JP2008543942A - ホップ酸の無機塩を含有する組成物、及び該組成物の製造方法 - Google Patents
ホップ酸の無機塩を含有する組成物、及び該組成物の製造方法 Download PDFInfo
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- JP2008543942A JP2008543942A JP2008518335A JP2008518335A JP2008543942A JP 2008543942 A JP2008543942 A JP 2008543942A JP 2008518335 A JP2008518335 A JP 2008518335A JP 2008518335 A JP2008518335 A JP 2008518335A JP 2008543942 A JP2008543942 A JP 2008543942A
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- acid
- slurry
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- salt
- calcium
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- 239000000203 mixture Substances 0.000 title claims abstract description 165
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- QRDZSRWEULKVNW-UHFFFAOYSA-N 6-hydroxy-2-oxo-1h-quinoline-4-carboxylic acid Chemical compound C1=C(O)C=C2C(C(=O)O)=CC(=O)NC2=C1 QRDZSRWEULKVNW-UHFFFAOYSA-N 0.000 claims description 119
- 150000001875 compounds Chemical class 0.000 claims description 100
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 13
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- RGLRXNKKBLIBQS-XNHQSDQCSA-N leuprolide acetate Chemical compound CC(O)=O.CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)CC1=CC=C(O)C=C1 RGLRXNKKBLIBQS-XNHQSDQCSA-N 0.000 claims description 7
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- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 4
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Abstract
Description
本願は、以下の米国仮特許出願:2005年6月21日出願の第60/692、746号;2005年6月21日出願の第60/692,910号、及び2005年12月12日出願の第60/749,966号の利益を主張する;本願は、米国特許出願第11/302,308号の一部継続出願であり、これは次に前記した各米国仮特許出願の利益を主張する。これらの各出願の全内容は、参照により本明細書に組み入れられる。
最近の報告では、ホップ由来の酸が、抗炎症剤及び栄養補助食品として有用であることが提案されている。これらの酸は、他の医薬用途も有すると思われる。ホップ酸は、粘性の油又は樹脂の形態で存在するため、活性成分は、消化又は局所適用された際の吸収が乏しく、また取り扱いが不便である。加えて、ホップ酸の製造方法は時間集約的であり、これは生産コストを増大させる。改善されたバイオアベイラビリティを有し、取り扱いが便利なホップ酸製剤が必要とされている。
例えば特許文献1に記載されているホップ酸の固体塩の以前の製造方法は、ホップ酸のアルカリ性水溶液を塩水溶液と共に加熱して、ホップ酸の固体塩を製造することを含む4ステップの工程を必要とする。この加熱ステップは、塩形成中にα酸の分解を加速し、望ましくない。加えて、この方法は、マグネシウム塩形成反応中、濃度4%〜7%のホップ酸を使用する。これらのホップ酸の低い濃度は、反応に必要な時間を延長して、コストを増大させる。ホップ酸を、該ホップ酸の固体塩に変換する改善された方法が必要とされている。
Z及びTは、独立してH及びPi軌道から選択されるが、T又はZの一方がPi軌道の場合、隣接するT又はZもPi軌道であることを条件とし、それにより二重結合を形成し;
Mは、一価又は二価カチオンであり;
Wは、Cl、OH、SO4 −、Br、I、又は式E、F、G若しくはH:
Rは、H、Na、K、Li又はM−Wである)の任意の一種又はそれ以上を含有する組成物を含む組成物を提供する。
有利には、β酸のマグネシウム塩は、β酸それ自体よりも相当吸湿性が低い。
Z及びTは、独立してH及びPi軌道から選択されるが、T又はZの一方がPi軌道の場合、隣接するT又はZもPi軌道であることを条件とし、それにより二重結合を形成し;
Mは、マグネシウム又はカルシウムであり;
Wは、Cl、OH、SO4 −、Br、I、又は式E、F、G若しくはH:
Rは、H、Na、K、Li又はM−Wである)の組み合わせを有する水性組成物を含む組成物に関する。
Z及びTは、独立してH及びPi軌道から選択されるが、T又はZの一方がPi軌道の場合、隣接するT又はZもPi軌道であることを条件とし、それにより二重結合を形成し;
Mは、マグネシウム又はカルシウムであり;
Wは、Cl、OH、SO4 −、Br、I、又は式E、F、G若しくはH:
Rは、H、Na、K、Li又はM−Wである)の少なくとも一つを含む組成物に関する。
R’’はアルキルであり;
R、T、X及びZは、独立してH、F、Cl、Br、I及びPi軌道からなる群より選択されるが、R、T、X、又はZがPi軌道の場合、隣接するR、T、X、又はZもPi軌道であることを条件とし、それにより二重結合を形成し;
Mは、マグネシウム又はカルシウムであり;
Wは、Cl、OH、SO4 −、Br、I、式C又は式Dである)の任意の一つ又はそれ以上を含むが、これらに限定されない。
Mは、リチウム、ナトリウム、カリウム、銀、銅、マグネシウム、カルシウム、バリウム、クロム、マンガン、鉄、銀、コバルト、ニッケル、銅、亜鉛、又はカドミウムであり;
Wは存在しないか、又はCl、OH、SO4 −、Br、若しくはIである)を有するヘキサヒドロイソα酸である。
本発明は、一種又はそれ以上のホップ酸又はホップ酸誘導体を含有する組成物、及び一種又はそれ以上のホップ酸又はホップ酸誘導体の製造方法を提供する。この方法は、イソα酸、ロイソα酸、テトラヒドロイソα酸、酸及びヘキサヒドロイソα酸、並びにβ酸、例えばルプロン、コルプロン、アドルプロン及びそれらの誘導体の製造に関して、効率が改善されている。特定の実施態様において、これらのβ酸は、ヘキサヒドロβ酸及びテトラヒドロβ酸を含む。
R’’はアルキルであり;
R、T、X及びZは、独立してH、F、Cl、Br、I及びPi軌道からなる群より選択されるが、R、T、X、又はZがPi軌道の場合、隣接するR、T、X、又ZもPi軌道であることを条件とし、それにより二重結合を形成し;
Mは、マグネシウム又はカルシウムであり;
Wは、Cl、OH、SO4 −、Br、I、式C又は式Dである)の任意の一つ又はそれ以上を含むが、これらに限定されない。
式A、B、C及びD:
Z及びTは、独立してH及びPi軌道から選択されるが、T又はZの一方がPi軌道の場合、隣接するT又はZもPi軌道であることを条件とし、それにより二重結合を形成し;
Mは、マグネシウム又はカルシウムであり;
Wは、Cl、OH、SO4 −、Br、I、又は式E、F、G若しくはH:
Rは、H、Na、K、Li又はM−Wである)の任意の一つ又はそれ以上を含むが、これらに限定されない。有利には、β酸のマグネシウム塩は、β酸それ自体よりも相当吸湿性が低い。
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Publishers (1999); T.W. Greene and P.G.M. Wuts、Protective
Groups in Organic Synthesis、3rd. Ed.、John Wiley and Sons (1999); L. Fieser and M. Fieser、Fieser and Fieser's Reagents for Organic Synthesis、John Wiley and Sons (1999); L. Paquette、ed.、Encyclopedia of Reagents for Organic Synthesis、John Wiley and Sons (1995)、及びM. Verzele and
D. De Keukeleire、Chemistry and Analysis of Hop and Beer
Bitter Acids、Elsevier (1991)、並びにそれらの改訂版に記載されているものを含む。
Chemistry 1988、31、318-322;
Bundgaard、H. Design of Prodrugs; Elsevier: Amsterdam、1985; pp 1〜92; Bundgaard、H.; Nielsen、N. M. Journal of Medical
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Friis、G. J.; Bundgaard、H.Textbook
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edition、by Alfred Burger、Donald
J. Abraham、ed.、Volumes 1 to 6、Wiley Interscience Publication、NY、2003である。
一般に、ホップ酸の無機塩は、以下のように調製される。β酸、α酸、イソα酸、ロイソα酸、テトラヒドロイソα酸、ヘキサヒドロイソα酸、又はそれらの任意の混合物として周知のホップ酸を含む、一つ又はそれ以上のホップ酸の水溶液又は樹脂質の調製物は、水及び適切な塩基(例、NaOH、KOH)を、ホップ酸混合物のpHが7〜12になる迄、またホップ酸混合物の濃度が50%〜1%になる迄、ホップ酸混合物に加えることにより調製する。次に、水溶液又は樹脂質調製物を、使用する金属塩の水溶性に応じて、カリウム塩、鉄塩、カルシウム塩、リチウム塩、若しくは亜鉛塩を含むが、これらに限定されない無機金属塩の水スラリー、又はそれら塩の水性製剤のいずれかと混合する。
ロイソα酸の無機塩は、当該技術分野にて周知の任意の標準的な方法を用いて製造される。一実施態様において、ロイソα酸は、以下の方法に従って製造される。
β酸マグネシウム塩を、以下のように調製した。β酸カリウム塩約500gを含むホップβ酸溶液5000mlを、室温で撹拌した。20%KOH溶液100mlを滴加して溶液のpHをpH11.50に調整した。次に、pH11.50に保ちながら溶液を脱イオン水(1100ml)で希釈した。
テトラヒドロβ酸マグネシウム塩を、以下のように調製した。20%テトラヒドロβ酸を含むアルカリ性水溶液1.25リットルを、6M炭酸カリウム水溶液1.25リットルと室温で混合した。30分間撹拌した後、20%KOH溶液50mlを滴加して溶液のpHをpH11.50に調整した。次に、pH11.50に保ちながら溶液を脱イオン水(550ml)で希釈した。室温での激しい撹拌下で、溶液に10%MgSO4溶液420mlを加えた。添加後、混合物を30分間撹拌し、次に白色沈殿をWhatman#45フィルター紙を用いて、ブフネルロートを通して濾過し、脱イオン水で洗浄し、乾燥してβ酸マグネシウム塩220g(純度:>95%、マグネシウム含有率として)を得た。
ロイソα酸の鉄塩を調製するために、pH10の30%ロイソα酸水溶液300グラムを、以前に500mL脱イオン水と混合してある70グラムのFeSO4 −7H2Oと混合した。このスラリーを均質となる迄、混合した。次に、スラリーを乾燥トレー上に直接注ぎ、乾燥した。
ロイソα酸のカルシウム塩を調製するために、pH11の30%ロイソα酸水溶液300グラムを、以前に脱イオン水200mLと混合してある37グラムのCaCl2−2H2Oと混合した。このスラリーを均質となる迄、混合した。次に、スラリーを乾燥トレー上に直接注ぎ、乾燥した。
ロイソα酸のリチウム塩を調製するために、pH9の30%ロイソα酸水溶液300グラムを、以前に300mL脱イオン水と混合してある21グラムのLiOH−H2Oと混合した。このスラリーを均質となる迄、混合した。次に、ブフネルロートを通してスラリーを濾過して過剰の水を除去し、乾燥トレー上に配置し、乾燥した。
ロイソα酸のカルシウム塩を調製するために、pH11の30%ロイソα酸水溶液300グラムを、以前に200mL脱イオン水と混合してある37グラムのCaCl2−2H2Oと混合した。このスラリーを均質となる迄、混合した。次に、スラリーを乾燥トレー上に直接注ぎ、乾燥した。
ロイソα酸の亜鉛塩を調製するために、pH8の30%ロイソα酸水溶液300グラムを、以前に500mL脱イオン水と混合してある72グラムのZnSO4 −7H2Oと混合した。このスラリーを均質となる迄、混合した。次に、スラリーを乾燥トレー上に直接注ぎ、乾燥した。
ロイソα酸のカリウム塩を調製するために、pH10の30%ロイソα酸水溶液300グラムを、以前に300mL脱イオン水と混合してある35グラムのK2CO3と混合した。このスラリーを均質となる迄、混合した。次に、スラリーを乾燥トレー上に直接注ぎ、乾燥した。
テトラヒドロイソα酸のカルシウム塩を調製するために、pH10.5の9%テトラヒドロイソα酸水溶液1000グラムを、以前に脱イオン水100mLと混合してある2グラムのCaCl2−2H2Oと混合した。このスラリーを均質となる迄、混合した。次に、ブフネルロートを通してスラリーを濾過して過剰の水を除去し、乾燥トレー上に配置し、乾燥した。
テトラヒドロイソα酸及びヘキサヒドロイソα酸の混合物の亜鉛塩を調製するために、pH10の水性10%ヘキサヒドロイソα450グラム及び水性10%テトラヒドロイソα溶液450グラムを、以前に脱イオン水200mLと混合してある73グラムのZnSO4 −7H2Oと混合した。このスラリーを均質となる迄、混合した。次に、ブフネルロートを通してスラリーを濾過して過剰の水を除去し、乾燥トレー上に配置し、乾燥した。
Claims (71)
- 式A、B、C及びD:
Z及びTは、独立してH及びPi軌道から選択されるが、T又はZの一方がPi軌道の場合、隣接するT又はZもPi軌道であることを条件とし、それにより二重結合を形成し;
Mは、リチウム、ナトリウム、カリウム、銀、銅、マグネシウム、カルシウム、バリウム、クロム、マンガン、鉄、銀、コバルト、ニッケル、銅、亜鉛、及びカドミウムからなる群より選択される一価又は二価カチオンであり;
Wは、存在しないか、又はCl、OH、SO4 −、Br、I、式E、F、G若しくはH:
Rは、H、Na、K、Li又はM−Wである)
で示される化合物の一種又はそれ以上を含有する組成物。 - 水性組成物が、β酸、ヘキサヒドロβ酸又はテトラヒドロβ酸を含む、請求項2に記載の組成物。
- R1がイソプロピル、イソブチル又はsec−ブチルである、請求項2に記載の組成物。
- 水性組成物のpHが7.0〜10.0である、請求項2に記載の組成物。
- 水性組成物のpHが7.0〜9.5である、請求項5に記載の組成物。
- 水性組成物のpHが7.0〜8.0である、請求項6に記載の組成物。
- 水性組成物のpHが7.2〜7.4である、請求項7に記載の組成物。
- 水性組成物の含水率が1〜20%である、請求項2に記載の組成物。
- 水性組成物の含水率が1〜10%である、請求項2に記載の組成物。
- 塩組成物の含有率が20〜90%である、請求項2に記載の組成物。
- ホップ酸の無機塩の製造方法であって:
a)10〜50%のホップ酸を含有する水溶液を提供するステップと、ここで溶液は、室温であることと;
b)撹拌しながら該水溶液に無機塩を加えて、スラリーを形成するステップと、ここでスラリーは、室温であることと;
c)スラリーが均質となる迄、混合するステップと;
d)スラリーを乾燥して、ホップ酸の無機塩を得るステップとを含む方法。 - イソα酸の無機塩の製造方法であって:
(a)10〜50%のイソα酸を含有するアルカリ性水溶液を提供するステップと、ここで溶液は、室温であることと;
(b)撹拌しながら該アルカリ性水溶液に無機塩を加えて、スラリーを形成するステップと、ここでスラリーは、室温であることと;
(c)スラリーが均質となる迄、混合するステップと;
(d)スラリーを乾燥して、イソα酸の無機塩を得るステップとを含む方法。 - β酸の無機塩の製造方法であって:
(a)10〜50%のβ酸を含有するアルカリ性水溶液を提供するステップと、ここで溶液は、室温であることと;
(b)撹拌しながら該アルカリ性水溶液に無機塩を加えて、スラリーを形成するステップと、ここでスラリーは、室温であることと;
(c)スラリーが均質となる迄、混合するステップと;
(d)スラリーを乾燥して、イソα酸の無機塩を得るステップとを含む方法。 - 無機塩が、リチウム、ナトリウム、カリウム、銀、銅、マグネシウム、カルシウム、バリウム、クロム、マンガン、鉄、銀、コバルト、ニッケル、銅、亜鉛、又はカドミウム塩である、請求項14〜16のいずれか一項に記載の方法。
- 無機塩が、マグネシウム、カルシウム、カリウム、リチウム、鉄、又は亜鉛塩である、請求項14〜16のいずれか一項に記載の方法。
- ホップ酸が、イソα酸、ロイソα酸、テトラヒドロイソα酸、及びヘキサヒドロ−イソα酸、並びにそれらの誘導体又は混合物からなる群より選択されるイソα酸である、請求項14又は請求項15に記載の方法。
- ホップ酸が、ルプロン、コルプロン、アドルプロン及びそれらの誘導体又は混合物からなる群より選択されるβ酸である、請求項14又は請求項15に記載の方法。
- β酸が、ヘキサヒドロβ酸又はテトラヒドロβ酸である、請求項14又は請求項15に記載の方法。
- 更にステップ(d)の前に、ステップ(c)の均質なスラリーを濾過するステップを含む、請求項14〜16のいずれか一項に記載の方法。
- イソα酸又はロイソα酸のマグネシウム塩の製造方法であって:
(a)10〜50%のイソα酸又はロイソα酸を含有する水溶液を提供するステップと、ここで溶液は、室温であることと;
(b)撹拌しながら該アルカリ性水溶液に無機マグネシウム塩を加えて、スラリーを形成するステップと、ここでスラリーは、室温であることと;
(c)スラリーが均質となる迄、混合するステップと;
(d)スラリーを乾燥して、イソα酸又はロイソα酸の無機マグネシウム塩を得るステップとを含む方法。 - 水溶液がアルカリ性水溶液である、請求項22に記載の方法。
- マグネシウム塩が硫酸マグネシウムである、請求項22に記載の方法。
- イソα酸又は還元イソα酸のカルシウム塩の製造方法であって:
(a)10〜50%のイソα酸又は還元イソα酸を含有する水溶液を提供するステップと、ここで溶液は、室温であることと;
(b)撹拌しながら該水溶液に無機カルシウム塩を加えて、スラリーを形成するステップと、ここでスラリーは、室温であることと;
(c)スラリーが均質となる迄、混合するステップと;
(d)スラリーを乾燥して、イソα酸又は還元イソα酸の無機カルシウム塩を得るステップとを含む、請求項22に記載の方法。 - 水溶液がアルカリ性水溶液である、請求項25に記載の方法。
- カルシウム塩が、炭酸カルシウム、塩化カルシウム、又は水酸化カルシウムのうちの少なくとも一つである、請求項25に記載の方法。
- 水溶液中に存在するイソα酸又はロイソα酸の濃度が、10%〜45%である、請求項14、15、及び17〜27のいずれか一項に記載の方法。
- 水溶液中に存在するイソα酸又はロイソα酸の濃度が、15%〜45%である、請求項28に記載の方法。
- 水溶液中に存在するイソα酸又はロイソα酸の濃度が15%である、請求項29に記載の方法。
- マグネシウム/イソα酸若しくはロイソα酸、又はカルシウム/イソα酸若しくはロイソα酸のモル比が、0.3〜0.8の範囲内にある、請求項14、15、及び17〜27のいずれか一項に記載の方法。
- 乾燥が、スプレードライ、真空乾燥、ドラム乾燥、パン・ドライ、ウィンドウ・ドライ及び凍結乾燥、又はそれらの任意の組み合わせからなる群より選択される方法により達成される、請求項14、15、及び17〜27のいずれか一項に記載の方法。
- 還元イソα酸が、テトラヒドロイソα酸及びヘキサヒドロイソα酸からなる群より選択される、請求項14、15、及び17〜27のいずれか一項に記載の方法。
- 室温が15℃〜25℃である、請求項14、15、及び17〜27のいずれか一項に記載の方法。
- 更にステップ(d)の前に、ステップ(c)の均質なスラリーを濾過するステップを含む、請求項14、15、及び17〜27のいずれか一項に記載の方法。
- 請求項14〜35のいずれか一項に記載の方法により形成される、還元イソα酸又は還元イソα酸の無機塩。
- イソα酸が、ロイソα酸、テトラヒドロイソα酸、及びヘキサヒドロイソα酸からなる群より選択される、還元イソα酸の無機塩。
- 塩が一価又は二価カチオンを含む、請求項37に記載の無機塩。
- 一価カチオンが、リチウム、ナトリウム、カリウム、銀、銅からなる群より選択される、請求項38に記載の無機塩。
- 二価カチオンが、マグネシウム、カルシウム、バリウム、クロム、マンガン、鉄、コバルト、ニッケル、銅、亜鉛、カドミウムである、請求項38に記載の無機塩。
- β酸のマグネシウム塩の製造方法であって:
(a)10〜50%のβ酸を含有するアルカリ性水溶液を提供するステップと、ここで溶液は、室温であることと;
(b)撹拌しながら該アルカリ性水溶液に無機マグネシウム塩を加えて、スラリーを形成するステップと、ここでスラリーは、室温であることと;
(c)スラリーが均質となる迄、混合するステップと;
(d)スラリーを乾燥して、β酸のマグネシウム塩を得るステップとを含む方法。 - マグネシウム塩が硫酸マグネシウムである、請求項41に記載の方法。
- β酸のカルシウム塩の製造方法であって:
(a)10〜50%のβ酸を含有するアルカリ性水溶液を提供するステップと、ここで溶液は、室温であることと;
(b)撹拌しながら該アルカリ性水溶液に無機カルシウム塩を加えて、スラリーを形成するステップと、ここでスラリーは、室温であることと;
(c)スラリーが均質となる迄、混合するステップと;
(d)スラリーを乾燥して、β酸のカルシウム塩を得るステップとを含む方法。 - カルシウム塩が、炭酸カルシウム、塩化カルシウム、又は水酸化カルシウムのうちの少なくとも一つである、請求項43に記載の方法。
- アルカリ性水溶液中に存在するβ酸の濃度が、10%〜45%である、請求項41〜45のいずれか一項に記載の方法。
- アルカリ性水溶液中に存在するβ酸の濃度が、15%〜45%である、請求項45に記載の方法。
- アルカリ性水溶液中に存在するβ酸の濃度が、20%である、請求項46に記載の方法。
- マグネシウム/β酸又はカルシウム/β酸のモル比が、0.3〜0.8の範囲内にある、請求項41〜47のいずれか一項に記載の方法。
- 更にステップ(d)の前に、ステップ(c)の均質なスラリーを濾過するステップを含む、請求項41〜47のいずれか一項に記載の方法。
- 乾燥が、スプレードライ、真空乾燥、ドラム乾燥、パン・ドライ、ウィンドウ・ドライ及び凍結乾燥、又はそれらの任意の組み合わせからなる群より選択される方法により達成される、請求項41〜47のいずれか一項に記載の方法。
- β酸が、テトラヒドロβ酸、及びヘキサヒドロβ酸からなる群より選択される、請求項41〜47のいずれか一項に記載の方法。
- 室温が15℃〜25℃である、請求項41〜47のいずれか一項に記載の方法。
- 請求項35〜46のいずれか一項に記載の方法により製造されるβ酸。
- β酸が、ルプロン、コルプロン、アドルプロン、ヘキサヒドロβ酸及びテトラヒドロβ酸からなる群より選択される、β酸の無機塩。
- 塩が一価又は二価カチオンを含む、請求項54に記載の無機塩。
- 一価カチオンが、リチウム、ナトリウム、カリウム、銀、銅からなる群より選択される、請求項55に記載の無機塩。
- 二価カチオンが、マグネシウム、カルシウム、バリウム、クロム、マンガン、鉄、コバルト、ニッケル、銅、亜鉛、カドミウムである、請求項55に記載の無機塩。
- 請求項1〜11、36及び52のいずれか一項に記載の組成物を、薬学的に許容される担体中に含む抗炎症組成物。
- 更に少なくとも一種の更なる治療薬を含む、請求項58に記載の組成物。
- 更なる治療薬が、テトラサイクリン、ドキシサイクリン、シクロフルキサシン、アジスロマイシン、ミノサイクリン、クラリスロマイシン、オーグメンチン、ペニシリン、ペニシリンG、ペニシリンV、メチシリン、オキサシリン、カルベニシリン、ナフシリン、アンピシリン、セファロスポリン、セファクロル、セファゾリン、セフロキシム、モキサラクタム、カルバペネム、モノバクタム、アミノグリコシド、マクロライド、リンコマイシン、ポリミキシン、スルホンアミド、キノロン、クロラムフェニコール(cloramphenical)、メトロニダゾール、スペクチノマイシン、トリメトプリム、及びバンコマイシンからなる群より選択される抗生物質である、請求項59に記載の組成物。
- 細菌感染の抑制方法であって、そのような処置を必要とする対象に、有効量の請求項1〜11、34及び46のいずれか一項に記載の組成物を投与することを含む方法。
- 細菌が、尋常性ざ瘡に関連する、請求項61に記載の方法。
- 細菌が、プロピオニバクテリウム・アクネである、請求項61に記載の方法。
- 細菌が、ヘリコバクター・ピロリ又は結核菌である、請求項61に記載の方法。
- 対象に、有効量の請求項1〜11、36及び52のいずれか一項に記載の組成物を投与することを含む、尋常性ざ瘡の処置方法。
- 組成物が局所的に投与される、請求項65に記載の方法。
- 組成物が全身に投与される、請求項65に記載の方法。
- 対象に、有効量の請求項1〜11、36及び52のいずれか一項に記載の組成物を投与することを含む、メタボリック症候群の処置又は予防方法。
- 組成物が全身に投与される、請求項68に記載の方法。
- 心疾患又は糖尿病の危険性を低下させる、請求項68に記載の方法。
- アレルギー、喘息、アレルギー性鼻炎、又はこれらの病状に関連した炎症の処置方法であって、対象に、有効量の請求項1〜11、36及び52のいずれか一項に記載の組成物を投与することを含む方法。
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US69274605P | 2005-06-21 | 2005-06-21 | |
US69291005P | 2005-06-21 | 2005-06-21 | |
US74996605P | 2005-12-12 | 2005-12-12 | |
US11/302,308 US20060287554A1 (en) | 2005-06-21 | 2006-04-24 | Process for producing inorganic salts of hop acids |
PCT/US2006/024045 WO2007002128A2 (en) | 2005-06-21 | 2006-06-21 | Compositions comprising and processes for producing inorganic salts of hop acids |
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US (2) | US20060287554A1 (ja) |
EP (1) | EP1898729A4 (ja) |
JP (1) | JP2008543942A (ja) |
KR (1) | KR20080032105A (ja) |
AU (1) | AU2006262321A1 (ja) |
WO (1) | WO2007002128A2 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2012101931A1 (ja) | 2011-01-24 | 2012-08-02 | 富士フイルム株式会社 | 経口用組成物 |
JP2017101019A (ja) * | 2010-10-30 | 2017-06-08 | カインデックス ファーマシューティカルズ インコーポレイテッド | シス3,4−ジヒドロキシ−2−(3−メチルブタノイル)−5−(3−メチルブチル)−4−(4−メチルペンタノイル)シクロペンタ−2−エン−1−オン誘導体、実質的に鏡像異性的に純粋な組成物及び方法 |
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US20060287554A1 (en) * | 2005-06-21 | 2006-12-21 | Madsen Kevin K | Process for producing inorganic salts of hop acids |
WO2009142736A1 (en) * | 2008-05-19 | 2009-11-26 | Betal, Llc | Method for preparing alpha acid-enriched hop compositions |
DE102009006539A1 (de) * | 2008-11-11 | 2010-05-20 | Boon Rawd Brewery Co., Ltd. | Verfahren zur Erhöhung der Extraktionsausbeute von funktionellen Inhaltsstoffen des Hopfens sowie Vorrichtung zur Durchführung des Verfahrens als auch hierfür geeignete Mischung und damit hergestelltes Getränk |
WO2021062607A1 (en) | 2019-09-30 | 2021-04-08 | The Procter & Gamble Company | Oral care compositions comprising hops beta acid and amino acid |
JP7428790B2 (ja) | 2019-09-30 | 2024-02-06 | ザ プロクター アンド ギャンブル カンパニー | 抗う蝕活性を有する口腔ケア組成物 |
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- 2006-06-21 WO PCT/US2006/024045 patent/WO2007002128A2/en active Application Filing
- 2006-06-21 EP EP06785221A patent/EP1898729A4/en not_active Withdrawn
- 2006-06-21 US US11/922,731 patent/US20110039927A1/en not_active Abandoned
- 2006-06-21 AU AU2006262321A patent/AU2006262321A1/en not_active Abandoned
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WO2007002128A2 (en) | 2007-01-04 |
EP1898729A4 (en) | 2009-05-06 |
US20060287554A1 (en) | 2006-12-21 |
EP1898729A2 (en) | 2008-03-19 |
WO2007002128A3 (en) | 2007-06-28 |
KR20080032105A (ko) | 2008-04-14 |
AU2006262321A1 (en) | 2007-01-04 |
US20110039927A1 (en) | 2011-02-17 |
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