JP5116476B2 - 2−アミノ−1,3−プロパンジオール誘導体を有効成分とする肝臓疾患治療剤および肝臓疾患治療方法 - Google Patents
2−アミノ−1,3−プロパンジオール誘導体を有効成分とする肝臓疾患治療剤および肝臓疾患治療方法 Download PDFInfo
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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Description
Annu. Rev. Biochem, 56: 651 (1987) Proc. Natl. Acad. Sci. USA, 87: 6547 (1990) 総合臨床, 54: 449 (2005). N. Engl. J. Med., 348:848 (2003) N. Engl. J. Med., 347: 975 (2002) J. Clin. Invest., 99: 1472 (1997)
1)一般式(1)
2)前記一般式(1)で表される誘導体が2−アミノ−2−[4−(3−ベンジルオキシフェニルチオ)−2−クロロフェニル]エチル−1,3−プロパンジオール及び薬学的に許容されるその塩ならびに水和物を有効成分とすることを特徴とする1)に記載の肝臓疾患治療剤、
3)前記一般式(1)で表される化合物が2−アミノ−2−[4−(3−ベンジルオキシフェニルチオ)−2−クロロフェニル]エチル−1,3−プロパンジオール塩酸塩ならびにその水和物を有効成分とすることを特徴とする1)に記載の肝臓疾患治療剤、
4)肝臓疾患が、肝炎、脂肪肝、中毒性肝障害、肝硬変又は糖尿病由来の肝臓疾患である上記1)〜3)に記載の肝臓疾患治療剤。
5)一般式(1)
6)肝臓疾患が、肝炎、脂肪肝、中毒性肝障害、肝硬変又は糖尿病由来の肝臓疾患である上記5)に記載の肝臓疾患の治療方法、に関するものである。
以下に実施例を挙げて本発明を具体的に説明する。本実施例では特に一般式の化合物のうち、2−アミノ−2−[4−(3−ベンジルオキシフェニルチオ)−2−クロロフェニル]エチル−1,3−プロパンジオール塩酸塩(以下、「KRP−203」と略記する)について述べるが、本発明はこれらの実施例によって何ら限定されるものではない。
マウスは日本チャールズリバーから雄性BALB/c8〜12週齢のものを購入し使用した。Concanavalin A(以下 Con A)をリン酸緩衝液(PBS)に溶解し、マウスの静脈内に40mg/kgになるように0.2mlを投与した。KRP−203は蒸留水に懸濁し、必要用量になるように体重10g当たりに0.1mgをCon A投与24時間前に経口投与した。マウスをConA投与24時間後に屠殺し、血清中のトランスアミナーゼ活性を測定した。また、30mLの0.1% EDTA−PBSで肝臓を還流し、肝浸潤物を回収した(文献、Eur.
J. Immunol., 17: 37,1987)。抹消血中のリンパ球の混入を避けるため、回収されるはじめの0.1% EDTA−PBS 2.5mLは廃棄した。収集された細胞は抗CD4抗体、抗CD8抗体、抗CD3抗体、抗CD45/B220抗体、抗CD11b抗体、抗Ly−49C抗体で染色しFACS Caliburで計数した。
(結果)
Con A誘発肝炎モデルにおけるALT活性値を測定した結果を図1に示した。KRP−203をCon A投与24時間前に経口投与し、Con A投与24時間後の血清中ATL活性値を図1に示した。Con Aにより肝炎が誘発されると肝障害の指標となるATLが上昇するが、KRP−203の0.1mg/kgおよび1mg/kgの前投与によってATLの上昇が有意に抑制された。さらに、0.01mg/kgの低投与量群でも抑制する傾向が観察された。
肝臓に浸潤した細胞の種類と数について表1に示した。KRP−203の投与群では浸潤細胞の総数が約50%減少した。特にCD3+、CD4+のT細胞やB220+のB細胞の浸潤は著明に抑制された。CD8+のT細胞およびNK−T細胞の浸潤抑制は軽度であり、NK細胞や単球の浸潤にはほとんど影響が見られなかった。
組成
化合物(KRP−203) 0.1mg
D−マンニトール 247.5mg
ステアリン酸マグネシウム 2.5mg
即ち、化合物とD−マンニトールを混合し、さらにステアリン酸マグネシウムを混合して混合末を調製した。この混合末をカプセルに充填してカプセル剤を製造した。
Claims (2)
- 2−アミノ−2−[4−(3−ベンジルオキシフェニルチオ)−2−クロロフェニル]エチル−1,3−プロパンジオール又は薬学的に許容されるその塩又はそれらの水和物を有効成分とすることを特徴とする肝炎治療剤。
- 2−アミノ−2−[4−(3−ベンジルオキシフェニルチオ)−2−クロロフェニル]エチル−1,3−プロパンジオール塩酸塩又はその水和物を有効成分とすることを特徴とする請求項1に記載の肝炎治療剤。
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JP2007539899A JP5116476B2 (ja) | 2005-10-07 | 2006-10-05 | 2−アミノ−1,3−プロパンジオール誘導体を有効成分とする肝臓疾患治療剤および肝臓疾患治療方法 |
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JP2005295478 | 2005-10-07 | ||
JP2005295478 | 2005-10-07 | ||
PCT/JP2006/319961 WO2007043433A1 (ja) | 2005-10-07 | 2006-10-05 | 2-アミノ-1,3-プロパンジオール誘導体を有効成分とする肝臓疾患治療剤および肝臓疾患治療方法 |
JP2007539899A JP5116476B2 (ja) | 2005-10-07 | 2006-10-05 | 2−アミノ−1,3−プロパンジオール誘導体を有効成分とする肝臓疾患治療剤および肝臓疾患治療方法 |
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JPWO2007043433A1 JPWO2007043433A1 (ja) | 2009-04-16 |
JP5116476B2 true JP5116476B2 (ja) | 2013-01-09 |
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US (1) | US8048928B2 (ja) |
EP (1) | EP1932522B1 (ja) |
JP (1) | JP5116476B2 (ja) |
KR (1) | KR101297302B1 (ja) |
CN (1) | CN101277687B (ja) |
AU (1) | AU2006300485B2 (ja) |
BR (1) | BRPI0617077A2 (ja) |
CA (1) | CA2624909C (ja) |
CY (1) | CY1112911T1 (ja) |
DK (1) | DK1932522T3 (ja) |
ES (1) | ES2385580T3 (ja) |
PL (1) | PL1932522T3 (ja) |
PT (1) | PT1932522E (ja) |
RU (1) | RU2421214C2 (ja) |
SI (1) | SI1932522T1 (ja) |
WO (1) | WO2007043433A1 (ja) |
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KR101297302B1 (ko) | 2013-08-19 |
SI1932522T1 (sl) | 2012-08-31 |
CN101277687B (zh) | 2012-07-18 |
JPWO2007043433A1 (ja) | 2009-04-16 |
BRPI0617077A2 (pt) | 2015-01-06 |
EP1932522A4 (en) | 2010-07-07 |
EP1932522B1 (en) | 2012-05-23 |
US20090253802A1 (en) | 2009-10-08 |
ES2385580T3 (es) | 2012-07-26 |
WO2007043433A1 (ja) | 2007-04-19 |
CY1112911T1 (el) | 2016-04-13 |
PL1932522T3 (pl) | 2012-09-28 |
US8048928B2 (en) | 2011-11-01 |
KR20080064962A (ko) | 2008-07-10 |
RU2008115613A (ru) | 2009-11-20 |
CA2624909C (en) | 2013-10-01 |
AU2006300485B2 (en) | 2011-08-25 |
EP1932522A1 (en) | 2008-06-18 |
CN101277687A (zh) | 2008-10-01 |
PT1932522E (pt) | 2012-06-26 |
CA2624909A1 (en) | 2007-04-19 |
DK1932522T3 (da) | 2012-07-02 |
RU2421214C2 (ru) | 2011-06-20 |
AU2006300485A1 (en) | 2007-04-19 |
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