AR028815A1 - Epotilonas c-21 modificadas - Google Patents
Epotilonas c-21 modificadasInfo
- Publication number
- AR028815A1 AR028815A1 ARP000100744A ARP000100744A AR028815A1 AR 028815 A1 AR028815 A1 AR 028815A1 AR P000100744 A ARP000100744 A AR P000100744A AR P000100744 A ARP000100744 A AR P000100744A AR 028815 A1 AR028815 A1 AR 028815A1
- Authority
- AR
- Argentina
- Prior art keywords
- epothilones
- modified
- compounds
- fungicidal
- epotilones
- Prior art date
Links
- 229930013356 epothilone Natural products 0.000 abstract 3
- 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 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000000855 fungicidal effect Effects 0.000 abstract 2
- 102000029749 Microtubule Human genes 0.000 abstract 1
- 108091022875 Microtubule Proteins 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 abstract 1
- 210000004027 cell Anatomy 0.000 abstract 1
- 230000001472 cytotoxic effect Effects 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 150000002596 lactones Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 210000004688 microtubule Anatomy 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 230000035755 proliferation Effects 0.000 abstract 1
- 230000006641 stabilisation Effects 0.000 abstract 1
- 238000011105 stabilization Methods 0.000 abstract 1
Classifications
-
- 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
-
- 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
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
Se refiere a epotilonas en las cuales el sustituyente tiazol se ha modificado, con métodos para su preparacion y con composiciones fungicidas o farmacéuticas que contienen estas epotilonas. Los compuestos de la invencion tienen la formula 1 en la cual G, P, Q y R tienen los significados dados en la descripcion de la solicitud. Los compuestos 1 son lactonas macrocíclicas denominadas epotilonas y presentan valiosas propiedades fungicidas y citotoxicas. Su accion se basa en la estabilizacion de los microtubulos que ocasiona la inhibicion de los tumores y la proliferacion de células que se dividen rápidamente.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1999107588 DE19907588A1 (de) | 1999-02-22 | 1999-02-22 | C-21 Modifizierte Epothilone |
| DE1999130111 DE19930111A1 (de) | 1999-07-01 | 1999-07-01 | C-21 Modifizierte Epothilone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR028815A1 true AR028815A1 (es) | 2003-05-28 |
Family
ID=26051995
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP000100744A AR028815A1 (es) | 1999-02-22 | 2000-02-22 | Epotilonas c-21 modificadas |
Country Status (37)
| Country | Link |
|---|---|
| US (1) | US6262094B1 (es) |
| EP (1) | EP1157023B1 (es) |
| JP (1) | JP4598957B2 (es) |
| KR (1) | KR100685336B1 (es) |
| CN (1) | CN1205208C (es) |
| AR (1) | AR028815A1 (es) |
| AT (1) | ATE254615T1 (es) |
| AU (1) | AU771089B2 (es) |
| BG (1) | BG64987B1 (es) |
| BR (1) | BR0008379A (es) |
| CA (1) | CA2360452C (es) |
| CO (1) | CO5140093A1 (es) |
| CZ (1) | CZ301498B6 (es) |
| DE (1) | DE60006649T2 (es) |
| DK (1) | DK1157023T3 (es) |
| EE (1) | EE04852B1 (es) |
| ES (1) | ES2209831T3 (es) |
| GE (1) | GEP20033067B (es) |
| HK (1) | HK1038923B (es) |
| HU (1) | HUP0200076A3 (es) |
| ID (1) | ID29829A (es) |
| IL (1) | IL144501A0 (es) |
| LT (1) | LT4944B (es) |
| LV (1) | LV12755B (es) |
| MX (1) | MXPA01008374A (es) |
| MY (1) | MY120601A (es) |
| NO (1) | NO320806B1 (es) |
| NZ (1) | NZ513629A (es) |
| PE (1) | PE20001546A1 (es) |
| PL (1) | PL212545B1 (es) |
| PT (1) | PT1157023E (es) |
| RU (1) | RU2253652C2 (es) |
| SK (1) | SK287200B6 (es) |
| TR (1) | TR200102401T2 (es) |
| TW (1) | TWI270546B (es) |
| UY (1) | UY26024A1 (es) |
| WO (1) | WO2000050423A1 (es) |
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| US6242469B1 (en) * | 1996-12-03 | 2001-06-05 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
| US6194181B1 (en) * | 1998-02-19 | 2001-02-27 | Novartis Ag | Fermentative preparation process for and crystal forms of cytostatics |
| GB9810659D0 (en) * | 1998-05-18 | 1998-07-15 | Ciba Geigy Ag | Organic compounds |
| US6780620B1 (en) * | 1998-12-23 | 2004-08-24 | Bristol-Myers Squibb Company | Microbial transformation method for the preparation of an epothilone |
| US6589968B2 (en) * | 2001-02-13 | 2003-07-08 | Kosan Biosciences, Inc. | Epothilone compounds and methods for making and using the same |
| PL362225A1 (en) * | 2000-09-22 | 2004-10-18 | GESELLSCHAFT FüR BIOTECHNOLOGISCHE FORSCHUNG MBH (GBF) | Triazolo-epothilones |
| WO2002030356A2 (en) * | 2000-10-13 | 2002-04-18 | The University Of Mississipi | Synthesis of epothilones and relates analogs |
| CN1489466A (zh) * | 2001-01-25 | 2004-04-14 | ����˹�ж�-����˹˹������˾ | 包含埃博霉素类似物的非肠道制剂 |
| US6893859B2 (en) | 2001-02-13 | 2005-05-17 | Kosan Biosciences, Inc. | Epothilone derivatives and methods for making and using the same |
| CN1610549A (zh) * | 2001-02-20 | 2005-04-27 | 布里斯托尔-迈尔斯斯奎布公司 | 用于治疗难治肿瘤的埃坡霉素衍生物 |
| MXPA03007394A (es) | 2001-02-20 | 2003-12-04 | Bristol Myers Squibb Co | Tratamiento de tumores refractarios mediante uso de derivados de epotilona. |
| CA2440555A1 (en) * | 2001-03-14 | 2002-09-19 | Bristol-Myers Squibb Company | Combination of epothilone analogs and chemotherapeutic agents for the treatment of proliferative diseases |
| MXPA04006822A (es) * | 2002-01-14 | 2004-12-08 | Novartis Ag | Combinaciones que comprenden epotilonas y anti-metabolitos. |
| TW200303202A (en) * | 2002-02-15 | 2003-09-01 | Bristol Myers Squibb Co | Method of preparation of 21-amino epothilone derivatives |
| AU2003212457A1 (en) * | 2002-03-01 | 2003-09-16 | University Of Notre Dame | Derivatives of epothilone b and d and synthesis thereof |
| SI1485090T1 (sl) * | 2002-03-08 | 2008-06-30 | Novartis Ag | Kombinacija vključujoča derivat epotilona in imidazotetrazinon |
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| EP2186811A1 (en) | 2002-08-23 | 2010-05-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto, analogues and uses thereof |
| 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 |
| BRPI0314133A8 (pt) | 2002-09-23 | 2017-09-19 | Bristol Myers Squibb Co | Processo para isolamento de epotilona b, métodos para cultivo de microorganismo que produza epotilona a ou b e para purifiação de apotilona |
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| EP2227296B1 (en) | 2008-01-08 | 2015-11-25 | Bristol-Myers Squibb Company | Combination of anti-ctla4 antibody with tubulin modulating agents for the treatment of proliferative diseases |
| HRP20140783T1 (hr) * | 2008-04-24 | 2014-09-12 | Bristol-Myers Squibb Company | Uporaba epotilona d u lijeäśenju tau-povezanih bolesti ukljuäśujuä†i alzheimerovu bolest |
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| HRP20171537T1 (hr) | 2009-11-05 | 2017-12-15 | Rhizen Pharmaceuticals S.A. | Novi modulatori benzopiran kinaze |
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| WO2011146638A1 (en) | 2010-05-18 | 2011-11-24 | Cerulean Pharma Inc. | Compositions and methods for treatment of autoimmune and other diseases |
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| WO2014075391A1 (zh) | 2012-11-17 | 2014-05-22 | 北京市丰硕维康技术开发有限责任公司 | 离去基团是含氨基或烷氨基的丙二酸衍生物的铂类化合物 |
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| EP3066127A1 (en) | 2013-11-06 | 2016-09-14 | Bristol-Myers Squibb Company | Immunotherapeutic dosing regimens and combinations thereof |
| BR112017011538A2 (pt) | 2014-12-04 | 2018-03-13 | Bristol-Myers Squibb Company | combinação de anticorpos anti-cs1 e anti-pd1 para tratar câncer (mieloma) |
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| CN105153177B (zh) * | 2015-09-28 | 2017-08-08 | 湖南大学 | 呋喃并色满肟烯/炔丙基醚及其制备方法与应用 |
| WO2017197045A1 (en) | 2016-05-11 | 2017-11-16 | Movassaghi Mohammad | Convergent and enantioselective total synthesis of communesin analogs |
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| US10640508B2 (en) | 2017-10-13 | 2020-05-05 | Massachusetts Institute Of Technology | Diazene directed modular synthesis of compounds with quaternary carbon centers |
| US11535634B2 (en) | 2019-06-05 | 2022-12-27 | Massachusetts Institute Of Technology | Compounds, conjugates, and compositions of epipolythiodiketopiperazines and polythiodiketopiperazines and uses thereof |
| WO2022182415A1 (en) | 2021-02-24 | 2022-09-01 | Massachusetts Institute Of Technology | Himastatin derivatives, and processes of preparation thereof, and uses thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE301115C (es) | ||||
| DE75883C (de) | W. schulte in Siegen und F. A. SAPP in Hillnhütten, Kreis Siegen | Ofen zur Erzeugung von Cyanammonium | ||
| GB8909737D0 (en) * | 1989-04-27 | 1989-06-14 | Shell Int Research | Thiazole derivatives |
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| DE19713970B4 (de) | 1997-04-04 | 2006-08-31 | R&D-Biopharmaceuticals Gmbh | Epothilone-Synthesebausteine II - Prenylderivate |
| DE59805900D1 (de) | 1997-04-18 | 2002-11-14 | 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 |
| DK1001951T3 (da) | 1997-07-16 | 2002-12-23 | Schering Ag | Thiazolderivater, fremgangsmåde til fremstilling deraf og anvendelse af disse |
| AU9340998A (en) | 1997-08-09 | 1999-03-01 | Schering Aktiengesellschaft | New epothilone derivatives, method for producing same and their pharmaceutical use |
| US6498257B1 (en) * | 1998-04-21 | 2002-12-24 | Bristol-Myers Squibb Company | 2,3-olefinic epothilone derivatives |
| EP1140928A4 (en) * | 1998-12-23 | 2002-10-02 | Bristol Myers Squibb Co | MICROBIAL CONVERSION METHOD FOR PRODUCING AN EPOTHILONE |
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2000
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