WO2009156182A3 - Uracilderivate und deren verwendung - Google Patents
Uracilderivate und deren verwendung Download PDFInfo
- Publication number
- WO2009156182A3 WO2009156182A3 PCT/EP2009/004698 EP2009004698W WO2009156182A3 WO 2009156182 A3 WO2009156182 A3 WO 2009156182A3 EP 2009004698 W EP2009004698 W EP 2009004698W WO 2009156182 A3 WO2009156182 A3 WO 2009156182A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- uracil derivatives
- uracil
- derivatives
- cytostatic
- suppressing
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/20—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D239/22—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (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)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Die Erfindung betrifft Uracilderivate sowie deren Anwendung als therapeutischer Wirkstoff. Die Uracilderivate werden dabei insbesondere zusammen mit einem Zytostatikum zur Unterdrückung oder Reduzierung der Resistenzenbildung bei der Zytostatikabehandlung eingesetzt.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09769031A EP2303848A2 (de) | 2008-06-25 | 2009-06-25 | Uracilderivate und deren verwendung |
US13/000,900 US9181199B2 (en) | 2008-06-25 | 2009-06-25 | Uracil derivatives and use thereof |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102008030091A DE102008030091B4 (de) | 2008-06-25 | 2008-06-25 | Uracilderivate und deren Verwendung |
DE102008030091.8 | 2008-06-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009156182A2 WO2009156182A2 (de) | 2009-12-30 |
WO2009156182A3 true WO2009156182A3 (de) | 2010-03-11 |
Family
ID=41351434
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2009/004698 WO2009156182A2 (de) | 2008-06-25 | 2009-06-25 | Uracilderivate und deren verwendung |
Country Status (4)
Country | Link |
---|---|
US (1) | US9181199B2 (de) |
EP (1) | EP2303848A2 (de) |
DE (1) | DE102008030091B4 (de) |
WO (1) | WO2009156182A2 (de) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103242242A (zh) * | 2012-02-08 | 2013-08-14 | 河南师范大学 | 5-位缺电子烯基取代嘧啶碳环核苷及制备方法 |
CN103242400B (zh) * | 2012-02-08 | 2016-06-08 | 河南师范大学 | 具有抗hiv活性的5-取代嘧啶核苷-噻唑啉酮杂化体及其制备方法 |
UA112897C2 (uk) | 2012-05-09 | 2016-11-10 | Байєр Фарма Акцієнгезелльшафт | Біциклічно заміщені урацили та їх застосування для лікування і/або профілактики захворювань |
EP3066098A1 (de) | 2013-11-08 | 2016-09-14 | Bayer Pharma Aktiengesellschaft | Substituierte uracile und ihre verwendung |
US9695131B2 (en) | 2013-11-08 | 2017-07-04 | Bayer Pharma Aktiengesellschaft | Substituted uracils as chymase inhibitors |
US20170216297A1 (en) | 2014-07-28 | 2017-08-03 | Technische Universitaet Dresden | Efficient inhibition of hsp27 |
EP3133065A1 (de) | 2015-08-21 | 2017-02-22 | Merck Patent GmbH | Verbindungen für optisch aktive vorrichtungen |
EP3363793A1 (de) | 2017-02-15 | 2018-08-22 | Merck Patent GmbH | Hydrophobe verbindungen zur herstellung von optisch aktiven vorrichtungen |
EP3819006A1 (de) | 2019-11-05 | 2021-05-12 | Technische Universität Dresden | Verbindungen mit thymin-gerüst zur verwendung in der medizin |
US20230273455A1 (en) | 2020-07-15 | 2023-08-31 | Johnson & Johnson Surgical Vision, Inc. | Optically active devices |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996023506A1 (de) * | 1995-02-01 | 1996-08-08 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von 5' substituierten nukleosiden zur hemmung von resistenzbildung bei der zytostatikabehandlung und arzneimittel, enthaltend diese nukleoside |
US5859014A (en) * | 1995-06-09 | 1999-01-12 | Syntex (U.S.A.) Inc. | Pyrimidinedione, pyrimidinetrione, triazinedione and tetrahydroquinazolinedione derivatives as α1 -adrenergic receptor antagonists |
WO2002083651A2 (en) * | 2001-04-11 | 2002-10-24 | Queen's University At Kingston | Pyrimidine compounds as anti-ictogenic and/or anti-epileptogenic agents |
WO2006070292A2 (en) * | 2004-10-12 | 2006-07-06 | Queen's University At Kingston | Pyrimidine compounds as anti-ictogenic and/or anti-epileptogenic agents |
WO2008145562A1 (en) * | 2007-05-30 | 2008-12-04 | F. Hoffmann-La Roche Ag | Non-nucleoside reverse transcriptase inhibitors |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DD202873A1 (de) * | 1981-08-25 | 1983-10-05 | Akad Wissenschaften Ddr | Verfahren zur herstellung von 5-(2,2-disubstituierten) uracilderivaten |
DE3912100A1 (de) * | 1989-04-13 | 1990-10-25 | Bayer Ag | Substituierte uracile, verfahren zu ihrer herstellung und verwendung gegen parasitaere protozoen |
DK0748800T3 (da) | 1995-06-09 | 2001-08-27 | Hoffmann La Roche | Pyrimidindion-, pyrimidintrion- og triazindionderivater som alfa-1-adrenergiske receptorantagonister |
MXPA02000763A (es) * | 1999-07-22 | 2002-08-12 | Newbiotics Inc | Activacion terapeutica catalizada por enzima. |
JP4931314B2 (ja) * | 2000-01-25 | 2012-05-16 | ニューロクライン バイオサイエンシーズ,インコーポレイテッド | 性腺刺激ホルモン放出ホルモンレセプタアンタゴニストおよびそれに関連した方法 |
CA2570968A1 (en) * | 2004-06-17 | 2006-01-26 | Wyeth | Gonadotropin releasing hormone receptor antagonists |
-
2008
- 2008-06-25 DE DE102008030091A patent/DE102008030091B4/de not_active Expired - Fee Related
-
2009
- 2009-06-25 WO PCT/EP2009/004698 patent/WO2009156182A2/de active Application Filing
- 2009-06-25 US US13/000,900 patent/US9181199B2/en not_active Expired - Fee Related
- 2009-06-25 EP EP09769031A patent/EP2303848A2/de not_active Withdrawn
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996023506A1 (de) * | 1995-02-01 | 1996-08-08 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verwendung von 5' substituierten nukleosiden zur hemmung von resistenzbildung bei der zytostatikabehandlung und arzneimittel, enthaltend diese nukleoside |
US5859014A (en) * | 1995-06-09 | 1999-01-12 | Syntex (U.S.A.) Inc. | Pyrimidinedione, pyrimidinetrione, triazinedione and tetrahydroquinazolinedione derivatives as α1 -adrenergic receptor antagonists |
WO2002083651A2 (en) * | 2001-04-11 | 2002-10-24 | Queen's University At Kingston | Pyrimidine compounds as anti-ictogenic and/or anti-epileptogenic agents |
WO2006070292A2 (en) * | 2004-10-12 | 2006-07-06 | Queen's University At Kingston | Pyrimidine compounds as anti-ictogenic and/or anti-epileptogenic agents |
WO2008145562A1 (en) * | 2007-05-30 | 2008-12-04 | F. Hoffmann-La Roche Ag | Non-nucleoside reverse transcriptase inhibitors |
Non-Patent Citations (7)
Title |
---|
DATABASE CAPLUS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 14 February 1996 (1996-02-14), XP002560556, retrieved from STN Database accession no. 1996:94641 * |
DATABASE CAPLUS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; 30 April 1994 (1994-04-30), XP002560557, retrieved from STN Database accession no. 1994:218388 * |
G. T. CRISP ET AL.: "Palladium-catalyzed coupling of a propargylglycine derivative", TETRAHEDRON, vol. 48, no. 15, 1992, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM. NL, pages 3239 - 3250, XP002560558, ISSN: 0040-4020 * |
H. MATSUHASHI ET AL.: "Synthesis of 5-substituted pyrimidine nucleosides through a palladium-catalyzed cross-coupling of alkylhalosilanes", HETEROCYCLES, vol. 42, no. 1, 1996, ELSEVIER SCIENCE PUBLISHERS B.V. AMSTERDAM; NL, pages 375 - 384, ISSN: 0385-5414 * |
N. G. KUNDU ET AL.: "Studies in uracil derivatives and analogs. 19. Synthesis of 5-(acylethynyl)uracils and their corresponding 2'-deoxyribonucleosides through palladium-catalyzed reactions", JOURNAL OF THE CHEMICAL SOCIETY, PERKIN TRANSACTIONS 1: ORGANIC AND BIO-ORGANIC CHEMISTRY, vol. 21, 1993, Chemical Society, London; GB, pages 2657 - 2663, ISSN: 0300-922X * |
S. J. HANNON ET AL.: "A new synthesis of N-blocked dihydrouracil and dihydroorotic acid derivatives using lithium tri-sec-butyl borohydride as reducing agent", TETRAHEDRON LETTERS, vol. 21, 1980, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM. NL, pages 1105 - 1108, XP002560559, ISSN: 0040-4039 * |
See also references of EP2303848A2 * |
Also Published As
Publication number | Publication date |
---|---|
DE102008030091B4 (de) | 2011-03-03 |
EP2303848A2 (de) | 2011-04-06 |
US9181199B2 (en) | 2015-11-10 |
US20110166096A1 (en) | 2011-07-07 |
DE102008030091A1 (de) | 2009-12-31 |
WO2009156182A2 (de) | 2009-12-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2009156182A3 (de) | Uracilderivate und deren verwendung | |
IL260158B (en) | Pyrazine derivatives, preparations containing them and their uses | |
EP2153838A4 (de) | Anti-norovirus-wirkstoff und zusammensetzung damit | |
IL199151A (en) | Pyrimidine derivatives, their pharmaceutical preparations, their use in cancer treatment and their kits | |
AP2965A (en) | Therapeutic compositions and the use thereof | |
IL204621A0 (en) | Bicyclic - ?? - amino acid derivatives, compositions comprising the same and uses thereof | |
AP2490A (en) | Therapeutic compositions and the use thereof | |
ZA200901132B (en) | Human GLP-1 mimetibodies, compositions, methods and uses | |
MX2009007254A (es) | Composiciones de tableta en tableta. | |
IL211889A (en) | Pyrazolo pyridine derivatives, preparations containing them and their use as nadph oxidase inhibitors | |
IL211892A0 (en) | Pyrazolo pyridine derivatives, compositions comprising the same and uses thereof | |
IL201009A0 (en) | Pyrazolo pyridine derivatives, compositions comprising the same and uses thereof | |
IL212836A0 (en) | Azaquinolinone derivatives, compositions comprising the same and uses thereof | |
IL212278A0 (en) | Morpholinopurine derivatives, compositions comprising the same and uses thereof | |
IL185484A0 (en) | Aminopyrazole derivatives, their manufacture and use as pharmaceutical agents | |
IL206808A (en) | Indolyl-pyridone history, their pharmaceutical preparations and their uses | |
IL211891B (en) | Pyrazolo pyridine derivatives, preparations containing them and their uses | |
EP2262778B8 (de) | 1-benzyl-3-hydroxymethylindazolderivate und ihre verwendung bei der behandlung von auf der expression von mcp-1, cx3cr1 und p40 basierten erkrankungen | |
EP2160152A4 (de) | Kombinierter fibrinolytischer und antimikrobieller katheter und seine verwendungen | |
AU2008303948A8 (en) | Use of the peptide Asn-Asp-Asp-Cys-Glu- Leu-Cys-Val-Asn-Val-Ala-Cys-Thr-Gly-Cys-Leu alone or in combination with the peptide Thr-Thr-Ser-Gln-Val- Arg-Pro-Arg as a therapeutic agent | |
BRPI0917728A2 (pt) | composição, uso da composição, e, método de prevenção da formação de espuma em uma composição | |
IL204814A0 (en) | Quinazolinedione derivatives, preparation thereof and therapeutic uses thereof | |
PL2410047T3 (pl) | Oksydoreduktaza i jej zastosowanie do redukcji sekodionu | |
PL2012805T3 (pl) | Kompozycja lecznicza i jej zastosowanie | |
IL208168A0 (en) | Tetrahydroisoquinoline derivatives, compositions comprising the same and use thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 09769031 Country of ref document: EP Kind code of ref document: A2 |
|
DPE1 | Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101) | ||
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2009769031 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13000900 Country of ref document: US |