KR910000731A - 4-아미노 3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도 - Google Patents
4-아미노 3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도 Download PDFInfo
- Publication number
- KR910000731A KR910000731A KR1019890007791A KR890007791A KR910000731A KR 910000731 A KR910000731 A KR 910000731A KR 1019890007791 A KR1019890007791 A KR 1019890007791A KR 890007791 A KR890007791 A KR 890007791A KR 910000731 A KR910000731 A KR 910000731A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- compound
- hydrogen
- formula
- phenyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/58—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems with hetero atoms directly attached to the ring nitrogen atom
- C07D215/60—N-oxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Anesthesiology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pulmonology (AREA)
- Communicable Diseases (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (22)
- 라세미체 또는 거울상 이성질체 형태의 식(Ⅰ)의 화합물 및 그의 약학적으로 허용될 수 있는 산 또는 염기부가염.위 식에서, R1과 R2는 같거나 다르며 각기 수소, C1-C6의 알킬, C2-C6의 알킬렌, 페닐, 벤질중의 하나이거나, R1과 R2는 그들이 결합된 질소와 함께 C4-C8의 포화헤테로사이클을 형성하고, R3는 수소, C1-C6의 알킬, 페닐 또는 C7-C9의 페닐알킬중의 하나이고, R4는 수소 또는 C1-C4의 알킬중의 하나이고 R5와 R6는 같거나 다르며 각기 수소, 할로겐, C1-C3의 알킬 또는 알콕시, 니트로 또는 트리플루오로메틸 중의 하나이거나 같이 메틸렌디옥시그룹을 형성하고, Z는 R7이 수소 또는 C1-C6의 알킬중의 하나인 OR7이거나; R8과 R9가 각기 수소, C1-C4의 알킬, 페닐, 벤질중의 하나인 NR8R9이거나; C1-C4의 알킬이거나; 벤질이거나; 헤테로원자가 있거나 또는 없는 C4-C6의 아릴이고, R10은 Z가 벤질 또는 페닐이 아니고 R3가 수소가 아니고, 페닐 및 벤질 그룹이 할로겐, C1-C3의 알콕시, 알킬 또는 티오알킬, 니트로, 트리플루오로 메틸 또는 하이드록시로 치환될 수 있고, 알킬 및 알콕시 그룹이 직쇄, 분지 또는 고리모양이라는 조건하에 수소, C1-C4의 알킬 또는 페닐 중의 하나이다. n은 0,1 또는 2이고, p는 0또는 1이며, A, B, C, D의 하나는 N이고 나머지 CH이거나, A, B, C, D 모두는 각기 CH를 나타낸다.
- 제1항에 있어서, Z가 치환 또는 미치환된 페닐그룹인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제2항에 있어서, Z가 미치환된 페닐그룹인 것을 특징으로 하는 화합물.
- 제1항에 있어서, Z가 피리딜, 피롤릴, 푸릴, 티에닐 또는 이미다졸릴인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제1항에 있어서, Z가 OR7인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제5항에 있어서, R7이 알킬인 것을 특징으로 하는 화합물.
- 제5항에 있어서, Z가 C1-C3의 알킬인 것을 특징으로 하는 화합물.
- 제1항 내지 제7항 중 어느 한 항에 있어서, A, B, C, D가 각기 CH인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제1항 내지 제7항 중 어느 한항에 있어서, A, B, C 또는 D중 어느 하나가 N인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제9항에 있어서, A가 N인 것을 특징으로 하는 화합물.
- 제1항에 있어서, R1과 R2가 각기 의 C1-C6알킬이고, R3이 C1-C3의 알킬이고, R10이 수소이고, Z가 R7이 C1-C6의 알킬인 OR7인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제11항에 있어서, R4가 수소인 것을 특징으로 하는 화합물.
- 제11항에 있어서, R4가 수소이고, C가 치환된 것을 특징으로 하는 화합물.
- 제1항에 있어서, R1가 알킬이고, R2및 Z가 각기 치환될 수 있는 페닐인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제1항에 있어서, R1가 알킬이고, R2및 Z가 치환될 수 있는 페닐이고, R3과 R10이 각기 수소인 것을 특징으로 하는 식Ⅰ의 화합물.
- 제14항과 제15항중 어느 한항에 있어서, A, B, C, D가 각기 CH인 것을 특징으로 하는 화합물.
- 제14항과 제15항중 어느 한항에 있어서, A가 N이고 B, C 및 D가 CH인 것을 특징으로 하는 화합물.
- 에틸7-클로로4-(1-N,N-디프로필카르바모일)에틸 아미노 퀴놀린3-카르복시레이트 및 그의 약학적으로 허용할 수 있는 산부가염.
- 3-벤조일7-클로로4-(N-메틸N-4-클로로페닐)카르바모일 메틸아미노 퀴놀린 및 그의 약학적으로 허용될 수 있는 산부가염.
- 3-벤조일4-(N-메틸N-4-클로로페닐)카르바모일 메틸아미노 1,5-나프티리딘 및 그의 약학적으로 허용될 수 있는 산부가염.
- 식Ⅱ의 아민과 식Ⅲ의 화합물을 반응시키는 것을 특징으로 하는 식Ⅰ의 화합물을 제조하는 방법.위 식에서 R1, R2, R3, R4, R5, R6, R10, Z, A, B, C, D, n 및 p는 제1항과 같은 의미이고 X는 할로겐 또는 설포네이트 중의 하나이다.
- 양립할 수 있는 부형제 뿐만 아니라 제1항 내지 제20항중 어는 한 항에 의한 화합물을 유효성분으로 함유하는 약학적인 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8807498A FR2632305B1 (fr) | 1988-06-06 | 1988-06-06 | Amino-4 aroyl-3 quinoleines et naphtyridines, leur procede de preparation et leur application en therapeutique |
FR88-07498 | 1988-06-06 | ||
FR88-08025 | 1988-06-15 | ||
FR8808025A FR2632861B1 (fr) | 1988-06-15 | 1988-06-15 | Derives d'amino-4 carboxy-3 quinoleines et naphtyridines, leur procede de preparation et leur application comme medicaments |
Publications (1)
Publication Number | Publication Date |
---|---|
KR910000731A true KR910000731A (ko) | 1991-01-30 |
Family
ID=26226703
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890007791A KR910000731A (ko) | 1988-06-06 | 1989-06-05 | 4-아미노 3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도 |
Country Status (12)
Country | Link |
---|---|
US (1) | US5026711A (ko) |
EP (1) | EP0346208B1 (ko) |
JP (1) | JP2766672B2 (ko) |
KR (1) | KR910000731A (ko) |
AU (1) | AU624825B2 (ko) |
CA (1) | CA1337073C (ko) |
DE (1) | DE68914515T2 (ko) |
DK (1) | DK273689A (ko) |
ES (1) | ES2063153T3 (ko) |
IE (1) | IE63429B1 (ko) |
NZ (1) | NZ229413A (ko) |
PT (1) | PT90748B (ko) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04211661A (ja) * | 1990-03-28 | 1992-08-03 | Otsuka Pharmaceut Co Ltd | キノリン誘導体及び該誘導体を含有する抗潰瘍剤 |
US5395399A (en) * | 1993-06-14 | 1995-03-07 | Sport Wrapz, Inc. | Thermal wrap for a body member |
DE4405712A1 (de) * | 1994-02-23 | 1995-08-24 | Basf Ag | Substituierte Naphthyridine und deren Verwendung |
IL117659A (en) * | 1995-04-13 | 2000-12-06 | Dainippon Pharmaceutical Co | Substituted 2-phenyl pyrimidino amino acetamide derivative process for preparing the same and a pharmaceutical composition containing same |
KR0169813B1 (ko) * | 1995-07-12 | 1999-01-15 | 김종인 | 4-아미노-3-아실나프티리딘 유도체 |
AU7474998A (en) * | 1997-05-07 | 1998-11-27 | Emory University | Haloisoquinoline carboxamide |
ZA9810490B (en) | 1997-12-03 | 1999-05-20 | Dainippon Pharmaceutical Co | 2-Aryl-8-oxodihydropurine derivative process for the preparation thereof pharmaceutical composition containing the same and intermediate therefor |
WO1999058117A1 (fr) * | 1998-05-13 | 1999-11-18 | Sanofi-Synthelabo | Utilisation de composes reduisant l'apoptose |
FR2778564B1 (fr) * | 1998-05-13 | 2001-07-13 | Sanofi Sa | Utilisation de composes reduisant l'apoptose |
ATE333281T1 (de) | 1998-12-18 | 2006-08-15 | Scios Inc | Agonisten und antagonisten von benzodiazepinrezeptoren des peripheren typs |
DE69926535T2 (de) * | 1998-12-18 | 2006-03-30 | Scios Inc., Sunnyvale | Behandlung von erkrankungen mit zystenbildung |
DE19960924C2 (de) * | 1999-12-17 | 2002-08-01 | Therapeutics Gmbh G.O.T. | Amphiphile Polyamine, deren Anwendungen |
US20100074949A1 (en) | 2008-08-13 | 2010-03-25 | William Rowe | Pharmaceutical composition and administration thereof |
FR2862301B1 (fr) * | 2003-11-17 | 2007-12-21 | Aventis Pharma Sa | Nouveau procede de preparation de quinoleines 3-fluorees |
SE0400284D0 (sv) * | 2004-02-10 | 2004-02-10 | Astrazeneca Ab | Novel compounds |
US8354427B2 (en) | 2004-06-24 | 2013-01-15 | Vertex Pharmaceutical Incorporated | Modulators of ATP-binding cassette transporters |
BR122018075478B8 (pt) * | 2004-06-24 | 2023-10-31 | Vertex Pharma | moduladores de transportadores de cassete de ligação de atp |
US20090105272A1 (en) * | 2005-12-24 | 2009-04-23 | Grootenhuis Peter D J | Prodrugs of modulators of ABC transporters |
HUE049976T2 (hu) | 2005-12-28 | 2020-11-30 | Vertex Pharma | N-[2,4-bisz(1,1-dimetil-etil)-5-hidroxi-fenil]-1,4-dihidro-4-oxo-kinolin-3-karboxamid amorf alakjának gyógyászati kompozíciói |
TW200829555A (en) * | 2006-11-10 | 2008-07-16 | Astrazeneca Ab | Chemical compounds |
CL2008000191A1 (es) * | 2007-01-25 | 2008-08-22 | Astrazeneca Ab | Compuestos derivados de 4-amino-cinnotina-3-carboxamida; inhibidores de csf-1r quinasa; su proceso de preparacion; y su uso para tratar el cancer. |
US20110190272A1 (en) * | 2008-05-07 | 2011-08-04 | Astrazeneca Ab | Chemical compounds |
US8415333B2 (en) | 2009-02-24 | 2013-04-09 | Respiratorious Ab | Bronchodilating diazaheteroaryls |
SG10201504084QA (en) | 2009-03-20 | 2015-06-29 | Vertex Pharma | Process for making modulators of cystic fibrosis transmembrane conductance regulator |
US8802700B2 (en) | 2010-12-10 | 2014-08-12 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-Binding Cassette transporters |
EP2753329B1 (en) * | 2012-01-19 | 2017-08-09 | OncoTherapy Science, Inc. | 1,5-naphthyridine derivatives as melk inhibitors |
CN109966264A (zh) | 2012-02-27 | 2019-07-05 | 沃泰克斯药物股份有限公司 | 药物组合物及其施用 |
CN107250113B (zh) | 2014-10-07 | 2019-03-29 | 弗特克斯药品有限公司 | 囊性纤维化跨膜传导调节蛋白的调节剂的共晶 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4324893A (en) * | 1979-04-18 | 1982-04-13 | American Home Products Corporation | 4-Amino-3-carboxy or cyano-1,2-dihydro-2-oxo-1,8-naphthyridine derivatives |
FR2581382B1 (fr) * | 1985-05-06 | 1987-06-26 | Sanofi Sa | Derives n-(quinolyl) glycinamides, leur procede de preparation et leur application therapeutique en tant que psychotropes |
GB8610981D0 (en) * | 1986-05-06 | 1986-06-11 | Ici America Inc | Quinoline amides |
GB8621425D0 (en) * | 1986-09-05 | 1986-10-15 | Smith Kline French Lab | Compounds |
US5034393A (en) * | 1989-07-27 | 1991-07-23 | Dowelanco | Fungicidal use of pyridopyrimidine, pteridine, pyrimidopyrimidine, pyrimidopyridazine, and pyrimido-1,2,4-triazine derivatives |
AU634561B2 (en) * | 1989-07-27 | 1993-02-25 | Eli Lilly And Company | Naphthyridine derivatives |
-
1989
- 1989-06-02 DK DK273689A patent/DK273689A/da not_active Application Discontinuation
- 1989-06-05 EP EP89401548A patent/EP0346208B1/fr not_active Expired - Lifetime
- 1989-06-05 PT PT90748A patent/PT90748B/pt not_active IP Right Cessation
- 1989-06-05 ES ES89401548T patent/ES2063153T3/es not_active Expired - Lifetime
- 1989-06-05 KR KR1019890007791A patent/KR910000731A/ko not_active Application Discontinuation
- 1989-06-05 CA CA000601729A patent/CA1337073C/en not_active Expired - Fee Related
- 1989-06-05 DE DE68914515T patent/DE68914515T2/de not_active Expired - Fee Related
- 1989-06-05 JP JP1143956A patent/JP2766672B2/ja not_active Expired - Lifetime
- 1989-06-06 US US07/362,105 patent/US5026711A/en not_active Expired - Fee Related
- 1989-06-06 NZ NZ229413A patent/NZ229413A/en unknown
- 1989-06-06 AU AU36035/89A patent/AU624825B2/en not_active Ceased
- 1989-06-12 IE IE179789A patent/IE63429B1/en unknown
Also Published As
Publication number | Publication date |
---|---|
ES2063153T3 (es) | 1995-01-01 |
PT90748A (pt) | 1989-12-29 |
EP0346208A1 (fr) | 1989-12-13 |
DK273689D0 (da) | 1989-06-02 |
AU624825B2 (en) | 1992-06-25 |
DE68914515T2 (de) | 1994-08-18 |
JPH0232058A (ja) | 1990-02-01 |
EP0346208B1 (fr) | 1994-04-13 |
IE891797L (en) | 1989-12-06 |
US5026711A (en) | 1991-06-25 |
DE68914515D1 (de) | 1994-05-19 |
CA1337073C (en) | 1995-09-19 |
NZ229413A (en) | 1990-11-27 |
PT90748B (pt) | 1994-10-31 |
AU3603589A (en) | 1989-12-07 |
DK273689A (da) | 1989-12-07 |
JP2766672B2 (ja) | 1998-06-18 |
IE63429B1 (en) | 1995-04-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR910000731A (ko) | 4-아미노 3-카르복시 퀴놀린 및 나프티리딘, 그 제조방법 및 그의 의약품으로서 용도 | |
PT96324A (pt) | Processo para a preparacao de compostos peptidicos e de composicoes farmaceuticas que os contem | |
IE37538B1 (en) | New 1,4-dihydropyridine carboxylic acid compounds their production and their medicinal use | |
KR890000485A (ko) | 캠프토데신 유도체 및 그의 아미노기에 있어서의 산 부가염 및 4급 암모늄염 및 그의 제조방법 | |
ATE126216T1 (de) | Pyrazolderivate, verfahren zu deren herstellung und diese enthaltende pharmazeutische zusammenstellung. | |
NO900306D0 (no) | Fremgangsmaate for fremstilling av nye pyrazolopyridin-forbindelser. | |
NO990227D0 (no) | Heterocykliske forbindelser som farmas°ytika | |
DE3873612D1 (de) | Dithioacetal-verbindungen, verfahren zu deren herstellung und diese enthaltende pharmazeutische zusammensetzungen. | |
OA09039A (fr) | Acides 3-alcenyl-1-azabicyclo(3.2.0)hep-2-ene-2carboxyliques | |
KR900016220A (ko) | 매크로리드 조성물 | |
ES524236A0 (es) | Un procedimiento para la preparacion de 1,4-dihidropiridina | |
DK0516941T3 (da) | Pyrazolopyridinforbindelser og fremgangsmåder til fremstilling deraf | |
KR920021547A (ko) | 아졸 유도체 | |
KR890014522A (ko) | 사이클릭 이미드의 아릴피페라지닐알콕시 유도체, 이의 제조방법 및 약제로서의 이의 용도 | |
KR890001957A (ko) | N-아미노부틸-n-페닐아릴아미드 유도체, 그의 제법 및 치료에의 응용 | |
KR900014396A (ko) | 티에노-트리아졸로-디아제핀 유도체, 그의 제조 방법 및 그를 함유하는 치료 조성물 | |
FI874865A (fi) | Menetelmä lääkeaineena käyttökelpoisten imidatsolidinonijohdannaisten valmistamiseksi | |
KR910009672A (ko) | 피리다진 유도체, 이의 제조방법 및 이것을 함유하는 약학 조성물 | |
OA09119A (fr) | Nouveaux céphèmes et leur préparation. | |
HUT40080A (en) | Process for preparing 1,4-dihydro-pyridine-hydroxy-amine derivatives and pharmaceutical compositions comprising the same as active substance | |
DK160486C (da) | N-(4-amino-2,2-diphenyl-butyl)- eller n-(3-amino-2,2-diphenyl-propyl) urinstofforbindelser, fremgangsmaade til fremstilling af disse, samt en farmaceutisk komposition | |
KR960029312A (ko) | N-아릴알킬페닐아세트아미드 유도체와 그의 제조방법 | |
ATE50248T1 (de) | Ein imidazolidintrion-derivat oder ein seiner pharmazeutisch akzeptierbaren salze enthaltende pharmazeutische zusammenstellung. | |
DK417380A (da) | Analogifremgangsmaade til fremstilling af nitrosourinstofderivater eller syreadditionssalte deraf | |
AR013004A1 (es) | Derivados de aminospiropiperidina quinazolina, composicion farmaceutica, uso de dichos derivados en la preparacion de medicamentos, proceso para lapreparacion de dichos derivados y compuestos intermediarios para su exclusivo uso en dicho proceso. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |