JP2010509240A - 喘息、アレルギー性鼻炎および皮膚障害の治療方法 - Google Patents
喘息、アレルギー性鼻炎および皮膚障害の治療方法 Download PDFInfo
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- JP2010509240A JP2010509240A JP2009535499A JP2009535499A JP2010509240A JP 2010509240 A JP2010509240 A JP 2010509240A JP 2009535499 A JP2009535499 A JP 2009535499A JP 2009535499 A JP2009535499 A JP 2009535499A JP 2010509240 A JP2010509240 A JP 2010509240A
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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Abstract
Description
R1は、C2H5、CO2R、CONR2R3、CH2OR4、1,3,4−オキサジアゾール−2−イル、もしくはCH2NR5R6であり、ここで、
Rは、H、C1〜6直鎖もしくは分岐鎖アルキル、C3〜6シクロアルキル、もしくはフェニルであり
またはR1は、式CO2 −R+のカルボン酸塩であり、ここで、R+は、Li+、Na+、K+もしくは式+NR10R11R12R13のアンモニウム部分であり、
R2、R3は、R2、R3のうちの多くとも1つだけが、OH、OCH3もしくはOC2H5であるという条件で、独立してH、C1〜6アルキル、C3〜6シクロアルキル、ベンジル、フェニル、OH、OCH3もしくはOC2H5であり、
R4は、H、C(O)R14、C1〜6アルキル、C3〜6シクロアルキル、ベンジルもしくはフェニルであり、
R5、R6は、R2、R3のうちの多くとも1つだけが、OH、OCH3もしくはOC2H5であるという条件で、独立してH、C(O)R14、C1〜6アルキル、C3〜6シクロアルキル、ベンジル、フェニル、OH、OCH3もしくはOC2H5であり、
R7、R8およびR9は、独立してH、CH3、C2H5、C(O)R14もしくはCO2R15であり、
または、R7およびR8、もしくはR8およびR9は、一緒になってカルボニル基(C=O)を構成し、したがって環状カーボネートを形成し、
または、OR8R1は、一緒になって環状エステル(ラクトン)を形成し、
R10〜R13は、独立してHもしくはC1〜6アルキルであり、各アルキル基は場合によって置換基OHもしくはOCH3を有し、
R14は、H、C1〜6アルキル、C3〜6シクロアルキル、ベンジルもしくはフェニルであり、
R15は、C1〜6アルキル、C3〜6シクロアルキル、ベンジルもしくはフェニルであり、
および
R1が、C2H5、CO2R、CH2OR4、1,3,4−オキサジアゾール−2−イルもしくは式CO2 −R+のカルボン酸塩であり、
R+は、Li+、Na+、K+もしくはNH4 +であり、
Rは、H、CH3、C2H5、n−C3H7もしくはi−C3H7であり、
R4は、H、COCH3もしくはCH3であり、
R7、R8、R9は、独立してH、CH3もしくはCH3COであり、
または、R7およびR8、もしくはR8およびR9は、一緒になってカルボニル基(C=O)を構成し、したがって環状カーボネートを形成し、
または、OR8R1は、一緒になって環状エステル(ラクトン)を形成する、
化合物である。
化合物3の合成
化合物4の合成
化合物8の合成
化合物9の合成
本発明の方法に従った喘息の治療に有用な、本発明の化合物を含む噴霧形態の代表的な医薬品製剤を、以下に例示する。
本発明の方法に従った喘息の治療に有用な、本発明の化合物を含む経口投与用の製剤を、以下に例示する。
本発明の方法に従ったアレルギー性鼻炎の治療のための局所的な投与用の点鼻液を、以下に例示する。
本発明の方法に従ったアレルギー性皮膚炎、接触過敏症、蕁麻疹(urticaria)(蕁麻疹(hive))、酒さまたは乾癬などの皮膚障害の治療のための局所投与用の軟膏を、以下に例示する。
Claims (13)
- 哺乳動物の喘息、アレルギー性鼻炎または皮膚障害の治療方法であって、薬学的に受容可能な担体および式Iの化合物の薬学的有効量を含む組成物を該哺乳動物に投与すること含み、
R1は、C2H5、CO2R、CONR2R3、CH2OR4、1,3,4−オキサジアゾール−2−イルもしくはCH2NR5R6であり、ここで、
Rは、H、C1〜6直鎖もしくは分岐鎖アルキル、C3〜6シクロアルキル、もしくはフェニルであり、
またはR1は、式CO2 −R+のカルボン酸塩であり、ここで、R+は、Li+、Na+、K+もしくは式+NR10R11R12R13のアンモニウム部分であり、
R2、R3は、R2、R3の多くとも1つだけが、OH、OCH3もしくはOC2H5であるという条件で、独立してH、C1〜6アルキル、C3〜6シクロアルキル、ベンジル、フェニル、OH、OCH3もしくはOC2H5であり、
R4は、H、C(O)R14、C1〜6アルキル、C3〜6シクロアルキル、ベンジルもしくはフェニルであり、
R5、R6は、R2、R3の多くとも1つだけが、OH、OCH3もしくはOC2H5であるという条件で、独立してH、C(O)R14、C1〜6アルキル、C3〜6シクロアルキル、ベンジル、フェニル、OH、OCH3もしくはOC2H5であり、
R7、R8およびR9は、独立してH、CH3、C2H5、C(O)R14もしくはCO2R15であり、
または、R7およびR8、もしくはR8およびR9は、一緒になってカルボニル基(C=O)を構成し、したがって環状カーボネートを形成し、
または、OR8R1は、一緒になって環状エステル(ラクトン)を形成し、
R10〜R13は、独立してHもしくはC1〜6アルキルであり、各アルキル基は場合によって置換基OHもしくはOCH3を有し、
R14は、H、C1〜6アルキル、C3〜6シクロアルキル、ベンジルもしくはフェニルであり、
R15は、C1〜6アルキル、C3〜6シクロアルキル、ベンジルもしくはフェニルであり、
該皮膚障害が、アレルギー性皮膚炎、接触過敏症、蕁麻疹、酒さおよび乾癬からなる群より選択される方法。 - 式Iの化合物について、
R1が、C2H5、CO2R、CH2OR4、1,3,4−オキサジアゾール−2−イル、もしくは式CO2 −R+のカルボン酸塩であり、
R+が、Li+、Na+、K+もしくはNH4 +であり、
Rが、H、CH3、C2H5、n−C3H7もしくはi−C3H7であり、
R4が、H、COCH3もしくはCH3であり、
R7、R8、R9が、独立してH、CH3もしくはCH3COであり、
または、R7およびR8、もしくはR8およびR9が、一緒になってカルボニル基(C=O)を構成し、したがって環状カーボネートを形成し、
または、OR8R1が、一緒になって環状エステル(ラクトン)を形成する、
請求項1に記載の方法。 - 式Iの化合物が立体配置:
- 式Iの化合物が立体配置:
- 式Iの化合物が、喘息を治療するために使用される、請求項3に記載の方法。
- 式Iの化合物が、アレルギー性鼻炎に使用される、請求項3に記載の方法。
- 式Iの化合物が、
- 前記化合物の薬学的有効量が0.001%から5%(w/v)である、請求項7に記載の方法。
- 前記薬学的有効量が、0.1から5%(w/v)である、請求項8に記載の方法。
- 前記薬学的に受容可能な担体が、界面活性剤、等張剤、緩衝剤、保存剤、共溶媒および増粘剤からなる群より選択される1種または複数の成分を含む、請求項1に記載の方法。
- 喘息を治療するための方法である、請求項1に記載の方法。
- アレルギー性鼻炎を治療するための方法である、請求項1に記載の方法。
- アレルギー性皮膚炎、接触過敏症、蕁麻疹、酒さおよび乾癬からなる群より選択される皮膚障害を治療するための方法である、請求項1に記載の方法。
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WO2011096941A1 (en) * | 2010-02-08 | 2011-08-11 | Alcon Research, Ltd. | Method of treating ocular allergy |
EP2538934A1 (en) * | 2010-02-25 | 2013-01-02 | Alcon Research, Ltd. | Method of accelerating corneal wound healing |
CN110840878B (zh) * | 2019-11-05 | 2020-06-26 | 牡丹江医学院 | 一种用于治疗银屑病的化合物及其制备方法 |
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CA2668645A1 (en) | 2008-05-15 |
KR20090086573A (ko) | 2009-08-13 |
WO2008058098A2 (en) | 2008-05-15 |
BRPI0718540A2 (pt) | 2013-11-19 |
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