KR960705843A - 펩티딜 화합물과 메탈로프로테인아제의 억제제로서 그들의 치료학적 용도(peptidyl compounds and their therapeutic use as inhibitors of metalloproteinases) - Google Patents
펩티딜 화합물과 메탈로프로테인아제의 억제제로서 그들의 치료학적 용도(peptidyl compounds and their therapeutic use as inhibitors of metalloproteinases)Info
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Abstract
본 발명은 하기의 식(Ⅰ)의 화합물로서,
여기서 R1은 C1-6알킬, C2-6알케닐, 아릴, (C1-6알킬)아릴 또는 C1-6알킬-AR9이고, A는 O, NR9이고, 또는 S(O)m이고, m은 0 내지 2이고, R9은 H, C1-4알킬, 아릴 또는 (C1-4알킬)아릴; R2는 H 또는 C1-6알킬; R4는 H 또는 아미노(NH2), 아릴 아미노, 보호된 아미노, 아릴, 디(C1-6알킬)아미노, 모노(C1-6알킬)아미노, CO2H, 보호된 카르복실, 카르바모일, 모노(C1-6알킬)카르바모일 또는 디(C1-6알킬)카르바모일에 의해 선택적으로 치환된 C1-6알킬, 및 R5는 H 또는 C1-6알킬, 또는 NR4R5은 피롤리디노, 피페리디도 또는 모르포리노; R6는 선택적으로 치환된 C3-6시클로알킬, C3-6시클로알케닐, C1-6알킬, 벤질, (C1-6알콕시)벤질, 벤질옥시벤질 또는 3-인돌리메틸; Alk는 C1-6알킬 또는 C2-6알케닐 및 n=0 또는 1; R7은 H 또는 R10CO, 여기서 R10은 C1-4알킬, (C1-4알킬)아릴, C3-6시클로알킬, (C3-6시클로알킬) C1-4알킬, C2-6알케닐 또는 (C2-6알케닐)아릴; 및 R8은 H, C1-4알킬, (C1-4알킬)아릴 또는 아릴; 또는 그들의 염, 솔베이트 또는 수화물이다.
이런 화합물들은 메타로프로테인아제, TNF 및/또는 다른 활성도와 관련된 상태를 처리하는데 사용될 수 있다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (6)
- 하기 일반식(Ⅰ)의 화합물, 또는 그들의 염, 솔베이트 또는 수화물.여기서 R1은 C1-6알킬, C2-6알케닐, 아릴, (C1-6알킬)아릴 또는 C1-6알킬-AR9이고, A는 O, NR9이고, 또는 S(O)m이고, m은 0 내지 2이고, R9은 H, C1-4알킬, 아릴 또는 (C1-4알킬)아릴; R2는 H 또는 C1-6알킬; R4는 H 또는 아미노(NH2), 아릴 아미노, 보호된 아미노, 아릴, 디(C1-6알킬)아미노, 모노(C1-6알킬)아미노, CO2H, 보호된 카르복실, 카르바모일, 모노(C1-6알킬)카르바모일 또는 디(C1-6알킬)카르바모일에 의해 선택적으로 치환된 C1-6알킬, 및 R5는 H 또는 C1-6알킬, 또는 NR4R5은 피롤리디노, 피페리디노 또는 모르포리노; R6는 선택적으로 치환된 C3-6시클로알킬, C3-6시클로알케닐, C1-6알킬, 벤질, (C1-6알콕시)벤질, 벤질옥시벤질 또는 3-인돌리메틸, Alk는 C1-6알킬 또는 C2-6알케닐 및 n=0 또는 1; R7은 H 또는 R10CO, 여기서 R10은 C1-4알킬, (C1-4알킬)아릴, C3-6시클로알킬, (C3-6시클로알킬)C1-4알킬, C2-6알케닐 또는 (C2-6알케닐)아릴; 및 R8은 H, C1-4알킬, (C1-4알킬)아릴 또는 아릴이다; 또는 그들의 염, 솔베이트 또는 수화물.
- 제1항에 있어서, R1은 알킬, 알케닐, 아릴, 알킬아릴이고, R7및 R8은 각각 H인 화합물.
- 제1항에 있어서, 화합물은 N-〔N-(메르캅토아세틸)-L-레우실〕-L-페닐알라닌 메틸아미드, N-〔(아세토메르캅토아실)-L-레우실〕-L-페닐알라닌 메틸아미드, (RS)-2-(아세틸티오)펜타노일-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-(아세틸티오)프로파노일-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-(아세틸티오)-3-메틸부타노일-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-(아세틸티오)-2-페닐아세틸-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-(아세틸티오)-3-페닐프로파노일-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-(아세틸티오)-4-페닐부타노일-L-레우실-L-페닐알라닌 N-메틸아미드, N-(아세틸메르캅토아실)-L-트레오닐-L-페닐알라닌 메틸아미드, N-(아세틸메르캅토아실)-L-트레오닐-L-레우실-L-트립토판 메틸아미드, (RS)-2-메르캅토펜타노일-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-메르캅토프로파노일-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-메르캅토-3-메틸부타노일-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-메르캅토-2-페닐아세틸-L-레우실-L-페닐알라닌 N-메틸아미드, (RS)-2-메르캅토-3-페닐프로파노일-L-레우실-L-페닐알라닌 N-메틸아미드, N-〔N-(메르캅토아세틸)-L-트레오닐〕-L-페닐알라닌 메틸아미드 및 N-〔N-(메르캅토아세틸)-L-레우실〕-L-트립토판 메틸아미드로부터 선택된 화합물.
- 제1항 내지 제3항 중 어느 하나의 항의 화합물과 생리학적으로 허용가능한 희석액 또는 담체로 이루어지는 치료에 사용하기 위한 제약학적 조성물.
- 매트릭스 메탈로프로테인아제 또는 TNF 활성과 관련된 상태의 억제 또는 치료를 위한 약제의 제조를 위한 제1항 내지 제3항 중 어느 하나의 항의 화합물의 용도.
- 제5항에 있어서, 상기 상태는 염증, 발열, 심장맥관의 효과, 출혈, 응고 및 급성상태 반응, 악태증 및 식욕결핍, 급성 간염, 쇼크 상태, 조직이식 대 숙주 반응, 자가면역 질병, 말라리아, 리퍼퓨션(reperfusion)질병, 수막염, 건선, 류마토이드 관절염, 다중 경화증 및 종양들로부터 선택되는 화합물의 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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GB939323165A GB9323165D0 (en) | 1993-11-10 | 1993-11-10 | Compounds |
GB9323165.2 | 1993-11-10 | ||
PCT/GB1994/002471 WO1995013289A1 (en) | 1993-11-10 | 1994-11-10 | Peptidyl compounds and their therapeutic use as inhibitors of metalloproteinases |
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KR1019960702437A KR960705843A (ko) | 1993-11-10 | 1994-11-10 | 펩티딜 화합물과 메탈로프로테인아제의 억제제로서 그들의 치료학적 용도(peptidyl compounds and their therapeutic use as inhibitors of metalloproteinases) |
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NZ271893A (en) * | 1993-08-23 | 1997-11-24 | Immunex Corp | Inhibitors of tnf-alpha secretion |
GB9414157D0 (en) * | 1994-07-13 | 1994-08-31 | Smithkline Beecham Plc | Medical use |
GB9601042D0 (en) * | 1996-01-17 | 1996-03-20 | Smithkline Beecham Plc | Medical use |
CN1193978A (zh) * | 1994-10-05 | 1998-09-23 | 奇罗斯恩有限公司 | 肽基化合物和它们作为金属蛋白酶抑制剂的医疗用途 |
AU701279B2 (en) * | 1995-05-10 | 1999-01-21 | Darwin Discovery Limited | Peptide compounds which inhibit metalloproteinase and TNF liberation and their therapeutic uses |
EP0824543A1 (en) * | 1995-05-10 | 1998-02-25 | Chiroscience Limited | Peptide compounds which inhibit metalloproteinase and tnf liberation, and their therapeutic use |
DE69627483T2 (de) * | 1995-05-10 | 2004-04-01 | Darwin Discovery Ltd., Slough | Peptidartige stoffe, die metalloproteinasen und die tnf-freisetzung hemmen, und ihre therapeutische verwendung |
US5677282A (en) * | 1995-06-07 | 1997-10-14 | Proscript, Inc. | Amino acid amides of 1,3,4-thiadiazoles as matrix metalloproteinase |
GB9514867D0 (en) * | 1995-07-20 | 1995-09-20 | British Biotech Pharm | Metalloproteinase inhibitors |
GB2318353B (en) * | 1995-07-20 | 1999-10-06 | British Biotech Pharm | Metalloproteinase inhibitors |
JP2008024720A (ja) * | 1995-07-26 | 2008-02-07 | Mitsubishi Chemicals Corp | ペニシラミンアミド誘導体 |
ES2186803T3 (es) * | 1995-10-05 | 2003-05-16 | Darwin Discovery Ltd | Peptidos tio-sustituidos como inhibidores de metaloproteinasas y de la liberacion de tnf. |
AU7139996A (en) * | 1995-10-05 | 1997-04-28 | Chiroscience Limited | Mercaptoamide derivatives and their therapeutic use |
GB9523066D0 (en) * | 1995-11-10 | 1996-01-10 | Chiroscience Ltd | Compounds and their therapeutic use |
DE69620639T2 (de) * | 1995-11-22 | 2002-10-17 | Darwin Discovery Ltd., Cambridge | Mercaptoalkylpeptidylverbindungen mit einem imidazolsubstituenten und ihre verwendung als inhibitoren der matrix metalloproteinasen (mmp) und/oder des tumor necrosis faktors (tnf) |
CZ298814B6 (cs) | 1996-01-23 | 2008-02-13 | Shionogi & Co., Ltd. | Sulfonované deriváty aminokyselin a metaloproteasové inhibitory obsahující tyto deriváty |
US6919375B1 (en) | 1996-01-23 | 2005-07-19 | Shionogi & Co., Ltd. | Sulfonated amino acid derivatives and metalloproteinase inhibitors containing the same |
GB9607249D0 (en) * | 1996-04-04 | 1996-06-12 | Chiroscience Ltd | Compounds |
GB9607119D0 (en) * | 1996-04-04 | 1996-06-12 | Chiroscience Ltd | Compounds |
GB9607120D0 (en) * | 1996-04-04 | 1996-06-12 | Chiroscience Ltd | Compounds |
WO1997037658A1 (en) * | 1996-04-04 | 1997-10-16 | F.Hoffmann-La Roche Ag | Use of derivatives of tetrahydro-beta-carbolines as antimetastatic agents |
GB9609702D0 (en) | 1996-05-09 | 1996-07-10 | Royal Free Hosp School Med | Anticoagulant peptides |
US5852213A (en) * | 1996-07-10 | 1998-12-22 | American Cyanamid Company | Mercaptoketones and mercaptoalcohols and a process for their preparation |
AU714687B2 (en) * | 1996-07-22 | 2000-01-06 | Monsanto Company | Thiol sulfone metalloprotease inhibitors |
GB9616643D0 (en) * | 1996-08-08 | 1996-09-25 | Chiroscience Ltd | Compounds |
US6953788B1 (en) | 1996-09-19 | 2005-10-11 | Aventis Pharmaceuticals Inc. | 3-mercaptoacetylamino-1,5-substituted-2-oxo-azepan derivatives useful as inhibitors of matrix metalloproteinase |
GB9624817D0 (en) * | 1996-11-28 | 1997-01-15 | British Biotech Pharm | Metalloproteinase inhibitors |
ATE258063T1 (de) * | 1997-03-03 | 2004-02-15 | Darwin Discovery Ltd | Selektive mmp inhibitoren mit verringerten nebenwirkungen |
US6696449B2 (en) | 1997-03-04 | 2004-02-24 | Pharmacia Corporation | Sulfonyl aryl hydroxamates and their use as matrix metalloprotease inhibitors |
KR20000075955A (ko) | 1997-03-04 | 2000-12-26 | 죤 에이치. 뷰센 | 방향족 술포닐 알파-히드록시 히드록삼산 화합물 |
US6362183B1 (en) | 1997-03-04 | 2002-03-26 | G. D. Searle & Company | Aromatic sulfonyl alpha-hydroxy hydroxamic acid compounds |
US6794511B2 (en) | 1997-03-04 | 2004-09-21 | G. D. Searle | Sulfonyl aryl or heteroaryl hydroxamic acid compounds |
US7115632B1 (en) | 1999-05-12 | 2006-10-03 | G. D. Searle & Co. | Sulfonyl aryl or heteroaryl hydroxamic acid compounds |
WO1998039316A1 (en) | 1997-03-04 | 1998-09-11 | Monsanto Company | N-hydroxy 4-sulfonyl butanamide compounds |
US6638952B1 (en) | 1997-03-04 | 2003-10-28 | Pharmacia Corporation | Aromatic sulfonyl alpha-cycloamino hydroxamic acid compounds |
US6034136A (en) | 1997-03-20 | 2000-03-07 | Novartis Ag | Certain cyclic thio substituted acylaminoacid amide derivatives |
US5756545A (en) * | 1997-04-21 | 1998-05-26 | Warner-Lambert Company | Biphenysulfonamide matrix metal alloproteinase inhibitors |
WO1999007679A1 (en) * | 1997-08-08 | 1999-02-18 | Chiroscience Limited | Peptidyl compounds having mmp and tnf inhibitory activity |
PL341379A1 (en) | 1997-11-14 | 2001-04-09 | Searle & Co | Aromatic sulphone substituted hydroxamic acid as inhibitor of metalloprotease |
US6750228B1 (en) | 1997-11-14 | 2004-06-15 | Pharmacia Corporation | Aromatic sulfone hydroxamic acid metalloprotease inhibitor |
US20010039287A1 (en) | 1997-11-14 | 2001-11-08 | Thomas E Barta | Aromatic sulfone hydroxamic acid metalloprotease inhibitor |
US6329418B1 (en) | 1998-04-14 | 2001-12-11 | The Procter & Gamble Company | Substituted pyrrolidine hydroxamate metalloprotease inhibitors |
AUPP508798A0 (en) * | 1998-08-05 | 1998-08-27 | Biotech Australia Pty Limited | Method of treating psoriasis |
US6858598B1 (en) | 1998-12-23 | 2005-02-22 | G. D. Searle & Co. | Method of using a matrix metalloproteinase inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
US6329550B1 (en) | 1998-12-31 | 2001-12-11 | Aventis Pharmaceuticals Inc. | Amidomalonamides useful as inhibitors of MMP of matrix metalloproteinase |
AU1836800A (en) * | 1998-12-31 | 2000-07-24 | Aventis Pharmaceuticals Inc. | Amidomalonamides and their use as inhibitors of matrix metalloproteinase |
US6800646B1 (en) | 1999-02-08 | 2004-10-05 | Pharmacia Corporation | Sulfamato hydroxamic acid metalloprotease inhibitor |
AU775701B2 (en) | 1999-02-08 | 2004-08-12 | G.D. Searle & Co. | Sulfamato hydroxamic acid metalloprotease inhibitor |
JP2003521476A (ja) * | 1999-06-15 | 2003-07-15 | メルク エンド カムパニー インコーポレーテッド | チオール誘導体、メタロ−β−ラクタマーゼ阻害剤 |
US6869951B1 (en) | 1999-07-16 | 2005-03-22 | Pharmacia Corporation | Method of changing conformation of a matrix metalloproteinase |
US6696456B1 (en) * | 1999-10-14 | 2004-02-24 | The Procter & Gamble Company | Beta disubstituted metalloprotease inhibitors |
IL151125A0 (en) | 2000-03-21 | 2003-04-10 | Procter & Gamble | Heterocyclic side chain containing, n-substituted metalloprotease inhibitors |
PL357275A1 (en) * | 2000-03-21 | 2004-07-26 | The Procter & Gamble Company | Carbocyclic side chain containing metalloprotease inhibitors |
CA2401728A1 (en) * | 2000-03-21 | 2001-09-27 | The Procter & Gamble Company | Difluorobutyric acid metalloprotease inhibitors |
US6683093B2 (en) | 2000-05-12 | 2004-01-27 | Pharmacia Corporation | Aromatic sulfone hydroxamic acids and their use as protease inhibitors |
FR2823212B1 (fr) * | 2001-04-10 | 2005-12-02 | Inst Nat Sante Rech Med | Inhibiteurs de la toxine botulique de type b |
AP2003002908A0 (en) | 2001-05-11 | 2003-12-31 | Pharmacia Corp | Aromatic sulfone hydroxamates and their use as protease inhibitors |
WO2003091247A2 (en) | 2002-04-25 | 2003-11-06 | Pharmacia Corporation | Piperidinyl-and piperazinyl-sulfonylmethyl hydroxamic acids and their use as protease inhibitors |
ES2342378T3 (es) * | 2002-08-20 | 2010-07-06 | Astellas Pharma Inc. | Inhibidor de degradacion de matriz extracelular del cartilago artrodial. |
WO2004060346A2 (en) | 2002-12-30 | 2004-07-22 | Angiotech International Ag | Drug delivery from rapid gelling polymer composition |
US7570250B2 (en) * | 2006-05-04 | 2009-08-04 | Yi-Ming Tseng | Control device including a ball that stores data |
DE202010018378U1 (de) | 2009-04-10 | 2016-04-07 | Tufts Medical Center, Inc. | PAR-1-Aktivierung durch Metalloproteinase-1 (MMP-1) |
CA3026074A1 (en) | 2016-06-01 | 2017-12-07 | M3 Biotechnology, Inc. | N-hexanoic-l-tyrosine-l-isoleucine-(6)-aminohexanoic amide compounds and their use to treat neurodegenerative diseases |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3774858D1 (de) * | 1986-12-24 | 1992-01-09 | Beecham Group Plc | Derivate von n-(2-alkyl-3-mercaptoglutaryl)-alpha-aminosaeuren und deren verwendung als collagenase-inhibitoren. |
JP2586942B2 (ja) * | 1987-03-17 | 1997-03-05 | リサーチ コーポレーシヨン テクノロジーズ インコーポレーテツド | 哺乳動物コラゲナーゼの合成阻止剤 |
US5144043A (en) * | 1988-06-15 | 1992-09-01 | Centocor | Cleavable bifunctional coupling agents |
AU5292193A (en) * | 1992-10-02 | 1994-04-26 | Merck & Co., Inc. | N-(mercaptoacyl)peptidyl derivatives as antidegenerative agents |
-
1993
- 1993-11-10 GB GB939323165A patent/GB9323165D0/en active Pending
-
1994
- 1994-11-10 CZ CZ19961349A patent/CZ287780B6/cs not_active IP Right Cessation
- 1994-11-10 CA CA002173470A patent/CA2173470A1/en not_active Abandoned
- 1994-11-10 BR BR9408025A patent/BR9408025A/pt not_active Application Discontinuation
- 1994-11-10 DK DK95900237T patent/DK0728144T3/da active
- 1994-11-10 EP EP95900237A patent/EP0728144B1/en not_active Expired - Lifetime
- 1994-11-10 JP JP7513690A patent/JPH09505041A/ja not_active Ceased
- 1994-11-10 DE DE69422726T patent/DE69422726T2/de not_active Expired - Fee Related
- 1994-11-10 WO PCT/GB1994/002471 patent/WO1995013289A1/en active IP Right Grant
- 1994-11-10 KR KR1019960702437A patent/KR960705843A/ko active IP Right Grant
- 1994-11-10 HU HU9601244A patent/HU217344B1/hu not_active IP Right Cessation
- 1994-11-10 ES ES95900237T patent/ES2143611T3/es not_active Expired - Lifetime
- 1994-11-10 AU AU81133/94A patent/AU679286B2/en not_active Ceased
- 1994-11-10 PL PL94314300A patent/PL180403B1/pl unknown
- 1994-11-10 AT AT95900237T patent/ATE188969T1/de not_active IP Right Cessation
- 1994-11-10 CN CN94194051A patent/CN1134705A/zh active Pending
- 1994-11-10 PT PT95900237T patent/PT728144E/pt unknown
-
1996
- 1996-05-09 NO NO961888A patent/NO961888D0/no not_active Application Discontinuation
- 1996-05-09 FI FI961976A patent/FI961976A0/fi unknown
- 1996-05-10 US US08/644,383 patent/US5853623A/en not_active Expired - Fee Related
-
1998
- 1998-12-28 HK HK98115826A patent/HK1015139A1/xx not_active IP Right Cessation
-
2000
- 2000-03-29 GR GR20000400792T patent/GR3033103T3/el not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CA2173470A1 (en) | 1995-05-18 |
EP0728144B1 (en) | 2000-01-19 |
HK1015139A1 (en) | 1999-10-08 |
US5853623A (en) | 1998-12-29 |
HU217344B1 (hu) | 2002-02-28 |
CN1134705A (zh) | 1996-10-30 |
NO961888L (no) | 1996-05-09 |
GR3033103T3 (en) | 2000-08-31 |
FI961976A (fi) | 1996-05-09 |
CZ134996A3 (en) | 1996-10-16 |
GB9323165D0 (en) | 1994-01-05 |
HU9601244D0 (en) | 1996-07-29 |
ATE188969T1 (de) | 2000-02-15 |
PL314300A1 (en) | 1996-09-02 |
HUT73799A (en) | 1996-09-30 |
DE69422726D1 (de) | 2000-02-24 |
WO1995013289A1 (en) | 1995-05-18 |
DE69422726T2 (de) | 2000-06-08 |
PT728144E (pt) | 2000-07-31 |
AU8113394A (en) | 1995-05-29 |
NO961888D0 (no) | 1996-05-09 |
PL180403B1 (pl) | 2001-01-31 |
DK0728144T3 (da) | 2000-07-03 |
BR9408025A (pt) | 1996-12-17 |
AU679286B2 (en) | 1997-06-26 |
ES2143611T3 (es) | 2000-05-16 |
FI961976A0 (fi) | 1996-05-09 |
EP0728144A1 (en) | 1996-08-28 |
JPH09505041A (ja) | 1997-05-20 |
CZ287780B6 (en) | 2001-02-14 |
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