JP2013520443A5 - - Google Patents

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Publication number
JP2013520443A5
JP2013520443A5 JP2012554085A JP2012554085A JP2013520443A5 JP 2013520443 A5 JP2013520443 A5 JP 2013520443A5 JP 2012554085 A JP2012554085 A JP 2012554085A JP 2012554085 A JP2012554085 A JP 2012554085A JP 2013520443 A5 JP2013520443 A5 JP 2013520443A5
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JP
Japan
Prior art keywords
cancer
pharmaceutically acceptable
ring
acceptable salt
compound according
Prior art date
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Application number
JP2012554085A
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English (en)
Japanese (ja)
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JP2013520443A (ja
JP5805672B2 (ja
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Publication date
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Priority claimed from PCT/US2011/025661 external-priority patent/WO2011103546A1/en
Publication of JP2013520443A publication Critical patent/JP2013520443A/ja
Publication of JP2013520443A5 publication Critical patent/JP2013520443A5/ja
Application granted granted Critical
Publication of JP5805672B2 publication Critical patent/JP5805672B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2012554085A 2010-02-22 2011-02-22 脂肪酸合成酵素阻害剤としてのトリアゾロン類 Expired - Fee Related JP5805672B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US30670910P 2010-02-22 2010-02-22
US61/306,709 2010-02-22
US35758710P 2010-06-23 2010-06-23
US61/357,587 2010-06-23
PCT/US2011/025661 WO2011103546A1 (en) 2010-02-22 2011-02-22 Triazolones as fatty acid synthase inhibitors

Publications (3)

Publication Number Publication Date
JP2013520443A JP2013520443A (ja) 2013-06-06
JP2013520443A5 true JP2013520443A5 (US07094801-20060822-C00173.png) 2014-03-13
JP5805672B2 JP5805672B2 (ja) 2015-11-04

Family

ID=44483349

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012554085A Expired - Fee Related JP5805672B2 (ja) 2010-02-22 2011-02-22 脂肪酸合成酵素阻害剤としてのトリアゾロン類

Country Status (13)

Country Link
US (2) US8802864B2 (US07094801-20060822-C00173.png)
EP (1) EP2538787B1 (US07094801-20060822-C00173.png)
JP (1) JP5805672B2 (US07094801-20060822-C00173.png)
KR (1) KR20120133386A (US07094801-20060822-C00173.png)
CN (1) CN102858175A (US07094801-20060822-C00173.png)
AU (1) AU2011217809A1 (US07094801-20060822-C00173.png)
BR (1) BR112012020976A2 (US07094801-20060822-C00173.png)
CA (1) CA2790692A1 (US07094801-20060822-C00173.png)
EA (1) EA201290822A1 (US07094801-20060822-C00173.png)
ES (1) ES2509951T3 (US07094801-20060822-C00173.png)
MX (1) MX2012009720A (US07094801-20060822-C00173.png)
SG (1) SG183260A1 (US07094801-20060822-C00173.png)
WO (1) WO2011103546A1 (US07094801-20060822-C00173.png)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2012009720A (es) * 2010-02-22 2012-10-09 Glaxosmithkline Llc Triazolonas como inhibidores de acido graso sintasa.
US9505728B2 (en) 2012-03-09 2016-11-29 Inception 2, Inc. Triazolone compounds and uses thereof
MX2015007433A (es) 2012-12-20 2015-12-07 Inception 2 Inc Compuestos de triazolona y usos de los mismos.
EP2943484B1 (en) * 2013-01-10 2017-10-25 Glaxosmithkline Intellectual Property (No. 2) Limited Fatty acid synthase inhibitors
PE20160122A1 (es) 2013-03-13 2016-02-12 Forma Therapeutics Inc Compuestos nobles y composiciones para la inhibicion de fasn
EP3041849A4 (en) 2013-09-05 2017-04-19 Dow AgroSciences LLC Methods for producing borylated arenes
WO2015035059A1 (en) 2013-09-06 2015-03-12 Inception 2, Inc. Triazolone compounds and uses thereof
CA2934257C (en) * 2013-12-17 2022-06-07 Janssen Pharmaceutica Nv Imidazolin-5-one derivative useful as fasn inhibitors for the treatment of cancer
TW201625354A (zh) 2014-06-16 2016-07-16 陶氏農業科學公司 用於製備氧硼基化芳烴之方法
CN104876917B (zh) * 2015-06-16 2017-09-19 上海皓元医药股份有限公司 用作脂肪酸合成酶抑制剂的三唑酮的合成方法
MX2017016669A (es) 2015-06-18 2018-04-13 Cephalon Inc Derivados de piperidina 1,4-sustituidos.
EP3310773B1 (en) 2015-06-18 2020-12-02 89Bio Ltd. Substituted 4-benzyl and 4-benzoyl piperidine derivatives
TW201722957A (zh) * 2015-09-15 2017-07-01 葛蘭素史克智慧財產(第二)有限公司 化學化合物
TWI767148B (zh) 2018-10-10 2022-06-11 美商弗瑪治療公司 抑制脂肪酸合成酶(fasn)
CN113382633A (zh) 2018-10-29 2021-09-10 福马治疗股份有限公司 (4-(2-氟-4-(1-甲基-1H-苯并[d]咪唑-5-基)苯甲酰基)哌嗪-1-基)(1-羟基环丙基)甲酮的固体形式
CN114539193A (zh) * 2022-01-20 2022-05-27 海南普利制药股份有限公司 一种盐酸胺碘酮中间体的制备方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5728834A (en) * 1996-11-14 1998-03-17 Wyckoff Chemical Company, Inc. Process for preparation of 4-aryl-1,2,4-triazol-3-ones
WO2004064730A2 (en) * 2003-01-14 2004-08-05 Cytokinetics, Inc. Compounds, compositions and methods
SE0400850D0 (sv) * 2004-03-30 2004-03-31 Astrazeneca Ab Novel Compounds
EP1784396B8 (en) * 2004-08-26 2011-04-20 Pfizer Inc. Pyrazole-substituted aminoheteroaryl compounds as protein kinase inhibitors
WO2007056170A2 (en) * 2005-11-02 2007-05-18 Bayer Healthcare Ag Pyrrolo[2,1-f] [1,2,4] triazin-4-ylamines igf-1r kinase inhibitors for the treatment of cancer and other hyperproliferative diseases
US8236792B2 (en) * 2008-05-23 2012-08-07 Janssen Pharmaceutica Nv Substituted pyrrolidine amides as modulators of the histamine H3 receptor
MX2012009720A (es) * 2010-02-22 2012-10-09 Glaxosmithkline Llc Triazolonas como inhibidores de acido graso sintasa.

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