WO2013177349A3 - Quinazolinediones as tankyrase inhibitors - Google Patents
Quinazolinediones as tankyrase inhibitors Download PDFInfo
- Publication number
- WO2013177349A3 WO2013177349A3 PCT/US2013/042332 US2013042332W WO2013177349A3 WO 2013177349 A3 WO2013177349 A3 WO 2013177349A3 US 2013042332 W US2013042332 W US 2013042332W WO 2013177349 A3 WO2013177349 A3 WO 2013177349A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- quinazolinediones
- hydrogen
- relates
- tankyrase inhibitors
- tankyrase
- 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.)
- Ceased
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
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
- C07D239/96—Two oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
This invention relates to compounds of Formula (I) and (l)(a) wherein R1, R2 and R3 are each independently hydrogen, halo, C1-C4alkyl, or C1-C4alkoxy; R4 is hydrogen or methyl; provided that at least one of R1, R2 and R3 is not hydrogen; or a pharmaceutically acceptable salt thereof. As well as the use of quinazolinediones for the modulation, notably the inhibition of the activity of tankyrases (TNKS1 and TNKS2). Suitably, the present invention relates to the use of quinazolinediones in the treatment of cancer, fibrosis and other hyperproliferative diseases through this mechanism.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261651687P | 2012-05-25 | 2012-05-25 | |
| US61/651,687 | 2012-05-25 | ||
| US201361773300P | 2013-03-06 | 2013-03-06 | |
| US61/773,300 | 2013-03-06 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2013177349A2 WO2013177349A2 (en) | 2013-11-28 |
| WO2013177349A3 true WO2013177349A3 (en) | 2014-01-16 |
Family
ID=49624519
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2013/042332 Ceased WO2013177349A2 (en) | 2012-05-25 | 2013-05-23 | Quinazolinediones as tankyrase inhibitors |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2013177349A2 (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX346147B (en) | 2012-03-07 | 2017-03-09 | Inst Of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use. |
| JP6456392B2 (en) | 2013-09-11 | 2019-01-23 | インスティチュート オブ キャンサー リサーチ:ロイヤル キャンサー ホスピタル | 3-Aryl-5-substituted isoquinolin-1-one compounds and therapeutic uses thereof |
| UY36060A (en) | 2014-04-02 | 2015-10-30 | Bayer Pharma AG | AZOL COMPOUNDS REPLACED WITH AMIDA |
| WO2017055316A1 (en) | 2015-10-01 | 2017-04-06 | Bayer Pharma Aktiengesellschaft | Amido-substituted azole compounds |
| WO2017055313A1 (en) | 2015-10-01 | 2017-04-06 | Bayer Pharma Aktiengesellschaft | Amido-substituted azole compounds |
| WO2017156350A1 (en) | 2016-03-09 | 2017-09-14 | K-Gen, Inc. | Methods of cancer treatment |
| WO2018078009A1 (en) | 2016-10-29 | 2018-05-03 | Bayer Pharma Aktiengesellschaft | Amido-substituted cyclohexane derivatives |
| WO2018078005A1 (en) | 2016-10-29 | 2018-05-03 | Bayer Pharma Aktiengesellschaft | Amido-substituted azaspiro derivatives as tankyrase inhibitors |
| WO2018087126A1 (en) | 2016-11-09 | 2018-05-17 | Bayer Pharma Aktiengesellschaft | Amido-substituted cyclohexane derivatives as inhibitors of tankyrase |
| CN112898221B (en) * | 2019-12-03 | 2023-12-08 | 浙江京新药业股份有限公司 | Preparation method of benzoxazine diketone compound C and intermediate thereof |
| CN112624911A (en) * | 2021-01-15 | 2021-04-09 | 阿里生物新材料(常州)有限公司 | 2-chloro-3-fluoro-4- (trifluoromethyl) benzaldehyde and synthetic method thereof |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011042145A1 (en) * | 2009-10-07 | 2011-04-14 | Siena Biotech S.P.A. | Wnt pathway antagonists |
| US20110136813A1 (en) * | 2008-05-27 | 2011-06-09 | Lawrence Lum | Wnt protein signalling inhibitors |
| US20120058987A1 (en) * | 2009-03-27 | 2012-03-08 | Sanofi | Therapeutic uses of quinazolinedione derivatives |
| US20120122863A1 (en) * | 2007-08-16 | 2012-05-17 | Boehringer Ingelheim International Gmbh | Quinazolinedione Chymase Inhibitors |
-
2013
- 2013-05-23 WO PCT/US2013/042332 patent/WO2013177349A2/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20120122863A1 (en) * | 2007-08-16 | 2012-05-17 | Boehringer Ingelheim International Gmbh | Quinazolinedione Chymase Inhibitors |
| US20110136813A1 (en) * | 2008-05-27 | 2011-06-09 | Lawrence Lum | Wnt protein signalling inhibitors |
| US20120058987A1 (en) * | 2009-03-27 | 2012-03-08 | Sanofi | Therapeutic uses of quinazolinedione derivatives |
| WO2011042145A1 (en) * | 2009-10-07 | 2011-04-14 | Siena Biotech S.P.A. | Wnt pathway antagonists |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2013177349A2 (en) | 2013-11-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
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| 122 | Ep: pct application non-entry in european phase |
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