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JP2008001722A - サイトカインおよび造血因子の内因性産生増強因子とその利用方法 - Google Patents

サイトカインおよび造血因子の内因性産生増強因子とその利用方法 Download PDF

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JP2008001722A
JP2008001722A JP2007238577A JP2007238577A JP2008001722A JP 2008001722 A JP2008001722 A JP 2008001722A JP 2007238577 A JP2007238577 A JP 2007238577A JP 2007238577 A JP2007238577 A JP 2007238577A JP 2008001722 A JP2008001722 A JP 2008001722A
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endogenous production
glutathione disulfide
cytokines
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cytokine
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Mark Borisovich Balazovsky
ボリソビチ バラツォフスキィ マルク
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Cellectar Biosciences Inc
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Abstract

【課題】内因性のサイトカインおよび造血因子産生を誘導することができる活性物質、および当該物質と/あるいはその誘導体と、その活性のエキステンダーや/もしくはエンハンサーあるいはモジュレーターの有益な組み合わせをそれを必要としている個体あるいは対象に提供すること。
【解決手段】サイトカインもしくは造血因子またはその両方に対する刺激を必要とする哺乳動物の体内に、治療効果を得るためにサイトカインおよび造血因子の内因性産生を刺激できるだけの時間、酸化型グルタチオン、医薬として許容される酸化型グルタチオン塩、医薬として許容されるグルタチオン誘導体またはこれらの混合物より選択された酸化型製剤の有効量を導入することを含んでなる、サイトカインおよび造血因子の内因性産生を刺激する方法。
【選択図】なし

Description

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本発明の上記およびその他の目的、特徴および利点については、明細書と添付した図面を一緒に読むとさらに良く理解できいるだろう;
図1a,1b、1cおよび1dはそれぞれ細胞HL−60(対照あるいは本発明の調整品存在下)の蛍光フローサウイトメトリー分析、ヒトリンパ球(対照あるいは本発明の調整物存在下)の蛍光フローサウイトメトリー分析を示しており、実施例4の考察に記載の如く、培養した哺乳動物細胞でのアポトーシス−誘導標本活性の研究に関するものである。 図2はGSSG塩および誘導体を作成したときの化学修飾のための箇所を印したGSSG構造の図である。 図3,4,5,6,および7はGSSGを共有結合により:システアミン(S−チオエチルアミン−グルタチオンジスルフィド、図.3);リポ酸(ビス−[6,8−チオオキタニル]1グルタチオンジスルフィド、図.4);カルノシン([b−アラニル−ヒスチジル]1グルタチオンジスルフィド、図.5)、アデノシン([9−β−D−リボフラノシルアデニル]1グルタチオンジスルフィド、図.6)、あるいはメチオニン(ビス−[2−アミノ−4−[メチルチオ]ブタノイル]1グルタチオンジスルフィド、図.7)に結合した化合物の図である。 図3,4,5,6,および7はGSSGを共有結合により:システアミン(S−チオエチルアミン−グルタチオンジスルフィド、図.3);リポ酸(ビス−[6,8−チオオキタニル]1グルタチオンジスルフィド、図.4);カルノシン([b−アラニル−ヒスチジル]1グルタチオンジスルフィド、図.5)、アデノシン([9−β−D−リボフラノシルアデニル]1グルタチオンジスルフィド、図.6)、あるいはメチオニン(ビス−[2−アミノ−4−[メチルチオ]ブタノイル]1グルタチオンジスルフィド、図.7)に結合した化合物の図である。 図3,4,5,6,および7はGSSGを共有結合により:システアミン(S−チオエチルアミン−グルタチオンジスルフィド、図.3);リポ酸(ビス−[6,8−チオオキタニル]1グルタチオンジスルフィド、図.4);カルノシン([b−アラニル−ヒスチジル]1グルタチオンジスルフィド、図.5)、アデノシン([9−β−D−リボフラノシルアデニル]1グルタチオンジスルフィド、図.6)、あるいはメチオニン(ビス−[2−アミノ−4−[メチルチオ]ブタノイル]1グルタチオンジスルフィド、図.7)に結合した化合物の図である。 図3,4,5,6,および7はGSSGを共有結合により:システアミン(S−チオエチルアミン−グルタチオンジスルフィド、図.3);リポ酸(ビス−[6,8−チオオキタニル]1グルタチオンジスルフィド、図.4);カルノシン([b−アラニル−ヒスチジル]1グルタチオンジスルフィド、図.5)、アデノシン([9−β−D−リボフラノシルアデニル]1グルタチオンジスルフィド、図.6)、あるいはメチオニン(ビス−[2−アミノ−4−[メチルチオ]ブタノイル]1グルタチオンジスルフィド、図.7)に結合した化合物の図である。 図3,4,5,6,および7はGSSGを共有結合により:システアミン(S−チオエチルアミン−グルタチオンジスルフィド、図.3);リポ酸(ビス−[6,8−チオオキタニル]1グルタチオンジスルフィド、図.4);カルノシン([b−アラニル−ヒスチジル]1グルタチオンジスルフィド、図.5)、アデノシン([9−β−D−リボフラノシルアデニル]1グルタチオンジスルフィド、図.6)、あるいはメチオニン(ビス−[2−アミノ−4−[メチルチオ]ブタノイル]1グルタチオンジスルフィド、図.7)に結合した化合物の図である。

Claims (1)

  1. 本明細書に記載されるような、サイトカインおよび造血因子の内因性産生増強因子とその利用方法。
JP2007238577A 1995-12-14 2007-09-13 サイトカインおよび造血因子の内因性産生増強因子とその利用方法 Pending JP2008001722A (ja)

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RU95120403/14A RU2089179C1 (ru) 1995-12-14 1995-12-14 Стимулятор эндогенной продукции цитокинов и гепопоэтических факторов и способ его использования
PCT/RU1996/000226 WO1997021443A1 (en) 1995-12-14 1996-08-08 Cytokine and hemopoietic factor endogenous production enhancer and methods of use thereof

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CN1152711C (zh) * 1997-03-21 2004-06-09 株式会社资生堂 免疫激活剂及谷光甘肽的应用
AU728488B2 (en) * 1997-04-02 2001-01-11 Sankyo Company Limited Dithiolan derivatives, their preparation and their therapeutic effect
EP1066370A1 (en) 1998-03-30 2001-01-10 I.D.M. Immuno-Designed Molecules Stimulated monocyte derived cells, their preparation and uses
JP2000169371A (ja) * 1998-10-02 2000-06-20 Sankyo Co Ltd ジチオラン誘導体を含有する医薬
US6312734B1 (en) * 1998-11-23 2001-11-06 Novelos Therapeutics, Inc. Methods for production of the oxidized glutathione composite with cis-diamminedichloroplatinum and pharmaceutical compositions based thereof regulating metabolism, proliferation, differentiation and apoptotic mechanisms for normal and transformed cells
RU2144374C1 (ru) 1998-11-23 2000-01-20 Закрытое акционерное общество "ВАМ" Способ получения композита окисленного глутатиона с cis-диаминодихлорплатиной и фармацевтических композиций на его основе, регулирующих метаболизм, пролиферацию, дифференцировку и механизмы апоптоза нормальных и трансформированных клеток
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AU1113097A (en) 1997-07-03
ES2174124T3 (es) 2002-11-01
WO1997021444A1 (en) 1997-06-19
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JP2000515111A (ja) 2000-11-14
EP0869809B1 (en) 2002-03-27

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