JP2008520630A5 - - Google Patents
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- JP2008520630A5 JP2008520630A5 JP2007541980A JP2007541980A JP2008520630A5 JP 2008520630 A5 JP2008520630 A5 JP 2008520630A5 JP 2007541980 A JP2007541980 A JP 2007541980A JP 2007541980 A JP2007541980 A JP 2007541980A JP 2008520630 A5 JP2008520630 A5 JP 2008520630A5
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- groups
- alkyl
- alkenyl group
- formulation
- 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.)
- Pending
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- 239000000203 mixture Substances 0.000 claims 11
- 125000003342 alkenyl group Chemical group 0.000 claims 10
- 125000004432 carbon atom Chemical group C* 0.000 claims 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 9
- 238000009472 formulation Methods 0.000 claims 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 7
- 229940106189 ceramide Drugs 0.000 claims 4
- WTVHAMTYZJGJLJ-UHFFFAOYSA-N (+)-(4S,8R)-8-epi-beta-bisabolol Natural products CC(C)=CCCC(C)C1(O)CCC(C)=CC1 WTVHAMTYZJGJLJ-UHFFFAOYSA-N 0.000 claims 3
- RGZSQWQPBWRIAQ-CABCVRRESA-N (-)-alpha-Bisabolol Chemical compound CC(C)=CCC[C@](C)(O)[C@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-CABCVRRESA-N 0.000 claims 3
- -1 2-hydroxypropyl Chemical group 0.000 claims 3
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 3
- RGZSQWQPBWRIAQ-LSDHHAIUSA-N alpha-Bisabolol Natural products CC(C)=CCC[C@@](C)(O)[C@@H]1CCC(C)=CC1 RGZSQWQPBWRIAQ-LSDHHAIUSA-N 0.000 claims 3
- 229940036350 bisabolol Drugs 0.000 claims 3
- HHGZABIIYIWLGA-UHFFFAOYSA-N bisabolol Natural products CC1CCC(C(C)(O)CCC=C(C)C)CC1 HHGZABIIYIWLGA-UHFFFAOYSA-N 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
- 230000004888 barrier function Effects 0.000 claims 2
- 150000001783 ceramides Chemical class 0.000 claims 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims 2
- 239000002537 cosmetic Substances 0.000 claims 2
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 claims 2
- 125000001419 myristoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
- HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 claims 1
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims 1
- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 claims 1
- CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 claims 1
- 235000021314 Palmitic acid Nutrition 0.000 claims 1
- 235000021355 Stearic acid Nutrition 0.000 claims 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 claims 1
- 239000004473 Threonine Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000004442 acylamino group Chemical group 0.000 claims 1
- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 claims 1
- 235000012000 cholesterol Nutrition 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- 230000002708 enhancing effect Effects 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 claims 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 235000002378 plant sterols Nutrition 0.000 claims 1
- 239000008117 stearic acid Substances 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63043304P | 2004-11-22 | 2004-11-22 | |
| PCT/EP2005/056156 WO2006053912A1 (en) | 2004-11-22 | 2005-11-22 | Formulations comprising ceramides and/or pseudoceramides and (alpha-)bisabolol for combating skin damage |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008520630A JP2008520630A (ja) | 2008-06-19 |
| JP2008520630A5 true JP2008520630A5 (enExample) | 2009-01-15 |
Family
ID=35874368
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007541980A Pending JP2008520630A (ja) | 2004-11-22 | 2005-11-22 | 皮膚損傷に有効なセラミド及び/又は偽セラミドと(α−)ビサボロールを含む製剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20100286102A1 (enExample) |
| EP (1) | EP1816998B1 (enExample) |
| JP (1) | JP2008520630A (enExample) |
| AT (1) | ATE425732T1 (enExample) |
| DE (1) | DE602005013422D1 (enExample) |
| ES (1) | ES2321218T3 (enExample) |
| WO (1) | WO2006053912A1 (enExample) |
Families Citing this family (83)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP5191991B2 (ja) * | 2006-10-13 | 2013-05-08 | エヴォニク ゴールドシュミット ゲーエムベーハー | 皮膚処置組成物 |
| EA025328B1 (ru) | 2007-04-19 | 2016-12-30 | Мэри Кэй Инк. | Способ увеличения упругости кожи или уменьшения ее дряблости в области вокруг глаз |
| US9241893B2 (en) | 2007-11-19 | 2016-01-26 | Stiefel Laboratories, Inc. | Topical cosmetic skin lightening compositions and methods of use thereof |
| US9364424B2 (en) | 2007-11-19 | 2016-06-14 | Stiefel Laboratories, Inc. | Topical cosmetic skin lightening compositions and methods of use thereof |
| JP2009221110A (ja) * | 2008-03-13 | 2009-10-01 | Shiseido Co Ltd | 基底膜安定化剤 |
| KR101018818B1 (ko) | 2008-07-11 | 2011-03-04 | (주)아모레퍼시픽 | 유사지질 복합체 및 이를 함유하는 피부 외용제 조성물 |
| EP2317981B1 (en) * | 2008-07-24 | 2013-11-13 | Amorepacific Corporation | Multi-layered lamellar granule and skin external application composition containing same |
| US10463891B2 (en) | 2008-09-30 | 2019-11-05 | Symrise Ag | Extracts of Isochrysis sp. |
| MX2010005549A (es) * | 2008-11-19 | 2010-08-16 | Stiefel Laboratories | Composiciones cosmeticas topicas para aclaracion de la piel y metodos de uso de las mismas. |
| EP3348255B1 (en) | 2008-12-05 | 2021-11-10 | Symrise AG | Extracts of tetraselmis sp. for cosmetic and therapeutic purposes |
| KR101676375B1 (ko) | 2009-04-09 | 2016-11-15 | 시므라이즈 아게 | 피부 자극-완화제로서 트랜스-텔트-부틸 사이클로헥사놀을 포함하는 조성물 |
| BRPI0924661B1 (pt) | 2009-04-28 | 2018-12-11 | Symrise Ag | Ômega-ciclo-hexilalcan-1-óis, seus métodos de produção, suas composições, suas formulações cosméticas, uso dos mesmos como ativos microbianos e método parareduzir a taxa de crescimento de corynebacterium xerosis e/ou staphylococcus epidermidis e/ou brevibacterium epidermidis |
| EP2295031B1 (de) | 2009-08-05 | 2018-01-10 | Symrise AG | Verwendung von Pterocarpanen als Anti-Cellulite-Wirkstoffe |
| KR101443927B1 (ko) * | 2009-08-20 | 2014-09-25 | (주)아모레퍼시픽 | 헥사미딘류 및 레티노이드류를 함유하는 피부 개선 조성물 |
| ES2547309T3 (es) | 2009-10-19 | 2015-10-05 | Symrise Ag | Composiciones que contienen fragancias, que comprenden nonanoato de cetilo y/o nonanoato de estearilo |
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| CN106687100B (zh) * | 2014-09-12 | 2020-09-04 | 宝洁公司 | 用于抑制黑素合成的化妆品组合物和方法 |
| EP3206659B1 (en) * | 2014-10-17 | 2019-12-25 | DSM IP Assets B.V. | Use of a cosmetic composition comprising 10-hydroxystearic acid |
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| CN107405305B (zh) * | 2015-01-20 | 2020-12-25 | 泰特拉德姆集团有限责任公司 | 提供粘膜和皮肤屏障恢复的通用局部药物递送载体和多因子组织保湿剂 |
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| JP2023158912A (ja) * | 2022-04-19 | 2023-10-31 | 小林製薬株式会社 | タイトジャンクション形成促進用組成物 |
| CN116035944B (zh) * | 2022-12-29 | 2023-09-22 | 植然天成(北京)生物科技有限公司 | 一种仿生胎脂组合物、化妆品及其制备方法 |
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|---|---|---|---|---|
| EP0644764B1 (en) | 1992-06-19 | 2000-05-17 | The Regents of the University of California | Lipids for epidermal moisturization and repair of barrier function |
| US5391373A (en) * | 1992-07-01 | 1995-02-21 | Chanel, Inc. | Skin cream composition |
| FR2725622A1 (fr) * | 1994-10-14 | 1996-04-19 | Fabre Pierre Dermo Cosmetique | Ceramide greffee anti-elastase |
| US6060612A (en) * | 1996-12-26 | 2000-05-09 | Pacific Corporation | Ceramide-like compounds and a method for preparation thereof, and a cosmetic composition containing the same |
| DE19710612A1 (de) * | 1997-03-14 | 1998-09-17 | Haarmann & Reimer Gmbh | N-Acyl-hydroxyaminosäureester und ihre Verwendung |
| US6335388B1 (en) * | 1997-10-03 | 2002-01-01 | Lavipharm Laboratories Inc. | Prolamine-plant polar lipid composition, its method of preparation and applications thereof |
| US5882665A (en) * | 1997-11-18 | 1999-03-16 | Elizabeth Arden Co., Division Of Conopco, Inc. | Phytosphingosine salicylates in cosmetic compositions |
| JP2003063942A (ja) * | 2001-08-27 | 2003-03-05 | Kose Corp | 皮膚外用剤 |
| US6495123B1 (en) * | 2001-09-12 | 2002-12-17 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Cosmetic composition with organic sunscreen and porous powder particles |
| GB0205504D0 (en) * | 2002-03-08 | 2002-04-24 | Accantia Holdings Ltd | Formulation |
| US7235250B2 (en) * | 2002-10-17 | 2007-06-26 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Personal care towelette article |
-
2005
- 2005-11-22 JP JP2007541980A patent/JP2008520630A/ja active Pending
- 2005-11-22 EP EP05823823A patent/EP1816998B1/en not_active Expired - Lifetime
- 2005-11-22 ES ES05823823T patent/ES2321218T3/es not_active Expired - Lifetime
- 2005-11-22 DE DE602005013422T patent/DE602005013422D1/de not_active Expired - Lifetime
- 2005-11-22 US US11/719,800 patent/US20100286102A1/en not_active Abandoned
- 2005-11-22 AT AT05823823T patent/ATE425732T1/de not_active IP Right Cessation
- 2005-11-22 WO PCT/EP2005/056156 patent/WO2006053912A1/en not_active Ceased
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