MXPA02009165A - Proceso para la preparacion de analogos de epotilona. - Google Patents
Proceso para la preparacion de analogos de epotilona.Info
- Publication number
- MXPA02009165A MXPA02009165A MXPA02009165A MXPA02009165A MXPA02009165A MX PA02009165 A MXPA02009165 A MX PA02009165A MX PA02009165 A MXPA02009165 A MX PA02009165A MX PA02009165 A MXPA02009165 A MX PA02009165A MX PA02009165 A MXPA02009165 A MX PA02009165A
- Authority
- MX
- Mexico
- Prior art keywords
- epothilone analogs
- preparation
- intermediates
- analogs
- epothilones
- Prior art date
Links
- 229930013356 epothilone Natural products 0.000 title abstract 4
- 238000000034 method Methods 0.000 title abstract 4
- 150000003883 epothilone derivatives Chemical class 0.000 title abstract 3
- 238000002360 preparation method Methods 0.000 title abstract 2
- 239000000543 intermediate Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- HESCAJZNRMSMJG-KKQRBIROSA-N epothilone A Chemical class C/C([C@@H]1C[C@@H]2O[C@@H]2CCC[C@@H]([C@@H]([C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1)O)C)=C\C1=CSC(C)=N1 HESCAJZNRMSMJG-KKQRBIROSA-N 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/38—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
-
- 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
- A61P27/02—Ophthalmic 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- 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
- C07D417/02—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 two hetero rings
- C07D417/06—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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Neurology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52852600A | 2000-03-20 | 2000-03-20 | |
| PCT/US2001/007749 WO2001070716A1 (en) | 2000-03-20 | 2001-03-12 | A process for the preparation of epothilone analogs and intermediates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA02009165A true MXPA02009165A (es) | 2004-08-12 |
Family
ID=24106039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA02009165A MXPA02009165A (es) | 2000-03-20 | 2001-03-12 | Proceso para la preparacion de analogos de epotilona. |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US6518421B1 (enExample) |
| EP (2) | EP1265878B1 (enExample) |
| JP (1) | JP4966468B2 (enExample) |
| KR (1) | KR100758069B1 (enExample) |
| AT (1) | ATE516280T1 (enExample) |
| AU (2) | AU2001245608B2 (enExample) |
| CA (1) | CA2404212C (enExample) |
| ES (1) | ES2367703T3 (enExample) |
| HU (1) | HU229348B1 (enExample) |
| IL (2) | IL151474A0 (enExample) |
| MX (1) | MXPA02009165A (enExample) |
| PE (1) | PE20011104A1 (enExample) |
| TW (1) | TWI310383B (enExample) |
| UY (1) | UY26624A1 (enExample) |
| WO (1) | WO2001070716A1 (enExample) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6867305B2 (en) * | 1996-12-03 | 2005-03-15 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US6242469B1 (en) | 1996-12-03 | 2001-06-05 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
| US6204388B1 (en) * | 1996-12-03 | 2001-03-20 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US20050043376A1 (en) * | 1996-12-03 | 2005-02-24 | Danishefsky Samuel J. | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
| US6605599B1 (en) | 1997-07-08 | 2003-08-12 | Bristol-Myers Squibb Company | Epothilone derivatives |
| US6780620B1 (en) * | 1998-12-23 | 2004-08-24 | Bristol-Myers Squibb Company | Microbial transformation method for the preparation of an epothilone |
| US20020058286A1 (en) * | 1999-02-24 | 2002-05-16 | Danishefsky Samuel J. | Synthesis of epothilones, intermediates thereto and analogues thereof |
| UA75365C2 (en) | 2000-08-16 | 2006-04-17 | Bristol Myers Squibb Co | Epothilone analog polymorph modifications, a method for obtaining thereof (variants), a pharmaceutical composition based thereon |
| EP1414384A4 (en) | 2000-10-13 | 2005-07-27 | Univ Mississippi | SYNTHESIS OF EPOTHILONES AND TRANSFORMATION ANALOGUE |
| JP2004521122A (ja) * | 2001-01-25 | 2004-07-15 | ブリストル−マイヤーズ スクイブ カンパニー | エポチロン類似体の非経口製剤 |
| IL156988A0 (en) | 2001-02-20 | 2004-02-08 | Bristol Myers Squibb Co | Pharmaceutical compositions containing epothilone derivatives |
| IL157312A0 (en) | 2001-02-27 | 2004-02-19 | Biotechnolog Forschung Gmbh | Processes for the preparation of epothilone derivatives and compounds produced thereby |
| TW200403994A (en) * | 2002-04-04 | 2004-03-16 | Bristol Myers Squibb Co | Oral administration of EPOTHILONES |
| TW200400191A (en) * | 2002-05-15 | 2004-01-01 | Bristol Myers Squibb Co | Pharmaceutical compositions and methods of using C-21 modified epothilone derivatives |
| KR101173510B1 (ko) * | 2002-08-23 | 2012-08-21 | 슬로안-케테링인스티튜트퍼캔서리서치 | 에포틸론, 이의 중간물질과 유사체의 합성 및 이들의 용도 |
| US6921769B2 (en) | 2002-08-23 | 2005-07-26 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US7649006B2 (en) * | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| DE10331004A1 (de) * | 2003-07-03 | 2005-02-24 | Schering Ag | Verfahren für die Herstellung von C1-C15-Fragmenten von Epothilonen und deren Derivaten |
| US20050171167A1 (en) * | 2003-11-04 | 2005-08-04 | Haby Thomas A. | Process and formulation containing epothilones and analogs thereof |
| EP1559447A1 (en) * | 2004-01-30 | 2005-08-03 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Use of epothilones in the treatment of neuronal connectivity defects such as schizophrenia and autism |
| US20090004277A1 (en) * | 2004-05-18 | 2009-01-01 | Franchini Miriam K | Nanoparticle dispersion containing lactam compound |
| EP1958625A1 (en) | 2004-11-18 | 2008-08-20 | Brystol-Myers Squibb Company | Enteric coate bead comprising ixabepilone and preparation thereof |
| WO2006055742A1 (en) * | 2004-11-18 | 2006-05-26 | Bristol-Myers Squibb Company | Enteric coated bead comprising epothilone or epothilone analog, and preparation and administration thereof |
| EP1674098A1 (en) | 2004-12-23 | 2006-06-28 | Schering Aktiengesellschaft | Stable and tolerable parental formulations of highly reactive organic drug substances with low or no solubility in water |
| CA2597647A1 (en) | 2005-02-11 | 2007-08-02 | University Of Southern California | Method of expressing proteins with disulfide bridges |
| EP2029156A4 (en) * | 2006-05-01 | 2010-07-21 | Univ Southern California | COMBINATION THERAPY FOR CANCER TREATMENT |
| US8463852B2 (en) * | 2006-10-06 | 2013-06-11 | Oracle International Corporation | Groupware portlets for integrating a portal with groupware systems |
| EP2065054A1 (en) | 2007-11-29 | 2009-06-03 | Bayer Schering Pharma Aktiengesellschaft | Combinations comprising a prostaglandin and uses thereof |
| EP2070521A1 (en) | 2007-12-10 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Surface-modified nanoparticles |
| DE102007059752A1 (de) | 2007-12-10 | 2009-06-18 | Bayer Schering Pharma Aktiengesellschaft | Funktionalisierte, feste Polymernanopartikel enthaltend Epothilone |
| US8802394B2 (en) | 2008-11-13 | 2014-08-12 | Radu O. Minea | Method of expressing proteins with disulfide bridges with enhanced yields and activity |
| EP2210584A1 (en) | 2009-01-27 | 2010-07-28 | Bayer Schering Pharma Aktiengesellschaft | Stable polymeric composition comprising an epothilone and an amphiphilic block copolymer |
| JP2013527239A (ja) | 2010-06-01 | 2013-06-27 | プラス・ケミカルス・エスアー | イクサベピロンの固体形 |
| WO2013008091A1 (en) * | 2011-07-13 | 2013-01-17 | Xellia Pharmaceuticals Aps | Manufacturing of epothilone derivatives and the use thereof |
| CA2858806A1 (en) | 2011-12-23 | 2013-06-27 | Innate Pharma | Enzymatic conjugation of polypeptides |
| WO2013164102A1 (en) | 2012-04-30 | 2013-11-07 | Xellia Pharmaceuticals Aps | Process for preparation of ixabepilone and intermediates useful in said process. |
| US10132799B2 (en) | 2012-07-13 | 2018-11-20 | Innate Pharma | Screening of conjugated antibodies |
| EP2916872B1 (en) | 2012-11-09 | 2019-02-27 | Innate Pharma | Recognition tags for tgase-mediated conjugation |
| US9309259B2 (en) | 2013-03-08 | 2016-04-12 | Scinopharm Taiwan, Ltd. | Process for ixabepilone, and intermediates thereof |
| WO2014140300A1 (en) | 2013-03-15 | 2014-09-18 | Innate Pharma | Solid phase tgase-mediated conjugation of antibodies |
| EP3010547B1 (en) | 2013-06-20 | 2021-04-21 | Innate Pharma | Enzymatic conjugation of polypeptides |
| CN105517577A (zh) | 2013-06-21 | 2016-04-20 | 先天制药公司 | 多肽的酶促偶联 |
| WO2019092148A1 (en) | 2017-11-10 | 2019-05-16 | Innate Pharma | Antibodies with functionalized glutamine residues |
| JP2023509871A (ja) * | 2020-04-08 | 2023-03-10 | 北京華昊中天生物医薬股▲ふん▼有限公司 | ウチデロン半水和物単結晶、並びにその調製方法及び応用 |
| CN112409366A (zh) * | 2020-11-30 | 2021-02-26 | 湖北宏中药业股份有限公司 | 一种伊沙匹隆二聚体的高收率制备方法 |
| CN112375085A (zh) * | 2020-11-30 | 2021-02-19 | 湖北宏中药业股份有限公司 | 一种伊沙匹隆反应液的高收率高纯度处理方法 |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4138042C2 (de) | 1991-11-19 | 1993-10-14 | Biotechnolog Forschung Gmbh | Epothilone, deren Herstellungsverfahren sowie diese Verbindungen enthaltende Mittel |
| US6288237B1 (en) | 1995-11-17 | 2001-09-11 | Gesellschaft Fur Biotechnologische Forschung Mbh (Gbf) | Epothilons C and D, preparation and compositions |
| DE19542986A1 (de) | 1995-11-17 | 1997-05-22 | Biotechnolog Forschung Gmbh | Epothilon-Derivate und deren Verwendung |
| DE19639456A1 (de) | 1996-09-25 | 1998-03-26 | Biotechnolog Forschung Gmbh | Epothilon-Derivate, Herstellung und Mittel |
| DE19636343C1 (de) | 1996-08-30 | 1997-10-23 | Schering Ag | Zwischenprodukte innerhalb der Totalsynthese von Epothilon A und B |
| DE19645361A1 (de) | 1996-08-30 | 1998-04-30 | Ciba Geigy Ag | Zwischenprodukte innerhalb der Totalsynthese von Epothilon A und B, Teil II |
| EP0923583A1 (de) | 1996-08-30 | 1999-06-23 | Novartis AG | Verfahren zur herstellung von epothilonen und zwischenprodukte innerhalb des verfahrens |
| DE19645362A1 (de) | 1996-10-28 | 1998-04-30 | Ciba Geigy Ag | Verfahren zur Herstellung von Epothilon A und B und Derivaten |
| DE19647380A1 (de) | 1996-11-15 | 1998-05-20 | Hoechst Ag | 5-Ring-Heterocyclen als Inhibitoren der Leukozytenadhäsion und VLA-4-Antagonisten |
| KR100538095B1 (ko) | 1996-11-18 | 2005-12-21 | 게젤샤프트 퓌어 비오테크놀로기쉐 포르슝 엠베하(게베에프) | 에포틸론 씨, 디, 이 및 에프, 그 제조방법 및 세포증식 억제제와 식물 위생제로서의 이들의 용도 |
| US6515016B2 (en) | 1996-12-02 | 2003-02-04 | Angiotech Pharmaceuticals, Inc. | Composition and methods of paclitaxel for treating psoriasis |
| US6204388B1 (en) | 1996-12-03 | 2001-03-20 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US6242469B1 (en) | 1996-12-03 | 2001-06-05 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
| US6380394B1 (en) | 1996-12-13 | 2002-04-30 | The Scripps Research Institute | Epothilone analogs |
| US6441186B1 (en) | 1996-12-13 | 2002-08-27 | The Scripps Research Institute | Epothilone analogs |
| DE19701758A1 (de) | 1997-01-20 | 1998-07-23 | Wessjohann Ludgar A Dr | Epothilone-Synthesebausteine |
| DE19707053B4 (de) | 1997-02-21 | 2008-03-27 | Sipra Patententwicklungs- Und Beteiligungsgesellschaft Mbh | Hoch/Tief-Plüschstrickware sowie Verfahren und Vorrichtung zu ihrer Herstellung |
| CZ298027B6 (cs) | 1997-02-25 | 2007-05-30 | Gesellschaft Fuer Biotechnologische Forschung Mbh(Gbf) | Zpusob prípravy epothilon-N-oxidu a N-oxidy epothilonu |
| DE19713970B4 (de) | 1997-04-04 | 2006-08-31 | R&D-Biopharmaceuticals Gmbh | Epothilone-Synthesebausteine II - Prenylderivate |
| ATE225783T1 (de) | 1997-04-18 | 2002-10-15 | Studiengesellschaft Kohle Mbh | Selektive olefinmetathese von bi- oder polyfunktionellen substraten in komprimiertem kohlendioxid als reaktionsmedium |
| DE19821954A1 (de) | 1997-05-15 | 1998-11-19 | Biotechnolog Forschung Gmbh | Verfahren zur Herstellung eines Epothilon-Derivats |
| DE19720312A1 (de) | 1997-05-15 | 1998-11-19 | Hoechst Ag | Zubereitung mit erhöhter in vivo Verträglichkeit |
| DE19726627A1 (de) | 1997-06-17 | 1998-12-24 | Schering Ag | Zwischenprodukte, Verfahren zu ihrer Herstellung und ihre Verwendung zur Herstellung von Epothilon |
| US6605599B1 (en) | 1997-07-08 | 2003-08-12 | Bristol-Myers Squibb Company | Epothilone derivatives |
| PT1001951E (pt) | 1997-07-16 | 2003-02-28 | Schering Ag | Derivados de tiazolo, processo para a sua preparacao e utilizacao |
| JP2001512723A (ja) | 1997-08-09 | 2001-08-28 | シエーリング アクチエンゲゼルシヤフト | 新規エポチロン誘導体、その製法およびその薬学的使用 |
| US6320045B1 (en) | 1997-12-04 | 2001-11-20 | Bristol-Myers Squibb Company | Process for the reduction of oxiranyl epothilones to olefinic epothilones |
| US6365749B1 (en) * | 1997-12-04 | 2002-04-02 | Bristol-Myers Squibb Company | Process for the preparation of ring-opened epothilone intermediates which are useful for the preparation of epothilone analogs |
| TR200002299T2 (tr) | 1998-02-05 | 2000-11-21 | Novartis Ag | Epotilon kompozisyonları. |
| US6194181B1 (en) | 1998-02-19 | 2001-02-27 | Novartis Ag | Fermentative preparation process for and crystal forms of cytostatics |
| FR2775187B1 (fr) | 1998-02-25 | 2003-02-21 | Novartis Ag | Utilisation de l'epothilone b pour la fabrication d'une preparation pharmaceutique antiproliferative et d'une composition comprenant l'epothilone b comme agent antiproliferatif in vivo |
| AU758526B2 (en) | 1998-02-25 | 2003-03-20 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues therof |
| DE19820599A1 (de) | 1998-05-08 | 1999-11-11 | Biotechnolog Forschung Gmbh | Epothilonderivate, Verfahren zu deren Herstellung und deren Verwendung |
| AU5036999A (en) | 1998-06-30 | 2000-01-17 | Schering Aktiengesellschaft | Epothilon derivatives, their preparation process, intermediate products and their pharmaceutical use |
| WO2000031247A2 (en) | 1998-11-20 | 2000-06-02 | Kosan Biosciences, Inc. | Recombinant methods and materials for producing epothilone and epothilone derivatives |
| DE69910831T2 (de) | 1998-12-22 | 2004-07-15 | Novartis Ag | Epothilonderivate und ihre verwendung als antitumormittel |
| NZ513268A (en) | 1999-02-18 | 2004-05-28 | Schering Ag | 16-halogen-epothilone derivatives, method for producing them and their pharmaceutical use |
| US6211412B1 (en) | 1999-03-29 | 2001-04-03 | The University Of Kansas | Synthesis of epothilones |
| PE20010116A1 (es) | 1999-04-30 | 2001-02-15 | Schering Ag | Derivados de 6-alquenil-, 6-alquinil- y 6-epoxi-epotilona, procedimientos para su preparacion |
| US6593115B2 (en) | 2000-03-24 | 2003-07-15 | Bristol-Myers Squibb Co. | Preparation of epothilone intermediates |
| UA75365C2 (en) * | 2000-08-16 | 2006-04-17 | Bristol Myers Squibb Co | Epothilone analog polymorph modifications, a method for obtaining thereof (variants), a pharmaceutical composition based thereon |
| TWI291464B (en) | 2002-09-23 | 2007-12-21 | Bristol Myers Squibb Co | Methods for the preparation, isolation and purification of epothilone B, and X-ray crystal structures of epothilone B |
-
2001
- 2001-02-01 US US09/775,361 patent/US6518421B1/en not_active Ceased
- 2001-03-12 AU AU2001245608A patent/AU2001245608B2/en not_active Ceased
- 2001-03-12 AU AU4560801A patent/AU4560801A/xx active Pending
- 2001-03-12 EP EP01918544A patent/EP1265878B1/en not_active Expired - Lifetime
- 2001-03-12 WO PCT/US2001/007749 patent/WO2001070716A1/en not_active Ceased
- 2001-03-12 MX MXPA02009165A patent/MXPA02009165A/es active IP Right Grant
- 2001-03-12 EP EP07020071A patent/EP1882690A3/en not_active Withdrawn
- 2001-03-12 IL IL15147401A patent/IL151474A0/xx unknown
- 2001-03-12 AT AT01918544T patent/ATE516280T1/de not_active IP Right Cessation
- 2001-03-12 JP JP2001568920A patent/JP4966468B2/ja not_active Expired - Fee Related
- 2001-03-12 ES ES01918544T patent/ES2367703T3/es not_active Expired - Lifetime
- 2001-03-12 HU HU0300693A patent/HU229348B1/hu not_active IP Right Cessation
- 2001-03-12 CA CA2404212A patent/CA2404212C/en not_active Expired - Fee Related
- 2001-03-12 KR KR1020027012290A patent/KR100758069B1/ko not_active Expired - Fee Related
- 2001-03-14 TW TW090105973A patent/TWI310383B/zh not_active IP Right Cessation
- 2001-03-19 UY UY26624A patent/UY26624A1/es not_active Application Discontinuation
- 2001-03-20 PE PE2001000256A patent/PE20011104A1/es not_active Application Discontinuation
-
2002
- 2002-08-26 IL IL151474A patent/IL151474A/en not_active IP Right Cessation
-
2005
- 2005-02-11 US US11/056,606 patent/USRE39356E1/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| KR100758069B1 (ko) | 2007-09-11 |
| HUP0300693A2 (hu) | 2003-08-28 |
| HU229348B1 (en) | 2013-11-28 |
| KR20020081463A (ko) | 2002-10-26 |
| HUP0300693A3 (en) | 2005-11-28 |
| HK1050680A1 (en) | 2003-07-04 |
| ATE516280T1 (de) | 2011-07-15 |
| EP1882690A3 (en) | 2008-04-23 |
| EP1882690A2 (en) | 2008-01-30 |
| AU2001245608B2 (en) | 2006-09-14 |
| WO2001070716A1 (en) | 2001-09-27 |
| IL151474A (en) | 2009-09-01 |
| US6518421B1 (en) | 2003-02-11 |
| USRE39356E1 (en) | 2006-10-17 |
| UY26624A1 (es) | 2001-10-25 |
| IL151474A0 (en) | 2003-04-10 |
| EP1265878B1 (en) | 2011-07-13 |
| PE20011104A1 (es) | 2001-12-02 |
| CA2404212A1 (en) | 2001-09-27 |
| CA2404212C (en) | 2012-05-01 |
| EP1265878A1 (en) | 2002-12-18 |
| JP4966468B2 (ja) | 2012-07-04 |
| TWI310383B (en) | 2009-06-01 |
| AU4560801A (en) | 2001-10-03 |
| JP2003528090A (ja) | 2003-09-24 |
| ES2367703T3 (es) | 2011-11-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MXPA02009165A (es) | Proceso para la preparacion de analogos de epotilona. | |
| WO2002060904A3 (en) | A process for the preparation of epothilone analogs | |
| CA2312098A1 (en) | A process for the preparation of ring-opened epothilone intermediates which are useful for the preparation of epothilone analogs | |
| Stephen et al. | Synthesis of brevetoxin sub-units by sequential ring-closing metathesis and hydroboration | |
| NZ534374A (en) | Method of synthesizing camptothecin-relating compounds | |
| Feng et al. | Stereoselective construction of a key hydroindole precursor of epidithiodiketopiperazine (ETP) natural products | |
| Denmark et al. | Tandem [4+ 2]/[3+ 2] cycloadditions: facile and stereoselective construction of polycyclic frameworks | |
| Alexandra | Synthetic application of biotransformations: absolute stereochemistry and Diels–Alder reactions of the (1 S, 2 R)-1, 2-dihydroxycyclohexa-3, 5-diene-1-carboxylic acid from Pseudomonas putida | |
| Montenegro et al. | Highly diastereoselective Pauson-Khand reactions of a stable, internally chelated, dicobalt pentacarbonyl complex of a chiral acetylene thioether | |
| Bach et al. | Synthesis of syn-and anti-1, 2-amino alcohols by regioselective ring opening reactions of cis-3-aminooxetanes | |
| WO2001027308A2 (en) | 13-alkyl epothilone derivatives | |
| EP0147317A2 (fr) | Nouveaux dérivés ortho-condensés du pyrrole, leur préparation et les médicaments qui les contiennent | |
| Lee et al. | Enantioselective synthesis of the C14–C25 portion of the cytotoxic natural product, amphidinolide B1 | |
| Page et al. | Asymmetric oxidation of dithiane derivatives: enantiomerically pure 1, 3-dithiane 1-oxide | |
| Lee et al. | Stereoselective synthesis of 2, 4, 6-trisubstituted tetrahydropyrans by the use of cyclopropanols as homoenols | |
| Rammeloo et al. | A new and short method for the synthesis of 2, 4-methanoproline | |
| Williams et al. | Total synthesis of myxovirescin A1 | |
| Schinzer et al. | Synthesis of epothilones: stereoselective routes to epothilone B | |
| Tanaka et al. | Formation of tetracyclic oxazolidinones from cycloadducts of benzylidene ketones with 4-phenyl-4, 5-dihydro-3 H-1, 2, 4-triazole-3, 5-dione (PTAD) by base-promoted backbone participation and rearrangement | |
| AU2001212914A1 (en) | Friedel-craft process for the preparation of thioxanthones | |
| Benningshof et al. | Studies towards the total synthesis of solanoeclepin A: synthesis of the 7-oxabicyclo [2.2. 1] heptane moiety and attempted seven-membered ring formation | |
| AU2767292A (en) | Cyclic peroxyacetal compounds | |
| Holland et al. | Biotransformation of organic sulfides. Part 11. Preparation of functionalised phenyl propyl sulfoxides using Helminthosporium species and Mortierella isabellina | |
| Guerra et al. | Synthesis of disubstituted 1, 2-dioxolanes, 1, 2-dioxanes, and 1, 2-dioxepanes | |
| Ishibashi et al. | A short synthesis of (±)-cuparene |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration |