JP2013545728A5 - - Google Patents
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- Publication number
- JP2013545728A5 JP2013545728A5 JP2013535012A JP2013535012A JP2013545728A5 JP 2013545728 A5 JP2013545728 A5 JP 2013545728A5 JP 2013535012 A JP2013535012 A JP 2013535012A JP 2013535012 A JP2013535012 A JP 2013535012A JP 2013545728 A5 JP2013545728 A5 JP 2013545728A5
- Authority
- JP
- Japan
- Prior art keywords
- chloro
- dichloroamino
- ethoxy
- absent
- methoxyethoxy
- 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
Links
- 150000001875 compounds Chemical class 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 14
- 239000001257 hydrogen Substances 0.000 claims 13
- -1 bromoamino Chemical group 0.000 claims 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000004404 heteroalkyl group Chemical group 0.000 claims 4
- LOTBYPQQWICYBB-UHFFFAOYSA-N methyl n-hexyl-n-[2-(hexylamino)ethyl]carbamate Chemical compound CCCCCCNCCN(C(=O)OC)CCCCCC LOTBYPQQWICYBB-UHFFFAOYSA-N 0.000 claims 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- 125000002252 acyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical group 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- VVEBJJFCVTUFKQ-NZFPMDFQSA-N (2s,3s,4s,5r,6s)-2-[[3-(dichloroamino)-3-methylbutyl]sulfonylmethyl]-6-methoxyoxane-3,4,5-triol Chemical compound CO[C@H]1O[C@H](CS(=O)(=O)CCC(C)(C)N(Cl)Cl)[C@@H](O)[C@H](O)[C@H]1O VVEBJJFCVTUFKQ-NZFPMDFQSA-N 0.000 claims 1
- LCWLUUNLZNVFKH-UHFFFAOYSA-N 1-chloro-2,2,5,5-tetramethylimidazolidin-4-one Chemical compound CC1(C)NC(=O)C(C)(C)N1Cl LCWLUUNLZNVFKH-UHFFFAOYSA-N 0.000 claims 1
- SLSOXGNKLOXNMR-UHFFFAOYSA-N 1-chloro-3-(2,3-dihydroxypropyl)-2,2,5,5-tetramethylimidazolidin-4-one Chemical compound CC1(C)N(Cl)C(C)(C)C(=O)N1CC(O)CO SLSOXGNKLOXNMR-UHFFFAOYSA-N 0.000 claims 1
- VDCCAVCXWWCKGK-UHFFFAOYSA-N 1-chloro-3-(2-hydroxyethyl)imidazolidin-2-one Chemical compound OCCN1CCN(Cl)C1=O VDCCAVCXWWCKGK-UHFFFAOYSA-N 0.000 claims 1
- GGHNWPLYHCXJBF-UHFFFAOYSA-N 1-chloro-3-(4-hydroxybutyl)-2,2,5,5-tetramethylimidazolidin-4-one Chemical compound CC1(C)N(Cl)C(C)(C)C(=O)N1CCCCO GGHNWPLYHCXJBF-UHFFFAOYSA-N 0.000 claims 1
- JTSDNKYYLMCKQO-UHFFFAOYSA-N 1-chloro-3-[2-(2-methoxyethoxy)ethyl]-2,2,5,5-tetramethylimidazolidin-4-one Chemical compound COCCOCCN1C(=O)C(C)(C)N(Cl)C1(C)C JTSDNKYYLMCKQO-UHFFFAOYSA-N 0.000 claims 1
- VOESVEGHDFKVMA-UHFFFAOYSA-N 1-chloro-3-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]-2,2,5,5-tetramethylimidazolidin-4-one Chemical compound COCCOCCOCCN1C(=O)C(C)(C)N(Cl)C1(C)C VOESVEGHDFKVMA-UHFFFAOYSA-N 0.000 claims 1
- QSQVWAGTISKHJB-UHFFFAOYSA-N 1-chloro-3-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]-5,5-dimethylimidazolidine-2,4-dione Chemical compound COCCOCCOCCN1C(=O)N(Cl)C(C)(C)C1=O QSQVWAGTISKHJB-UHFFFAOYSA-N 0.000 claims 1
- ROXTYZWLJJWEGZ-UHFFFAOYSA-N 1-chloro-3-[3-[2-(2-methoxyethoxy)ethoxy]propyl]-2,2,5,5-tetramethylimidazolidin-4-one Chemical compound COCCOCCOCCCN1C(=O)C(C)(C)N(Cl)C1(C)C ROXTYZWLJJWEGZ-UHFFFAOYSA-N 0.000 claims 1
- QRERCGJKTGBQFS-UHFFFAOYSA-N 1-chloro-5-(hydroxymethyl)-5-methylpyrrolidin-2-one Chemical compound OCC1(C)CCC(=O)N1Cl QRERCGJKTGBQFS-UHFFFAOYSA-N 0.000 claims 1
- DSCWHNKZIWFACR-UHFFFAOYSA-N 1-methylimidazolidin-4-one Chemical compound CN1CNC(=O)C1 DSCWHNKZIWFACR-UHFFFAOYSA-N 0.000 claims 1
- BGYXUNRFOXPGHE-UHFFFAOYSA-M 2-(3-chloro-4,4-dimethyl-2-oxoimidazolidin-1-yl)ethyl-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]-dimethylazanium;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.COCCOCCOCC[N+](C)(C)CCN1CC(C)(C)N(Cl)C1=O BGYXUNRFOXPGHE-UHFFFAOYSA-M 0.000 claims 1
- VMNZWUHUEGOGBG-UHFFFAOYSA-N 2-(chloroamino)-2-methylpropan-1-ol Chemical compound OCC(C)(C)NCl VMNZWUHUEGOGBG-UHFFFAOYSA-N 0.000 claims 1
- PKKXBKITPRFKPB-UHFFFAOYSA-N 2-(dibromoamino)-2-methylpropan-1-ol Chemical compound OCC(C)(C)N(Br)Br PKKXBKITPRFKPB-UHFFFAOYSA-N 0.000 claims 1
- VLSDNXBFQAMHHH-UHFFFAOYSA-N 2-(dichloroamino)-2-methylpropan-1-ol Chemical compound OCC(C)(C)N(Cl)Cl VLSDNXBFQAMHHH-UHFFFAOYSA-N 0.000 claims 1
- SZZQJABBPBAERE-UHFFFAOYSA-N 2-[2-(dichloroamino)-2-methylpropyl]sulfonylethanol Chemical compound ClN(Cl)C(C)(C)CS(=O)(=O)CCO SZZQJABBPBAERE-UHFFFAOYSA-N 0.000 claims 1
- FUUBLSWEFFLUEK-UHFFFAOYSA-N 2-[2-[2-[3-(dichloroamino)-3-methylbutyl]sulfonylethoxy]ethoxy]ethanol Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)CCOCCOCCO FUUBLSWEFFLUEK-UHFFFAOYSA-N 0.000 claims 1
- QOBSMEMOWLACMK-UHFFFAOYSA-N 2-[3-(dichloroamino)-3-methylbutyl]sulfonylethanol Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)CCO QOBSMEMOWLACMK-UHFFFAOYSA-N 0.000 claims 1
- BQCPZBNJVGHZDH-UHFFFAOYSA-M 2-butoxyethyl-[3-(dichloroamino)-3-methylbutyl]-dimethylazanium;chloride Chemical compound [Cl-].CCCCOCC[N+](C)(C)CCC(C)(C)N(Cl)Cl BQCPZBNJVGHZDH-UHFFFAOYSA-M 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- OLDAILRQGKQIFX-UHFFFAOYSA-N 3-(dichloroamino)-n-(2-hydroxyethyl)-n,3-dimethylbutane-1-sulfonamide Chemical compound OCCN(C)S(=O)(=O)CCC(C)(C)N(Cl)Cl OLDAILRQGKQIFX-UHFFFAOYSA-N 0.000 claims 1
- HZNGASGJKDPCFK-UHFFFAOYSA-N 3-[3-(dichloroamino)-3-methylbutyl]sulfonylbutane-1,2,4-triol Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)C(CO)C(O)CO HZNGASGJKDPCFK-UHFFFAOYSA-N 0.000 claims 1
- UYFVCFFXWMBGHH-UHFFFAOYSA-N 3-[3-(dichloroamino)-3-methylbutyl]sulfonylpropan-1-ol Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)CCCO UYFVCFFXWMBGHH-UHFFFAOYSA-N 0.000 claims 1
- CFJZCOCBJRFVDT-UHFFFAOYSA-N 3-[3-(dichloroamino)-3-methylbutyl]sulfonylpropane-1,2-diol Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)CC(O)CO CFJZCOCBJRFVDT-UHFFFAOYSA-N 0.000 claims 1
- GWJXADZLTUXLGH-UHFFFAOYSA-N 3-chloro-1-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethylsulfonyl]ethyl]-4,4-dimethylimidazolidin-2-one Chemical compound COCCOCCOCCS(=O)(=O)CCN1CC(C)(C)N(Cl)C1=O GWJXADZLTUXLGH-UHFFFAOYSA-N 0.000 claims 1
- WAUUAAGOJUGNGB-UHFFFAOYSA-N 3-chloro-4,4-bis(hydroxymethyl)-1,3-oxazolidin-2-one Chemical compound OCC1(CO)COC(=O)N1Cl WAUUAAGOJUGNGB-UHFFFAOYSA-N 0.000 claims 1
- ZKUKLPIJLOJPOO-UHFFFAOYSA-N 3-chloro-4-(hydroxymethyl)-1,4-dimethylimidazolidin-2-one Chemical compound CN1CC(C)(CO)N(Cl)C1=O ZKUKLPIJLOJPOO-UHFFFAOYSA-N 0.000 claims 1
- BQWNVQMQLCHRCD-UHFFFAOYSA-N 3-chloro-4-[2-[2-(2-methoxyethoxy)ethoxy]ethylsulfonylmethyl]-4-methyl-1,3-oxazolidin-2-one Chemical compound COCCOCCOCCS(=O)(=O)CC1(C)COC(=O)N1Cl BQWNVQMQLCHRCD-UHFFFAOYSA-N 0.000 claims 1
- RZJLGJAXSMBVNM-UHFFFAOYSA-N 3-chloro-4-methyl-4-(2,3,4-trihydroxybutylsulfonylmethyl)-1,3-oxazolidin-2-one Chemical compound OCC(O)C(O)CS(=O)(=O)CC1(C)COC(=O)N1Cl RZJLGJAXSMBVNM-UHFFFAOYSA-N 0.000 claims 1
- UZSSTEZNHQFDQL-UHFFFAOYSA-N 3-chloro-5-(hydroxymethyl)-4,4-dimethyl-1,3-oxazolidin-2-one Chemical compound CC1(C)C(CO)OC(=O)N1Cl UZSSTEZNHQFDQL-UHFFFAOYSA-N 0.000 claims 1
- IQNFVWDGRIVKOO-UHFFFAOYSA-N 4-[3-(dichloroamino)-3-methylbutyl]sulfonylbutane-1,2,3-triol Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)CC(O)C(O)CO IQNFVWDGRIVKOO-UHFFFAOYSA-N 0.000 claims 1
- GYBJFPVRNGMPTN-UHFFFAOYSA-N 4-[3-(dichloroamino)-3-methylbutyl]sulfonylbutane-1,2-diol Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)CCC(O)CO GYBJFPVRNGMPTN-UHFFFAOYSA-N 0.000 claims 1
- SIXKMUTXKVBKPB-UHFFFAOYSA-N 4-chloro-1-(2-hydroxyethyl)-3,3,5,5-tetramethylpiperazin-2-one Chemical compound CC1(C)CN(CCO)C(=O)C(C)(C)N1Cl SIXKMUTXKVBKPB-UHFFFAOYSA-N 0.000 claims 1
- TUTRAMZUORQNJK-UHFFFAOYSA-N 4-chloro-1-(2-hydroxyethyl)-3,3-dimethylpiperazine-2,5-dione Chemical compound CC1(C)N(Cl)C(=O)CN(CCO)C1=O TUTRAMZUORQNJK-UHFFFAOYSA-N 0.000 claims 1
- 208000035143 Bacterial infection Diseases 0.000 claims 1
- BZNAGDUKBMZXLQ-UHFFFAOYSA-M [3-(dichloroamino)-3-methylbutyl]-(2-hexoxyethyl)-dimethylazanium;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.CCCCCCOCC[N+](C)(C)CCC(C)(C)N(Cl)Cl BZNAGDUKBMZXLQ-UHFFFAOYSA-M 0.000 claims 1
- JLEPHOCCKAJGAC-UHFFFAOYSA-M [3-(dichloroamino)-3-methylbutyl]-(2-methoxyethyl)-dimethylazanium;chloride Chemical compound [Cl-].COCC[N+](C)(C)CCC(C)(C)N(Cl)Cl JLEPHOCCKAJGAC-UHFFFAOYSA-M 0.000 claims 1
- VYCXTMWECWUDKK-UHFFFAOYSA-M [3-(dichloroamino)-3-methylbutyl]-(3-hydroxypropyl)-dimethylazanium;chloride Chemical compound [Cl-].ClN(Cl)C(C)(C)CC[N+](C)(C)CCCO VYCXTMWECWUDKK-UHFFFAOYSA-M 0.000 claims 1
- LAXNGDQFCYSTEO-UHFFFAOYSA-M [3-(dichloroamino)-3-methylbutyl]-(3-methoxypropyl)-dimethylazanium;chloride Chemical compound [Cl-].COCCC[N+](C)(C)CCC(C)(C)N(Cl)Cl LAXNGDQFCYSTEO-UHFFFAOYSA-M 0.000 claims 1
- RLQKEJPRKWRTIL-UHFFFAOYSA-N [3-[3-(dichloroamino)-3-methylbutyl]sulfonyl-2-hydroxypropyl] acetate Chemical compound CC(=O)OCC(O)CS(=O)(=O)CCC(C)(C)N(Cl)Cl RLQKEJPRKWRTIL-UHFFFAOYSA-N 0.000 claims 1
- 239000000443 aerosol Substances 0.000 claims 1
- 230000000845 anti-microbial effect Effects 0.000 claims 1
- 239000004599 antimicrobial Substances 0.000 claims 1
- 208000022362 bacterial infectious disease Diseases 0.000 claims 1
- 239000006071 cream Substances 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 230000000249 desinfective effect Effects 0.000 claims 1
- 125000003963 dichloro group Chemical group Cl* 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 239000000499 gel Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- GVONPBONFIJAHJ-UHFFFAOYSA-N imidazolidin-4-one Chemical compound O=C1CNCN1 GVONPBONFIJAHJ-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000006210 lotion Substances 0.000 claims 1
- 210000004400 mucous membrane Anatomy 0.000 claims 1
- WEKKHJLHFSSBNI-UHFFFAOYSA-N n,n-dichloro-2-methyl-4-(1,4,7,10-tetraoxacyclododec-2-ylmethylsulfonyl)butan-2-amine Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)CC1COCCOCCOCCO1 WEKKHJLHFSSBNI-UHFFFAOYSA-N 0.000 claims 1
- SOOBYIHTPZGBKF-UHFFFAOYSA-N n,n-dichloro-2-methyl-4-(oxolan-3-ylsulfonyl)butan-2-amine Chemical compound ClN(Cl)C(C)(C)CCS(=O)(=O)C1CCOC1 SOOBYIHTPZGBKF-UHFFFAOYSA-N 0.000 claims 1
- FMUSNVQRVQIHIS-UHFFFAOYSA-N n,n-dichloro-2-methyl-4-[2-[2-[2-[(2-methylpropan-2-yl)oxy]ethoxy]ethoxy]ethylsulfonyl]butan-2-amine Chemical compound CC(C)(C)OCCOCCOCCS(=O)(=O)CCC(C)(C)N(Cl)Cl FMUSNVQRVQIHIS-UHFFFAOYSA-N 0.000 claims 1
- JEKLRGBMACLUHA-UHFFFAOYSA-N n,n-dichloro-4-(2-methoxyethylsulfonyl)-2-methylbutan-2-amine Chemical compound COCCS(=O)(=O)CCC(C)(C)N(Cl)Cl JEKLRGBMACLUHA-UHFFFAOYSA-N 0.000 claims 1
- HXONALVXNOIIDY-UHFFFAOYSA-N n,n-dichloro-4-[2-(2-methoxyethoxy)ethylsulfonyl]-2-methylbutan-2-amine Chemical compound COCCOCCS(=O)(=O)CCC(C)(C)N(Cl)Cl HXONALVXNOIIDY-UHFFFAOYSA-N 0.000 claims 1
- YUGMGVWSECPAOM-UHFFFAOYSA-N n,n-dichloro-4-[2-[2-(2-ethoxyethoxy)ethoxy]ethylsulfonyl]-2-methylbutan-2-amine Chemical compound CCOCCOCCOCCS(=O)(=O)CCC(C)(C)N(Cl)Cl YUGMGVWSECPAOM-UHFFFAOYSA-N 0.000 claims 1
- XQMITGQTMVOVEW-UHFFFAOYSA-N n,n-dichloro-4-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethylsulfonyl]-2-methylbutan-2-amine Chemical compound COCCOCCOCCOCCS(=O)(=O)CCC(C)(C)N(Cl)Cl XQMITGQTMVOVEW-UHFFFAOYSA-N 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 239000002674 ointment Substances 0.000 claims 1
- 239000006072 paste Substances 0.000 claims 1
- XGQJZNCFDLXSIJ-UHFFFAOYSA-N pentadecanal Chemical compound CCCCCCCCCCCCCCC=O XGQJZNCFDLXSIJ-UHFFFAOYSA-N 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 claims 1
- OMZRUCUOACVGDX-UHFFFAOYSA-N CCC(C)(CO1)N(CC)C1=O Chemical compound CCC(C)(CO1)N(CC)C1=O OMZRUCUOACVGDX-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US39469710P | 2010-10-19 | 2010-10-19 | |
| US61/394,697 | 2010-10-19 | ||
| US41833410P | 2010-11-30 | 2010-11-30 | |
| US61/418,334 | 2010-11-30 | ||
| PCT/US2011/056764 WO2012054521A2 (en) | 2010-10-19 | 2011-10-18 | Antimicrobial polyether and polyol compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013545728A JP2013545728A (ja) | 2013-12-26 |
| JP2013545728A5 true JP2013545728A5 (enExample) | 2014-11-20 |
Family
ID=45975842
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013535012A Pending JP2013545728A (ja) | 2010-10-19 | 2011-10-18 | 抗菌性ポリエーテルおよびポリオール化合物 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US9248117B2 (enExample) |
| EP (1) | EP2629607A4 (enExample) |
| JP (1) | JP2013545728A (enExample) |
| KR (1) | KR20130123383A (enExample) |
| CN (1) | CN103260402A (enExample) |
| AU (1) | AU2011317223A1 (enExample) |
| BR (1) | BR112013009279A2 (enExample) |
| CA (1) | CA2814378A1 (enExample) |
| IL (1) | IL225838A0 (enExample) |
| MX (1) | MX2013004311A (enExample) |
| SG (1) | SG189857A1 (enExample) |
| WO (1) | WO2012054521A2 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7635390B1 (en) | 2000-01-14 | 2009-12-22 | Marctec, Llc | Joint replacement component having a modular articulating surface |
| GB201121768D0 (en) * | 2011-12-16 | 2012-02-01 | Univ Swansea | Compounds |
| US20150118179A1 (en) * | 2012-05-17 | 2015-04-30 | University Of Manitoba | Biocidal compounds and methods for using same |
| WO2017197518A1 (en) * | 2016-05-18 | 2017-11-23 | Exigence Technologies Inc. | Compounds with one or more functional groups and use thereof in liquid disinfectants |
| CA3117601C (en) * | 2018-10-26 | 2022-06-14 | University Of South Alabama | Functionalized materials and compounds |
| WO2022091091A1 (en) * | 2020-10-29 | 2022-05-05 | Technion Research & Development Foundation Ltd. | Polymeric disinfectants and uses thereof |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6269883A (ja) * | 1985-09-20 | 1987-03-31 | 日東紡績株式会社 | 繊維用抗菌剤 |
| JPH0813996B2 (ja) * | 1986-05-28 | 1996-02-14 | ライオン株式会社 | 漂白剤組成物 |
| DD300072A5 (de) * | 1989-12-28 | 1992-05-21 | Akad Wissenschaften Ddr | Desinfektionsmittellösung zur verbesserten Keimabtötung |
| DE4234188C2 (de) * | 1992-10-10 | 1996-01-11 | Beiersdorf Ag | Antimycotische kosmetische und dermatologische Verwendungen |
| US7173073B2 (en) * | 2002-01-14 | 2007-02-06 | Johnson & Johnson Vision Care, Inc. | Ophthalmic devices containing heterocyclic compounds and methods for their production |
| BRPI0413660A (pt) * | 2003-08-18 | 2006-10-24 | Novacal Pharmaceuticals Inc | Aminoácidos n,n-di-alogenado e derivados |
| WO2006099567A2 (en) * | 2005-03-11 | 2006-09-21 | Auburn University | Biocidal n-halamine epoxides |
| WO2007102705A1 (en) * | 2006-03-07 | 2007-09-13 | Hee Jung Kim | Anion receptor and electrolyte using the same |
| TW200843787A (en) * | 2006-12-29 | 2008-11-16 | Novabay Pharmaceuticals Inc | N-halogenated amino compounds and derivatives; compositions and methods of using them |
| WO2008094664A1 (en) * | 2007-01-31 | 2008-08-07 | Adam Heller | Methods and compositions for the treatment of pain |
| WO2009126912A1 (en) * | 2008-04-10 | 2009-10-15 | Novabay Pharmaceuticals, Inc. | Compositions comprising n-halogenated or n, n-dihalogenated amine for treatment and prophylaxis of bronchopulmonary infections |
| WO2010017405A1 (en) * | 2008-08-06 | 2010-02-11 | Adam Heller | Methods and compositions for the treatment of pain |
| JP5681630B2 (ja) * | 2008-08-12 | 2015-03-11 | ノバベイ・ファーマシューティカルズ・インコーポレイテッドＮｏｖａｂａｙ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ，Ｉｎｃ． | 抗菌性ゲル製剤 |
| WO2010054269A1 (en) * | 2008-11-07 | 2010-05-14 | Novabay Pharmaceuticals, Inc. | Antimicrobial n-chlorinated compositions |
| CA2741660A1 (en) * | 2008-11-07 | 2010-05-14 | Novabay Pharmaceuticals, Inc. | Antimicrobial oxazolidinone, hydantoin and imidazolidinone compositions |
| US20100272783A1 (en) * | 2009-04-24 | 2010-10-28 | Novabay Pharmaceuticals, Inc. | Methods of Treating Infections of the Nail |
| US20120101018A1 (en) * | 2010-10-22 | 2012-04-26 | Gregory Scot Miracle | Bis-azo colorants for use as bluing agents |
-
2011
- 2011-10-18 MX MX2013004311A patent/MX2013004311A/es unknown
- 2011-10-18 CN CN2011800611993A patent/CN103260402A/zh active Pending
- 2011-10-18 JP JP2013535012A patent/JP2013545728A/ja active Pending
- 2011-10-18 AU AU2011317223A patent/AU2011317223A1/en not_active Abandoned
- 2011-10-18 WO PCT/US2011/056764 patent/WO2012054521A2/en not_active Ceased
- 2011-10-18 KR KR1020137010129A patent/KR20130123383A/ko not_active Withdrawn
- 2011-10-18 CA CA2814378A patent/CA2814378A1/en not_active Abandoned
- 2011-10-18 EP EP11835017.2A patent/EP2629607A4/en not_active Withdrawn
- 2011-10-18 US US13/276,145 patent/US9248117B2/en active Active
- 2011-10-18 BR BR112013009279A patent/BR112013009279A2/pt not_active Application Discontinuation
- 2011-10-18 SG SG2013026349A patent/SG189857A1/en unknown
-
2013
- 2013-04-18 IL IL225838A patent/IL225838A0/en unknown
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