KR930700468A - 신규의 약학적 활성을 지닌 카테콜 유도체 - Google Patents

신규의 약학적 활성을 지닌 카테콜 유도체

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KR930700468A
KR930700468A KR1019920702604A KR920702604A KR930700468A KR 930700468 A KR930700468 A KR 930700468A KR 1019920702604 A KR1019920702604 A KR 1019920702604A KR 920702604 A KR920702604 A KR 920702604A KR 930700468 A KR930700468 A KR 930700468A
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compound
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dihydroxy
methylidene
group
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레이조 배크스트됨
에르키 혼카넨
인게-브리트 린덴
에르키 니시넨
아이노 피퓨리
펜티 포토
타피오 코르코라이넨
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펜티 포토, 라이자 맨티라
오리온 위티머 오위
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Abstract

내용 없음.

Description

신규의 약학적 활성을 지닌 카테콜 유도체
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (43)

  1. 일반식(I)의 화합물 또는 약학적으로 적용가능한 그이 염 또는 에스테르.
  2. 상기식중, R1은 니트로, 할로겐 또는 시아노기와 같은 전기적으로 음성인 치환체이며, R2
  3. [상기식중, X1,X2,Y 및 Z는 독립적으로 산소, 황 또는 NR(식중, R은 수소알킬, 시클로알킬, 아랄킬 또는 아릴기이다)을 나타낸다.]로 부터 선택된 그룹이다.
  4. 제1항에 있어서, R1이 시아노기인 화합물.
  5. 제1항에 있어서, R1이 니트로기인 화합물.
  6. 제1항에 있어서, R1이 할로겐인 화합물.
  7. 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 구조식(Ia)그룹인 화합물.
  8. 상기식중, X1및 X2는 모두 NR(식중, R은 수소 또는 알킬이다.)을 나타내며, Y는 산소 또는 황을 나타내며 Z도 산소 또는 황이다.
  9. 제5항에 있어서, 구조식(I)의 화합물이 4-〔(3,4-디히드록시-5-니트로페닐)메틸리덴〕-2-티옥소이미다졸리딘-5-온, 4-〔(3,4-디히드록시-5-클로로페닐)메틸리덴]-2-티옥소이미다졸리딘-5-온 및 4-〔(3,4-디히드록시-5-니트로페닐)메틸리덴〕-2,5-이미다졸리딘디온 중에서 선택된 화합물.
  10. 4-〔(3,4-디히드록시-5-시아노페닐)메틸리덴〕-2-티옥소이미다졸리딘-5-온 또는 약학적으로 적용 가능한 그의 염 또는 에스테르.
  11. 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 구조식 (Ia)인 화합물.
  12. 상기식중, X1,Y 및 Z는 각각 독립적으로 산소 또는 황을 NR(식중, R은 수소 또는알킬이다.)을 나타낸다.
  13. 제8항에 있어서, 구조식(I)의 화합물이 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴〕-2-티옥소티아졸리딘-4-온, 5-〔(3,4-디히드록시-5-니트로페닐)메틸리덴]-3-메틸-2-티옥소티아졸리딘-4-온, 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-티아졸리딘-2,4-디온, 5-[(3,4-디히드록시-5-클로로페닐)메틸리덴]-티아졸리딘-2,4-디온, 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-4-티옥소-2-옥사졸리딘 및 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-4-티옥소티아졸리딘-2-온 중에서 선택
  14. 5-[(3,4-디히드록시-5-시아노페닐)메틸리덴]-2-티옥소티아졸리딘-4-온 또는약학적으로 적용 가능한 그의 염 또는 에스테르.
  15. 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 구조식(Ia)그룹인 화합물.
  16. 상기식중, X, 및 Z는 독립적으로 산소 또는 황이며 Y 및 X2는 NR(식중, 은 수소이다.)을 나타낸다.
  17. 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-2-아미노티아졸리딘-4-온 또는 약학적으로 적용가능한 그의 염 또는 에스테르.
  18. 제1항 내지 4항중 어느 한 항에 있어서, 구조식(I) 화합물에서 R2가 (Ia) 그룹이며, 그중 R2
  19. [상기식중, Y는 산소 또는 황이며, X1은 NR(식중, R은 수소 또는 알킬이다.)을 나타낸다.]인 화합물.
  20. 제13항에 있어서, Y가 산소인 화합물.
  21. 5-[(3,4-디히드록시-5-니트로페닐)메틸리덴]-2,4,6(1H,3H,5h)-피리미딘트리온 또는 약학적으로 적용가능한 그의 염 또는 에스테르.
  22. 5-[(3,4,-디히드록시-5-니트로페닐)메틸]-(1H,3H,5H)-피리미딘-2,4,6-트리온 또는 약학적으로 적용가능한 그이 염 또는 에스테르.
  23. 제1항 낸지 16항에 있어서, 외과적 수술, 치료, 진단등의 의학적 방법에 사용되는 화합물.
  24. 제1항 내지 16항의 화합물과 약학적으로 적용가능한 담체 또는 희석제를 함유하는 약학적 조성물.
  25. 본 발명에서 사용하는 약제의 제조 및 지방 과산화에 의한 조직 손상의 치료를 위한 제1항 내지 16항의 화합물의 용도.
  26. 제19항에 있어서, 치료 또는 예방을 해야할 조직 손상의 상태가, 심장 질환, 류마티스 관절염, 종양, 염증 질환, 이식 부작용, 저혈, 노화인 화합물의 용도.
  27. 제1-16항의 화합물의 효과적인 양을 그 대상에 복용시키는 지방 과산화에 의한 조직 손상의 예방 및 치료방법.
  28. 구조식(Ⅱ) 화합물의 알데히드기를 활성 메틸렌기를 가진 구조식 (Ⅲ)또는 (Ⅳ)화합물과 축합시켜, R2가 구조식(Ia) 기인 구조식(Ⅰ)화합물을 얻은후, 구조식(Ⅰa) 기의 탄소 -탄소 이중결합을 환원시켜 R2가 본 발명의 구조식(Ib)기 인 구조식(Ⅰ) 화합물을 생성시키는 공정으로 행해지는 구조식(Ⅰ)화합물의 제조방법.
  29. 상기식중, R1은 니트로, 할로겐, 시아노기와 같은 전기적으로 음성인 치환체이며, R2
  30. 상기식중,X1,X2,및 Z는 각각 독립적으로 산소, 황 또는 NR(식중,R은 수소, 알킬,시클로알킬, 아랄킬 또는 아릴기이다.)을 나타낸다.
  31. 상기식중, R1은 상기한바와 같다.
  32. 상기식중,X1,X2,Y및 Z는 상기한 바와 같다.
  33. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019920702604A 1990-04-27 1992-10-21 New pharmacologically active catechol derivatives KR100207144B1 (en)

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GB909009565A GB9009565D0 (en) 1990-04-27 1990-04-27 New pharmacologically active catechol derivatives
GB9101563.6 1991-01-24
GB919101563A GB9101563D0 (en) 1991-01-24 1991-01-24 New pharmacologically active catechol derivatives
GB9009565.4 1991-01-24
PCT/FI1991/000124 WO1991017151A1 (en) 1990-04-27 1991-04-26 New pharmacologically active catechol derivatives

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KR100207144B1 KR100207144B1 (en) 1999-07-15

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AT (1) ATE146462T1 (ko)
AU (1) AU646464B2 (ko)
CA (1) CA2080917C (ko)
DE (1) DE69123738T2 (ko)
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IE (1) IE911430A1 (ko)
LT (1) LT3137B (ko)
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HUT65662A (en) 1994-07-28
FI95129C (fi) 1995-12-27
LV10097A (lv) 1994-05-10
PT97507A (pt) 1992-01-31
LT3137B (en) 1995-01-31
PL166269B1 (pl) 1995-04-28
NO301928B1 (no) 1997-12-29
KR100207144B1 (en) 1999-07-15
IE911430A1 (en) 1991-11-06
JP2972377B2 (ja) 1999-11-08
EP0526598A1 (en) 1993-02-10
PT97507B (pt) 1998-08-31
HU214872B (hu) 1998-07-28
US5362733A (en) 1994-11-08
NO924132L (no) 1992-12-23
LTIP227A (lt) 1994-08-25
FI924838A (fi) 1992-10-23
NO924132D0 (no) 1992-10-26
AU646464B2 (en) 1994-02-24
LV10097B (en) 1995-02-20
US5614541A (en) 1997-03-25
US5889037A (en) 1999-03-30
WO1991017151A1 (en) 1991-11-14
FI95129B (fi) 1995-09-15
CA2080917A1 (en) 1991-10-28
HU9203369D0 (en) 1993-01-28
CA2080917C (en) 2001-06-12
DE69123738T2 (de) 1997-07-03
EP0526598B1 (en) 1996-12-18
DE69123738D1 (en) 1997-01-30
ATE146462T1 (de) 1997-01-15
JPH05331148A (ja) 1993-12-14
FI924838A0 (fi) 1992-10-23
AU7761891A (en) 1991-11-27

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