JP2001525340A5 - - Google Patents
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- Publication number
- JP2001525340A5 JP2001525340A5 JP2000523249A JP2000523249A JP2001525340A5 JP 2001525340 A5 JP2001525340 A5 JP 2001525340A5 JP 2000523249 A JP2000523249 A JP 2000523249A JP 2000523249 A JP2000523249 A JP 2000523249A JP 2001525340 A5 JP2001525340 A5 JP 2001525340A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- general formula
- combination
- azide
- individually
- 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
- 125000000217 alkyl group Chemical group 0.000 description 21
- 0 CCC(C)(C)N(*)C(C)(*)* Chemical compound CCC(C)(C)N(*)C(C)(*)* 0.000 description 13
- 150000001540 azides Chemical class 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 10
- 150000001412 amines Chemical class 0.000 description 9
- 150000008064 anhydrides Chemical class 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 9
- 238000007254 oxidation reaction Methods 0.000 description 9
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 8
- 150000004820 halides Chemical class 0.000 description 7
- 125000004103 aminoalkyl group Chemical group 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 125000004181 carboxyalkyl group Chemical group 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 4
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 229930014626 natural product Natural products 0.000 description 3
- 238000006068 polycondensation reaction Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- -1 glycidyl ester Chemical class 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000005041 acyloxyalkyl group Chemical group 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CZ3867-97 | 1997-12-03 | ||
| CZ19973867A CZ293419B6 (cs) | 1997-12-03 | 1997-12-03 | Přípravek k prevenci a hojení zánětlivých onemocnění |
| PCT/CZ1998/000046 WO1999028359A1 (en) | 1997-12-03 | 1998-12-02 | Preparation for prevention and healing of inflammation affections |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001525340A JP2001525340A (ja) | 2001-12-11 |
| JP2001525340A5 true JP2001525340A5 (enExample) | 2006-01-26 |
| JP4298915B2 JP4298915B2 (ja) | 2009-07-22 |
Family
ID=5467367
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000523249A Expired - Lifetime JP4298915B2 (ja) | 1997-12-03 | 1998-12-02 | 炎症疾患の予防および治療のための製剤 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6610284B1 (enExample) |
| EP (1) | EP1058698B1 (enExample) |
| JP (1) | JP4298915B2 (enExample) |
| AU (1) | AU1331399A (enExample) |
| CA (1) | CA2312087C (enExample) |
| CZ (1) | CZ293419B6 (enExample) |
| DE (1) | DE69825319T2 (enExample) |
| SK (1) | SK284875B6 (enExample) |
| WO (1) | WO1999028359A1 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6492521B2 (en) * | 2000-11-03 | 2002-12-10 | Cytec Technology Corp. | Hindered amine light stabilizers based on multi-functional carbonyl compounds and methods of making same |
| JP4506955B2 (ja) * | 2004-07-07 | 2010-07-21 | 三菱瓦斯化学株式会社 | 安定ラジカルを持つ共重合体組成物の製造方法 |
| EP1888658B1 (en) * | 2005-06-08 | 2009-07-08 | Ciba Holding Inc. | Polymeric nitroxides their preparation and use |
| WO2011018472A2 (en) * | 2009-08-14 | 2011-02-17 | Basf Se | Methods in cell cultures, and related inventions, employing certain additives |
| US8835000B2 (en) * | 2011-12-23 | 2014-09-16 | General Electric Company | High-density fluorescent dye clusters |
| WO2014182713A1 (en) * | 2013-05-06 | 2014-11-13 | The Regents Of The University Of Minnesota | Sugar free, statistical copolymers made from at least three monomers |
| CZ2014825A3 (cs) * | 2014-11-28 | 2015-08-26 | Ústav makromolekulární chemie AV ČR, v. v. i. | Přípravek pro orální použití |
| US10660851B2 (en) | 2015-01-02 | 2020-05-26 | Rxos Medical | Polyfunctional radical scavenger hydrogel formulation |
| CZ309768B6 (cs) * | 2017-06-05 | 2023-09-27 | Pharmacy point s.r.o | Antibakteriální a antifungální hydrofilní gelová kompozice na bázi zesíťovaného kopolymeru 2-hydroxyethylmethakrylátu |
| CZ308284B6 (cs) * | 2018-03-15 | 2020-04-15 | Ústav makromolekulární chemie AV ČR, v. v. i. | Přípravek na bázi interpenetrujících polymerních sítí pro hojení ran |
| EP3765084B1 (en) | 2018-03-15 | 2021-09-15 | Ustav Makromolekularni Chemie AV CR, V. V. I. | Preparation based on interpenetrating polymer networks for wound healing |
| CN108863908B (zh) * | 2018-04-24 | 2020-06-09 | 宿迁联盛科技股份有限公司 | 一种聚合型橡胶稳定剂中间体及其制备方法 |
| CZ2018359A3 (cs) * | 2018-07-17 | 2019-11-20 | Ústav makromolekulární chemie AV ČR, v. v. i. | Tekutý krycí přípravek pro ošetření ran |
| WO2020015768A1 (en) * | 2018-07-17 | 2020-01-23 | Ustav Makromolekularni Chemie Av Cr, V. V. I. | Liquid wound dressing composition |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU76955A1 (enExample) * | 1977-03-15 | 1978-10-18 | ||
| US4987210A (en) * | 1988-11-03 | 1991-01-22 | Gaf Chemicals Corporation | Polymerizable derivatives of 5-oxo-pyrrolidinecarboxylic acid |
| FR2695800B1 (fr) * | 1992-09-23 | 1996-03-08 | Inst Textile De France | Compose antiseptique. |
| DE19630977A1 (de) * | 1996-07-31 | 1998-02-05 | Basf Ag | Wasserlösliche Polymerisate und deren Verwendung in kosmetischen Formulierungen |
-
1997
- 1997-12-03 CZ CZ19973867A patent/CZ293419B6/cs not_active IP Right Cessation
-
1998
- 1998-10-02 US US09/555,626 patent/US6610284B1/en not_active Expired - Lifetime
- 1998-12-02 DE DE69825319T patent/DE69825319T2/de not_active Expired - Lifetime
- 1998-12-02 SK SK823-2000A patent/SK284875B6/sk not_active IP Right Cessation
- 1998-12-02 JP JP2000523249A patent/JP4298915B2/ja not_active Expired - Lifetime
- 1998-12-02 EP EP98956767A patent/EP1058698B1/en not_active Expired - Lifetime
- 1998-12-02 WO PCT/CZ1998/000046 patent/WO1999028359A1/en not_active Ceased
- 1998-12-02 AU AU13313/99A patent/AU1331399A/en not_active Abandoned
- 1998-12-02 CA CA2312087A patent/CA2312087C/en not_active Expired - Lifetime
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