PE20100052A1 - 3-OXOISOINDOLIN-1-CARBOXAMIDE DERIVATIVES AS INHIBITORS OF SODIUM CHANNELS - Google Patents
3-OXOISOINDOLIN-1-CARBOXAMIDE DERIVATIVES AS INHIBITORS OF SODIUM CHANNELSInfo
- Publication number
- PE20100052A1 PE20100052A1 PE2009000757A PE2009000757A PE20100052A1 PE 20100052 A1 PE20100052 A1 PE 20100052A1 PE 2009000757 A PE2009000757 A PE 2009000757A PE 2009000757 A PE2009000757 A PE 2009000757A PE 20100052 A1 PE20100052 A1 PE 20100052A1
- Authority
- PE
- Peru
- Prior art keywords
- carboxamide
- oxoisoindolin
- inhibitors
- oxo
- methyl
- Prior art date
Links
- XRJWQHDBFCGEPW-UHFFFAOYSA-N 3-oxo-1,2-dihydroisoindole-1-carboxamide Chemical class C1=CC=C2C(C(=O)N)NC(=O)C2=C1 XRJWQHDBFCGEPW-UHFFFAOYSA-N 0.000 title abstract 2
- 108010052164 Sodium Channels Proteins 0.000 title abstract 2
- 102000018674 Sodium Channels Human genes 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 3
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 3
- 208000002193 Pain Diseases 0.000 abstract 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- VKYTVITWNRXGGT-UHFFFAOYSA-N 2,3-dihydro-1h-isoindole-1-carboxamide Chemical compound C1=CC=C2C(C(=O)N)NCC2=C1 VKYTVITWNRXGGT-UHFFFAOYSA-N 0.000 abstract 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- -1 4,4-DIFLUOROCYCLOHEXYL Chemical class 0.000 abstract 1
- 208000000094 Chronic Pain Diseases 0.000 abstract 1
- 208000005298 acute pain Diseases 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- 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
- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE 3-OXOISOINDOLIN-1-CARBOXAMIDA DE FORMULA (I) DONDE R1 ES H, ALQUILO(C1-C3), ALCOXI(C1-C3), CN, ENTRE OTROS; m ES 1 O 2; R2 Y R3 SON CADA UNO H, HALOALQUILO(C1-C4), HALOALCOXI(C1-C4), HALO, ENTRE OTROS; D ES CICLOALQUILO(C3-C7) O HETEROCICLOALQUILO(C3-C7); L1 ES ALQUILENO(C1-C4) O UN ENLACE; L2 ES ALQUILENO(C1-C3). SON COMPUESTOS PREFERIDOS: 2-(OXAN-4-IL)-3-OXO-N-[[4-(TRIFLUOROMETOXI)FENIL]METIL]-1H-ISOINDOL-1-CARBOXAMIDA, 2-(4,4-DIFLUOROCICLOHEXIL)-3-OXO-N-[4-(TRIFLUOROMETOXI)BENCIL]ISOINDOLIN-1-CARBOXAMIDA, 3-OXO-2-[[(2S)-OXOLAN-2-IL]METIL]-N-[[4-(TRIFLUOROMETOXI)FENIL]METIL]-1H-ISOINDOL-1-CARBOXAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LOS CANALES DE SODIO NaV1,7 SIENDO UTILES EN EL TRATAMIENTO DEL DOLOR AGUDO, DOLOR CRONICO, DOLOR NEUROPATICO, LUMBALGIAREFERS TO COMPOUNDS DERIVED FROM 3-OXOISOINDOLIN-1-CARBOXAMIDE OF FORMULA (I) WHERE R1 IS H, ALKYL (C1-C3), ALCOXY (C1-C3), CN, AMONG OTHERS; m IS 1 O 2; R2 AND R3 ARE EACH H, HALOALKYL (C1-C4), HALOALCOXY (C1-C4), HALO, AMONG OTHERS; D IS CYCLOALKYL (C3-C7) OR HETERO CYCLOALKYL (C3-C7); L1 IS ALKYLENE (C1-C4) OR A LINK; L2 IS ALKYLENE (C1-C3). PREFERRED COMPOUNDS ARE: 2- (OXAN-4-IL) -3-OXO-N - [[4- (TRIFLUOROMETOXY) PHENYL] METHYL] -1H-ISOINDOL-1-CARBOXAMIDE, 2- (4,4-DIFLUOROCYCLOHEXYL) - 3-OXO-N- [4- (TRIFLUOROMETOXI) BENZYL] ISOINDOLIN-1-CARBOXAMIDE, 3-OXO-2 - [[(2S) -OXOLAN-2-IL] METHYL] -N - [[4- (TRIFLUOROMETOXI) PHENYL] METHYL] -1H-ISOINDOL-1-CARBOXAMIDE, AMONG OTHERS. IT ALSO REFERS TO A PHARMACEUTICAL COMPOSITION. SUCH COMPOUNDS ARE INHIBITORS OF NaV1,7 SODIUM CHANNELS, BEING USEFUL IN THE TREATMENT OF ACUTE PAIN, CHRONIC PAIN, NEUROPATHIC PAIN, LOW BACK
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5731008P | 2008-05-30 | 2008-05-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20100052A1 true PE20100052A1 (en) | 2010-02-20 |
Family
ID=41377346
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2009000757A PE20100052A1 (en) | 2008-05-30 | 2009-05-29 | 3-OXOISOINDOLIN-1-CARBOXAMIDE DERIVATIVES AS INHIBITORS OF SODIUM CHANNELS |
Country Status (6)
| Country | Link |
|---|---|
| AR (1) | AR071954A1 (en) |
| CL (1) | CL2009001328A1 (en) |
| PE (1) | PE20100052A1 (en) |
| TW (1) | TW201000446A (en) |
| UY (1) | UY31854A (en) |
| WO (1) | WO2009145721A1 (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8278302B2 (en) | 2009-04-08 | 2012-10-02 | Boehringer Ingelheim International Gmbh | Substituted piperidines as CCR3 antagonists |
| UA109290C2 (en) | 2010-10-07 | 2015-08-10 | Common Crystals and Salts of CCR3 Inhibitors | |
| CN106478497B (en) | 2010-10-18 | 2020-05-08 | 拉夸里亚创药株式会社 | Arylamine derivatives as TTX-S blockers |
| AR090566A1 (en) | 2012-04-02 | 2014-11-19 | Boehringer Ingelheim Int | PROCESS FOR THE PRODUCTION OF CRR INHIBITORS |
| US10213421B2 (en) | 2012-04-04 | 2019-02-26 | Alkahest, Inc. | Pharmaceutical formulations comprising CCR3 antagonists |
| JP7120549B2 (en) | 2016-12-15 | 2022-08-17 | 小野薬品工業株式会社 | Activator of TREK (TWIK-associated K channel) channels |
| PL3851436T3 (en) | 2018-09-10 | 2024-12-16 | Kaken Pharmaceutical Co., Ltd. | NEW HETEROAROMATIC AMIDE DERIVATIVE AND DRUG CONTAINING IT |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6995144B2 (en) * | 2002-03-14 | 2006-02-07 | Eisai Co., Ltd. | Nitrogen containing heterocyclic compounds and medicines containing the same |
| TW200613272A (en) * | 2004-08-13 | 2006-05-01 | Astrazeneca Ab | Isoindolone compounds and their use as metabotropic glutamate receptor potentiators |
| GB0514017D0 (en) * | 2005-07-07 | 2005-08-17 | Ionix Pharmaceuticals Ltd | Chemical compounds |
| TW200812962A (en) * | 2006-07-12 | 2008-03-16 | Astrazeneca Ab | New compounds I/418 |
| WO2008008020A1 (en) * | 2006-07-12 | 2008-01-17 | Astrazeneca Ab | 3-oxoisoindoline-1-carboxamide derivatives as analgesic agents |
| GB0705882D0 (en) * | 2007-03-27 | 2007-05-02 | Glaxo Group Ltd | Novel compounds |
-
2009
- 2009-05-26 TW TW098117487A patent/TW201000446A/en unknown
- 2009-05-29 WO PCT/SE2009/050618 patent/WO2009145721A1/en not_active Ceased
- 2009-05-29 UY UY0001031854A patent/UY31854A/en unknown
- 2009-05-29 CL CL2009001328A patent/CL2009001328A1/en unknown
- 2009-05-29 AR ARP090101936A patent/AR071954A1/en unknown
- 2009-05-29 PE PE2009000757A patent/PE20100052A1/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CL2009001328A1 (en) | 2010-01-15 |
| UY31854A (en) | 2010-01-05 |
| WO2009145721A1 (en) | 2009-12-03 |
| TW201000446A (en) | 2010-01-01 |
| AR071954A1 (en) | 2010-07-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |