KR101664525B1 - 스피로시클릭 아미드 유도체 - Google Patents
스피로시클릭 아미드 유도체 Download PDFInfo
- Publication number
- KR101664525B1 KR101664525B1 KR1020127005165A KR20127005165A KR101664525B1 KR 101664525 B1 KR101664525 B1 KR 101664525B1 KR 1020127005165 A KR1020127005165 A KR 1020127005165A KR 20127005165 A KR20127005165 A KR 20127005165A KR 101664525 B1 KR101664525 B1 KR 101664525B1
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- South Korea
- Prior art keywords
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- 0 CC(C(C)(*)*1)C=*N1C(I)(I)IC(C)(C)C(C)(*)C(C)(C)* Chemical compound CC(C(C)(*)*1)C=*N1C(I)(I)IC(C)(C)C(C)(*)C(C)(C)* 0.000 description 8
- UWXZFZOFLHKSEY-UHFFFAOYSA-N CCCCN(CCNCCc(ccc(O)c1N2)c1OCC2=O)C(CCOCCc1cccc(CCN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)c1)=O Chemical compound CCCCN(CCNCCc(ccc(O)c1N2)c1OCC2=O)C(CCOCCc1cccc(CCN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)c1)=O UWXZFZOFLHKSEY-UHFFFAOYSA-N 0.000 description 2
- VOWNCVKLMNRNKL-UHFFFAOYSA-N CC(C)(C)[Si+](C)(C)OCCSc1cccc(C(O)=O)c1 Chemical compound CC(C)(C)[Si+](C)(C)OCCSc1cccc(C(O)=O)c1 VOWNCVKLMNRNKL-UHFFFAOYSA-N 0.000 description 1
- MBOSFUDMKYOTQC-UHFFFAOYSA-N CC(C)(C)[Si+](C)(C)OCCc1cccc(Br)c1C Chemical compound CC(C)(C)[Si+](C)(C)OCCc1cccc(Br)c1C MBOSFUDMKYOTQC-UHFFFAOYSA-N 0.000 description 1
- JWSRKCRFLQMJQV-MRVPVSSYSA-N CC(C)[C@@H](C)NCC(OC)OC Chemical compound CC(C)[C@@H](C)NCC(OC)OC JWSRKCRFLQMJQV-MRVPVSSYSA-N 0.000 description 1
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- BSHGQKBSTZBPNI-UHFFFAOYSA-N CC(C)c1nc(C(N2CC3(CCN(Cc(cccc4CCOCCC(N(CCNCCc(c(OC5)c6NC5=O)ccc6O)Cc5cccc(OC)c5)=O)c4F)CC3)OCC2)=O)c[s]1 Chemical compound CC(C)c1nc(C(N2CC3(CCN(Cc(cccc4CCOCCC(N(CCNCCc(c(OC5)c6NC5=O)ccc6O)Cc5cccc(OC)c5)=O)c4F)CC3)OCC2)=O)c[s]1 BSHGQKBSTZBPNI-UHFFFAOYSA-N 0.000 description 1
- KXSAPGBHMYZRSW-UHFFFAOYSA-N CC(C)c1nc(C(N2CC3(CCN(Cc(cccc4CCOCCC(N(CCNCCc(ccc(O)c5N6)c5OCC6=O)C5CCCCCC5)=O)c4F)CC3)OCC2)=O)c[s]1 Chemical compound CC(C)c1nc(C(N2CC3(CCN(Cc(cccc4CCOCCC(N(CCNCCc(ccc(O)c5N6)c5OCC6=O)C5CCCCCC5)=O)c4F)CC3)OCC2)=O)c[s]1 KXSAPGBHMYZRSW-UHFFFAOYSA-N 0.000 description 1
- GXJQZQWSVCNMBC-UHFFFAOYSA-N CC(C)c1nc(C(N2CC3(CCN(Cc(cccc4CCO[Si+](C)(C)C(C)(C)C)c4F)CC3)OCC2)=O)c[s]1 Chemical compound CC(C)c1nc(C(N2CC3(CCN(Cc(cccc4CCO[Si+](C)(C)C(C)(C)C)c4F)CC3)OCC2)=O)c[s]1 GXJQZQWSVCNMBC-UHFFFAOYSA-N 0.000 description 1
- SCOHVIWSLZMAFR-UHFFFAOYSA-N CC(C)c1nc(C(N2CC3(CCN(Cc4c(C)c(CCOCCC(N(CCNCCc(ccc(O)c5N6)c5OCC6=O)C5CCCC5)=O)ccc4)CC3)OCC2)=O)c[s]1 Chemical compound CC(C)c1nc(C(N2CC3(CCN(Cc4c(C)c(CCOCCC(N(CCNCCc(ccc(O)c5N6)c5OCC6=O)C5CCCC5)=O)ccc4)CC3)OCC2)=O)c[s]1 SCOHVIWSLZMAFR-UHFFFAOYSA-N 0.000 description 1
- QDLPQRSSBFWKTI-UHFFFAOYSA-N CC(C)c1nc(C(N2CC3(CCN(Cc4cccc(CCOCCC(N(CCNCCc(c(OC5)c6NC5=O)ccc6O)CCOC)=O)c4Cl)CC3)OCC2)=O)c[s]1 Chemical compound CC(C)c1nc(C(N2CC3(CCN(Cc4cccc(CCOCCC(N(CCNCCc(c(OC5)c6NC5=O)ccc6O)CCOC)=O)c4Cl)CC3)OCC2)=O)c[s]1 QDLPQRSSBFWKTI-UHFFFAOYSA-N 0.000 description 1
- MLUFYZIJDOJUNS-UHFFFAOYSA-N CC(C)c1nc(C(N2CC3(CCN(Cc4cccc(CCOCCC(N(CCNCCc(ccc(O)c5N6)c5OCC6=O)CCF)=O)c4F)CC3)OCC2)=O)c[s]1 Chemical compound CC(C)c1nc(C(N2CC3(CCN(Cc4cccc(CCOCCC(N(CCNCCc(ccc(O)c5N6)c5OCC6=O)CCF)=O)c4F)CC3)OCC2)=O)c[s]1 MLUFYZIJDOJUNS-UHFFFAOYSA-N 0.000 description 1
- LAMKGDXLXPFNDD-UHFFFAOYSA-N CCCCN(CCNCCc(ccc(O)c1N2)c1OCC2=O)C(CCOCCc1ccc(CCN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)cc1)=O Chemical compound CCCCN(CCNCCc(ccc(O)c1N2)c1OCC2=O)C(CCOCCc1ccc(CCN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)cc1)=O LAMKGDXLXPFNDD-UHFFFAOYSA-N 0.000 description 1
- QGNGLQHRHIOVPL-UHFFFAOYSA-N CCCCNCC(OC)OC Chemical compound CCCCNCC(OC)OC QGNGLQHRHIOVPL-UHFFFAOYSA-N 0.000 description 1
- BJZXYOLWNCMEMB-JGCGQSQUSA-N CCCC[C@@H](C)N(CCNCCc(c(OC1)c2NC1=O)ccc2O)C(CCOCCc1ccc(CCN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C)n2)=O)cc1)=O Chemical compound CCCC[C@@H](C)N(CCNCCc(c(OC1)c2NC1=O)ccc2O)C(CCOCCc1ccc(CCN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C)n2)=O)cc1)=O BJZXYOLWNCMEMB-JGCGQSQUSA-N 0.000 description 1
- JZJUWLXMSBVCFG-UHFFFAOYSA-N CCCN(CCNCCc(ccc(O)c1N2)c1OCC2=O)C(CCOCCc(cccc1CN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)c1Cl)=O Chemical compound CCCN(CCNCCc(ccc(O)c1N2)c1OCC2=O)C(CCOCCc(cccc1CN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)c1Cl)=O JZJUWLXMSBVCFG-UHFFFAOYSA-N 0.000 description 1
- HXFNTZUWVHSQSS-UHFFFAOYSA-N CCN(CCNCCc(c(S1)c2NC1=O)ccc2O)C(CCOCCCc1cccc(CN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)c1F)=O Chemical compound CCN(CCNCCc(c(S1)c2NC1=O)ccc2O)C(CCOCCCc1cccc(CN(CC2)CCC2(C2)OCCN2C(c2c[s]c(C(C)C)n2)=O)c1F)=O HXFNTZUWVHSQSS-UHFFFAOYSA-N 0.000 description 1
- VKIJFZGAAPOULL-UHFFFAOYSA-N CCOC(CCSc1cc(C(O)=O)ccc1)=O Chemical compound CCOC(CCSc1cc(C(O)=O)ccc1)=O VKIJFZGAAPOULL-UHFFFAOYSA-N 0.000 description 1
- AMOXIYVNQPNJRD-UHFFFAOYSA-N CCOC(COc1ccccc1CCO)OCC Chemical compound CCOC(COc1ccccc1CCO)OCC AMOXIYVNQPNJRD-UHFFFAOYSA-N 0.000 description 1
- SDUZFUDOIIIRKV-UHFFFAOYSA-N CCc1nc(C(N2CC3(CCN(Cc(cccc4CCOCCC(N(CCNCCc(c(OC5)c6NC5=O)ccc6O)C5CCCC5)=O)c4Cl)CC3)OCC2)=O)c[s]1 Chemical compound CCc1nc(C(N2CC3(CCN(Cc(cccc4CCOCCC(N(CCNCCc(c(OC5)c6NC5=O)ccc6O)C5CCCC5)=O)c4Cl)CC3)OCC2)=O)c[s]1 SDUZFUDOIIIRKV-UHFFFAOYSA-N 0.000 description 1
- WYBPAJYFPAUEJR-UHFFFAOYSA-N COC(CNC1CCCC1)OC Chemical compound COC(CNC1CCCC1)OC WYBPAJYFPAUEJR-UHFFFAOYSA-N 0.000 description 1
- LQXFYESLKHNKJL-UHFFFAOYSA-N Cc1nc(C(N2CC3(CCNCC3)OCC2)=O)c[s]1 Chemical compound Cc1nc(C(N2CC3(CCNCC3)OCC2)=O)c[s]1 LQXFYESLKHNKJL-UHFFFAOYSA-N 0.000 description 1
- ZHHNUIUNWSNZNY-UHFFFAOYSA-N OCCc(cc1CN(CC2)CCC2(C2)OCCN2C(C(F)(F)F)=O)ccc1F Chemical compound OCCc(cc1CN(CC2)CCC2(C2)OCCN2C(C(F)(F)F)=O)ccc1F ZHHNUIUNWSNZNY-UHFFFAOYSA-N 0.000 description 1
- KJOPFDPXKUBNAM-UHFFFAOYSA-N OCCc(cc1CN(CC2)CCC22OCCNC2)ccc1F Chemical compound OCCc(cc1CN(CC2)CCC22OCCNC2)ccc1F KJOPFDPXKUBNAM-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C07D519/04—Dimeric indole alkaloids, e.g. vincaleucoblastine
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0913342.2A GB0913342D0 (en) | 2009-07-31 | 2009-07-31 | Compounds - 801 |
| GB0913342.2 | 2009-07-31 | ||
| PCT/GB2010/051242 WO2011012896A2 (en) | 2009-07-31 | 2010-07-29 | Compounds - 801 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20120056838A KR20120056838A (ko) | 2012-06-04 |
| KR101664525B1 true KR101664525B1 (ko) | 2016-10-11 |
Family
ID=41129405
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020127005165A Expired - Fee Related KR101664525B1 (ko) | 2009-07-31 | 2010-07-29 | 스피로시클릭 아미드 유도체 |
Country Status (33)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2713322C (en) | 2008-02-06 | 2017-01-17 | Astrazeneca Ab | Diazaspiro [5.5] undecane derivatives and their use in the treatment of pulmonary disorders |
| TWI466885B (zh) | 2009-07-31 | 2015-01-01 | Japan Tobacco Inc | 含氮螺環化合物及其醫藥用途 |
| GB0913342D0 (en) | 2009-07-31 | 2009-09-16 | Astrazeneca Ab | Compounds - 801 |
| GB201021992D0 (en) * | 2010-12-23 | 2011-02-02 | Astrazeneca Ab | Compound |
| GB201021979D0 (en) * | 2010-12-23 | 2011-02-02 | Astrazeneca Ab | New compound |
| WO2016179349A1 (en) * | 2015-05-05 | 2016-11-10 | Northwestern University | Cxcr4 chemokine receptor modulators |
| CN109195975B (zh) * | 2016-09-30 | 2022-01-04 | 四川海思科制药有限公司 | 一种二氮杂螺[5.5]十一碳烷衍生物及其用途 |
| ES2836113T3 (es) | 2016-12-14 | 2021-06-24 | Beijing Showby Pharmaceutical Co Ltd | Clase de compuestos bifuncionales con estructura de sal de amonio cuaternario |
| US10501449B2 (en) | 2017-06-01 | 2019-12-10 | Bristol-Myers Squibb Company | Substituted nitrogen containing compounds |
| EP3682906A1 (en) * | 2019-01-17 | 2020-07-22 | Julius-Maximilians-Universität Würzburg | Compound targeting norepinephrine transporter |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008096127A2 (en) | 2007-02-07 | 2008-08-14 | Argenta Discovery Ltd | Bicyclo[2.2.1]hept-7-ylamine derivatives and their use as m3 muscarinic receptor modulators |
Family Cites Families (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2707186A (en) | 1954-05-06 | 1955-04-26 | Hoffmann La Roche | Imidazolone derivatives |
| AU565621B2 (en) | 1983-04-26 | 1987-09-24 | Smithkline Beckman Corporation | Dopaminergic carbostyrils |
| FR2665440B1 (fr) | 1990-07-31 | 1994-02-04 | Lipha | Nouveaux cycloalkylsulfonamides substitues, procedes de preparation et medicaments les contenant. |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| PL194689B1 (pl) | 1996-02-13 | 2007-06-29 | Astrazeneca Uk Ltd | Pochodne chinazoliny, ich kompozycje farmaceutyczne oraz ich zastosowania |
| GB9604578D0 (en) | 1996-03-04 | 1996-05-01 | Sericol Ltd | Photocurable compositions |
| EP0885198B1 (en) | 1996-03-05 | 2001-12-19 | AstraZeneca AB | 4-anilinoquinazoline derivatives |
| SE9602263D0 (sv) | 1996-06-07 | 1996-06-07 | Astra Ab | New amino acid derivatives |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| TWI258462B (en) | 1999-12-17 | 2006-07-21 | Astrazeneca Ab | Adamantane derivative compounds, process for preparing the same and pharmaceutical composition comprising the same |
| EP1289952A1 (en) | 2000-05-31 | 2003-03-12 | AstraZeneca AB | Indole derivatives with vascular damaging activity |
| WO2002008213A1 (en) | 2000-07-07 | 2002-01-31 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as angiogenesis inhibitors |
| CN1255391C (zh) | 2000-07-07 | 2006-05-10 | 安吉奥金尼药品有限公司 | 作为血管破坏剂的colchinol衍生物 |
| ES2329586T3 (es) * | 2003-11-21 | 2009-11-27 | Theravance, Inc. | Compuestos que tienen actividad agonista del receptor beta2 adrenergico y antagonista del receptor muscarino. |
| TW200531692A (en) | 2004-01-12 | 2005-10-01 | Theravance Inc | Aryl aniline derivatives as β2 adrenergic receptor agonists |
| PT1751131E (pt) | 2004-03-10 | 2009-02-13 | Janssen Pharmaceutica Nv | Aril-piperidinas ou aril-piperazinas substituídas com heterociclos de 5 membros inibidoras de mtp |
| WO2005092841A1 (en) | 2004-03-23 | 2005-10-06 | Pfizer Limited | Compounds having beta-agonist activity |
| US20050215542A1 (en) | 2004-03-23 | 2005-09-29 | Pfizer Inc | Compounds for the treatment of diseases |
| DE102004024453A1 (de) * | 2004-05-14 | 2006-01-05 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue langwirksame Bronchodilatoren zur Behandlung von Atemwegserkrankungen |
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