JP2013525494A5 - - Google Patents

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JP2013525494A5
JP2013525494A5 JP2013509219A JP2013509219A JP2013525494A5 JP 2013525494 A5 JP2013525494 A5 JP 2013525494A5 JP 2013509219 A JP2013509219 A JP 2013509219A JP 2013509219 A JP2013509219 A JP 2013509219A JP 2013525494 A5 JP2013525494 A5 JP 2013525494A5
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Claims (10)

  1. 高脂肪食摂取に関連する疾患または閉経後肥満に関連する疾患の治療、予防、発症遅延、発生率低下、あるいは重症度低下のための、下記の化学構造式XIで表されるエストロゲン受容体リガンド化合物の使用
    Figure 2013525494
    及びは、互いに独立的に、水素、アルデヒド、COOH、−C(=NH)−OH、CHNOH、CH=CHCOH、CH=CHCOR、−CH=CH、ヒドロキシアルキル、ハロゲン、ヒドロキシル、アルコキシ、シアノ、ニトロ、CF、NH4−メトキシフェニル、4−ヒドロキシフェニル、SH、COR、COOR、OCOR、アルケニル、アリル、2−メチルアリル、アルキニル、プロパルギル、OSOCF、OSOCH、NHR、NHCOR、N(R)、スルホンアミド、SOR、アルキル、シクロアルキル、ハロアルキル、アリール、フェニル、またはベンジルであり;
    は、水素、アルデヒド、−C(=NH)−OH、CHNOH、CH=CHCO H、CH=CHCO R、−CH=CH 、ヒドロキシアルキル、ハロゲン、ヒドロキシル、アルコキシ、シアノ、ニトロ、CF 、NH 、4−メトキシフェニル、4−ヒドロキシフェニル、SH、COR、OCOR、アルケニル、アリル、2−メチルアリル、アルキニル、プロパルギル、OSO CF 、OSO CH 、NHR、NHCOR、N(R) 、スルホンアミド、SO R、アルキル、シクロアルキル、ハロアルキル、アリール、フェニル、またはベンジルであり;
    Rは、アルキル、シクロアルキル、水素、ハロアルキル、ジハロアルキル、トリハロアルキル、CHF、CHF、CF、CFCF、アリール、フェニル、ベンジル、−Ph−CF、−Ph−CHF、−Ph−CHF、−Ph−CFCF、ハロゲン、アルケニル、CN、NO、またはOHであり;
    R´は、水素、Alk、またはCORであり;
    R´´は、水素、Alk、またはCORであり
    は、0、1、2、または3であり;
    iは、0、1、2、3、または4であり;
    nは、1、2、3、または4であり;
    mは、1であり;
    pは、0、1、2、3、4、または5であり;
    Alkは、炭素数1〜7個の直鎖アルキル、炭素数1〜7個の分鎖アルキル、または炭素数3〜8個のシクロアルキルである。
    ただし、h及びiの少なくとも一方は、0ではない。
  2. 前記高脂肪食摂取に関連する疾患が、肥満、体重増加、脂肪形成、骨無機質含量低下、白色脂肪組織重量増加、コレステロール値上昇、レプチン値上昇、インスリン耐性、II型糖尿病、血糖値上昇、炎症性疾患、変形性関節症、心臓血管疾患、脂肪肝疾患(肝臓への脂肪の蓄積)、脱共役タンパク質−1(UCP−1)値低下、脂質生成増加、あるいはそれらの任意の組み合わせから選択されることを特徴とする請求項1に記載の使用
  3. 前記閉経後肥満に関連する疾患が、肥満、体重増加、脂肪形成、骨無機質含量低下、白色脂肪組織重量増加、コレステロール値上昇、レプチン値上昇、インスリン耐性、II型糖尿病、血糖値上昇、炎症性疾患、変形性関節症、心臓血管疾患、脂肪肝疾患(肝臓への脂肪の蓄積)、脱共役タンパク質−1(UCP−1)値低下、脂質生成増加、あるいはそれらの任意の組み合わせから選択されることを特徴とする請求項に記載の使用
  4. 対象のエネルギー消費増大または除脂肪体重の増加のための、下記の化学構造式XIで表される化合物の使用。
    Figure 2013525494
    及びは、互いに独立的に、水素、アルデヒド、COOH、−C(=NH)−OH、CHNOH、CH=CHCOH、CH=CHCOR、−CH=CH、ヒドロキシアルキル、ハロゲン、ヒドロキシル、アルコキシ、シアノ、ニトロ、CF、NH4−メトキシフェニル、4−ヒドロキシフェニル、SH、COR、COOR、OCOR、アルケニル、アリル、2−メチルアリル、アルキニル、プロパルギル、OSOCF、OSOCH、NHR、NHCOR、N(R)、スルホンアミド、SOR、アルキル、シクロアルキル、ハロアルキル、アリール、フェニル、またはベンジルであり;
    は、水素、アルデヒド、−C(=NH)−OH、CHNOH、CH=CHCO H、CH=CHCO R、−CH=CH 、ヒドロキシアルキル、ハロゲン、ヒドロキシル、アルコキシ、シアノ、ニトロ、CF 、NH 、4−メトキシフェニル、4−ヒドロキシフェニル、SH、COR、OCOR、アルケニル、アリル、2−メチルアリル、アルキニル、プロパルギル、OSO CF 、OSO CH 、NHR、NHCOR、N(R) 、スルホンアミド、SO R、アルキル、シクロアルキル、ハロアルキル、アリール、フェニル、またはベンジルであり;
    Rは、アルキル、シクロアルキル、水素、ハロアルキル、ジハロアルキル、トリハロアルキル、CHF、CHF、CF、CFCF、アリール、フェニル、ベンジル、−Ph−CF、−Ph−CHF、−Ph−CHF、−Ph−CFCF、ハロゲン、アルケニル、CN、NO、またはOHであり;
    R´は、水素、Alk、またはCORであり;
    R´´は、水素、Alk、またはCORであり
    は、0、1、2、または3であり;
    iは、0、1、2、3、または4であり;
    nは、1、2、3、または4であり;
    mは、1であり;
    pは、0、1、2、3、4、または5であり;
    Alkは、炭素数1〜7個の直鎖アルキル、炭素数1〜7個の分鎖アルキル、または炭素数3〜8個のシクロアルキルであり、
    前記アルキル、アルケニル、アリール、及び複素環は、置換または非置換である。
    ただし、h及びiの少なくとも一方は、0ではない。
  5. 前記対象が、高脂肪食を摂取していることを特徴とする請求項に記載の使用
  6. 前記対象が、閉経後肥満を有していることを特徴とする請求項4に記載の使用
  7. 前記エストロゲン受容体リガンド化合物が、エストロゲン受容体βアゴニストであることを特徴とする請求項1ないし3のいずれか一項に記載の使用
  8. 前記化合物が、立体異性体、薬学的に許容される塩、医薬品、多形体、結晶、水和物、エステル、またはN−オキシド、あるいはそれらの任意の組み合わせを含むことを特徴とする請求項1ないし6のいずれか一項に記載の使用
  9. 前記化合物が、
    4−ブロモ−6,8−ジヒドロキシ−2−(4−ヒドロキシフェニル)イソキノリン−1(2H)−オン、または
    4−シアノ−6,8−ジヒドロキシ−2−(4−ヒドロキシフェニル)イソキノリン−1(2H)−オンであることを特徴とする請求項1ないし6のいずれか一項に記載の使用
  10. 前記化合物を0.01〜50mg/kg/日の用量で投与することを特徴とする請求項1ないし3のいずれか一項に記載の使用
JP2013509219A 2010-05-04 2011-05-04 核内受容体結合薬 Expired - Fee Related JP5792799B2 (ja)

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US12/773,515 US9623021B2 (en) 2007-01-22 2010-05-04 Nuclear receptor binding agents
PCT/US2011/035206 WO2011140228A1 (en) 2010-05-04 2011-05-04 Nuclear receptor binding agents

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EP (1) EP2566330A4 (ja)
JP (2) JP5792799B2 (ja)
KR (1) KR20130061151A (ja)
CN (2) CN102970870A (ja)
AU (1) AU2011248154B2 (ja)
CA (1) CA2798259A1 (ja)
IL (1) IL222823A0 (ja)
MX (1) MX2012012777A (ja)
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