CN102816194A - 大环化合物以及其制作和使用方法 - Google Patents
大环化合物以及其制作和使用方法 Download PDFInfo
- Publication number
- CN102816194A CN102816194A CN2012102533942A CN201210253394A CN102816194A CN 102816194 A CN102816194 A CN 102816194A CN 2012102533942 A CN2012102533942 A CN 2012102533942A CN 201210253394 A CN201210253394 A CN 201210253394A CN 102816194 A CN102816194 A CN 102816194A
- Authority
- CN
- China
- Prior art keywords
- saturated
- unsaturated
- membered
- mmol
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 0 CC(C1)=*OC1O Chemical compound CC(C1)=*OC1O 0.000 description 28
- GTCSKAJTBIGWMQ-UHFFFAOYSA-N C#CCNCc1ccc(CCO)cc1 Chemical compound C#CCNCc1ccc(CCO)cc1 GTCSKAJTBIGWMQ-UHFFFAOYSA-N 0.000 description 1
- SOEWUJYXVUKYDK-BQYBEJQRSA-N C/C(/CCO)=C\C=C(/C)\CBr Chemical compound C/C(/CCO)=C\C=C(/C)\CBr SOEWUJYXVUKYDK-BQYBEJQRSA-N 0.000 description 1
- FKMCGAZOJQYGLC-PKNBQFBNSA-N C/N=C/C=C1CCCCCC1 Chemical compound C/N=C/C=C1CCCCCC1 FKMCGAZOJQYGLC-PKNBQFBNSA-N 0.000 description 1
- NEUKCSXPEGXYKF-UHFFFAOYSA-N CC(C)(C)OC(N(Cc1ccc(CCO)cc1)CC#C)=O Chemical compound CC(C)(C)OC(N(Cc1ccc(CCO)cc1)CC#C)=O NEUKCSXPEGXYKF-UHFFFAOYSA-N 0.000 description 1
- PSLHDALTMIBUKZ-CTQIIAAMSA-N CC(CC1C(O)O2)[C@@H]1C2=O Chemical compound CC(CC1C(O)O2)[C@@H]1C2=O PSLHDALTMIBUKZ-CTQIIAAMSA-N 0.000 description 1
- OIWCTDIWQKPQHU-MKRHZNTKSA-N CC[C@H]([C@](C)([C@@H]([C@@H](C)C([C@H](C)C[C@](C)([C@@H]([C@@H](C)[C@@H]([C@H]1C)O[C@@H](C[C@@]2(C)OC)O[C@@H](C)[C@@H]2O)O[C@@H](C2)O[C@H](C)C[C@@H]2NC)OC)=O)O)O)OC1=O Chemical compound CC[C@H]([C@](C)([C@@H]([C@@H](C)C([C@H](C)C[C@](C)([C@@H]([C@@H](C)[C@@H]([C@H]1C)O[C@@H](C[C@@]2(C)OC)O[C@@H](C)[C@@H]2O)O[C@@H](C2)O[C@H](C)C[C@@H]2NC)OC)=O)O)O)OC1=O OIWCTDIWQKPQHU-MKRHZNTKSA-N 0.000 description 1
- VZEWKEMJEQKTRL-CBPOBEHUSA-N CC[C@H]([C@](C)([C@@H]([C@@H](C)N(C)C[C@H](C)C[C@](C)([C@@H]([C@@H](C)[C@@H]([C@H]1C)O[C@@H](C[C@@]2(C)OC)O[C@@H](C)[C@@H]2O)O[C@@H](C2)O[C@H](C)C[C@@H]2NC)O)O)O)OC1=O Chemical compound CC[C@H]([C@](C)([C@@H]([C@@H](C)N(C)C[C@H](C)C[C@](C)([C@@H]([C@@H](C)[C@@H]([C@H]1C)O[C@@H](C[C@@]2(C)OC)O[C@@H](C)[C@@H]2O)O[C@@H](C2)O[C@H](C)C[C@@H]2NC)O)O)O)OC1=O VZEWKEMJEQKTRL-CBPOBEHUSA-N 0.000 description 1
- FWUQLBBPJWSTQE-CBUWHHKMSA-N CC[C@H]([C@](C)([C@@H]([C@@H](C)N(C)C[C@H](C)C[C@](C)([C@@H]([C@@H](C)[C@H](C(CC1(C)C)O[C@@H](C)[C@@H]1O)[C@H]1C)O[C@@H](C2)O[C@H](C)C[C@@H]2N(C)CCc2c[n]([C@H](C)[C@@H](c3ccccc3)O)nn2)O)O)O)OC1=O Chemical compound CC[C@H]([C@](C)([C@@H]([C@@H](C)N(C)C[C@H](C)C[C@](C)([C@@H]([C@@H](C)[C@H](C(CC1(C)C)O[C@@H](C)[C@@H]1O)[C@H]1C)O[C@@H](C2)O[C@H](C)C[C@@H]2N(C)CCc2c[n]([C@H](C)[C@@H](c3ccccc3)O)nn2)O)O)O)OC1=O FWUQLBBPJWSTQE-CBUWHHKMSA-N 0.000 description 1
- DTJUJXBNASAHJF-UHFFFAOYSA-N CN(C=C1)OC1=O Chemical compound CN(C=C1)OC1=O DTJUJXBNASAHJF-UHFFFAOYSA-N 0.000 description 1
- AYIRNRDRBQJXIF-NXEZZACHSA-N CS(c1ccc([C@H]([C@@H](CF)NC(C(Cl)Cl)=O)O)cc1)(=O)=O Chemical compound CS(c1ccc([C@H]([C@@H](CF)NC(C(Cl)Cl)=O)O)cc1)(=O)=O AYIRNRDRBQJXIF-NXEZZACHSA-N 0.000 description 1
- FPQOQDFWCJXVKF-BQBZGAKWSA-N C[C@@H]1C[C@H](C)OCC1 Chemical compound C[C@@H]1C[C@H](C)OCC1 FPQOQDFWCJXVKF-BQBZGAKWSA-N 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N Cc(cc1)ccc1S(N)(=O)=O Chemical compound Cc(cc1)ccc1S(N)(=O)=O LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- QNJHTLTUBNXLFS-UHFFFAOYSA-N NS(c1ccc(CBr)cc1)(=O)=O Chemical compound NS(c1ccc(CBr)cc1)(=O)=O QNJHTLTUBNXLFS-UHFFFAOYSA-N 0.000 description 1
- WCOCCXZFEJGHTC-UHFFFAOYSA-N OC(Cc1ccc(CBr)cc1)=O Chemical compound OC(Cc1ccc(CBr)cc1)=O WCOCCXZFEJGHTC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
- C07H17/04—Heterocyclic radicals containing only oxygen as ring hetero atoms
- C07H17/08—Hetero rings containing eight or more ring members, e.g. erythromycins
-
- 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
-
- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P1/10—Laxatives
-
- 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
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- 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]
-
- 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
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- 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
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H17/00—Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nutrition Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Materials For Medical Uses (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54828004P | 2004-02-27 | 2004-02-27 | |
| US60/548,280 | 2004-02-27 | ||
| US57594904P | 2004-06-01 | 2004-06-01 | |
| US60/575,949 | 2004-06-01 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200580013532 Division CN1950388A (zh) | 2004-02-27 | 2005-02-25 | 大环化合物以及其制作和使用方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102816194A true CN102816194A (zh) | 2012-12-12 |
Family
ID=34922681
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2012102533942A Pending CN102816194A (zh) | 2004-02-27 | 2005-02-25 | 大环化合物以及其制作和使用方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (4) | US8202843B2 (https=) |
| EP (2) | EP2716647A3 (https=) |
| JP (5) | JP5383037B2 (https=) |
| CN (1) | CN102816194A (https=) |
| WO (1) | WO2005085266A2 (https=) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR043050A1 (es) | 2002-09-26 | 2005-07-13 | Rib X Pharmaceuticals Inc | Compuestos heterociclicos bifuncionales y metodos para preparar y usar los mismos |
| JP5383037B2 (ja) | 2004-02-27 | 2014-01-08 | リブ−エックス ファーマシューティカルズ,インコーポレイテッド | 大環状化合物およびそれらを製造し使用する方法 |
| DE102004045870A1 (de) * | 2004-04-07 | 2005-12-01 | Dynamit Nobel Gmbh Explosivstoff- Und Systemtechnik | Verfahren zur Herstellung von Azidoalkylaminen |
| EP1807439A2 (en) * | 2004-10-25 | 2007-07-18 | Ranbaxy Laboratories Limited | Ketolide derivatives as antibacterial agents |
| UA90720C2 (en) * | 2005-05-25 | 2010-05-25 | Басф Акциенгезелльшафт | Heteroaroyl-substituted serine amides |
| EP3290427A1 (en) * | 2005-08-24 | 2018-03-07 | Melinta Therapeutics, Inc. | Triazole compounds and methods of making and using the same |
| JP2009506063A (ja) * | 2005-08-24 | 2009-02-12 | リブ−エックス ファーマシューティカルズ,インコーポレイテッド | トリアゾール化合物ならびにこれを作製する方法および使用する方法 |
| WO2007054904A2 (en) * | 2005-11-08 | 2007-05-18 | Ranbaxy Laboratories Limited | Macrolides as anti-inflammatory agents |
| WO2007060518A2 (en) * | 2005-11-23 | 2007-05-31 | Ranbaxy Laboratories Limited | Ketolide derivatives as antibacterial agents |
| EA017878B1 (ru) * | 2006-12-12 | 2013-03-29 | Замбон С.П.А. | Макролидные соединения, обладающие противовоспалительной активностью |
| WO2008106224A1 (en) * | 2007-02-28 | 2008-09-04 | Rib-X Pharmaceuticals, Inc. | Macrolide compounds and methods of making and using the same |
| CA2733706A1 (en) * | 2007-08-10 | 2009-02-19 | Y's Therapeutics Co., Ltd. | Modulation of immune responses by administration of roxithromycin or its derivative |
| JP2011529977A (ja) | 2008-07-31 | 2011-12-15 | スリーエム イノベイティブ プロパティズ カンパニー | フルオロポリマー組成物並びにその製造及び使用方法 |
| EP2315802A4 (en) * | 2008-07-31 | 2012-04-18 | 3M Innovative Properties Co | AZIUM COMPOSITIONS AND METHOD FOR THEIR PREPARATION AND USE |
| WO2011018510A1 (en) | 2009-08-13 | 2011-02-17 | Basilea Pharmaceutica Ag | New macrolides and their use |
| JP2013506676A (ja) * | 2009-09-30 | 2013-02-28 | トランザイム・ファーマ,インコーポレイテッド | 大環状グレリン受容体アゴニストの塩、溶媒和物、および薬学的組成物、ならびにその使用方法 |
| EP2694707B1 (en) | 2011-04-07 | 2018-08-15 | Cornell University | Monomers capable of dimerizing in an aqueous solution, and methods of using same |
| PT2782922T (pt) * | 2011-11-25 | 2018-02-05 | The Kitasato Inst | Derivados antibacterianos de tilosina e processos para a sua preparação |
| WO2017150341A1 (ja) * | 2016-03-04 | 2017-09-08 | 株式会社カネカ | アーク防護服用布帛及びアーク防護服 |
| WO2018191682A1 (en) * | 2017-04-15 | 2018-10-18 | Melinta Therapeutics, Inc. | Triazole compounds and methods of making and using the same |
| CU24717B1 (es) | 2018-10-02 | 2024-08-15 | Lunella Biotech Inc | Derivados de azitromicina y roxitromicina como fármacos senolíticos |
Family Cites Families (117)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3629232A (en) | 1969-08-19 | 1971-12-21 | Abbott Lab | 2'-o-alkanoyl-4'-alkanoyloxy derivatives of erythromycin |
| US3681325A (en) | 1970-09-30 | 1972-08-01 | Abbott Lab | De(n-methyl)-n-substituted derivatives of erythromycin |
| US4404201A (en) | 1981-11-13 | 1983-09-13 | Warner-Lambert Company | Cephalosporins |
| US4546176A (en) | 1982-12-14 | 1985-10-08 | Eisai Co., Ltd. | 7-Carboxymethoxyphenylacetamido-3-cephem derivatives and antibacterial preparations containing the same |
| US5008249A (en) | 1985-08-31 | 1991-04-16 | Kitasato Kenkyusho | Therapeutic method of stimulating digestive tract contractile motion in mammals |
| EP0215355B1 (en) | 1985-08-31 | 1994-04-06 | Kitasato Kenkyusho | Erythromycin derivative and process for preparing the same |
| US5232918A (en) | 1987-07-23 | 1993-08-03 | Imperial Chemical Industries Plc | Cephalosporin derivatives |
| US5336768A (en) | 1988-05-24 | 1994-08-09 | Hoffmann-La Roche Inc. | Antibacterial cephalosporin compounds |
| US5180719A (en) | 1988-10-24 | 1993-01-19 | Norwich Eaton Pharmaceuticals, Inc. | Antimicrobial quinolonyl lactam esters |
| US6446032B1 (en) | 1990-09-21 | 2002-09-03 | Massachusetts Institute Of Technology | Designing compounds specifically inhibiting ribonucleic acid by binding to the minor groove |
| IL114589A (en) | 1990-11-21 | 1999-12-22 | Roussel Uclaf | Intermediates for the preparation of erythromycin derivatives |
| US5686065A (en) | 1991-03-27 | 1997-11-11 | Special Advanced Biomaterials, Inc. | Topical siloxane sunscreen compositions having enhanced performance and safety |
| ES2101119T3 (es) | 1991-10-01 | 1997-07-01 | Procter & Gamble Pharma | Procedimiento para preparar quinolonil-lactamas antimicrobianas. |
| US5215980A (en) | 1992-01-17 | 1993-06-01 | Merck & Co., Inc. | 10-AZA-9-deoxo-11-deoxy-erythromycin A and derivatives thereof |
| MY113693A (en) * | 1992-05-26 | 2002-05-31 | Chugai Pharmaceutical Co Ltd | Erythromycin derivatives having an enterokinesis stimulating action |
| TW355711B (en) | 1992-11-04 | 1999-04-11 | Chugai Pharmaceutical Co Ltd | Erythromycin derivatives |
| FR2697524B1 (fr) | 1992-11-05 | 1994-12-23 | Roussel Uclaf | Nouveaux dérivés de l'érythromycine, leur procédé de préparation et leur application comme médicaments. |
| US5527780A (en) | 1992-11-05 | 1996-06-18 | Roussel Uclaf | Erythromycin derivatives |
| MY115155A (en) | 1993-09-09 | 2003-04-30 | Upjohn Co | Substituted oxazine and thiazine oxazolidinone antimicrobials. |
| FR2719587B1 (fr) | 1994-05-03 | 1996-07-12 | Roussel Uclaf | Nouveaux dérivés de l'érythromycine, leur procédé de préparation et leur application comme médicaments. |
| IT1276901B1 (it) | 1994-12-13 | 1997-11-03 | Zambon Spa | Derivati dell'eritromicina a 9-0-ossina dotati di attivita' antibiotica |
| US5693791A (en) | 1995-04-11 | 1997-12-02 | Truett; William L. | Antibiotics and process for preparation |
| US6274715B1 (en) | 1995-11-08 | 2001-08-14 | Abbott Laboratories | Tricyclic erythromycin derivatives |
| US5891643A (en) | 1995-11-14 | 1999-04-06 | Abbott Laboratories | Use of nuclear magnetic resonance to design ligands to target biomolecules |
| FR2742757B1 (fr) | 1995-12-22 | 1998-01-30 | Roussel Uclaf | Nouveaux derives de l'erythromycine, leur procede de preparation et leur application comme medicaments |
| DE19604223A1 (de) | 1996-02-06 | 1997-08-07 | Bayer Ag | Neue substituierte Oxazolidinone |
| WO1997035195A1 (en) | 1996-03-19 | 1997-09-25 | The Salk Institute For Biological Studies | In vitro methods for identifying modulators of members of the steroid/thyroid superfamily of receptors |
| FR2748746B1 (fr) * | 1996-05-14 | 1998-08-14 | Hoechst Marion Roussel Inc | Nouveau procede d'isomerisation du radical methyle en 10 de derives de l'erythromycine |
| US5712253A (en) | 1996-06-18 | 1998-01-27 | Abbott Laboratories | Macrocyclic 13-membered ring derivatives of erythromycins A and B |
| UA51730C2 (uk) | 1996-09-04 | 2002-12-16 | Ебботт Лабораторіз | 6-o-заміщені кетоліди з антибактеріальною активністю, спосіб їх одержання (варіанти), фармацевтична композиція та спосіб регулювання бактеріальної інфекції у ссавців |
| HN1998000074A (es) | 1997-06-11 | 1999-01-08 | Pfizer Prod Inc | Derivados de macrolidos c-4 sustituidos |
| CZ9904388A3 (cs) | 1997-06-11 | 2002-10-16 | Pfizer Products Inc. | 9-Oximové deriváty erythromycinu |
| EP0895999A1 (en) | 1997-08-06 | 1999-02-10 | Pfizer Products Inc. | C-4" substituted macrolide antibiotics |
| US5780605A (en) | 1997-09-08 | 1998-07-14 | Abbott Laboratories | 6,9-bridged erythromycin derivatives |
| DK1025114T3 (da) * | 1997-09-30 | 2004-07-05 | Abbott Lab | 3'-N-modificerede 6-O-substituerede erythromycin-ketolidderivater med antibakteriel aktivitet |
| US6034069A (en) | 1997-09-30 | 2000-03-07 | Abbott Laboratories | 3-'N-modified 6-O-substituted erythromycin ketolide derivatives having antibacterial activity |
| ZA989885B (en) * | 1997-10-31 | 1999-05-05 | Abbott Lab | Use of macrolides for the treatment of cancer and macular degeneration |
| WO1999028308A1 (en) | 1997-11-29 | 1999-06-10 | Truett William L | Antibiotics and process for preparation |
| AU1694099A (en) | 1997-12-26 | 1999-07-19 | Cheil Jedang Corporation | Cephem derivatives and a method for producing the compounds and an antibacterialcomposition containing the compounds |
| US5955440A (en) | 1998-03-27 | 1999-09-21 | Abbott Laboratories | Macrolide LHRH antagonists |
| US6437119B1 (en) | 1998-05-07 | 2002-08-20 | William Lawrence Truett | Compounds formed from two or three antibiotics and their processes of preparation |
| TR200003595T2 (tr) | 1998-06-05 | 2001-07-23 | Astrazeneca Ab | Kimyasal bileşikler |
| GB9812019D0 (en) | 1998-06-05 | 1998-07-29 | Zeneca Ltd | Chemical compounds |
| WO1999063929A2 (en) | 1998-06-08 | 1999-12-16 | Advanced Medicine, Inc. | Multibinding inhibitors of microsomal triglyceride transferase protein |
| EP1086065A4 (en) | 1998-06-08 | 2001-03-28 | Advanced Medicine Inc | Combinatorial synthesis of multibinding libraries |
| US6541669B1 (en) | 1998-06-08 | 2003-04-01 | Theravance, Inc. | β2-adrenergic receptor agonists |
| WO1999063994A1 (en) | 1998-06-08 | 1999-12-16 | Advanced Medicine, Inc. | MULTIBINDING INHIBITORS OF HMG-CoA REDUCTASE |
| US6420354B1 (en) | 1998-06-08 | 2002-07-16 | Advanced Medicine, Inc. | Sodium channel drugs and uses |
| EP1085845A2 (en) | 1998-06-08 | 2001-03-28 | Advanced Medicine, Inc. | Multibinding inhibitors of cyclooxygenase-2 |
| IT1301968B1 (it) | 1998-07-30 | 2000-07-20 | Zambon Spa | Derivati di eritromicina ad attivita' antibiotica |
| US6020521A (en) | 1998-08-26 | 2000-02-01 | Abbott Laboratories | Macrolide LHRH antagonists |
| GB9821938D0 (en) | 1998-10-09 | 1998-12-02 | Zeneca Ltd | Chemical compounds |
| HRP980646B1 (en) * | 1998-12-30 | 2008-02-29 | GlaxoSmithKline istra�iva�ki centar Zagreb d.o.o. | Novel oleandomycin derivatives |
| IT1306205B1 (it) | 1999-01-15 | 2001-05-30 | Zambon Spa | Macrolidi ad attivita' antiinfiammatoria. |
| US6479498B1 (en) | 1999-06-04 | 2002-11-12 | Theravance, Inc. | Sodium channel drugs and uses |
| HRP990192A2 (en) | 1999-06-11 | 2001-04-30 | Pliva D D | 4'-DEMICAROZYL-8a-AZA-8a-HOMOTHILOSINE DERIVATIVES |
| US6413981B1 (en) | 1999-08-12 | 2002-07-02 | Ortho-Mcneil Pharamceutical, Inc. | Bicyclic heterocyclic substituted phenyl oxazolidinone antibacterials, and related compositions and methods |
| GB9928568D0 (en) | 1999-12-03 | 2000-02-02 | Zeneca Ltd | Chemical compounds |
| IT1314261B1 (it) | 1999-12-03 | 2002-12-06 | Enichem Spa | Composti metallocenici pontati, processo per la loro preparazione eloro uso come catalizzatori per la polimerizzazione di olefine. |
| GB9928499D0 (en) | 1999-12-03 | 2000-02-02 | Zeneca Ltd | Chemical processes and intermediates |
| JP2003522763A (ja) | 2000-02-10 | 2003-07-29 | ファルマシア・アンド・アップジョン・カンパニー | ピペラジンアミド置換基を持つオキサゾリジノンチオアミド |
| JP2001261694A (ja) | 2000-03-06 | 2001-09-26 | Pfizer Prod Inc | ケトライド抗生物質 |
| GB0009803D0 (en) | 2000-04-25 | 2000-06-07 | Astrazeneca Ab | Chemical compounds |
| EP1299109B1 (en) | 2000-04-27 | 2009-07-15 | The Scripps Research Institute | Bifunctional antibiotics |
| DE10034627A1 (de) | 2000-07-17 | 2002-01-31 | Bayer Ag | Aryl-substituierte Oxazolidinone mit Cytokin inhibitorischer Wirkung |
| IL180679A0 (en) | 2000-10-27 | 2009-02-11 | Pfizer Prod Inc | Process for the preparation of non-steroidal glucocorticoid receptor modulators |
| ES2262612T3 (es) | 2000-10-28 | 2006-12-01 | Pfizer Products Inc. | Moduladpres del receptor de glucocorticoides. |
| AU2002225724A1 (en) * | 2000-12-01 | 2002-07-08 | Kosan Biosciences, Inc. | Motilide compounds |
| US6440942B1 (en) | 2000-12-22 | 2002-08-27 | Enanta Pharmaceuticals, Inc. | 14-membered macrolides derived from leucomycins |
| GB0108764D0 (en) | 2001-04-07 | 2001-05-30 | Astrazeneca Ab | Chemical compounds |
| ES2268011T3 (es) | 2001-04-07 | 2007-03-16 | Astrazeneca Ab | Oxazolidinonas que contienen un grupo sulfonimida como antibioticos. |
| GB0108793D0 (en) | 2001-04-07 | 2001-05-30 | Astrazeneca Ab | Chemical compounds |
| GB0108794D0 (en) | 2001-04-07 | 2001-05-30 | Astrazeneca Ab | Chemical compound |
| GB0113299D0 (en) | 2001-06-01 | 2001-07-25 | Astrazeneca Ab | Chemical process & intermediates |
| GB0113297D0 (en) | 2001-06-01 | 2001-07-25 | Astrazeneca Ab | Chemical Process |
| US6680299B2 (en) | 2001-07-27 | 2004-01-20 | Enanta Pharmaceuticals, Inc. | 4'-substituted leucomycins |
| US20030158093A1 (en) | 2001-08-17 | 2003-08-21 | Binyuan Sun | Bifunctional glycopeptide antibiotics and combinatorial libararies thereof |
| US7396847B2 (en) | 2001-09-11 | 2008-07-08 | Astrazeneca Ab | Oxazolidinone and/or isoxazoline as antibacterial agents |
| EP1443930A1 (en) | 2001-10-25 | 2004-08-11 | AstraZeneca AB | Isoxazoline derivatives useful as antimicrobials |
| GB2396350A (en) | 2001-10-25 | 2004-06-23 | Astrazeneca Ab | Aryl substituted oxazolidinones with antibacterial activity |
| US6576615B2 (en) | 2001-11-08 | 2003-06-10 | Enanta Pharmaceuticals, Inc. | 4′-O-substituted tylosin analogs |
| GB0127349D0 (en) | 2001-11-14 | 2002-01-02 | Glaxo Group Ltd | Macrolides |
| US6664240B2 (en) | 2001-11-15 | 2003-12-16 | Enanta Pharmaceuticals, Inc. | Tylosin derivatives having antibacterial activity |
| PL371335A1 (en) | 2002-01-22 | 2005-06-13 | Pharmacia & Upjohn Company | Infection-resistant medical devices |
| AU2003211113B2 (en) | 2002-02-15 | 2007-08-09 | Merckle Gmbh | Antibiotic conjugates |
| WO2003070173A2 (en) | 2002-02-15 | 2003-08-28 | Sympore Gmbh | Conjugates of biologically active compounds, methods for their preparation and use, formulation and pharmaceutical applications thereof |
| AU2003219770B2 (en) | 2002-02-15 | 2008-10-09 | Merckle Gmbh | Conjugates of biologically active compounds, methods for their preparation and use, formulation and pharmaceutical applications thereof |
| JP2005524661A (ja) | 2002-02-28 | 2005-08-18 | アストラゼネカ アクチボラグ | 3−シクリル−5−(窒素含有5員環)メチル−オキサゾリジノン誘導体と抗菌剤としてのその使用 |
| US6710034B2 (en) | 2002-04-19 | 2004-03-23 | Enanta Pharmaceuticals, Inc. | 5-O-mycaminosyltylonide derivatives |
| US6753415B2 (en) | 2002-04-19 | 2004-06-22 | Enanta Pharmaceuticals, Inc. | 23-O-substituted 5-O-mycaminosyltylonide derivatives |
| US6878691B2 (en) | 2002-05-13 | 2005-04-12 | Enanta Pharmaceuticals, Inc. | 6-11 bicyclic ketolide derivatives |
| US7064110B2 (en) | 2002-05-13 | 2006-06-20 | Enanta Pharmaceuticals, Inc. | 6-11 bicycle ketolide derivatives |
| KR100661973B1 (ko) | 2002-05-13 | 2006-12-28 | 이난타 파마슈티칼스, 인코포레이티드 | 6,11 바이사이클릭 에리스로마이신 유도체 |
| RU2330858C2 (ru) | 2002-07-08 | 2008-08-10 | Глаксомитклайн Истраживацки Центар Загреб Д.О.О. | Новые соединения, составы и способы лечения воспалительных заболеваний и состояний |
| PL374646A1 (en) | 2002-07-08 | 2005-10-31 | Pliva-Istrazivacki Institutt D.O.O. | Novel nonsteroidal anti-inflammatory substances, compositions and methods for their use |
| US7157433B2 (en) | 2002-07-08 | 2007-01-02 | Glaxosmithkline Istrazivacki Centar Zagreb | Compounds, compositions as carriers for steroid/nonsteroid anti-inflammatory; antienoplastic and antiviral active molecules |
| ITMI20021726A1 (it) * | 2002-08-01 | 2004-02-02 | Zambon Spa | Macrolidi ad attivita' antiinfiammatoria. |
| AR043050A1 (es) | 2002-09-26 | 2005-07-13 | Rib X Pharmaceuticals Inc | Compuestos heterociclicos bifuncionales y metodos para preparar y usar los mismos |
| HRP20020886A2 (en) | 2002-11-11 | 2005-06-30 | PLIVA-ISTRAŽIVAČKI INSTITUT d.o.o. | SUBSTITUTED 9a-N-[N'-(BENZENSULFONYL)CARBAMOYL-γ-AMINOPROPYL) AND 9a-N(N' -(?-CYANOETHIL)-N' -(b |
| US20060116400A1 (en) | 2002-11-28 | 2006-06-01 | Astrazeneca Ab | Oxazolidinone and/or isoxazoline derivatives as antibacterial agents |
| GB0229526D0 (en) | 2002-12-19 | 2003-01-22 | Astrazeneca Ab | Chemical compounds |
| GB0229518D0 (en) | 2002-12-19 | 2003-01-22 | Astrazeneca Ab | Chemical compounds |
| GB0229521D0 (en) | 2002-12-19 | 2003-01-22 | Astrazeneca Ab | Chemical compounds |
| CN1780846A (zh) | 2003-03-05 | 2006-05-31 | Rib-X医药品有限公司 | 双官能杂环化合物及其制备和使用方法 |
| ES2552682T3 (es) | 2003-03-10 | 2015-12-01 | Merck Sharp & Dohme Corp. | Agentes antibacterianos novedosos |
| HRP20030324A2 (en) | 2003-04-24 | 2005-02-28 | Pliva-Istra�iva�ki institut d.o.o. | Compounds of antiinflammatory effect |
| NZ543757A (en) | 2003-04-30 | 2009-02-28 | Morphochem Ag Komb Chemie | Use of oxazolidinone-quinoline hybrid antibiotics for the treatment of anthrax and other infections |
| WO2004108745A2 (en) | 2003-06-05 | 2004-12-16 | Enanta Pharmaceuticals, Inc. | 11-12 bicyclic erythromycin derivatives |
| US20040254126A1 (en) | 2003-06-05 | 2004-12-16 | Yao-Ling Qiu | 11-12 Bicyclic erythromycin derivatives |
| US20070270484A1 (en) | 2003-09-25 | 2007-11-22 | Biswajit Das | 3'-N-Substituted-3-O-Substituted Erythronolide a Derivatives |
| WO2005042554A1 (en) * | 2003-10-30 | 2005-05-12 | Rib-X Pharmaceuticals, Inc. | Bifunctional macrolide heterocyclic compounds and methods of making and using the same |
| JP2007512256A (ja) | 2003-11-18 | 2007-05-17 | リブ−エックス ファーマシューティカルズ,インコーポレイテッド | 二官能性マクロライド複素環化合物ならびにこれらを製造する方法およびこれらを使用する方法 |
| ITMI20040124A1 (it) | 2004-01-29 | 2004-04-29 | Zambon Spa | Macrolidi ad attivita' antiinfiammatoria |
| JP5383037B2 (ja) | 2004-02-27 | 2014-01-08 | リブ−エックス ファーマシューティカルズ,インコーポレイテッド | 大環状化合物およびそれらを製造し使用する方法 |
| WO2005118610A2 (en) | 2004-06-01 | 2005-12-15 | Rib-X Pharmaceuticals, Inc. | Macrocyclic compounds and methods of making and using the same |
| JP2009506063A (ja) | 2005-08-24 | 2009-02-12 | リブ−エックス ファーマシューティカルズ,インコーポレイテッド | トリアゾール化合物ならびにこれを作製する方法および使用する方法 |
| EP3290427A1 (en) | 2005-08-24 | 2018-03-07 | Melinta Therapeutics, Inc. | Triazole compounds and methods of making and using the same |
-
2005
- 2005-02-25 JP JP2007501005A patent/JP5383037B2/ja not_active Expired - Fee Related
- 2005-02-25 EP EP13178998.4A patent/EP2716647A3/en not_active Withdrawn
- 2005-02-25 WO PCT/US2005/006082 patent/WO2005085266A2/en not_active Ceased
- 2005-02-25 EP EP05723790.1A patent/EP1723159B1/en not_active Expired - Lifetime
- 2005-02-25 US US10/590,782 patent/US8202843B2/en not_active Expired - Fee Related
- 2005-02-25 CN CN2012102533942A patent/CN102816194A/zh active Pending
-
2012
- 2012-02-20 JP JP2012034350A patent/JP5631909B2/ja not_active Expired - Fee Related
- 2012-06-18 US US13/525,900 patent/US8841263B2/en not_active Expired - Lifetime
-
2014
- 2014-07-09 US US14/327,452 patent/US20150158901A1/en not_active Abandoned
- 2014-08-07 JP JP2014161364A patent/JP2014208707A/ja active Pending
-
2016
- 2016-07-11 JP JP2016136733A patent/JP2017019786A/ja active Pending
-
2017
- 2017-04-21 US US15/493,344 patent/US20180066007A1/en not_active Abandoned
-
2018
- 2018-01-24 JP JP2018009418A patent/JP2018104437A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| US20150158901A1 (en) | 2015-06-11 |
| WO2005085266A8 (en) | 2005-12-01 |
| US20180066007A1 (en) | 2018-03-08 |
| JP2012102147A (ja) | 2012-05-31 |
| JP2007525520A (ja) | 2007-09-06 |
| US20080045585A1 (en) | 2008-02-21 |
| JP5383037B2 (ja) | 2014-01-08 |
| JP2017019786A (ja) | 2017-01-26 |
| WO2005085266A2 (en) | 2005-09-15 |
| EP2716647A3 (en) | 2014-08-20 |
| EP2716647A2 (en) | 2014-04-09 |
| US8841263B2 (en) | 2014-09-23 |
| EP1723159A2 (en) | 2006-11-22 |
| WO2005085266A3 (en) | 2006-01-05 |
| JP5631909B2 (ja) | 2014-11-26 |
| EP1723159B1 (en) | 2019-06-12 |
| JP2018104437A (ja) | 2018-07-05 |
| JP2014208707A (ja) | 2014-11-06 |
| US20120252747A1 (en) | 2012-10-04 |
| US8202843B2 (en) | 2012-06-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5631909B2 (ja) | 大環状化合物およびそれらを製造し使用する方法 | |
| JP5981401B2 (ja) | トリアゾール化合物ならびにこれを作製する方法および使用する方法 | |
| WO2008106226A2 (en) | Macrolide compounds and methods of making and using the same | |
| ES2216581T3 (es) | Azalidas de 13 miembros y su uso como agentes antibioticos. | |
| US9085600B2 (en) | Triazole compounds and methods of making and using the same | |
| CN108101948A (zh) | 大环化合物以及其制作和使用方法 | |
| JP2006523229A (ja) | 二官能性複素環式化合物ならびにその製造および使用方法 | |
| JP2007509980A (ja) | 二官能性マクロライド複素環式化合物およびそれらの化合物を調製および使用する方法 | |
| WO2018191682A1 (en) | Triazole compounds and methods of making and using the same | |
| HK1178906A (en) | Macrocyclic compounds and methods of making and using the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 1178906 Country of ref document: HK |
|
| C53 | Correction of patent for invention or patent application | ||
| CB02 | Change of applicant information |
Address after: American Connecticut Applicant after: MELINTA THERAPEUTICS INC. Address before: American Connecticut Applicant before: Rib X. Pharmaceuticals Inc. |
|
| COR | Change of bibliographic data |
Free format text: CORRECT: APPLICANT; FROM: RIB X. PHARMACEUTICALS INC. TO: MELINTA THERAPEUTICS INC. |
|
| RJ01 | Rejection of invention patent application after publication | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20121212 |
|
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: WD Ref document number: 1178906 Country of ref document: HK |