CN1069024A - 用作降低血中胆甾醇药剂的取代的β-内酰胺化合物及其制备方法 - Google Patents
用作降低血中胆甾醇药剂的取代的β-内酰胺化合物及其制备方法 Download PDFInfo
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- CN1069024A CN1069024A CN92108760A CN92108760A CN1069024A CN 1069024 A CN1069024 A CN 1069024A CN 92108760 A CN92108760 A CN 92108760A CN 92108760 A CN92108760 A CN 92108760A CN 1069024 A CN1069024 A CN 1069024A
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- Prior art keywords
- lower alkyl
- compound
- phenyl
- substituted
- formula
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- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- 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
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/06—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D205/08—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams
- C07D205/085—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with one oxygen atom directly attached in position 2, e.g. beta-lactams with a nitrogen atom directly attached in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
- C07F7/1872—Preparation; Treatments not provided for in C07F7/20
- C07F7/1892—Preparation; Treatments not provided for in C07F7/20 by reactions not provided for in C07F7/1876 - C07F7/1888
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Pyrrole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Quinoline Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73442691A | 1991-07-23 | 1991-07-23 | |
| US73465291A | 1991-07-23 | 1991-07-23 | |
| US734,652 | 1991-07-23 | ||
| US734,426 | 1991-07-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1069024A true CN1069024A (zh) | 1993-02-17 |
Family
ID=27112730
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN92108760A Pending CN1069024A (zh) | 1991-07-23 | 1992-07-22 | 用作降低血中胆甾醇药剂的取代的β-内酰胺化合物及其制备方法 |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US5306817A (cg-RX-API-DMAC7.html) |
| EP (2) | EP0596015B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2525125B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN1069024A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE158789T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU658441B2 (cg-RX-API-DMAC7.html) |
| BG (1) | BG61118B2 (cg-RX-API-DMAC7.html) |
| CZ (1) | CZ14294A3 (cg-RX-API-DMAC7.html) |
| DE (1) | DE69222532T2 (cg-RX-API-DMAC7.html) |
| EE (1) | EE9400342A (cg-RX-API-DMAC7.html) |
| ES (1) | ES2107548T3 (cg-RX-API-DMAC7.html) |
| FI (1) | FI940296A7 (cg-RX-API-DMAC7.html) |
| HU (1) | HUT67341A (cg-RX-API-DMAC7.html) |
| IE (1) | IE922374A1 (cg-RX-API-DMAC7.html) |
| IL (1) | IL102582A0 (cg-RX-API-DMAC7.html) |
| MX (1) | MX9204327A (cg-RX-API-DMAC7.html) |
| MY (1) | MY131273A (cg-RX-API-DMAC7.html) |
| NO (1) | NO940221D0 (cg-RX-API-DMAC7.html) |
| NZ (1) | NZ243669A (cg-RX-API-DMAC7.html) |
| OA (1) | OA09878A (cg-RX-API-DMAC7.html) |
| SK (1) | SK7994A3 (cg-RX-API-DMAC7.html) |
| TW (1) | TW223059B (cg-RX-API-DMAC7.html) |
| WO (1) | WO1993002048A1 (cg-RX-API-DMAC7.html) |
| YU (1) | YU72092A (cg-RX-API-DMAC7.html) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1050830C (zh) * | 1993-09-21 | 2000-03-29 | 先灵公司 | 氮杂环丁烷酮类化合物及其医药用途 |
| CN1071745C (zh) * | 1993-07-09 | 2001-09-26 | 先灵公司 | 合成氮杂环丁酮类化合物的方法 |
| CN1083833C (zh) * | 1994-11-18 | 2002-05-01 | 先灵公司 | 用作降胆固醇剂的硫取代的氮杂环丁烷酮类化合物 |
| CN1090479C (zh) * | 1992-12-23 | 2002-09-11 | 先灵公司 | 一种胆固醇生物合成抑制剂与一种β-内酰胺胆固醇吸收抑制剂的联合 |
| CN100522159C (zh) * | 2001-01-26 | 2009-08-05 | 先灵公司 | 取代的氮杂环丁烷酮化合物在制备治疗谷甾醇血症的药物中的应用 |
| CN103254107A (zh) * | 2013-05-09 | 2013-08-21 | 东华大学 | 一种依泽替米贝类似物及其制备方法 |
| CN103524486A (zh) * | 2013-09-18 | 2014-01-22 | 中国科学院昆明植物研究所 | N-喹啉基取代的β-内酰胺类化合物及其药物组合物和合成方法与应用 |
Families Citing this family (86)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5688787A (en) * | 1991-07-23 | 1997-11-18 | Schering Corporation | Substituted β-lactam compounds useful as hypochlesterolemic agents and processes for the preparation thereof |
| US5688785A (en) * | 1991-07-23 | 1997-11-18 | Schering Corporation | Substituted azetidinone compounds useful as hypocholesterolemic agents |
| CA2139104A1 (en) * | 1992-06-26 | 1994-01-06 | Michael P. Deninno | Steroidal glycosides for treating hypercholesterolemia |
| CA2106840A1 (en) * | 1992-09-25 | 1994-03-26 | Marco Baroni | Heteroarylazetidines and -pyrrolidines, process for their preparation and pharmaceutical compositions containing them |
| LT3595B (en) * | 1993-01-21 | 1995-12-27 | Schering Corp | Spirocycloalkyl-substituted azetidinones useful as hypocholesterolemic agents |
| US5627176A (en) * | 1994-03-25 | 1997-05-06 | Schering Corporation | Substituted azetidinone compounds useful as hypocholesterolemic agents |
| WO1995035277A1 (en) * | 1994-06-20 | 1995-12-28 | Schering Corporation | Substituted azetidinone compounds useful as hypocholesterolemic agents |
| US5624920A (en) * | 1994-11-18 | 1997-04-29 | Schering Corporation | Sulfur-substituted azetidinone compounds useful as hypocholesterolemic agents |
| US5656624A (en) * | 1994-12-21 | 1997-08-12 | Schering Corporation | 4-[(heterocycloalkyl or heteroaromatic)-substituted phenyl]-2-azetidinones useful as hypolipidemic agents |
| JP3023179B2 (ja) * | 1995-09-27 | 2000-03-21 | シェーリング コーポレイション | 立体選択的微生物還元プロセス |
| JPH11515025A (ja) | 1995-11-02 | 1999-12-21 | ワーナー−ランバート・コンパニー | 脂質濃度を調節するための方法および医薬組成物 |
| WO1997016424A1 (en) * | 1995-11-02 | 1997-05-09 | Schering Corporation | Process for preparing 1-(4-fluorophenyl)-3(r)-(3(s)-hydroxy-3-([phenyl or 4-fluorophenyl])-propyl)-4(s)-(4-hydroxyphenyl)-2-azetidinone |
| IL126696A0 (en) * | 1996-04-26 | 1999-08-17 | Smithkline Beecham Plc | Azetidinone derivatives for the treatment of atherosclerosis |
| US5756470A (en) * | 1996-10-29 | 1998-05-26 | Schering Corporation | Sugar-substituted 2-azetidinones useful as hypocholesterolemic agents |
| US6593078B1 (en) | 1999-04-16 | 2003-07-15 | Schering Corporation | Use of azetidinone compounds |
| DE10042447A1 (de) * | 2000-08-29 | 2002-03-28 | Aventis Pharma Gmbh | Protein aus dem Darm von Wirbeltieren, welches Cholesterin absorbiert, sowie Verwendung dieses Proteins zur Identifizierung von Inhibitoren des intestinalen Cholesterintransports |
| US6584357B1 (en) * | 2000-10-17 | 2003-06-24 | Sony Corporation | Method and system for forming an acoustic signal from neural timing difference data |
| US6982251B2 (en) | 2000-12-20 | 2006-01-03 | Schering Corporation | Substituted 2-azetidinones useful as hypocholesterolemic agents |
| MEP27808A (en) * | 2001-01-26 | 2010-10-10 | Schering Corp | Combinations of peroxisome proliferator-activated receptor (ppar) activator(s) and sterol absorption inhibitor(s) and treatments for vascular indications |
| US7071181B2 (en) | 2001-01-26 | 2006-07-04 | Schering Corporation | Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors |
| EP1911462A3 (en) | 2001-01-26 | 2011-11-30 | Schering Corporation | Compositions comprising a sterol absorption inhibitor |
| US20060287254A1 (en) * | 2001-01-26 | 2006-12-21 | Schering Corporation | Use of substituted azetidinone compounds for the treatment of sitosterolemia |
| AU2005246926B2 (en) * | 2001-01-26 | 2008-02-28 | Merck Sharp & Dohme Corp. | The use of substituted azetidinone compounds for the treatment of sitosterolemia |
| TW200840563A (en) * | 2001-01-26 | 2008-10-16 | Schering Corp | Combinations of nicotinic acid and derivatives thereof and sterol absorption inhibitor(S) and treatments for vascular indications |
| TWI291957B (en) * | 2001-02-23 | 2008-01-01 | Kotobuki Pharmaceutical Co Ltd | Beta-lactam compounds, process for repoducing the same and serum cholesterol-lowering agents containing the same |
| AU2002258605B2 (en) | 2001-03-28 | 2006-01-12 | Merck Sharp & Dohme Corp. | Enantioselective synthesis of azetidinone intermediate compounds |
| EP1417187A1 (en) | 2001-07-16 | 2004-05-12 | Euro-Celtique S.A. | Aryl substituted thiazolidinones and the use thereof |
| MXPA04002572A (es) * | 2001-09-21 | 2004-05-31 | Schering Corp | Metodos para el tratamiento o prevencion de inflamacion vascular usando inhibidores de absorcion de esterol. |
| US7132415B2 (en) * | 2001-09-21 | 2006-11-07 | Schering Corporation | Methods and therapeutic combinations for the treatment of xanthoma using sterol absorption inhibitors |
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| US7056906B2 (en) | 2001-09-21 | 2006-06-06 | Schering Corporation | Combinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women |
| US20030204096A1 (en) * | 2002-03-25 | 2003-10-30 | Schering Corporation | Enantioselective synthesis of azetidinone intermediate compounds |
| GB0215579D0 (en) | 2002-07-05 | 2002-08-14 | Astrazeneca Ab | Chemical compounds |
| US7135556B2 (en) * | 2002-07-19 | 2006-11-14 | Schering Corporation | NPC1L1 (NPC3) and methods of use thereof |
| US20040132058A1 (en) | 2002-07-19 | 2004-07-08 | Schering Corporation | NPC1L1 (NPC3) and methods of use thereof |
| AR040588A1 (es) | 2002-07-26 | 2005-04-13 | Schering Corp | Formulacion farmaceutica que comprende un inhibidor de la absorcion del colesterol y un inhibidor de una hmg- co a reductasa |
| AU2003254261B2 (en) * | 2002-07-30 | 2008-04-17 | Children's Medical Center Corporation | Compositions of ezetimibe and methods for the treatment of cholesterol-associated benign and malignant tumors |
| AU2003291227A1 (en) | 2002-11-05 | 2004-06-07 | Smithkline Beecham Corporation | Antibacterial agents |
| CA2504878A1 (en) | 2002-11-06 | 2004-05-27 | Schering Corporation | Cholesterol absorption inhibitors for the treatment of demyelination |
| WO2004081002A1 (en) | 2003-03-07 | 2004-09-23 | Schering Corporation | Substituted azetidinone compounds, formulations and uses thereof for the treatment of hypercholesterolemia |
| CN1756755A (zh) | 2003-03-07 | 2006-04-05 | 先灵公司 | 取代的2-吖丁啶酮化合物、其制剂及其治疗高胆甾醇血症的用途 |
| WO2004081003A1 (en) | 2003-03-07 | 2004-09-23 | Schering Corporation | Substituted azetidinone compounds, formulations and uses thereof for the treatment of hypercholeterolemia |
| US7459442B2 (en) | 2003-03-07 | 2008-12-02 | Schering Corporation | Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof |
| JP2005015434A (ja) * | 2003-06-27 | 2005-01-20 | Kotobuki Seiyaku Kk | 血清コレステロール低下剤或はアテローム性硬化症の予防又は治療剤 |
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| GB0329778D0 (en) * | 2003-12-23 | 2004-01-28 | Astrazeneca Ab | Chemical compounds |
| US7871998B2 (en) | 2003-12-23 | 2011-01-18 | Astrazeneca Ab | Diphenylazetidinone derivatives possessing cholesterol absorption inhibitory activity |
| AU2004308332B2 (en) * | 2003-12-23 | 2008-04-10 | Merck Sharp & Dohme Corp. | Anti-hypercholesterolemic compounds |
| JP4590417B2 (ja) * | 2004-01-16 | 2010-12-01 | メルク・シャープ・エンド・ドーム・コーポレイション | Npc1l1(npc3)およびこのリガンドの同定方法 |
| WO2005113496A1 (de) * | 2004-05-21 | 2005-12-01 | Sanofi-Aventis Deutschland Gmbh | Verfahren zur herstellung von 1,4-diphenylazetidinon-derivaten |
| DE102004025072A1 (de) * | 2004-05-21 | 2005-12-15 | Sanofi-Aventis Deutschland Gmbh | Verfahren zur Herstellung von Diphenyl-azetidinon-Derivaten |
| EP1807070A1 (en) * | 2004-09-29 | 2007-07-18 | Schering Corporation | Combinations of substituted azetidinones and cb1 antagonists |
| WO2006050634A1 (en) * | 2004-11-15 | 2006-05-18 | Xiamen Mchem Pharma (Group) Ltd. | A preparation method of 1-(4-fluorophenyl)-(3r)-[3-(4-fluorophenyl)-(3s)-hydroxypropyl]-(4s)-(4-hydroxyphenyl)-2-azetidinone |
| EP1819684B1 (en) | 2004-12-03 | 2013-08-07 | Intervet International B.V. | Substituted piperazines as cb1 antagonists |
| MX2007007473A (es) * | 2004-12-20 | 2007-09-04 | Schering Corp | Procedimiento para la sintesis de azetidinonas. |
| EP1851197A2 (en) * | 2005-02-09 | 2007-11-07 | Microbia, Inc. | Phenylazetidinone derivatives |
| EP1877067A1 (en) * | 2005-04-26 | 2008-01-16 | Microbia, Inc. | 4-biarylyl-1-phenylazetidin-2-one glucuronide derivatives for hypercholesterolemia |
| TW200726746A (en) * | 2005-05-06 | 2007-07-16 | Microbia Inc | Processes for production of 4-biphenylylazetidin-2-ones |
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1992
- 1992-07-21 TW TW081105745A patent/TW223059B/zh active
- 1992-07-21 EP EP92916790A patent/EP0596015B1/en not_active Expired - Lifetime
- 1992-07-21 CZ CS94142A patent/CZ14294A3/cs unknown
- 1992-07-21 AT AT92916790T patent/ATE158789T1/de not_active IP Right Cessation
- 1992-07-21 WO PCT/US1992/005972 patent/WO1993002048A1/en not_active Ceased
- 1992-07-21 HU HU9400185A patent/HUT67341A/hu unknown
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- 1992-07-21 DE DE69222532T patent/DE69222532T2/de not_active Expired - Lifetime
- 1992-07-21 IL IL102582A patent/IL102582A0/xx unknown
- 1992-07-21 SK SK79-94A patent/SK7994A3/sk unknown
- 1992-07-21 MY MYPI92001303A patent/MY131273A/en unknown
- 1992-07-21 ES ES92916790T patent/ES2107548T3/es not_active Expired - Lifetime
- 1992-07-21 AU AU23980/92A patent/AU658441B2/en not_active Ceased
- 1992-07-21 JP JP5502964A patent/JP2525125B2/ja not_active Expired - Fee Related
- 1992-07-22 CN CN92108760A patent/CN1069024A/zh active Pending
- 1992-07-22 IE IE237492A patent/IE922374A1/en not_active Application Discontinuation
- 1992-07-22 NZ NZ243669A patent/NZ243669A/en unknown
- 1992-07-22 YU YU72092A patent/YU72092A/sh unknown
- 1992-07-23 MX MX9204327A patent/MX9204327A/es not_active IP Right Cessation
- 1992-10-19 US US07/962,768 patent/US5306817A/en not_active Expired - Fee Related
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1994
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- 1994-01-21 NO NO940221A patent/NO940221D0/no unknown
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1090479C (zh) * | 1992-12-23 | 2002-09-11 | 先灵公司 | 一种胆固醇生物合成抑制剂与一种β-内酰胺胆固醇吸收抑制剂的联合 |
| CN1071745C (zh) * | 1993-07-09 | 2001-09-26 | 先灵公司 | 合成氮杂环丁酮类化合物的方法 |
| CN1050830C (zh) * | 1993-09-21 | 2000-03-29 | 先灵公司 | 氮杂环丁烷酮类化合物及其医药用途 |
| CN1083833C (zh) * | 1994-11-18 | 2002-05-01 | 先灵公司 | 用作降胆固醇剂的硫取代的氮杂环丁烷酮类化合物 |
| CN100522159C (zh) * | 2001-01-26 | 2009-08-05 | 先灵公司 | 取代的氮杂环丁烷酮化合物在制备治疗谷甾醇血症的药物中的应用 |
| CN103254107A (zh) * | 2013-05-09 | 2013-08-21 | 东华大学 | 一种依泽替米贝类似物及其制备方法 |
| CN103254107B (zh) * | 2013-05-09 | 2015-10-21 | 东华大学 | 一种依泽替米贝类似物及其制备方法 |
| CN103524486A (zh) * | 2013-09-18 | 2014-01-22 | 中国科学院昆明植物研究所 | N-喹啉基取代的β-内酰胺类化合物及其药物组合物和合成方法与应用 |
| CN103524486B (zh) * | 2013-09-18 | 2016-03-02 | 中国科学院昆明植物研究所 | N-喹啉基取代的β-内酰胺类化合物及其药物组合物和合成方法与应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| US5306817A (en) | 1994-04-26 |
| MX9204327A (es) | 1994-07-29 |
| MY131273A (en) | 2007-07-31 |
| JP2525125B2 (ja) | 1996-08-14 |
| DE69222532T2 (de) | 1998-02-26 |
| CZ14294A3 (en) | 1994-07-13 |
| NO940221L (no) | 1994-01-21 |
| FI940296A0 (fi) | 1994-01-21 |
| OA09878A (en) | 1994-09-15 |
| EP0596015A1 (en) | 1994-05-11 |
| WO1993002048A1 (en) | 1993-02-04 |
| ATE158789T1 (de) | 1997-10-15 |
| FI940296A7 (fi) | 1994-01-21 |
| AU2398092A (en) | 1993-02-23 |
| DE69222532D1 (de) | 1997-11-06 |
| HU9400185D0 (en) | 1994-05-30 |
| YU72092A (sh) | 1995-12-04 |
| EP0596015B1 (en) | 1997-10-01 |
| NZ243669A (en) | 1994-12-22 |
| BG61118B2 (bg) | 1996-11-29 |
| TW223059B (cg-RX-API-DMAC7.html) | 1994-05-01 |
| JPH06508637A (ja) | 1994-09-29 |
| HUT67341A (en) | 1995-03-28 |
| US6093812A (en) | 2000-07-25 |
| IE922374A1 (en) | 1993-01-27 |
| AU658441B2 (en) | 1995-04-13 |
| EP0524595A1 (en) | 1993-01-27 |
| IL102582A0 (en) | 1993-01-14 |
| NO940221D0 (no) | 1994-01-21 |
| SK7994A3 (en) | 1994-07-06 |
| ES2107548T3 (es) | 1997-12-01 |
| EE9400342A (et) | 1996-04-15 |
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