JP2010539073A5 - - Google Patents
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- Publication number
- JP2010539073A5 JP2010539073A5 JP2010523486A JP2010523486A JP2010539073A5 JP 2010539073 A5 JP2010539073 A5 JP 2010539073A5 JP 2010523486 A JP2010523486 A JP 2010523486A JP 2010523486 A JP2010523486 A JP 2010523486A JP 2010539073 A5 JP2010539073 A5 JP 2010539073A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- polymer
- halogen
- unsubstituted
- 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.)
- Withdrawn
Links
- 125000000217 alkyl group Chemical group 0.000 claims 81
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 43
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 claims 30
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 30
- 239000000203 mixture Substances 0.000 claims 25
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 22
- 229910052736 halogen Inorganic materials 0.000 claims 21
- 150000002367 halogens Chemical class 0.000 claims 21
- 229920000642 polymer Polymers 0.000 claims 20
- 150000003863 ammonium salts Chemical class 0.000 claims 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 16
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 15
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 15
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 14
- 125000003545 alkoxy group Chemical group 0.000 claims 12
- 229920001577 copolymer Polymers 0.000 claims 12
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 claims 10
- 125000005157 alkyl carboxy group Chemical group 0.000 claims 10
- 230000000845 anti-microbial effect Effects 0.000 claims 10
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 8
- 229920006395 saturated elastomer Polymers 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 7
- 238000009472 formulation Methods 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 239000001257 hydrogen Substances 0.000 claims 7
- 125000001624 naphthyl group Chemical group 0.000 claims 7
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 230000007935 neutral effect Effects 0.000 claims 5
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 4
- 150000001768 cations Chemical class 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 4
- 239000002184 metal Substances 0.000 claims 4
- 229910052751 metal Inorganic materials 0.000 claims 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims 3
- 229920002118 antimicrobial polymer Polymers 0.000 claims 3
- 238000000576 coating method Methods 0.000 claims 3
- 244000005700 microbiome Species 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- 238000002360 preparation method Methods 0.000 claims 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 150000001409 amidines Chemical class 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 2
- 239000004566 building material Substances 0.000 claims 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 2
- 239000011248 coating agent Substances 0.000 claims 2
- 239000008199 coating composition Substances 0.000 claims 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 229920005615 natural polymer Polymers 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- 229920001059 synthetic polymer Polymers 0.000 claims 2
- 208000001840 Dandruff Diseases 0.000 claims 1
- -1 alkenoyl Chemical group 0.000 claims 1
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- 239000000412 dendrimer Substances 0.000 claims 1
- 229920000736 dendritic polymer Polymers 0.000 claims 1
- 230000000249 desinfective effect Effects 0.000 claims 1
- IIRVGTWONXBBAW-UHFFFAOYSA-M disodium;dioxido(oxo)phosphanium Chemical compound [Na+].[Na+].[O-][P+]([O-])=O IIRVGTWONXBBAW-UHFFFAOYSA-M 0.000 claims 1
- 239000004744 fabric Substances 0.000 claims 1
- 229920000587 hyperbranched polymer Polymers 0.000 claims 1
- 239000010985 leather Substances 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 210000004379 membrane Anatomy 0.000 claims 1
- 230000000813 microbial effect Effects 0.000 claims 1
- 210000004400 mucous membrane Anatomy 0.000 claims 1
- 239000004745 nonwoven fabric Substances 0.000 claims 1
- 239000000123 paper Substances 0.000 claims 1
- 150000003009 phosphonic acids Chemical class 0.000 claims 1
- 229920000223 polyglycerol Polymers 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims 1
- 239000002023 wood Substances 0.000 claims 1
- 239000002759 woven fabric Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US99325907P | 2007-09-11 | 2007-09-11 | |
| US6263308P | 2008-01-28 | 2008-01-28 | |
| PCT/EP2008/061462 WO2009033970A1 (en) | 2007-09-11 | 2008-09-01 | Polyglycerol anti-microbial agents and compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010539073A JP2010539073A (ja) | 2010-12-16 |
| JP2010539073A5 true JP2010539073A5 (enExample) | 2011-10-20 |
Family
ID=40032522
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010523486A Withdrawn JP2010539073A (ja) | 2007-09-11 | 2008-09-01 | ポリグリセロール系抗微生物剤及び組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20090068138A1 (enExample) |
| EP (1) | EP2190901A1 (enExample) |
| JP (1) | JP2010539073A (enExample) |
| KR (1) | KR20100080905A (enExample) |
| CN (1) | CN101883810A (enExample) |
| BR (1) | BRPI0816251A2 (enExample) |
| WO (1) | WO2009033970A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9260817B2 (en) | 2009-09-18 | 2016-02-16 | The Procter & Gamble Company | Freshening compositions comprising malodor binding polymers and malodor counteractants |
| US9273427B2 (en) * | 2009-09-18 | 2016-03-01 | The Procter & Gamble Company | Freshening compositions comprising malodor binding polymers |
| CN102396515B (zh) * | 2010-08-20 | 2016-01-20 | 中国科学院成都有机化学有限公司 | 一类支化型有机硅聚胍耐久性皮革抗菌剂及其制备方法 |
| BR112013025591B1 (pt) | 2011-04-06 | 2020-11-17 | Stepan Company | composição dispersível em água ou solúvel em água, composição de limpeza e de limpeza de vidro |
| CN104725627B (zh) * | 2015-01-28 | 2017-07-07 | 浙江大学 | 一种聚甘油结构树枝状大分子及其制备方法和应用 |
| EP3429651B1 (en) * | 2016-03-17 | 2022-12-21 | TekCyte Limited | Anti-fouling and/or anti-thrombotic medical devices |
| CN114316241A (zh) * | 2021-11-30 | 2022-04-12 | 山东一诺威新材料有限公司 | 抗菌型聚氨酯慢回弹泡沫用聚醚多元醇的制备方法 |
| CN118591372A (zh) * | 2021-12-06 | 2024-09-03 | 俄亥俄州创新基金会 | 二氨基脂质(dal)化合物和包含免疫治疗剂的药物组合物 |
| KR102721932B1 (ko) * | 2021-12-30 | 2024-10-25 | 주식회사 아이센스 | 고분자 재료의 표면 처리용 조성물, 키트 및 표면 처리 방법 |
| CN115960469B (zh) * | 2022-12-13 | 2024-03-15 | 赛轮集团股份有限公司 | 防护蜡缓释微胶囊的制备方法及其应用 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6071866A (en) * | 1994-06-01 | 2000-06-06 | Lever Brothers Company, Division Of Conopco, Inc. | Mild antimicrobial liquid cleansing formulations comprising hydroxy acid buffering compound or compounds as potentiator of antimicrobial effectiveness |
| US5635462A (en) * | 1994-07-08 | 1997-06-03 | Gojo Industries, Inc. | Antimicrobial cleansing compositions |
| US6358906B1 (en) * | 1996-06-04 | 2002-03-19 | Ciba Specialty Chemicals Corporation | Concentrated liquid accumulations comprising a microbicidally active ingredient |
| US5955408A (en) * | 1996-07-10 | 1999-09-21 | Steris Inc. | Triclosan skin wash with enhanced efficacy |
| US6258368B1 (en) * | 1997-06-04 | 2001-07-10 | The Procter & Gamble Company | Antimicrobial wipes |
| US6440405B1 (en) * | 1999-06-07 | 2002-08-27 | University Of Delaware | Quaternary ammonium functionalized dendrimers and methods of use therefor |
| US6861397B2 (en) * | 1999-06-23 | 2005-03-01 | The Dial Corporation | Compositions having enhanced deposition of a topically active compound on a surface |
| FI19991705L (fi) * | 1999-08-11 | 2001-02-12 | Neste Chemicals Oy | Antimikrobinen hyperhaaroittunut polymeerikoostumus |
| JP2005508245A (ja) * | 2001-10-19 | 2005-03-31 | イノベイティブ コンストラクション アンド ビルディング マテリアルズ， エルエルシー | 感染性空気伝搬微生物に対する防御力を有する抗病原性空気濾過媒体および空気処理デバイス |
| DE10311163A1 (de) * | 2003-03-12 | 2004-09-23 | Albert-Ludwigs-Universität Freiburg, vertreten durch den Rektor | Proteinabweisende Oberflächen auf der Basis dendritischer Polymerfilme |
| GB0422401D0 (en) * | 2004-10-08 | 2004-11-10 | Syngenta Participations Ag | Fungicidal compositions |
| US8790672B2 (en) * | 2005-02-22 | 2014-07-29 | Nina M. Lamba-Kohli | Generation of antimicrobial surfaces using dendrimer biocides |
| CA2653541C (en) * | 2005-06-06 | 2014-12-23 | The University Of British Columbia | Polymer-based serum albumin substitute |
| JP2007217578A (ja) * | 2006-02-17 | 2007-08-30 | Mie Univ | 高分岐ポリマー及びそれを架橋してなるフィルム |
-
2008
- 2008-09-01 WO PCT/EP2008/061462 patent/WO2009033970A1/en not_active Ceased
- 2008-09-01 JP JP2010523486A patent/JP2010539073A/ja not_active Withdrawn
- 2008-09-01 EP EP08803445A patent/EP2190901A1/en not_active Withdrawn
- 2008-09-01 BR BRPI0816251 patent/BRPI0816251A2/pt not_active IP Right Cessation
- 2008-09-01 CN CN2008801065487A patent/CN101883810A/zh active Pending
- 2008-09-01 KR KR1020107007699A patent/KR20100080905A/ko not_active Withdrawn
- 2008-09-09 US US12/283,067 patent/US20090068138A1/en not_active Abandoned
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