KR900016238A - 신규 화합물 - Google Patents
신규 화합물 Download PDFInfo
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- KR900016238A KR900016238A KR1019900005135A KR900005135A KR900016238A KR 900016238 A KR900016238 A KR 900016238A KR 1019900005135 A KR1019900005135 A KR 1019900005135A KR 900005135 A KR900005135 A KR 900005135A KR 900016238 A KR900016238 A KR 900016238A
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- leucine
- hydrogen
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- phosphonopropyl
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
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- C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
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- A61P27/00—Drugs for disorders of the senses
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- A—HUMAN NECESSITIES
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- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
- C07F9/3804—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se) not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
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- C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
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- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
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Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (16)
- 일반식(Ⅰ)의 화합물 또는 그들의 염, 용매화합물 또는 수화물 :(여기에서 R은 수소, C1-6알킬 또는 임의적으로 치환된 벤질; R1은 수소 또는 C1-6알킬 : R2는 C3-6알킬 R3는 수소, 알킬, Z이 임의적으로치환된 페닐 또는 헤테로아릴인 -CH2-Z, 또는 R7이 수소, 알킬 또는 -CH2-Ph(여기서 Ph는 임의적으로 치환된 페닐임)이고 R8이 수소 또는 알킬기 기및 R4는 n은 1 내지 6의 정수이고, R5,R6및 R9가 수소 또는 C1-6알킬; R10은 히드록시 또는 -O-C1-6알킬 또는 -NR5R6(여기에서 R5및 R6은 연결되어 헤테로시클릭 고리를 형성할 수도 있다)인 -CH2-(CH2)nOR5또는 -CH2-(CH)nOCOR6또는이고 또는 R3및 R4는 m이 4 내지 12의 정수인 -(CH2)m-로서 함께 결합될 수 있다)
- 제1항에 있어서, R이 수소, 메틸 또는 에틸인 화합물.
- 제1항 또는 제2항에 있어서, R1이 수소, 메틸, 에틸, 이소프로필 또는 n-부틸인 화합물.
- 제1항 내지 제3항 중 어느 한 항에 있어서, R2가 n-부틸, 이소부틸 또는 섹크-부틸인 화합물.
- 제1항 내지 제4항중 어느 한 항에 있어서, R3가 벤질, 4-히드록시벤질, 4-메톡시벤질 또는 3-인돌일메틸이고, R4가 -(CH2)2OH, -(CH2)2OCH3또는 -CH(CH3)CO2CH3거나, R3및 R4가 m이 10인 -(CH2)m으로서 결합되는 화합물.
- 제1항 내지 제5항중 어느 한 항에 있어서, R이 수소 또는 에틸이고, R은 메틸, 에틸 또는 n-부틸이고; R2는 이소-부틸이고, R3는 4-메톡시 벤질 또는 3-인돌일 메틸이고 R4는 -(CH2)2OH 또는 -CH(CH3)CO2CH3이거나; R3및 R4가 함께 m이 10인 -(CH2)m인 화합물.
- 제1항 내지 제6항중 어느 한 항에 있어서, 일반식(Ⅰ)에서 별표로 표시된 키탈 중심이 R3가 수소가 아닐 때 S- 배치를 갖는 화합물.
- N-[N-[N-(1-포스포노에틸)-류실]-(S)-트리프토필]-(S)-알라닌, 메틸 에스터,N-[N-[N-(1-포스포노에틸)-류실]-Q-메틸-(S)-티로실]-(S)-알라닌, 메틸 에스터, 3-[N-[N-((S)-1-포스포노프로필)-(R)-류실]]-아미노-아자시클로트리데칸-2-온, 3-[N-[N-((S)-1-포스포노프로필)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온, 3-[N-[N-((R)-1-포스포노프로필)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온,N-[N-[N-(1-(R)-포스포노프로필)-(S)-류실]-O-메틸-(S)-티로신-(2-히드록시에틸)아미드, 3-[N-[N-((S)-포스포노프로필)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온, 모노에틸에스터, 나트륨 염 : 3-[N-[N-(1-프스포노프로필)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온, 이나트륨 염; 또는 3-[N-[N-(1-포스포노페틸)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온으로부터 선택한 화합물.
- 제1항 내지 제8항 중 어느 한 항에 있어서, 화합물의 제약학적으로 허용가능한 염, 용매화합물 또는 수화물.
- 하기 일반식(Ⅱ)의 화합물로부터 R20기를 분리시킴으로써 R20기를 수소로 전환시키고 필요하다면, R21을 수소로 전환시키는 것으로 구성되는 제1항의 일반식(Ⅰ)의 화합물의 제조방법.여기에서 R20은 알킬 또는 임의로 치환된 벤질이고 R21은 수소, 알킬 또는 임의로 치환된 벤질이고, R1,R2,R3및 R4는 제1항에서 일반식(Ⅰ)에 대해 정의한 바와 같다.
- 제10항에서 정의한 바와 같으나 단 R21이 수소가 아닌 일반식(Ⅱ)의 화합물.
- N-[N-[N-(1-디에톡시포스핀일에틸)-류실]-(S)-트립토필]-(S)알라닌, 메틸 에스터,N-[N-[N-(1-디에톡시포스핀일에틸)-류실]-O-메틸-(S)-티로실]-(S)-알라닌, 메틸에스터, 3-[N-[N-((S)-1-포스포노프로필)-(R)-류실]]-(-)-아미노-아자시클로트리데칸-2-온, 디에틸에스터, 3-[N-[N-((S)-1-포스포노프로필)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온, 디에틸 에스터, 3-[N-[N-(1-포스포노프로필)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온, 디벤질 에스터, N-[N-(1-(R)-포스포노프로필)-(S)-류실]-O-메틸-(S)-티로신-N-(2-히드록시에틸)아미드, 디벤질에스터, 또는 3-[N-[N-(1-포스포노펜틸)-(S)-류실]]-(-)-아미노-아자시클로트리데칸-2-온, 디벤질 에스터로부터 선택한 화합물.
- 제1항에서 정의한 바의 일반식(Ⅰ)의 화합물, 또는 그들의 제약학적으로 허용가능한 염, 용매화합물 또는 수화물, 및 제약학적으로 허용가능한 담체로 구성되는 제약학적 조성물.
- 활성적인 치료학적 물질 용도를 위한, 제1항에서 정의한 바의 일반식(Ⅰ)의 화합물, 또는 그들의 제약학적으로 허용 가능한 염, 용매화합물 또는 수화물.
- 결합조직 및 몸의 다른 단백질 성의 성분의 분해가 발생하는 증상의 치료 용도를 위한 제1항에서 정의한 바의 일반식(Ⅰ)의 화합물, 그들의 제약학적으로 허용가능한 염, 용매화합물 또는 그들의 수화물.
- 결합조직 및 몸의 다른 단백질 성분의 분해가 발생하는 증상의 치료용 약물 제조에 있어서 제1항에서 정의한 바의 일반식(Ⅰ)의 화합물, 또는 그들의 제약학적으로 허용 가능한 염, 용매화합물 또는 그들의 수화물의 용도.※참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB89083589 | 1989-04-13 | ||
GB898908353A GB8908353D0 (en) | 1989-04-13 | 1989-04-13 | Novel compounds |
GB898917756A GB8917756D0 (en) | 1989-08-03 | 1989-08-03 | Novel compounds |
GB8917756.2 | 1989-08-03 |
Publications (1)
Publication Number | Publication Date |
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KR900016238A true KR900016238A (ko) | 1990-11-13 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019900005135A KR900016238A (ko) | 1989-04-13 | 1990-04-13 | 신규 화합물 |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0401963A1 (ko) |
JP (1) | JPH0363294A (ko) |
KR (1) | KR900016238A (ko) |
AU (1) | AU618669B2 (ko) |
CA (1) | CA2014375A1 (ko) |
NZ (1) | NZ233288A (ko) |
PT (1) | PT93724A (ko) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8921326D0 (en) * | 1989-09-21 | 1989-11-08 | Beecham Group Plc | Novel treatment |
GB9008065D0 (en) * | 1990-04-10 | 1990-06-06 | Beecham Group Plc | Novel compounds |
EP0473936A1 (en) * | 1990-09-04 | 1992-03-11 | American Cyanamid Company | Renin Inhibitors |
US5189023A (en) * | 1990-09-04 | 1993-02-23 | American Cyanamid Company | Renin inhibitors |
GB9107368D0 (en) * | 1991-04-08 | 1991-05-22 | Smithkline Beecham Plc | Novel compounds |
US5155100A (en) * | 1991-05-01 | 1992-10-13 | Ciba-Geigy Corporation | Phosphono/biaryl substituted dipeptide derivatives |
US5294632A (en) * | 1991-05-01 | 1994-03-15 | Ciba-Geigy Corporation | Phosphono/biaryl substituted dipetide derivatives |
EP0520573A1 (en) * | 1991-06-27 | 1992-12-30 | Glaxo Inc. | Cyclic imide derivatives |
US5250522A (en) * | 1992-10-09 | 1993-10-05 | Ciba-Geigy Corporation | Phosphono/biaryl substituted amino acid derivatives |
GB9122859D0 (en) * | 1991-10-28 | 1991-12-11 | Smithkline Beecham Plc | Novel compounds |
JPH05148277A (ja) * | 1991-11-05 | 1993-06-15 | Banyu Pharmaceut Co Ltd | アミノホスホン酸誘導体 |
WO1993021942A2 (en) * | 1992-05-01 | 1993-11-11 | British Biotech Pharmaceuticals Limited | Use of mmp inhibitors |
US5326760A (en) * | 1992-06-29 | 1994-07-05 | Glaxo, Inc. | Aminobutanoic acid compounds having metalloprotease inhibiting properties |
US5594106A (en) * | 1993-08-23 | 1997-01-14 | Immunex Corporation | Inhibitors of TNF-α secretion |
US5840698A (en) * | 1994-10-27 | 1998-11-24 | Affymax Technologies N.V. | Inhibitors of collagenase-1 and stormelysin-I metalloproteases, pharmaceutical compositions comprising same and methods of their use |
US5831004A (en) * | 1994-10-27 | 1998-11-03 | Affymax Technologies N.V. | Inhibitors of metalloproteases, pharmaceutical compositions comprising same and methods of their use |
IT1296305B1 (it) | 1997-07-17 | 1999-06-25 | Polifarma Spa | Inibitori di metalloproteinasi loro uso terapeutico e procedimento per la produzione del composto di partenza nella loro |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
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CY1406A (en) * | 1980-12-18 | 1988-04-22 | Schering Corp | Substituted dipeptides, processes for their preparation and pharmaceutical compositions containing them and their use in the inhibition of enkephalinase |
US4558034A (en) * | 1984-01-31 | 1985-12-10 | The Board Of Trustees Of The University Of Kentucky | Inhibitors of bacterial collagenase |
GB8726714D0 (en) * | 1987-11-14 | 1987-12-16 | Beecham Group Plc | Compounds |
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1990
- 1990-04-10 EP EP90303851A patent/EP0401963A1/en not_active Withdrawn
- 1990-04-11 AU AU53158/90A patent/AU618669B2/en not_active Ceased
- 1990-04-11 CA CA002014375A patent/CA2014375A1/en not_active Abandoned
- 1990-04-11 PT PT93724A patent/PT93724A/pt not_active Application Discontinuation
- 1990-04-11 NZ NZ233288A patent/NZ233288A/en unknown
- 1990-04-13 KR KR1019900005135A patent/KR900016238A/ko not_active Application Discontinuation
- 1990-04-13 JP JP2096589A patent/JPH0363294A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
CA2014375A1 (en) | 1990-10-13 |
EP0401963A1 (en) | 1990-12-12 |
JPH0363294A (ja) | 1991-03-19 |
PT93724A (pt) | 1990-11-20 |
NZ233288A (en) | 1992-01-29 |
AU618669B2 (en) | 1992-01-02 |
AU5315890A (en) | 1990-10-18 |
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