WO2008013987A3 - N-alkyl substituted piperazinylmethylquinazolinones and azepanylmethylquinazolinones - Google Patents
N-alkyl substituted piperazinylmethylquinazolinones and azepanylmethylquinazolinones Download PDFInfo
- Publication number
- WO2008013987A3 WO2008013987A3 PCT/US2007/016996 US2007016996W WO2008013987A3 WO 2008013987 A3 WO2008013987 A3 WO 2008013987A3 US 2007016996 W US2007016996 W US 2007016996W WO 2008013987 A3 WO2008013987 A3 WO 2008013987A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- piperazinylmethylquinazolinones
- azepanylmethylquinazolinones
- compounds
- alkyl substituted
- cancer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Abstract
Compounds represented by Structural Formula (I) : are useful, for example, in the effective killing or reduction in rate of proliferation of cancer cells, such as in patients suffering from cancer. In addition to the compounds themselves, the invention provides pharmaceutical compositions of the compounds and method of treatment using the compounds.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US83402706P | 2006-07-27 | 2006-07-27 | |
US60/834,027 | 2006-07-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008013987A2 WO2008013987A2 (en) | 2008-01-31 |
WO2008013987A3 true WO2008013987A3 (en) | 2008-10-30 |
Family
ID=38951450
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2007/016996 WO2008013987A2 (en) | 2006-07-27 | 2007-07-27 | N-alkyl substituted piperazinylmethylquinazolinones and azepanylmethylquinazolinones |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2008013987A2 (en) |
Cited By (2)
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---|---|---|---|---|
US9255108B2 (en) | 2012-04-10 | 2016-02-09 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US9359365B2 (en) | 2013-10-04 | 2016-06-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
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US20110123486A1 (en) * | 2007-06-25 | 2011-05-26 | Prolexys Pharmaceuticals, Inc. | Methods of treating multiple myeloma and resistant cancers |
CN102391287B (en) * | 2011-09-28 | 2013-11-06 | 河南省健康伟业生物医药研究股份有限公司 | Levo-fluoroquinolone C3 bisazole methyl sulfide, preparation method and application thereof |
CN102443011B (en) * | 2011-09-28 | 2013-09-25 | 河南大学 | Levorotatory fluoroquinolone C3 diazole methyl sulfide quaternary ammonium salt, preparation method and application thereof |
US9751888B2 (en) | 2013-10-04 | 2017-09-05 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
JP6701088B2 (en) | 2014-03-19 | 2020-05-27 | インフィニティー ファーマシューティカルズ, インコーポレイテッド | Heterocyclic compounds for use in the treatment of PI3K-gamma mediated disorders |
CN106459011B (en) | 2014-04-01 | 2019-11-15 | 华盛顿大学 | σ -2 receptors ligand drug conjugate, its preparation method and use as antitumoral compounds |
US9708348B2 (en) | 2014-10-03 | 2017-07-18 | Infinity Pharmaceuticals, Inc. | Trisubstituted bicyclic heterocyclic compounds with kinase activities and uses thereof |
KR20180058741A (en) | 2015-09-14 | 2018-06-01 | 인피니티 파마슈티칼스, 인코포레이티드 | Solid form of isoquinolines, a process for their preparation, compositions comprising them and methods for using them |
WO2017161116A1 (en) | 2016-03-17 | 2017-09-21 | Infinity Pharmaceuticals, Inc. | Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors |
WO2017214269A1 (en) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
TW201815787A (en) | 2016-09-23 | 2018-05-01 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
TW201813963A (en) | 2016-09-23 | 2018-04-16 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
TW201825465A (en) | 2016-09-23 | 2018-07-16 | 美商基利科學股份有限公司 | Phosphatidylinositol 3-kinase inhibitors |
DE102017117369A1 (en) | 2017-08-01 | 2019-02-07 | Gustav Klauke Gmbh | Building with a metallic, electrically conductive pipe and laid in such a pipe electrical line and metallic, electrically conductive pipe for this purpose |
EP3806848A2 (en) | 2018-06-15 | 2021-04-21 | Flagship Pioneering Innovations V, Inc. | Increasing immune activity through modulation of postcellular signaling factors |
US20230114107A1 (en) | 2019-12-17 | 2023-04-13 | Flagship Pioneering Innovations V, Inc. | Combination anti-cancer therapies with inducers of iron-dependent cellular disassembly |
Citations (5)
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---|---|---|---|---|
WO2004018058A2 (en) * | 2002-08-21 | 2004-03-04 | Cytokinetics, Inc. | Compounds, compositions, and methods |
US20040248221A1 (en) * | 2003-01-29 | 2004-12-09 | Whitehead Institute For Biomedical Research | Identification of genotype-selective anti-tumor agents |
WO2006081331A2 (en) * | 2005-01-25 | 2006-08-03 | Prolexys Pharmaceuticals, Inc. | Quinoxaline derivatives as antitumor agents |
WO2006081337A2 (en) * | 2005-01-25 | 2006-08-03 | Whitehead Institute For Biomedical Research | Erastin analogues and their uses for killing cancer cells |
WO2007076087A2 (en) * | 2005-12-22 | 2007-07-05 | Prolexys Pharmaceuticals, Inc. | 3-aryl-substituted quinazolones, and uses thereof |
-
2007
- 2007-07-27 WO PCT/US2007/016996 patent/WO2008013987A2/en active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004018058A2 (en) * | 2002-08-21 | 2004-03-04 | Cytokinetics, Inc. | Compounds, compositions, and methods |
US20040248221A1 (en) * | 2003-01-29 | 2004-12-09 | Whitehead Institute For Biomedical Research | Identification of genotype-selective anti-tumor agents |
WO2006081331A2 (en) * | 2005-01-25 | 2006-08-03 | Prolexys Pharmaceuticals, Inc. | Quinoxaline derivatives as antitumor agents |
WO2006081337A2 (en) * | 2005-01-25 | 2006-08-03 | Whitehead Institute For Biomedical Research | Erastin analogues and their uses for killing cancer cells |
WO2007076087A2 (en) * | 2005-12-22 | 2007-07-05 | Prolexys Pharmaceuticals, Inc. | 3-aryl-substituted quinazolones, and uses thereof |
Non-Patent Citations (13)
Title |
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ABDEL-ALIM A-A M ET AL: "SYNTHESIS AND BIOLOGICAL ACTIVITIES OF 6-BROMO-2,3-DISUBSTITUTED-4-(3 H)-QUINAZOLINONES", INDIAN JOURNAL OF CHEMISTRY, SECTION B: ORGANIC, INCL.MEDICINAL, PUBLICATIONS & INFORMATIONS DIRECTORATE, NEW DELHI, vol. 33B, 1 March 1994 (1994-03-01), pages 260 - 265, XP008066973, ISSN: 0019-5103 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY LTD.: "CHEMICAL LIBRARY", XP002466896 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY LTD.: "CHEMICAL LIBRARY", XP002466897 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY LTD.: "CHEMICAL LIBRARY", XP002466898 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY LTD.: "CHEMICAL LIBRARY", XP002466899 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY LTD.: "CHEMICAL LIBRARY", XP002466900 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY LTD.: "CHEMICAL LIBRARY", XP002466902 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY LTD.: "CHEMICAL LIBRARY", XP002466903 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 29 May 2006 (2006-05-29), MICROCHEMISTRY: "CHEMICAL LIBRARY", XP002466901 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 8 August 2004 (2004-08-08), AMBINTER: "CHEMICAL LIBRARY", XP002466904 * |
DATABASE REGISTRY CHEMICAL ABSTRACTS, COLUMBUS, OHIO; 8 August 2004 (2004-08-08), AMBINTER: "CHEMICAL LIBRARY", XP002466905 * |
DOLMA S ET AL: "Identification of genotype-selective antitumor agnets using synthetic lethal chemical screening in engineered human tumor cells", CANCER CELL, XX, US, vol. 3, 2003, pages 285 - 296, XP002392895, ISSN: 1535-6108 * |
TANI J ET AL: "STUDIES ON BIOLOGICALLY ACTIVE HALOGENATED COMPOUNDS. ÖII. CHEMICAL MODIFICATIONS OF 6-AMINO-2-FLUOROMETHYL-3-(O-TOLY)-4(3H)-QUINAZOLINONE AND THE CNS DEPRESSANT ACTIVITIES OF RELATED COMPOUNDS", CHEMICAL AND PHARMACEUTICAL BULLETIN, PHARMACEUTICAL SOCIETY OF JAPAN, TOKYO, vol. 27, no. 11, 1 November 1979 (1979-11-01), pages 2675 - 2687, XP000608776, ISSN: 0009-2363 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9255108B2 (en) | 2012-04-10 | 2016-02-09 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US9359365B2 (en) | 2013-10-04 | 2016-06-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
Also Published As
Publication number | Publication date |
---|---|
WO2008013987A2 (en) | 2008-01-31 |
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