KR20090065508A - 나트륨 채널 차단제와 삼투질 처리에 의한 점막 수화와 점막 세척 촉진 방법 - Google Patents
나트륨 채널 차단제와 삼투질 처리에 의한 점막 수화와 점막 세척 촉진 방법 Download PDFInfo
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- KR20090065508A KR20090065508A KR1020097004814A KR20097004814A KR20090065508A KR 20090065508 A KR20090065508 A KR 20090065508A KR 1020097004814 A KR1020097004814 A KR 1020097004814A KR 20097004814 A KR20097004814 A KR 20097004814A KR 20090065508 A KR20090065508 A KR 20090065508A
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- Prior art keywords
- chor
- lower alkyl
- independently
- hydrogen
- phenyl
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Otolaryngology (AREA)
- Gynecology & Obstetrics (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Ophthalmology & Optometry (AREA)
- Toxicology (AREA)
- Dermatology (AREA)
- Inorganic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US84266906P | 2006-09-07 | 2006-09-07 | |
| US60/842,669 | 2006-09-07 | ||
| US84517106P | 2006-09-18 | 2006-09-18 | |
| US60/845,171 | 2006-09-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20090065508A true KR20090065508A (ko) | 2009-06-22 |
Family
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Family Applications (1)
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|---|---|---|---|
| KR1020097004814A Withdrawn KR20090065508A (ko) | 2006-09-07 | 2007-09-07 | 나트륨 채널 차단제와 삼투질 처리에 의한 점막 수화와 점막 세척 촉진 방법 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8058278B2 (enExample) |
| EP (1) | EP2059237A4 (enExample) |
| JP (1) | JP2010502738A (enExample) |
| KR (1) | KR20090065508A (enExample) |
| AR (1) | AR062741A1 (enExample) |
| AU (1) | AU2007294547A1 (enExample) |
| BR (1) | BRPI0716884A2 (enExample) |
| CA (1) | CA2663041A1 (enExample) |
| EA (1) | EA200970258A1 (enExample) |
| MX (1) | MX2009002602A (enExample) |
| TW (1) | TW200817343A (enExample) |
| WO (1) | WO2008031028A2 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6858615B2 (en) | 2002-02-19 | 2005-02-22 | Parion Sciences, Inc. | Phenyl guanidine sodium channel blockers |
| US7638138B2 (en) | 2003-02-21 | 2009-12-29 | Translational Research, Ltd. | Compositions for nasal administration of pharmaceuticals |
| MXPA05010379A (es) | 2003-03-27 | 2006-05-31 | Bioactis Ltd | Aparato para administrar una medicina en polvo en la cavidad intranasal. |
| PT1663235E (pt) * | 2003-08-18 | 2013-10-29 | Parion Sciences Inc | Novos bloqueadores dos canais do sódio de pirazinoílguanidina protegida |
| US8673360B2 (en) * | 2004-08-10 | 2014-03-18 | Shin Nippon Biomedical Laboratories, Ltd. | Compositions that enable rapid-acting and highly absorptive intranasal administration |
| US7399766B2 (en) * | 2004-08-18 | 2008-07-15 | Parion Sciences, Inc. | Soluble amide & ester pyrazinoylguanidine sodium channel blockers |
| US7807834B2 (en) | 2005-08-03 | 2010-10-05 | Parion Sciences, Inc. | Capped pyrazinoylguanidine sodium channel blockers |
| WO2007146867A2 (en) * | 2006-06-09 | 2007-12-21 | Parion Sciences Inc. | Aliphatic pyrazinoylguanidine sodium channel blockers with beta agonist activity |
| US8163758B2 (en) * | 2006-06-09 | 2012-04-24 | Parion Sciences, Inc. | Phenyl substituted pyrazinoylguanidine sodium channel blockers possessing beta agonist activity |
| JP2010502739A (ja) * | 2006-09-07 | 2010-01-28 | パリオン・サイエンシィズ・インコーポレーテッド | ナトリウムチャネル阻害剤及び浸透圧調節物質を用いた処置による粘膜水和及び粘液クリアランスの改善 |
| JP5415769B2 (ja) | 2006-12-26 | 2014-02-12 | 株式会社新日本科学 | 経鼻投与用製剤 |
| WO2008124496A1 (en) * | 2007-04-03 | 2008-10-16 | Parion Sciences, Inc. | Method of treating acid-sensing ion channel mediated pain, cough, and central nervous system disorders |
| WO2008124491A1 (en) * | 2007-04-03 | 2008-10-16 | Parion Sciences, Inc. | Pyrazinoylguanidine compounds for use taste modulators |
| DE102007040615A1 (de) * | 2007-08-27 | 2009-03-05 | Bitop Ag | Osmolyte zur Behandlung von allergisch oder viral bedingten Atemwegserkrankungen |
| EP2211956A4 (en) | 2007-10-10 | 2014-07-09 | Parion Sciences Inc | DISPOSAL OF OSMOLYTES WITH A NOSE CANNULA |
| DE102007052380A1 (de) * | 2007-10-31 | 2009-05-07 | Bitop Ag | Osmolythaltige Zubereitungen zur Anwendung bei trockenen Schleimhäuten |
| KR101654549B1 (ko) * | 2008-02-26 | 2016-09-07 | 패리온 사이언스 인코퍼레이티드 | 다중방향족 나트륨 채널 차단제 |
| US9486418B2 (en) * | 2008-04-08 | 2016-11-08 | Dynamis Pharmaceuticals, Inc. | Method for treating or preventing dry eye disorders using alkylamino-polyhydroxyalkanes |
| US20100074881A1 (en) * | 2008-07-11 | 2010-03-25 | Parion Sciences, Inc. | Multiple nebulizer systems |
| US9101539B2 (en) * | 2009-05-15 | 2015-08-11 | Shin Nippon Biomedical Laboratories, Ltd. | Intranasal pharmaceutical compositions with improved pharmacokinetics |
| GB2472327B (en) | 2009-07-31 | 2013-03-13 | Shin Nippon Biomedical Lab Ltd | Intranasal granisetron and nasal applicator |
| US8945605B2 (en) | 2011-06-07 | 2015-02-03 | Parion Sciences, Inc. | Aerosol delivery systems, compositions and methods |
| US8778383B2 (en) | 2011-06-07 | 2014-07-15 | Parion Sciences, Inc. | Methods of treatment |
| BR112013032771B1 (pt) | 2011-06-27 | 2021-01-12 | Parion Sciences, Inc. | dipeptídio quimicamente e metabolicamente estável possuindo potente atividade bloqueadora de canais de sódio |
| AR086745A1 (es) * | 2011-06-27 | 2014-01-22 | Parion Sciences Inc | 3,5-diamino-6-cloro-n-(n-(4-(4-(2-(hexil(2,3,4,5,6-pentahidroxihexil)amino)etoxi)fenil)butil)carbamimidoil)pirazina-2-carboxamida |
| DK2855435T3 (en) * | 2012-05-29 | 2018-07-16 | Parion Sciences Inc | DENDRIMER-LIKE AMINOAMIDES WITH SODIUM CHANNEL BLOCKING ACTIVITY FOR THE TREATMENT OF DRY EYES AND OTHER MILK DISEASES |
| WO2014036445A2 (en) * | 2012-08-31 | 2014-03-06 | Johnson Michael R | Novel mucolytic agents |
| CA2894279A1 (en) * | 2012-12-07 | 2014-06-12 | Paul Boucher | Nasal cannula for delivery of aerosolized medicaments |
| BR112015014349A2 (pt) | 2012-12-17 | 2017-07-11 | Parion Sciences Inc | derivados de cloro-pirazina carboxamida úteis para o tratamento de doenças favorecidas por hidratação mucosa insuficiente |
| ES2674665T3 (es) * | 2012-12-17 | 2018-07-03 | Parion Sciences, Inc. | Compuestos de 3,5-diamino-6-cloro-N-(N-(4-fenilbutilo)carbamimidoilo)-pirazina-2-carboxamida |
| US9029382B2 (en) | 2012-12-17 | 2015-05-12 | Parion Sciences, Inc. | 3,5-diamino-6-chloro-N-(N-(4-phenylbutyl)carbamimidoyl) pyrazine-2-carboxamide compounds |
| AU2014309251B2 (en) | 2013-08-23 | 2018-05-24 | Parion Sciences, Inc. | Dithiol mucolytic agents |
| US9102633B2 (en) | 2013-12-13 | 2015-08-11 | Parion Sciences, Inc. | Arylalkyl- and aryloxyalkyl-substituted epithelial sodium channel blocking compounds |
| US20150376145A1 (en) | 2014-06-30 | 2015-12-31 | Parion Sciences, Inc. | Stable sodium channel blockers |
| CN112321472A (zh) * | 2015-01-30 | 2021-02-05 | 帕里昂科学公司 | 新型单硫醇粘液溶解剂 |
| CN107708680A (zh) | 2015-04-30 | 2018-02-16 | 帕里昂科学公司 | 新的二硫醇粘液溶解剂的前药 |
| US11744967B2 (en) | 2017-09-26 | 2023-09-05 | Shin Nippon Biomedical Laboratories, Ltd. | Intranasal delivery devices |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4501729A (en) * | 1982-12-13 | 1985-02-26 | Research Corporation | Aerosolized amiloride treatment of retained pulmonary secretions |
| KR930701992A (ko) * | 1990-10-05 | 1993-09-08 | 웨인 알.조운즈 | 환자의 폐에 잔존하는 점액 분비물의 제거 방법 |
| AUPM411494A0 (en) * | 1994-02-25 | 1994-03-24 | Central Sydney Area Health Service | Method and device for the provocation of upper or lower airway narrowing and/or the induction of sputum |
| US5656256A (en) * | 1994-12-14 | 1997-08-12 | The University Of North Carolina At Chapel Hill | Methods of treating lung disease by an aerosol containing benzamil or phenamil |
| US6264975B1 (en) * | 1998-10-20 | 2001-07-24 | The University Of North Carolina At Chapel Hill | Methods of hydrating mucosal surfaces |
| US6926911B1 (en) * | 1998-12-22 | 2005-08-09 | The University Of North Carolina At Chapel Hill | Compounds and methods for the treatment of airway diseases and for the delivery of airway drugs |
| JP2004513870A (ja) * | 1999-07-19 | 2004-05-13 | ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル | ナトリウムチャネルブロッカーの結合物及びその使用法 |
| WO2001055390A1 (en) * | 2000-01-28 | 2001-08-02 | Human Genome Sciences, Inc. | Human serpin polynucleotides, polypeptides, and antibodies |
| US6858614B2 (en) * | 2002-02-19 | 2005-02-22 | Parion Sciences, Inc. | Phenolic guanidine sodium channel blockers |
| US6858615B2 (en) * | 2002-02-19 | 2005-02-22 | Parion Sciences, Inc. | Phenyl guanidine sodium channel blockers |
| US6903105B2 (en) * | 2003-02-19 | 2005-06-07 | Parion Sciences, Inc. | Sodium channel blockers |
| US20050090505A1 (en) * | 2003-08-18 | 2005-04-28 | Johnson Michael R. | Methods of reducing risk of infection from pathogens |
| AU2004264441A1 (en) * | 2003-08-18 | 2005-02-24 | Parion Sciences, Inc. | Cyclic pyrazinoylguanidine sodium channel blockers |
| PT1663235E (pt) * | 2003-08-18 | 2013-10-29 | Parion Sciences Inc | Novos bloqueadores dos canais do sódio de pirazinoílguanidina protegida |
| AU2004271945A1 (en) * | 2003-08-18 | 2005-03-24 | Parion Sciences, Inc. | Aliphatic pyrazinoylguanidine sodium channel blockers |
| US7745442B2 (en) * | 2003-08-20 | 2010-06-29 | Parion Sciences, Inc. | Methods of reducing risk of infection from pathogens |
| US7399766B2 (en) * | 2004-08-18 | 2008-07-15 | Parion Sciences, Inc. | Soluble amide & ester pyrazinoylguanidine sodium channel blockers |
| US7807834B2 (en) * | 2005-08-03 | 2010-10-05 | Parion Sciences, Inc. | Capped pyrazinoylguanidine sodium channel blockers |
| JP2010502739A (ja) * | 2006-09-07 | 2010-01-28 | パリオン・サイエンシィズ・インコーポレーテッド | ナトリウムチャネル阻害剤及び浸透圧調節物質を用いた処置による粘膜水和及び粘液クリアランスの改善 |
-
2007
- 2007-09-07 BR BRPI0716884-5A2A patent/BRPI0716884A2/pt not_active IP Right Cessation
- 2007-09-07 WO PCT/US2007/077880 patent/WO2008031028A2/en not_active Ceased
- 2007-09-07 TW TW096133769A patent/TW200817343A/zh unknown
- 2007-09-07 KR KR1020097004814A patent/KR20090065508A/ko not_active Withdrawn
- 2007-09-07 AU AU2007294547A patent/AU2007294547A1/en not_active Abandoned
- 2007-09-07 EP EP07842049A patent/EP2059237A4/en not_active Withdrawn
- 2007-09-07 AR ARP070103971A patent/AR062741A1/es unknown
- 2007-09-07 JP JP2009527584A patent/JP2010502738A/ja active Pending
- 2007-09-07 MX MX2009002602A patent/MX2009002602A/es unknown
- 2007-09-07 CA CA002663041A patent/CA2663041A1/en not_active Abandoned
- 2007-09-07 EA EA200970258A patent/EA200970258A1/ru unknown
- 2007-09-07 US US11/851,803 patent/US8058278B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US8058278B2 (en) | 2011-11-15 |
| EP2059237A2 (en) | 2009-05-20 |
| CA2663041A1 (en) | 2008-03-13 |
| AU2007294547A1 (en) | 2008-03-13 |
| JP2010502738A (ja) | 2010-01-28 |
| EA200970258A1 (ru) | 2009-08-28 |
| BRPI0716884A2 (pt) | 2013-10-15 |
| EP2059237A4 (en) | 2010-06-30 |
| WO2008031028A2 (en) | 2008-03-13 |
| TW200817343A (en) | 2008-04-16 |
| AU2007294547A2 (en) | 2009-03-19 |
| MX2009002602A (es) | 2009-05-28 |
| WO2008031028A3 (en) | 2008-11-13 |
| US20080090841A1 (en) | 2008-04-17 |
| AR062741A1 (es) | 2008-12-03 |
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