JP2002543249A5 - - Google Patents
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- Publication number
- JP2002543249A5 JP2002543249A5 JP2000615663A JP2000615663A JP2002543249A5 JP 2002543249 A5 JP2002543249 A5 JP 2002543249A5 JP 2000615663 A JP2000615663 A JP 2000615663A JP 2000615663 A JP2000615663 A JP 2000615663A JP 2002543249 A5 JP2002543249 A5 JP 2002543249A5
- Authority
- JP
- Japan
- Prior art keywords
- formula
- derivative according
- cyclodextrin
- nhco
- represent
- 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
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical class O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 15
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 10
- 239000000126 substance Substances 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000003431 steroids Chemical class 0.000 description 3
- 0 *CC(C*(C1O)O)OC1O Chemical compound *CC(C*(C1O)O)OC1O 0.000 description 2
- 229920000858 Cyclodextrin Polymers 0.000 description 2
- 108010052285 Membrane Proteins Proteins 0.000 description 2
- 102000018697 Membrane Proteins Human genes 0.000 description 2
- 238000003800 Staudinger reaction Methods 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- IEYFRQLMJACEQY-UHFFFAOYSA-N 16-iodo-3-methylhexadecanoic acid Chemical compound OC(=O)CC(C)CCCCCCCCCCCCCI IEYFRQLMJACEQY-UHFFFAOYSA-N 0.000 description 1
- PLXMOAALOJOTIY-FPTXNFDTSA-N Aesculin Natural products OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1Oc2cc3C=CC(=O)Oc3cc2O PLXMOAALOJOTIY-FPTXNFDTSA-N 0.000 description 1
- WNBCMONIPIJTSB-BGNCJLHMSA-N Cichoriin Natural products O([C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1)c1c(O)cc2c(OC(=O)C=C2)c1 WNBCMONIPIJTSB-BGNCJLHMSA-N 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- 229960004853 betadex Drugs 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- 150000008050 dialkyl sulfates Chemical class 0.000 description 1
- -1 dothiepine Chemical compound 0.000 description 1
- XHCADAYNFIFUHF-TVKJYDDYSA-N esculin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(C(=C1)O)=CC2=C1OC(=O)C=C2 XHCADAYNFIFUHF-TVKJYDDYSA-N 0.000 description 1
- 229940093496 esculin Drugs 0.000 description 1
- AWRMZKLXZLNBBK-UHFFFAOYSA-N esculin Natural products OC1OC(COc2cc3C=CC(=O)Oc3cc2O)C(O)C(O)C1O AWRMZKLXZLNBBK-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR99/05460 | 1999-04-29 | ||
| FR9905460A FR2792942B1 (fr) | 1999-04-29 | 1999-04-29 | Cyclodextrines amphiphiles, leur preparation et leur utilisation pour solubiliser des systemes organises et incorporer des molecules hydrophobes |
| PCT/FR2000/001102 WO2000066635A1 (fr) | 1999-04-29 | 2000-04-26 | Cyclodextrines amphiphiles, leur preparation et leur utilisation pour solubiliser des systemes organises et incorporer des molecules hydrophobes |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002543249A JP2002543249A (ja) | 2002-12-17 |
| JP2002543249A5 true JP2002543249A5 (enExample) | 2011-02-17 |
| JP4698842B2 JP4698842B2 (ja) | 2011-06-08 |
Family
ID=9545038
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000615663A Expired - Fee Related JP4698842B2 (ja) | 1999-04-29 | 2000-04-26 | 両親媒性シクロデキストリン、組織的系を溶解して疎水性分子を組み込むための、前記シクロデキストリンの調製及び使用 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6858723B1 (enExample) |
| EP (1) | EP1177217B1 (enExample) |
| JP (1) | JP4698842B2 (enExample) |
| AT (1) | ATE279446T1 (enExample) |
| DE (1) | DE60014885T2 (enExample) |
| FR (1) | FR2792942B1 (enExample) |
| WO (1) | WO2000066635A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1543841A4 (en) * | 2002-08-15 | 2011-03-16 | Yunqing Liu | SOLID PHARMACEUTICAL NANO FORMULATION AND MANUFACTURING METHOD THEREFOR |
| KR20140070676A (ko) | 2002-09-06 | 2014-06-10 | 인설트 테라페틱스, 인코퍼레이티드 | 공유결합된 치료제 전달을 위한 사이클로덱스트린-기초 중합체 |
| FR2850972B1 (fr) * | 2003-02-07 | 2005-03-11 | Commissariat Energie Atomique | Derives de per(3,6-anhydro) cyclodextrines, leur preparation et leur utilisation pour vehiculer des elements metalliques vers des cibles biologiques ou pour decontaminer des cibles ou fluides biologiques |
| FR2861396B1 (fr) | 2003-10-24 | 2005-12-16 | Commissariat Energie Atomique | Derives amphiphiles de cyclodextrines,leur procede de preparation et leurs utilisations |
| BRPI0417593A (pt) * | 2003-12-18 | 2007-03-20 | Ciba Sc Holding Ag | derivados de polissacarìdeo reativo, sua preparação e seu uso |
| WO2006001844A2 (en) * | 2004-01-29 | 2006-01-05 | Pinnacle Pharmaceuticals | β-CYCLODEXTRIN DERIVATIVES AND THEIR USE AGAINST ANTHRAX LETHAL TOXIN |
| EP1846006A4 (en) * | 2005-01-28 | 2011-04-20 | Pinnacle Pharmaceuticals Inc | BETA-CYCLODEXTRIN DERIVATIVES AS ANTIBACTERIAL AGENTS |
| EP2023896B8 (en) | 2006-05-19 | 2016-09-14 | Viroblock SA | A composition for inactivating an enveloped virus |
| FR2907455A1 (fr) * | 2006-10-18 | 2008-04-25 | Commissariat Energie Atomique | Oligosaccharides cycliques,notamment derives de cyclodextrines amphiphiles,substitues par un ou plusieurs groupements polycycles naturels,tels que les triterpenoides. |
| JP2010516625A (ja) | 2007-01-24 | 2010-05-20 | インサート セラピューティクス， インコーポレイテッド | 制御された薬物送達のためのテザー基を有するポリマー−薬物コンジュゲート |
| FR2919872B1 (fr) * | 2007-08-10 | 2009-12-18 | Commissariat Energie Atomique | Derives de cyclodextrines |
| JP5364923B2 (ja) * | 2009-01-28 | 2013-12-11 | 学校法人福岡大学 | 多機能性シクロデキストリン誘導体、その包接化合物およびそれらの製造方法。 |
| WO2014055493A1 (en) | 2012-10-02 | 2014-04-10 | Cerulean Pharma Inc. | Methods and systems for polymer precipitation and generation of particles |
| WO2014058438A1 (en) * | 2012-10-12 | 2014-04-17 | Empire Technology Development Llc | Paints and coatings containing cyclodextrin additives |
| CN105392804B (zh) | 2013-08-09 | 2018-07-10 | 生物辐射实验室股份有限公司 | 采用修饰的环糊精的蛋白质检测 |
| TW202009013A (zh) * | 2018-08-14 | 2020-03-01 | 優你康光學股份有限公司 | 具有功能性成分的隱形眼鏡及其產品 |
| US20220362401A1 (en) * | 2019-09-20 | 2022-11-17 | The University Of Kitakyushu | Particles, method for producing particles, drug, method for producing drug, and anti-cancer agent |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2681868A1 (fr) * | 1991-09-30 | 1993-04-02 | Sederma Sa | Nouvelles substances amphiphiles derivees de cyclodextrines et leur utilisation dans des compositions cosmetiques. |
| FR2726765B1 (fr) | 1994-11-14 | 1996-12-20 | Cis Bio Int | Compositions radiopharmaceutiques comprenant un complexe d'inclusion d'une cyclodextrine et d'un acide gras radiohalogene |
| FR2736056B1 (fr) * | 1995-06-29 | 1997-08-08 | Commissariat Energie Atomique | Derives de cyclodextrines, leur preparation et leur utilisation pour incorporer des molecules hydrophobes dans des systemes de tensioactifs organises |
| AU2002241823A1 (en) * | 2001-01-11 | 2002-07-24 | Eastman Chemical Company | Cyclodextrin sulfonates, guest inclusion complexes, methods of making the same and related materials |
-
1999
- 1999-04-29 FR FR9905460A patent/FR2792942B1/fr not_active Expired - Fee Related
-
2000
- 2000-04-26 US US09/926,413 patent/US6858723B1/en not_active Expired - Fee Related
- 2000-04-26 EP EP00922751A patent/EP1177217B1/fr not_active Expired - Lifetime
- 2000-04-26 DE DE60014885T patent/DE60014885T2/de not_active Expired - Lifetime
- 2000-04-26 WO PCT/FR2000/001102 patent/WO2000066635A1/fr not_active Ceased
- 2000-04-26 AT AT00922751T patent/ATE279446T1/de not_active IP Right Cessation
- 2000-04-26 JP JP2000615663A patent/JP4698842B2/ja not_active Expired - Fee Related
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