)C VQBSGHGICMYQGM-UHFFFAOYSA-N 0.000 claims 1
- NDLNYVBNKQVKIM-UHFFFAOYSA-N 2-(3,4-dimethylcyclohexyl)acetic acid Chemical compound CC1CCC(CC(O)=O)CC1C NDLNYVBNKQVKIM-UHFFFAOYSA-N 0.000 claims 1
- MLHVLSFCLWASNP-UHFFFAOYSA-N 2-[(1,4-dimethyl-2-bicyclo[3.1.0]hexanyl)methyl]-1-methylcyclopropane-1-carboxylic acid Chemical compound CC12CC1C(C)CC2CC1CC1(C)C(O)=O MLHVLSFCLWASNP-UHFFFAOYSA-N 0.000 claims 1
- DNSDREPILBQXKN-UHFFFAOYSA-N 2-[(4,5-dimethylspiro[2.4]heptan-7-yl)methyl]-1-methylcyclopropane-1-carboxylic acid Chemical compound C1CC21C(C)C(C)CC2CC1CC1(C)C(O)=O DNSDREPILBQXKN-UHFFFAOYSA-N 0.000 claims 1
- VRFZBVPLWNHCKL-UHFFFAOYSA-N 2-[1-[(1,4-dimethyl-2-bicyclo[3.1.0]hexanyl)methyl]cyclopropyl]propanoic acid Chemical compound C1C(C)C2CC2(C)C1CC1(C(C(O)=O)C)CC1 VRFZBVPLWNHCKL-UHFFFAOYSA-N 0.000 claims 1
- RZFCTOIYOWTBPT-UHFFFAOYSA-N 2-[1-[(1-methyl-2-bicyclo[3.1.0]hexanyl)methyl]cyclopropyl]acetic acid Chemical compound CC12CC1CCC2CC1(CC(O)=O)CC1 RZFCTOIYOWTBPT-UHFFFAOYSA-N 0.000 claims 1
- CXYZORLHNHLYAH-UHFFFAOYSA-N 3,3-dimethyl-4-(2,2,3-trimethylcyclopentyl)butanoic acid Chemical compound CC1CCC(CC(C)(C)CC(O)=O)C1(C)C CXYZORLHNHLYAH-UHFFFAOYSA-N 0.000 claims 1
- QTALZWUULKHVTK-UHFFFAOYSA-N 3-(2,2,6-trimethylcyclohexyl)propanoic acid Chemical compound CC1CCCC(C)(C)C1CCC(O)=O QTALZWUULKHVTK-UHFFFAOYSA-N 0.000 claims 1
- IZZFEHBOGAIUMT-UHFFFAOYSA-N 4-(1-methyl-2-bicyclo[3.1.0]hexanyl)butanoic acid Chemical compound C1CC(CCCC(O)=O)C2(C)C1C2 IZZFEHBOGAIUMT-UHFFFAOYSA-N 0.000 claims 1
- YRIPPWABYROTJJ-UHFFFAOYSA-N 4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enoic acid Chemical compound CC1=CCC(CC=CC(O)=O)C1(C)C YRIPPWABYROTJJ-UHFFFAOYSA-N 0.000 claims 1
- LYFXCRCUENNESS-UHFFFAOYSA-N 4-(2,2,3-trimethylcyclopentyl)butanoic acid Chemical compound CC1CCC(CCCC(O)=O)C1(C)C LYFXCRCUENNESS-UHFFFAOYSA-N 0.000 claims 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N Crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 1
- 239000001274 FEMA 4529 Substances 0.000 claims 1
- 239000002304 perfume Substances 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- 241000894007 species Species 0.000 claims 1
Claims (3)
- 4−(2,2,3−トリメチルシクロペンタ−3−エニル)ブタ−2−エン酸、4−(2,2,3−トリメチルシクロペンチル)ブタン酸、4−(2,2,6−トリメチルシクロヘキシル)ブタン酸、3−(2,2,6−トリメチルシクロヘキシル)プロパン酸、2−(3,4−ジメチルシクロヘキシル)酢酸、2−メチル−4−(2,6,6−トリメチルシクロヘキサ−2−エニル)ブタン酸、1−メチル−2−((1,2,2−トリメチルビシクロ[3.1.0]ヘキサン−3−イル)メチル)シクロプロパンカルボン酸;
(E)−3−(1−(2,2,3−トリメチルシクロペンタ−3−エニル)シクロプロピル)アクリル酸、(E)−4−(2,2,3−トリメチルシクロヘキサ−3−エニル)ブタ−2−エン酸、(E)−4−(2,2,3−トリメチルシクロペンチル)ブタ−3−エン酸、(E)−4−(2,2,3−トリメチルシクロペンチル)ブタ−2−エン酸、1−メチル−2−((1,2,2−トリメチルビシクロ[3.1.0]ヘキサン−3−イル)メチル)シクロプロパンカルボン酸、2,2−ジメチル−4−(2,2,3−トリメチルシクロペンチル)ブタン酸、2−((1,4−ジメチルビシクロ[3.1.0]ヘキサン−2−イル)メチル)−1−メチルシクロプロパンカルボン酸、2−(1−((1,2,2−トリメチルビシクロ[3.1.0]ヘキサン−3−イル)メチル)シクロプロピル)プロパン酸、2−(1−((1−メチルビシクロ[3.1.0]ヘキサン−2−イル)メチル)シクロプロピル)酢酸、3,3−ジメチル−4−(2,2,3−トリメチルシクロペンチル)ブタン酸、4−(1−メチルビシクロ[3.1.0]ヘキサン−2−イル)ブタン酸、(E)−1−(2−(1−メチルビシクロ[3.1.0]ヘキサン−2−イル)ビニル)シクロプロパンカルボン酸、(E)−1−(2−(7−メチルスピロ[2.4]ヘプタン−4−イル)ビニル)シクロプロパンカルボン酸、(E)−4−(1−メチルビシクロ[3.1.0]ヘキサン−2−イル)ブタ−3−エン酸、(E)−4−(7−メチルスピロ[2.4]ヘプタ−6−エン−4−イル)ブタ−2−エン酸、(E)−4−(7−メチルスピロ[2.4]ヘプタン−4−イル)ブタ−3−エン酸、(E)−4−(7−メチルスピロ[2.4]ヘプタン−4−イル)ブタ−2−エン酸、(E)−4−(8−メチルスピロ[2.5]オクタ−7−エン−4−イル)ブタ−2−エン酸、1−(2−(7−メチルスピロ[2.4]ヘプタン−4−イル)エチル)シクロプロパンカルボン酸、2−((6,7−ジメチルスピロ[2.4]ヘプタン−4−イル)メチル)−1−メチルシクロプロパンカルボン酸、2−(1−((1,4−ジメチルビシクロ[3.1.0]ヘキサン−2−イル)メチル)シクロプロピル)プロパン酸、2−(1−((1−メチルビシクロ[3.1.0]ヘキサン−2−イル)メチル)シクロプロピル)酢酸、2−(1−((7−メチルスピロ[2.4]ヘプタン−4−イル)メチル)シクロプロピル)酢酸、および4−(7−メチルスピロ[2.4]ヘプタン−4−イル)ブタン酸のうち、1種または2種以上から選択されるオフノ−ト遮断化合物。 - オフノート付与消耗品成分および請求項1に記載の1種または2種以上のオフノート遮断化合物を含む香料組成物。
- (a)オフノートを付与するために十分な濃度における1種または2種以上のオフノート付与成分、および(b)請求項1に記載された1種または2種以上のオフノート遮断化合物、を消耗品と混合することを含む、消耗品におけるオフノートを遮断する方法。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US90914307P | 2007-03-30 | 2007-03-30 | |
US60/909,143 | 2007-03-30 | ||
US96251507P | 2007-07-30 | 2007-07-30 | |
US60/962,515 | 2007-07-30 | ||
PCT/CH2008/000135 WO2008119196A1 (en) | 2007-03-30 | 2008-03-27 | Off-note blocking sensory organic compounds |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2010522700A JP2010522700A (ja) | 2010-07-08 |
JP2010522700A5 true JP2010522700A5 (ja) | 2011-05-12 |
JP5442595B2 JP5442595B2 (ja) | 2014-03-12 |
Family
ID=39580609
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2010500048A Active JP5442595B2 (ja) | 2007-03-30 | 2008-03-27 | オフノ−トを遮断する官能有機化合物 |
Country Status (6)
Country | Link |
---|---|
US (2) | US8409649B2 (ja) |
EP (1) | EP2139841B1 (ja) |
JP (1) | JP5442595B2 (ja) |
AT (1) | ATE555670T1 (ja) |
BR (1) | BRPI0809856B1 (ja) |
WO (1) | WO2008119196A1 (ja) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8546085B2 (en) | 2008-06-13 | 2013-10-01 | Givaudan Sa | Methods of identifying modulators of the bitter taste receptor TAS2R44 |
WO2010015097A1 (en) * | 2008-08-07 | 2010-02-11 | Givaudan Sa | Methods to identify modulators of the interaction between dextromethorphan and the bitter taste receptor tas2r46 |
US8329239B2 (en) * | 2009-03-03 | 2012-12-11 | Givandan S.A. | Off-taste masking |
JP6068330B2 (ja) | 2010-04-15 | 2017-01-25 | クロモセル コーポレーション | 苦味を低減または排除する化合物、組成物、および方法 |
CN103429098B (zh) * | 2011-03-14 | 2016-08-31 | 奇华顿股份有限公司 | 异味掩蔽 |
JP5883599B2 (ja) * | 2011-09-20 | 2016-03-15 | 花王株式会社 | カテキン類の苦味抑制剤の評価又は選択方法 |
RU2614776C2 (ru) | 2011-10-20 | 2017-03-29 | Хромоселл Корпорейшн | Соединения, композиции и способы для снижения или устранения горького вкуса |
JP6122858B2 (ja) | 2011-10-20 | 2017-04-26 | クロモセル コーポレーション | 苦味を調整する化合物を同定するための検定 |
WO2013072332A1 (en) | 2011-11-14 | 2013-05-23 | Givaudan Sa | Methods of using antagonists of bitter taste receptors |
US10798961B2 (en) * | 2013-03-15 | 2020-10-13 | Altria Client Services Llc | Functional food and beverage compositions with improved taste through the use of sensates |
WO2014150967A1 (en) | 2013-03-15 | 2014-09-25 | Altria Client Services Inc. | Oral energy products including encapsulated caffeine |
CA2910161A1 (en) | 2013-04-24 | 2014-10-30 | Chromocell Corporation | Assays for identifying compounds that modulate bitter taste |
US10407378B2 (en) * | 2014-04-21 | 2019-09-10 | Takasago International Corporation | Compound, and flavor and/or fragrance composition containing said compound |
CN105801636A (zh) * | 2016-03-24 | 2016-07-27 | 济南诚汇双达化工有限公司 | 一种柚皮苷二氢查尔酮的合成方法 |
WO2021214008A1 (en) | 2020-04-20 | 2021-10-28 | Givaudan Sa | Compositions |
CN113056202A (zh) | 2018-09-20 | 2021-06-29 | 贝特尔肉制品公司 | 用于生产可食用的真菌菌丝体共混肉和肉类似物组合物的增强的好氧发酵方法 |
CN109588688A (zh) * | 2019-01-22 | 2019-04-09 | 中国计量大学 | 一种采用山梨酸钾控制酱油中生物胺含量的方法 |
PL240449B1 (pl) * | 2019-05-06 | 2022-04-04 | Univ Medyczny Im Piastow Slaskich We Wroclawiu | Pochodna terpenoidowa do zastosowania w chemoprewencji i wspomaganiu chemioterapii nowotworów |
GB202007984D0 (en) | 2020-05-28 | 2020-07-15 | Givaudan Sa | Compositions |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1982003216A1 (fr) * | 1981-03-13 | 1982-09-30 | Baudin Josiane | Nouveaux composes odoriferants |
DE3278403D1 (en) * | 1981-09-09 | 1988-06-01 | Givaudan & Cie Sa | Perfuming and/or flavouring compositions containing unsaturated acids |
JPS60109537A (ja) | 1983-11-18 | 1985-06-15 | T Hasegawa Co Ltd | シクロペンテン誘導体 |
US20020004092A1 (en) * | 2000-02-02 | 2002-01-10 | Riha William E. | Low calorie beverages containing high intensity sweeteners and arabinogalactan |
WO2002080704A1 (en) * | 2001-04-03 | 2002-10-17 | Michigan Biotechnology Institute | Composition for improving the taste and sweetness profile of beverages having intense sweeteners |
EP2267130A3 (en) | 2002-09-25 | 2011-08-03 | Deutsches Institut für Ernährungsforschung Potsdam-Rehbrücke | Bitter taste receptors |
US7632531B2 (en) * | 2003-04-11 | 2009-12-15 | International Flavors & Fragnances Inc. | Alkyldienamides exhibiting taste and sensory effect in flavor compositions |
US20060024335A1 (en) * | 2004-07-29 | 2006-02-02 | Roger Stier E | Oral compositions which mask the bitter taste of a bitter-tasting agent |
US8367137B2 (en) * | 2005-11-23 | 2013-02-05 | The Coca-Cola Company | High-potency sweetener composition with fatty acid and compositions sweetened therewith |
-
2008
- 2008-03-27 EP EP08714785A patent/EP2139841B1/en active Active
- 2008-03-27 US US12/593,114 patent/US8409649B2/en active Active
- 2008-03-27 WO PCT/CH2008/000135 patent/WO2008119196A1/en active Application Filing
- 2008-03-27 AT AT08714785T patent/ATE555670T1/de active
- 2008-03-27 JP JP2010500048A patent/JP5442595B2/ja active Active
- 2008-03-27 BR BRPI0809856A patent/BRPI0809856B1/pt active IP Right Grant
-
2013
- 2013-03-29 US US13/853,575 patent/US9451784B2/en active Active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2010522700A5 (ja) | ||
RU2470910C9 (ru) | Соединения, представляющие собой алкинилфенильные производные, для лечения офтальмических заболеваний и расстройств | |
JP2009530282A5 (ja) | ||
JP2011502276A5 (ja) | ||
JP2003526724A5 (ja) | ||
CN1749240A (zh) | 作为加香成分的腈衍生物 | |
JP2009504793A5 (ja) | ||
JP2004505989A5 (ja) | ||
MX355214B (es) | Composiciones que contrarrestan el mal olor (moc). | |
JP2018522581A5 (ja) | ||
ATE488499T1 (de) | Phenoxypyrrolidinderivat, seine verwendung sowie zusammensetzungen daraus | |
JP2015508097A5 (ja) | ||
JP2004509955A5 (ja) | ||
JP2010510232A5 (ja) | ||
JP2010537991A5 (ja) | ||
JP2015536965A5 (ja) | ||
CN1250437A (zh) | 环烷基链烷羧酰胺及其制备和应用 | |
JP2019507176A5 (ja) | ||
JP2014502964A5 (ja) | 2−(アルコキシまたはアルコキシカルボニル)−4−メチル−6−(2,6,6−トリメチルシクロヘキサ−1エニル)ヘキサ−2−エン酸化合物、その調製およびその使用 | |
AR035990A1 (es) | Compuestos intermediarios y metodo para preparar cis-1-{2-[4-(6-metoxi-2-fenil-1,2,3,4-tetrahidronaftalen-1-il)fenoxi]etil}pirrolidina | |
WO2007146768A3 (en) | Compounds for the treatment of metabolic disorders | |
JP2007508392A5 (ja) | ||
JP2019532123A5 (ja) | ||
JP2012031382A5 (ja) | ||
JP6675875B2 (ja) | 含フッ素化合物の製造方法 |