KR930017881A - 술폰아미드 엔도텔린 길항제 - Google Patents
술폰아미드 엔도텔린 길항제 Download PDFInfo
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Abstract
본 발명은 엔도텔린을 억제하는 하기 일반식의 화합물에 관한 것이다.
상기 식에서, X및 Y중의 하나는 N이고, 다른 하나는 O이고, R은 나프틸 또는 R1,R2및 R3으로 치환된 나프틸이고, R1,R2및 R3은 각각 독립적으로 수소, Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬, 할로, 히드록실, 시아노, 니트로, -C(O)H,-C(O)R6,CO2H,-CO2R6,-SH,-S(O)nR6,-S(O)m-OH,-S(O)m-OR6,-O-S(O)m-R6,-O-S(O)mOH,-O-S-(O)-m-OR6,-Z4-NR7R8,또는 -Z4-N(R11)-Z5-NR9R10이고, R4및 R5는 각각 독립적으로 수소, Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬, 할로, 히드록실, 시아노, 니트로, -C(O)H,-C(O)R6,CO2H,-CO2R6,-SH,-S(O)nR6,-S(O)m-OH,-S(O)m-OR6,-O-S(O)m-R6,-O-S(O)mOH,-O-S-(O)-m-OR6,-Z4-NR7R8,또는 -Z4-N(R11)-Z5-NR9R10이거나, 또는 R4및R5는 함께 그들이 결합된 탄소 원자와 함께 4내지 8원 포화, 불포화, 또는 방향족 고리를 완성하고, Z1,Z2및 Z3으로 치환될 수 있는, 알킬렌 또는 알케닐렌이고, 여기에서, R6,R7,R8,R9,R10,R11,Z6,Z7,Z9, m및 n은 상기 정의한 바와 같다.
Description
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Claims (20)
- 하기 일반식의 화합물 또는 제약상 허용되는 그의 염.상기 식에서, X및 Y중의 하나는 N이고, 다른 하나는 O이고, R은 나프틸 또는 R1,R2및 R3으로 치환된 나프틸이고, R1,R2및 R3은 각각 독립적으로, (a)수소, (b)Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬, (c)할로, (d)히드록실, (e)시아노, (f)니트로, (g)-C(O)H또는-C(O)R6, (h)CO2H,-CO2R|6,(i)-SH,-S(O)n-R6,-S(O)m-OH,-S(O)m-R6,-O-S(O)m-R|6,-S(O)mOH또는-S-(O)m-OR6,-Z4-NR7R|8,또는 (k)-Z4-N(R11)-Z5-NR9R10이고, R4및 R5는 각각 독립적으로 (a)수소, (b)Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬, (c)할로, (d)히드록실, (e)시아노, (f)니트로, (g)-C(O)H 또는-C(O)R6,(h)CO2H또는-CO2R6,(i)-SH,-S(O)|n-R6,-S(O)m-OH,-S(O)m-OR6,-O-S(O)m-R6,-O-S(O)mOH 또는-S(O)|m-OR6,(j)-Z4-NR7R8또는 (k)-Z4-N(R11)-Z5-NR9R10이거나, 또는 (1)R4및R5는 함께 그들이 결합된 탄소 원자와 함께 4내지 8원 포화, 불포화, 또는 방향족 고리를 완성하는 Z1,Z2및 Z3으로 치환될 수 있는 알킬렌 또는 알케닐렌이고, R6은Z1,Z2및Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴, 또는 아랄킬이고, R7은, (a)수소, (b)Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬, (c)시아노, (d)히드록실, (e)-C(O)H 또는-C(O)R6,(f)CO2H또는-CO2R6,또는(g)-SH,-S(O)nR6,-S(O)m-OH,-S(O)m-OR6,-O-S(O)m-R6,-O-S(O)mOH 또는-0-S(O)m-OR6이고,(단,Z4가 -S(0)m-인 경우는 제외함),R8은, (a)수소, (b)-C(O)H 또는C(O)R6(단, Z4가 -C(O)-이고, R7이 -C(O)H, -C(O)R6,-CO|2H 또는 -CO2R6인 경우는 제외함),또는 (c) Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬이거나, 또는 R7및R8은 함께 그들이 결합된 질소 원자와 함께 3내지 8원 포화, 불포화 또는 방향족 고리를 완성하는 Z1,Z2및 Z3으로 치환될 수 있는 알킬렌 또는 알케닐렌이고, R9는, (a)수소, (b)히드록실, (c)-C(O)H 또는-C(O)R6,(d)-CO2H또는-CO2R6,(e)-SH,-S(O)n-R6,-S(O)m-OH,-S(O)m-OR|6,-O-S(O)m-R6,-O-S(O)mOH 또는-S(O)m-OR6,또는 (f) Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬이고,R10은, (a)수소,(b)-C(O)H 또는 -C(O)R6(단, Z5가 -C(O)-이고, R9가-C(O)H,-C(O)R|6,-CO2H 또는 CO2R6인 경우는 제외함),또는 (c)Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬이고,R11은, (a)수소,(b)히드록실, -CO2R6또는 CO|2H(단, R9및R10중의 하나가 히드록실, CO2R6또는CO2H인 경우는 제외함),(c) -C(O)H 또는-C(O)R6,또는 (d) Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 알콕시, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬이거나, R9,R10및 R11중의 임의의 2개는 함께 그들이 결합된 원자들과 함께 3내지 8원 포화, 불포화 또는 방향족 고리를 완성하는, Z1,Z2및 Z3으로 치환될 수 있는 알킬렌 또는 알케닐렌이고, Z1,Z2및 Z3은 각각 독립적으로, (a)수소,(b)할로, (c)히드록시, (d)알콕시, (e)-SH, -S(O)nZ6,-S(O)m-OH,-S(O)m-OZ6,-O-S(O)|m-Z6,-O-S(O)mOH또는-S(O)m-OZ6,(f)옥소,(g)니트로,(h)시아노,(i)-C(O)H 또는 -C(O)Z6,(j)-CO|2H또는CO2Z6, 또는(k)-NZ7Z8,-C(O)NZ7Z8또는-S(O)nZ7Z|8이고, Z4및Z5는 각각 독립적으로, (a)단일결합, (b)-S(O)n-,(c)-C(O)-,(d)-C(S)또는(e)Z1,Z2및 Z3으로 치환될 수 있는, 알킬, 알케닐, 알키닐, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬이고,Z6,Z7및 Z8은 각각 독립적으로 수소,알킬, 알케닐, 알키닐, 시클로알킬, 시클로알킬알킬, 시클로알케닐, 시클로알케닐알킬, 아릴 또는 아랄킬이거나, 또는 Z7및 Z8은 함께 그들이 결합된 질소 원자와 함께 3내지 8원 포호, 불포화 도는 방향족 고리를 완성하는 알킬렌 또는 알케닐이고, m은 1또는 2이고,n은 0,1또는 2이다.
- 제1항에 있어서, R1,R2및 R3중의 하나가 -NR7R8인 화합물,
- 제2항에 있어서, R7및 R8이 각각 독립적으로 수소, 알킬, 또는 C(O)알킬인 화합물.
- 제1항에 있어서, R이이고, 여기에서, 1또는 2위치에는 술폰아미드가 결합되고, 5또는 6위치에는 R1,R2및 R3중의 하나가 결합된 화합물.
- 제4항에 있어서, R1,R2및 R3중의 하나가 -NR6R8인 화합물.
- 제5항에 있어서, R7및 R8이 각각 독립적으로 수소,알킬 또는 C(O)알킬인 화합물.
- 제6항에 있어서, R7및 R8이 각각 독립적으로 수소, 메틸, 메틸에틸 또는 아세틸인 화합물.
- 제1항에 있어서, 하기 식을 갖는 화합물.
- 제8항에 있어서, R7및 R8이 각각 독립적으로 수소,알킬 또는 C(O)알킬인 화합물.
- 제9항에 있어서, R7및 R8이 각각 독립적으로 수소, 메틸, 메틸에틸 또는 아세틸인 화합물.
- 제1항에 있어서, R4및 R5가 알킬인 화합물.
- 제4항에 있어서, R4및 R5가 알킬인 화합물.
- 제1항에 있어서, R4및 R5가 메틸인 화합물.
- 제4항에 있어서, R4및 R5가 메틸인 화합물.
- 제1항에 있어서, 5-(디메틸아미노)-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,N-[5-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈레닐]아세트아미드, 5-아미노-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,N-[6-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈레닐]아세트아미드,5-아미노-N-(3,4-디메틸-5-이속사졸릴)-2-나프탈렌술폰아미드,N-[4-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈레닐]아세트아미드,N-[6-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-2-나프탈레닐]아세트아미드,6-아미노-N-(3,4-디메틸-5-이속사졸릴)-2-나프탈렌술폰아미드,4-아미노-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,5-디메틸아미노-N-(4,5-디메틸-3-이속사졸릴)-1-나프탈렌술폰아미드,N-[5-[[(4,5-디메틸-3-이속사졸릴)아미노]술포닐]-1-나프탈레닐]아세트아미드,N-[5-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-2-나프탈레닐]아세트아미드,N-[8-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-2-나프탈레닐]아세트아미드,N-[7-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-2-나프탈레닐]아세트아미드,N-[7-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈레닐]아세트아미드,N-(3,4-디메틸-5-이속사졸릴)-5-메톡시-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,5-[(1-메틸에틸)아미노]-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,N-[5-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈레닐]-2-메틸프로판아미드,5-클로로-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-5-[(페닐메틸)아미노]-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-5-히드록시-1-나프탈렌술폰아미드,7-(디메틸아미노)-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-5-[메틸(1-메틸에틸)-아미노]-1-나프탈렌술폰아미드,2-[[5-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈레닐]아미노]프로판산, 에틸 에스테르, N-(3,4-디메틸-5-이속사졸릴-5-(2-옥소-1-피롤리디닐)-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-5-(2-옥소-1-피페리디닐)-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-5-[[(페닐아미노)-티옥소메틸]아미노]-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-5-(1-피롤리디닐)-1-나프탈렌술폰아미드,5-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈렌카르복실산,5-[[[5-(디메틸아미노)-1-나프탈레닐]술포닐]아미노]-3-메틸-4-이속사졸카르복실산,에틸 에스테르,5-[[(3,4-디메틸-5-이속사졸릴)아미노]술포닐]-1-나프탈렌카르복실산,메틸 에스테르,5-(디메틸아미노)-N-(3-메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,5-[(디메틸아미노)메틸]-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,트리플루오로아세테이트(1:1)염,N-(3,4-디메틸-5-이속사졸릴)-5-(1-히드록시-1-메틸에틸)-1-나프탈렌술폰아미드,N-(3,4-디메틸-5-이속사졸릴)-5-(1-메틸에테닐)-1-나프탈렌술폰아미드, N-(3,4,-디메틸-5-이속사졸릴-5-(1-피페리디닐)-1-나프탈렌술폰아미드.트리플루오로아세테이트(2;1) 염, N-(3,4-디메틸-5-이속사졸릴)-5-(메틸아미노)-1-나프탈렌술폰아디므, N-(3,4-디메틸-5-이속사졸릴)-5-(에틸아미노)-1-나프탈렌술폰아미드, N-(3-메틸-4-페닐메틸-5-이속사졸릴)-5-[디메틸아미노]-1-나프탈렌술폰아미드, N-(3-메틸-4-페닐-5-이속사졸릴)-5-(디메틸아미노)-1-나프탈렌술폰아미드,N-(3-에틸-4-메틸-5-이속사졸릴)-5-(디메틸아미노)-1나프탈렌술폰아미드,5-(디부틸아미노)-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,일나트륨염, 4-[1-[[(3,4-디메틸-5-이속사졸릴]아미노]술포닐]나프탈렌-5-일]아미노]부탄산, 6-아미노-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,7-아미노-N-(3,4-디메틸-5-이속사졸릴)-2-나프탈렌술폰아미드,8-아미노-N-(3,4-디메틸-5-이속사졸릴)-2-나프탈렌술폰아미드,7-아미노-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,7-(디메틸아미노)-N-(3,4-디메틸-5-이속사졸릴)-2-나프탈렌술폰아미드,8-(디메틸아미노-N-(3,4-디메틸-5-이속사졸릴)-2-나프탈렌술폰아미드,6-(디메틸아미노)-N-(3,4-디메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,5-(디메틸아미노)-N-(3-메틸-4-니트로-5-이속사졸릴)-1-나프탈렌술폰아미드,5-(디메틸아미노)-N-(4,5,6,7-테트라히드로-2,1-벤즈이속사졸릴-3-일)-1-나프탈렌술폰아미드,5-(디메틸아미노)-N-(4-에틸-3-메틸-5-이속사졸릴)-1-나프탈렌술폰아미드,및 5-(디메틸아니노)-N-(4-메틸-5-이속사졸릴)-1-나프탈렌술폰아미드로 이루어진 군 중에서 선택된 화합물.
- 유효량의 제1항에 따른 화합물을 투여하는 것으로 이루어진 포유류에 있어서 엔도텔린 관련 질환을 치료하는 방법.
- 유효량의 제1항에 따른 화합물을 투여하는 것으로 이루어진 고혈압을 치료하는 방법.
- 유효량의 제1항에 따른 화합물을 투여하는 것으로 이루어진 신장, 시구체 또는 사구체 간질 세포 관련 질환을 치료하는 방법.
- 유효량의 제1항에 따른 화합물을 투여하는 것으로 이루어진 내독소혈병을 치료하는 방법.
- 유효량의 제1항에 따른 화합물을 투여하는 것으로 이루어진 빈혈을 치료하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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Families Citing this family (64)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5591761A (en) * | 1993-05-20 | 1997-01-07 | Texas Biotechnology Corporation | Thiophenyl-, furyl-and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
US5514691A (en) * | 1993-05-20 | 1996-05-07 | Immunopharmaceutics, Inc. | N-(4-halo-isoxazolyl)-sulfonamides and derivatives thereof that modulate the activity of endothelin |
US5594021A (en) * | 1993-05-20 | 1997-01-14 | Texas Biotechnology Corporation | Thienyl-, furyl- and pyrrolyl sulfonamides and derivatives thereof that modulate the activity of endothelin |
US5571821A (en) * | 1993-05-20 | 1996-11-05 | Texas Biotechnology Corporation | Sulfonamides and derivatives thereof that modulate the activity of endothelin |
US5962490A (en) | 1987-09-25 | 1999-10-05 | Texas Biotechnology Corporation | Thienyl-, furyl- and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
US5736509A (en) * | 1990-12-14 | 1998-04-07 | Texas Biotechnology Corporation | Cyclic peptide surface feature mimics of endothelin |
NZ247440A (en) * | 1992-05-06 | 1995-04-27 | Squibb & Sons Inc | Phenyl sulphonamide derivatives, preparation and pharmaceutical compositions thereof |
US5514696A (en) * | 1992-05-06 | 1996-05-07 | Bristol-Myers Squibb Co. | Phenyl sulfonamide endothelin antagonists |
US5767310A (en) * | 1993-03-19 | 1998-06-16 | Merck & Co., Inc. | Phenoxyphenylacetic acid derivatives |
CA2121724A1 (en) | 1993-04-21 | 1994-10-22 | Toshifumi Watanabe | Methods and compositions for the prophylactic and/or therapeutic treatment of organ hypofunction |
US6613804B2 (en) | 1993-05-20 | 2003-09-02 | Encysive Pharmaceuticals, Inc. | Biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin |
US6030991A (en) * | 1993-05-20 | 2000-02-29 | Texas Biotechnology Corp. | Benzenesulfonamides and the use thereof to modulate the activity of endothelin |
US6376523B1 (en) | 1994-05-20 | 2002-04-23 | Texas Biotechnology Corporation | Benzenesulfonamides and the use thereof to modulate the activity of endothelin |
US6541498B2 (en) | 1993-05-20 | 2003-04-01 | Texas Biotechnology | Benzenesulfonamides and the use thereof to modulate the activity of endothelin |
US6342610B2 (en) | 1993-05-20 | 2002-01-29 | Texas Biotechnology Corp. | N-aryl thienyl-, furyl-, and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin |
US5391566A (en) * | 1993-07-20 | 1995-02-21 | Merck & Co., Inc. | Benzimidazolinones substituted with phenoxyphenylacetic acid derivatives |
US5686478A (en) * | 1993-07-20 | 1997-11-11 | Merck & Co. Inc. | Endothelin antagonists |
ES2081251B1 (es) * | 1993-08-04 | 1996-10-16 | Squibb & Sons Inc | Antagonistas de endotelina, a base de sulfonamida. |
US5965732A (en) * | 1993-08-30 | 1999-10-12 | Bristol-Myers Squibb Co. | Sulfonamide endothelin antagonists |
US5780498A (en) * | 1993-11-01 | 1998-07-14 | Ciba-Geigy Japan Limited | Endothelin receptor antagonists |
GB9504854D0 (en) * | 1994-03-31 | 1995-04-26 | Zeneca Ltd | Nitrogen derivatives |
GB9409618D0 (en) * | 1994-05-13 | 1994-07-06 | Zeneca Ltd | Pyridine derivatives |
US5612359A (en) * | 1994-08-26 | 1997-03-18 | Bristol-Myers Squibb Company | Substituted biphenyl isoxazole sulfonamides |
US5538991A (en) * | 1994-09-14 | 1996-07-23 | Merck & Co., Inc. | Endothelin antagonists bearing 5-membered heterocyclic amides |
US5559135A (en) * | 1994-09-14 | 1996-09-24 | Merck & Co., Inc. | Endothelin antagonists bearing pyridyl amides |
US5780473A (en) * | 1995-02-06 | 1998-07-14 | Bristol-Myers Squibb Company | Substituted biphenyl sulfonamide endothelin antagonists |
ES2201181T3 (es) * | 1995-04-04 | 2004-03-16 | Encysive Pharmaceuticals Inc. | Tienil-, furil-, pirrolil- y bifenilsulfonamidas y derivados de los mismos que modulan la actividad de endotelina. |
UA58494C2 (uk) * | 1995-06-07 | 2003-08-15 | Зенека Лімітед | Похідні n-гетероарилпіридинсульфонаміду, фармацевтична композиція, спосіб одержання та спосіб протидії впливам ендотеліну |
GB9512697D0 (en) * | 1995-06-22 | 1995-08-23 | Zeneca Ltd | Heterocyclic compounds |
US5846990A (en) * | 1995-07-24 | 1998-12-08 | Bristol-Myers Squibb Co. | Substituted biphenyl isoxazole sulfonamides |
JPH09124620A (ja) * | 1995-10-11 | 1997-05-13 | Bristol Myers Squibb Co | 置換ビフェニルスルホンアミドエンドセリン拮抗剤 |
US5977117A (en) * | 1996-01-05 | 1999-11-02 | Texas Biotechnology Corporation | Substituted phenyl compounds and derivatives thereof that modulate the activity of endothelin |
US5856507A (en) * | 1997-01-21 | 1999-01-05 | Bristol-Myers Squibb Co. | Methods for the preparation of biphenyl isoxazole sulfonamides |
SG87051A1 (en) | 1996-02-20 | 2002-03-19 | Bristol Myers Squibb Co | Process for preparing biphenyl isoxazole sulfonamide intermediates |
US5958905A (en) * | 1996-03-26 | 1999-09-28 | Texas Biotechnology Corporation | Phosphoramidates, phosphinic amides and related compounds and the use thereof to modulate the activity of endothelin |
US5939446A (en) * | 1996-04-09 | 1999-08-17 | Bristol-Myers Squibb Co. | Heteroaryl substituted phenyl isoxazole sulfonamide endothelin antagonists |
US5804585A (en) * | 1996-04-15 | 1998-09-08 | Texas Biotechnology Corporation | Thieno-pyridine sulfonamides derivatives thereof and related compounds that modulate the activity of endothelin |
WO1998033781A1 (en) * | 1997-01-30 | 1998-08-06 | Bristol-Myers Squibb Company | Method for preventing or treating low renin hypertension by administering an endothelin antagonist |
TW536540B (en) * | 1997-01-30 | 2003-06-11 | Bristol Myers Squibb Co | Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe |
US5783705A (en) * | 1997-04-28 | 1998-07-21 | Texas Biotechnology Corporation | Process of preparing alkali metal salys of hydrophobic sulfonamides |
IL131318A (en) | 1997-04-28 | 2004-08-31 | Encysive Pharmaceuticals Inc | Pharmaceutically acceptable salts of sulfonamides for treatment of endothelin-mediated disorders |
JP3783411B2 (ja) | 1997-08-15 | 2006-06-07 | 富士ゼロックス株式会社 | 表面発光型半導体レーザ |
US6638937B2 (en) | 1998-07-06 | 2003-10-28 | Bristol-Myers Squibb Co. | Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists |
IL144708A0 (en) | 1999-03-19 | 2002-06-30 | Bristol Myers Squibb Co | Methods for the preparation of biphenyl isoxazole sulfonamide derivatives |
US7566452B1 (en) | 1999-05-04 | 2009-07-28 | New York University | Cancer treatment with endothelin receptor antagonists |
KR20020072285A (ko) | 1999-12-31 | 2002-09-14 | 텍사스 바이오테크놀로지 코포레이션 | 엔도텔린의 활성을 조절하는 설폰아미드 및 이의 유도체 |
US6639082B2 (en) | 2000-10-17 | 2003-10-28 | Bristol-Myers Squibb Company | Methods for the preparation of biphenyl isoxazole sulfonamides |
JP4293734B2 (ja) * | 2001-01-17 | 2009-07-08 | 三菱電機株式会社 | 電動式パワーステアリング制御装置 |
JP4448902B2 (ja) | 2001-06-08 | 2010-04-14 | 株式会社医薬分子設計研究所 | スルホンアミド誘導体 |
GB0219660D0 (en) | 2002-08-23 | 2002-10-02 | Astrazeneca Ab | Therapeutic use |
DE10256186A1 (de) * | 2002-12-02 | 2004-06-09 | Bayer Ag | Cyclopenta(c)isoxazol-3-amine als Materialschutzmittel |
GB0403744D0 (en) | 2004-02-20 | 2004-03-24 | Astrazeneca Ab | Chemical process |
BRPI0517263A (pt) * | 2004-10-29 | 2008-10-07 | Astrazeneca Ab | novos derivados de sulfonamida como moduladores do receptor de glicocorticóide para o tratamento de doenças inflamatórias |
JP5204662B2 (ja) | 2005-11-22 | 2013-06-05 | アムジエン・インコーポレーテツド | 11−β−ヒドロキシステロイドデヒドロゲナーゼ1型の阻害剤 |
WO2008011453A2 (en) | 2006-07-20 | 2008-01-24 | Amgen Inc. | SUBSTITUTED AZOLE AROMATIC HETEROCYCLES AS INHIBITORS OF LLβ-HSD-1 |
JP4518065B2 (ja) * | 2006-10-25 | 2010-08-04 | 宇部興産株式会社 | 新規ジアルコキシアミドオキシム誘導体及びその製法 |
JP4518066B2 (ja) * | 2006-10-25 | 2010-08-04 | 宇部興産株式会社 | ジアルコキシニトリル誘導体及びその製法 |
TW200829578A (en) | 2006-11-23 | 2008-07-16 | Astrazeneca Ab | Chemical compounds 537 |
JO2754B1 (en) | 2006-12-21 | 2014-03-15 | استرازينكا ايه بي | Amylendazoleil derivatives for the treatment of glucocorticoid-mediated disorders |
US8211930B2 (en) | 2008-05-20 | 2012-07-03 | Astrazeneca Ab | Phenyl and benzodioxinyl substituted indazoles derivatives |
CN101818056B (zh) * | 2010-05-27 | 2013-07-31 | 中南大学 | 一类丹磺酰类分子探针及其合成方法和应用 |
JP6144631B2 (ja) * | 2012-01-31 | 2017-06-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | シタキセンタン誘導体 |
GB201810581D0 (en) | 2018-06-28 | 2018-08-15 | Ctxt Pty Ltd | Compounds |
RS64931B1 (sr) | 2019-06-18 | 2023-12-29 | Pfizer | Derivati benzizoxazol sulfonamida |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2888455A (en) * | 1956-09-04 | 1959-05-26 | Shionogi & Co | New sulfonamide and process for producing the same |
US3300488A (en) * | 1963-12-23 | 1967-01-24 | Shionogi & Co | Nu, nu'-bis [4-halogenated-5-alkyl-3-isoxazolylsulfamoyl)-phenyl]-ureas |
GB1473433A (ko) * | 1975-10-09 | 1977-05-11 | Banyu Pharmaceutical Co Ltd Hi | |
FI97540C (fi) * | 1989-11-06 | 1997-01-10 | Sanofi Sa | Menetelmä terapeuttisesti käyttökelpoisten, aromaattisesti substituoitujen piperidiini- ja piperatsiinijohdannaisten valmistamiseksi |
NZ239846A (en) * | 1990-09-27 | 1994-11-25 | Merck & Co Inc | Sulphonamide derivatives and pharmaceutical compositions thereof |
TW270116B (ko) * | 1991-04-25 | 1996-02-11 | Hoffmann La Roche | |
RU2086544C1 (ru) * | 1991-06-13 | 1997-08-10 | Хоффманн-Ля Рош АГ | Бензолсульфонамидные производные пиримидина или их соли, фармацевтическая композиция для лечения заболеваний, связанных с активностью эндотелина |
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1993
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1997
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