WO2010022055A3 - 1, 3, 5 -triaz ine derivatives useful in the treatment of chronic pain disorders - Google Patents
1, 3, 5 -triaz ine derivatives useful in the treatment of chronic pain disorders Download PDFInfo
- Publication number
- WO2010022055A3 WO2010022055A3 PCT/US2009/054169 US2009054169W WO2010022055A3 WO 2010022055 A3 WO2010022055 A3 WO 2010022055A3 US 2009054169 W US2009054169 W US 2009054169W WO 2010022055 A3 WO2010022055 A3 WO 2010022055A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- treatment
- chronic pain
- pain disorders
- derivatives useful
- ine derivatives
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (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
The present invention provides compounds that are inhibitors of voltage-gated sodium channel (Nav), in particular Nav 1.7 and are therefore useful for the treatment of diseases 5 treatable by inhibition of these channels, in particular, chronic pain disorders. Also provided are pharmaceutical compositions containing such compounds and processes for preparing such compounds.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18950108P | 2008-08-20 | 2008-08-20 | |
| US61/189,501 | 2008-08-20 | ||
| US19601208P | 2008-10-14 | 2008-10-14 | |
| US61/196,012 | 2008-10-14 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2010022055A2 WO2010022055A2 (en) | 2010-02-25 |
| WO2010022055A3 true WO2010022055A3 (en) | 2010-06-17 |
Family
ID=41707632
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2009/054169 Ceased WO2010022055A2 (en) | 2008-08-20 | 2009-08-18 | Inhibitors of voltage-gated sodium channels |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2010022055A2 (en) |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011103196A1 (en) * | 2010-02-17 | 2011-08-25 | Amgen Inc. | Aryl carboxamide derivatives as sodium channel inhibitors for treatment of pain |
| ES2533990T3 (en) * | 2010-02-24 | 2015-04-16 | Research Triangle Institute | Arylpiperazine opioid receptor antagonists |
| US8871996B2 (en) | 2010-06-09 | 2014-10-28 | Regeneron Pharmaceuticals, Inc. | Mice expressing human voltage-gated sodium channels |
| US8486647B2 (en) | 2010-06-09 | 2013-07-16 | Regeneron Pharmaceuticals, Inc. | Neuropeptide release assay for sodium channels |
| CN102344407A (en) * | 2010-08-03 | 2012-02-08 | 艾琪康医药科技(上海)有限公司 | 3-droperidol derivative and preparation method thereof |
| HRP20160094T1 (en) * | 2010-09-13 | 2016-02-26 | Novartis Ag | Triazine-oxadiazoles |
| EP2681193B1 (en) | 2011-03-02 | 2016-01-06 | Lead Discovery Center GmbH | Pharmaceutically active disubstituted pyridine derivatives |
| CA2826464C (en) | 2011-03-02 | 2020-07-28 | Lead Discovery Center Gmbh | Pharmaceutically active disubstituted triazine derivatives |
| CN102285969B (en) * | 2011-06-28 | 2013-06-19 | 山东大学 | N-1-substituted piperidin-4-arylamine derivatives and preparation method and use thereof |
| KR20140105445A (en) | 2011-10-31 | 2014-09-01 | 제논 파마슈티칼스 인크. | Biaryl ether sulfonamides and their use as therapeutic agents |
| BR112014010271A2 (en) | 2011-10-31 | 2017-04-18 | Xenon Pharmaceuticals Inc | benzenesulfonamide compounds and their use as therapeutic agents |
| PE20150400A1 (en) | 2012-05-22 | 2015-03-27 | Genentech Inc | N-SUBSTITUTED BENZAMIDES AND ITS USE IN THE TREATMENT OF PAIN |
| CA2878478A1 (en) | 2012-07-06 | 2014-01-09 | Genentech, Inc. | N-substituted benzamides and methods of use thereof |
| WO2014106238A1 (en) * | 2012-12-31 | 2014-07-03 | Fang, Qun, Kevin | Heterocyclic compounds and methods of use thereof |
| US9040712B2 (en) * | 2013-01-23 | 2015-05-26 | Novartis Ag | Thiadiazole analogs thereof and methods for treating SMN-deficiency-related-conditions |
| WO2014127116A1 (en) | 2013-02-13 | 2014-08-21 | Novartis Ag | Topical ocular analgesic agents |
| JP6096370B2 (en) | 2013-03-14 | 2017-03-15 | ジェネンテック, インコーポレイテッド | Substituted triazolopyridines and methods of use |
| JP6227112B2 (en) | 2013-03-15 | 2017-11-08 | ジェネンテック, インコーポレイテッド | Substituted benzoxazole and methods of use |
| EP2970231A1 (en) | 2013-03-15 | 2016-01-20 | Blueprint Medicines Corporation | Piperazine derivatives and their use as kit modulators |
| GB2516303A (en) * | 2013-07-18 | 2015-01-21 | Redx Pharma Ltd | Compounds |
| EP3039019B1 (en) * | 2013-08-26 | 2020-04-22 | Purdue Pharma L.P. | Azaspiro[4.5]decane derivatives and use thereof |
| US20160237071A1 (en) * | 2013-10-02 | 2016-08-18 | Nissan Chemical Industries, Ltd. | T-type calcium channel inhibitor |
| EP3409674B1 (en) | 2013-10-17 | 2022-04-06 | Blueprint Medicines Corporation | Process for preparing compositions useful for treating disorders related to kit |
| WO2015058129A1 (en) * | 2013-10-17 | 2015-04-23 | Blueprint Medicines Corporation | Compositions useful for treating disorders related to kit |
| WO2015078374A1 (en) | 2013-11-27 | 2015-06-04 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
| CN106103422B (en) * | 2014-02-12 | 2020-09-18 | 普渡制药公司 | Isoquinoline derivatives and their uses |
| PE20161368A1 (en) * | 2014-03-17 | 2016-12-25 | Pfizer | DIACILGLICEROL ACILTRANFERASE 2 INHIBITORS |
| CN104016977B (en) * | 2014-06-13 | 2016-06-22 | 山东大学 | A kind of replacement thiadiazine diketone derivative and preparation method thereof and application |
| CN106715418A (en) | 2014-07-07 | 2017-05-24 | 基因泰克公司 | Therapeutic compounds and methods of use thereof |
| WO2016022569A1 (en) | 2014-08-04 | 2016-02-11 | Blueprint Medicines Corporation | Compositions useful for treating disorders related to kit |
| AU2016268120A1 (en) | 2015-05-22 | 2017-11-30 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
| JP2018521076A (en) | 2015-07-24 | 2018-08-02 | ブループリント メディシンズ コーポレイション | Compounds useful for treating diseases associated with KIT and PDGFR |
| JP2018526371A (en) | 2015-08-27 | 2018-09-13 | ジェネンテック, インコーポレイテッド | Therapeutic compounds and methods of use thereof |
| WO2017058821A1 (en) | 2015-09-28 | 2017-04-06 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| EP3380466A1 (en) | 2015-11-25 | 2018-10-03 | Genentech, Inc. | Substituted benzamides useful as sodium channel blockers |
| CN105837525B (en) * | 2016-03-25 | 2019-05-28 | 浙江工业大学 | 2, 4-diamine-1, 3,5-triazine compound and preparation method and application thereof |
| JP2019513714A (en) | 2016-03-30 | 2019-05-30 | ジェネンテック, インコーポレイテッド | Substituted benzamides and methods of use thereof |
| CA3039853A1 (en) | 2016-10-17 | 2018-04-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| CN110099898B (en) | 2016-10-24 | 2023-07-25 | 优曼尼蒂治疗公司 | Compounds and uses thereof |
| FI3541784T3 (en) | 2016-11-18 | 2023-10-02 | Integrative Res Laboratories Sweden Ab | Novel azetidine derivatives useful as modulators of cortical catecholaminergic neurotransmission |
| EA037318B1 (en) | 2016-12-16 | 2021-03-11 | Пфайзер Инк. | Glp-1 receptor agonists and uses thereof |
| WO2018129403A1 (en) | 2017-01-06 | 2018-07-12 | Yumanity Therapeutics | Methods for the treatment of neurological disorders |
| WO2018175707A1 (en) | 2017-03-24 | 2018-09-27 | Genentech, Inc. | 4-piperidin-n-(pyrimidin-4-yl)chroman-7-sulfonamide derivatives as sodium channel inhibitors |
| CN106995380B (en) * | 2017-03-31 | 2018-12-28 | 九江善水科技股份有限公司 | A kind of synthetic method of 2- Amino-4-nitrophenol |
| WO2018183712A1 (en) | 2017-03-31 | 2018-10-04 | Blueprint Medicines Corporation | Pyrrolo[1,2-b]pyridazine compounds and compositions useful for treating disorders related to kit and pdgfr |
| WO2019018795A1 (en) * | 2017-07-20 | 2019-01-24 | Yumanity Therapeutics | Compounds and uses thereof |
| EP3700934A4 (en) | 2017-10-24 | 2021-10-27 | Yumanity Therapeutics, Inc. | COMPOUNDS AND USES OF THESE COMPOUNDS |
| WO2019165290A1 (en) | 2018-02-26 | 2019-08-29 | Genentech, Inc. | Pyridine-sulfonamide compounds and their use against pain and related conditions |
| CN112312913B (en) | 2018-03-23 | 2024-03-08 | 詹森药业有限公司 | Compounds and their uses |
| WO2019191702A1 (en) | 2018-03-30 | 2019-10-03 | F. Hoffmann-La Roche Ag | Substituted hydro-pyrido-azines as sodium channel inhibitors |
| JP2021522253A (en) | 2018-04-25 | 2021-08-30 | ユマニティ セラピューティクス,インコーポレーテッド | Compounds and their use |
| TW202003490A (en) | 2018-05-22 | 2020-01-16 | 瑞士商赫孚孟拉羅股份公司 | Therapeutic compounds and methods of use thereof |
| AU2020212034A1 (en) | 2019-01-24 | 2021-09-16 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
| EP3856341B1 (en) | 2019-04-12 | 2023-09-06 | Blueprint Medicines Corporation | Crystalline forms of (s)-1-(4-fluorophenyl)-1-(2-(4-(6-(1-methyl-1h-pyrazol-4-yl)pyrrolo[2,1-f][1,2,4]triazin-4-yl)piperazinyl)-pyrimidin-5-yl)ethan-1-amine and methods of making |
| MX2021012469A (en) | 2019-04-12 | 2022-01-18 | Blueprint Medicines Corp | Pyrrolotriazine derivatives for treating kit- and pdgfra-mediated diseases. |
| EA202192047A1 (en) | 2019-11-13 | 2021-12-08 | Юманити Терапьютикс, Инк. | COMPOUNDS AND THEIR APPLICATIONS |
| CN111057021B (en) * | 2019-12-11 | 2023-05-23 | 中国药科大学 | s-triazine compound and its preparation method and use |
| NZ788624A (en) * | 2019-12-23 | 2025-08-29 | Lg Chemical Ltd | Novel amino aryl derivative useful as diacylglycerol acyltransferase 2 inhibitor and use thereof |
| ES2969310T3 (en) * | 2019-12-23 | 2024-05-17 | Lg Chemical Ltd | New amide derivative useful as a diacylglycerol acyltransferase 2 inhibitor, and use thereof |
| JPWO2023132208A1 (en) * | 2022-01-07 | 2023-07-13 | ||
| WO2023229685A2 (en) * | 2022-02-24 | 2023-11-30 | Microbiotix, Inc. | Broad-spectrum inhibitors of cytomegalovirus |
| CN116178465A (en) * | 2023-03-06 | 2023-05-30 | 中国科学院成都生物研究所 | Four-membered ring-containing polyphenol compound and application thereof |
| AU2024289298A1 (en) | 2023-07-06 | 2026-01-15 | Integrative Research Laboratories Sweden Ab | Pharmaceutically acceptable salts of 3-(2,3-difluorophenoxy)azetidine and uses thereof |
| CN117384091B (en) * | 2023-12-08 | 2024-02-20 | 四川大学华西第二医院 | Amide derivative, synthesis method and application |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002083653A1 (en) * | 2001-04-11 | 2002-10-24 | Amgen Inc. | Triazinyl acrylamide derivatives as kinase inhibitors |
| WO2002092576A1 (en) * | 2001-05-16 | 2002-11-21 | Boehringer Ingelheim Pharmaceuticals, Inc. | Diarylurea derivatives useful as anti-inflammatory agents |
-
2009
- 2009-08-18 WO PCT/US2009/054169 patent/WO2010022055A2/en not_active Ceased
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002083653A1 (en) * | 2001-04-11 | 2002-10-24 | Amgen Inc. | Triazinyl acrylamide derivatives as kinase inhibitors |
| WO2002092576A1 (en) * | 2001-05-16 | 2002-11-21 | Boehringer Ingelheim Pharmaceuticals, Inc. | Diarylurea derivatives useful as anti-inflammatory agents |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010022055A2 (en) | 2010-02-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2010022055A3 (en) | 1, 3, 5 -triaz ine derivatives useful in the treatment of chronic pain disorders | |
| WO2009012242A3 (en) | Sodium channel inhibitors | |
| WO2007095124A3 (en) | Benzazole derivatives, compositions, and methods of use as aurora kinase inhibitors | |
| IL196543A (en) | Pyridazinone derivatives and pharmaceutical compositions comprising them for use in the treatment of disorders | |
| WO2006107451A3 (en) | Honokiol derivatives for the treatment of proliferative disorders | |
| WO2010017545A3 (en) | Triazole compounds that modulate hsp90 activity | |
| WO2005110994A8 (en) | Substituted pyrazolyl urea derivatives useful in the treatment of cancer | |
| WO2008135826A3 (en) | 2 -pyridine carboxamide derivatives as sodium channel modulators | |
| WO2007021941A3 (en) | Inhibitors of voltage-gated sodium channels | |
| WO2008089307A3 (en) | Delta 5 desaturase inhibitors for the treatment of pain, inflammation and cancer | |
| MX346186B (en) | Protein kinase inhibitors. | |
| WO2008147797A3 (en) | Ion channel modulators and methods of use | |
| WO2005111039A3 (en) | Compounds and methods for inhibiting mitotic progression by inhibition of aurora kinase | |
| WO2009076454A3 (en) | Compounds that modulate intracellular calcium | |
| WO2008070016A3 (en) | Inhibitors of akt activity | |
| MX2009008253A (en) | Kinase inhibitors. | |
| WO2006135627A3 (en) | Inhibitors of akt activity | |
| WO2009036996A3 (en) | Small molecule bradykinin b1 receptor antagonists | |
| WO2005046603A3 (en) | Pyridine compounds | |
| WO2008097924A3 (en) | Pharmaceutical compositions comprising dextromethorphan analogs for the treatment of neurological disorders | |
| WO2008021038A3 (en) | Pyridobenzazepine compounds and methods for inhibiting mitotic progression | |
| WO2010011772A3 (en) | Tri-cyclic pyrazolopyridine kinase inhibitors | |
| WO2007109279A3 (en) | Tetrahydropyridothienopyrimidine compounds and methods of use thereof | |
| WO2008013987A3 (en) | N-alkyl substituted piperazinylmethylquinazolinones and azepanylmethylquinazolinones | |
| WO2010042925A3 (en) | Compositions and methods for treating alcohol use disorders, pain and other diseases |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 09791616 Country of ref document: EP Kind code of ref document: A2 |