PE20120589A1 - DERIVADOS DE N-FENIL-1H-BENZIMIDAZOL-2-AMINA COMO INHIBIDORES DE PROSTAGLANDINA MICROSOMICA E2 SINTASA-1 (mPGES-1) - Google Patents
DERIVADOS DE N-FENIL-1H-BENZIMIDAZOL-2-AMINA COMO INHIBIDORES DE PROSTAGLANDINA MICROSOMICA E2 SINTASA-1 (mPGES-1)Info
- Publication number
- PE20120589A1 PE20120589A1 PE2011001560A PE2011001560A PE20120589A1 PE 20120589 A1 PE20120589 A1 PE 20120589A1 PE 2011001560 A PE2011001560 A PE 2011001560A PE 2011001560 A PE2011001560 A PE 2011001560A PE 20120589 A1 PE20120589 A1 PE 20120589A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- methyl
- microsomic
- mpges
- benzimidazol
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory 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
- A61P25/04—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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D405/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE UNO DE X e Y ES -N-H Y EL OTRO -N=; UNO DE Z1, Z2, Z3 ES CH Y EL OTRO -CR7; Q2, Q3 Y Q4 SON CADA UNO CR2, CR3, CR4; R1 ES HALO, OH, CN, ALQUILO C1-C3, O-(ALQUILO C1-C3), ENTRE OTROS; R2, R3 Y R4 SON CADA UNO H, HALO, -CN, ALQUILO C1-C3, ENTRE OTROS; Ra Y Rb SON CADA UNO H, ALQUILO C1-C3, O AMBOS JUNTO AL CARBONO QUE LOS UNE FORMAN CICLOALQUILENO C3-C7, HETEROCICLOALQUILENO DE 4-6-MIEMBROS; Rc ES H, ALQUILO C1-C3; W ES -C(O)-, S(O)-, S(O)2, ENTRE OTROS; M ES ALQUILO C1-C7, CICLOALQUILO C3-C7, SUSTITUIDOS O NO POR F, OH, CN, ENTRE OTROS; R5 ES H, ALQUILO C1-C3; R7 ES H, HALO, -CN, ALQUILO C1-C7, ALQUILO C1-C5-O-, ENTRE OTROS; A-L JUNTOS REPRESENTAN 1-PIRROLIDINCARBONIL, 1-METILCICLOHEXILAMIDO, N-CICLOPENTILSULFAMOIL, N-CICLOHEXILMETIL-CARBAMOIL, ENTRE OTROS. UN COMPUESTO PREFERIDO ES 2-{2-CLORO-5-[(1-METILCICLOHEXILAMIDO)METIL]FENILAMINO}-N-CICLOPENTIL-1-METILBENCIMIDAZOL-5-CARBOXAMIDA; N-(4-BROMOFENIL)-2-{2-CLORO-5-[(1-METILCICLOHEXILAMIDO)METIL]FENILAMINO}-1-METILBENCIMIDAZOL-5-CARBOXAMIDA; ENTRE OTROS. DICHOS COMPUESTOS SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES INFLAMATORIAS Y AFECCIONES ASOCIADAS
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09154414 | 2009-03-05 | ||
EP09179618 | 2009-12-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20120589A1 true PE20120589A1 (es) | 2012-05-26 |
Family
ID=42111729
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2011001560A PE20120589A1 (es) | 2009-03-05 | 2010-03-05 | DERIVADOS DE N-FENIL-1H-BENZIMIDAZOL-2-AMINA COMO INHIBIDORES DE PROSTAGLANDINA MICROSOMICA E2 SINTASA-1 (mPGES-1) |
Country Status (37)
Country | Link |
---|---|
US (3) | US20100256188A1 (es) |
EP (1) | EP2403852B8 (es) |
JP (1) | JP5433708B2 (es) |
KR (1) | KR20110123764A (es) |
CN (1) | CN102341395B (es) |
AP (1) | AP2806A (es) |
AR (1) | AR075789A1 (es) |
AU (1) | AU2010220263B2 (es) |
BR (1) | BRPI1009118A2 (es) |
CA (1) | CA2753149A1 (es) |
CL (1) | CL2011002180A1 (es) |
CO (1) | CO6450668A2 (es) |
CY (1) | CY1115959T1 (es) |
DK (1) | DK2403852T3 (es) |
EA (1) | EA020282B1 (es) |
EC (1) | ECSP11011324A (es) |
ES (1) | ES2528730T3 (es) |
GE (1) | GEP20146034B (es) |
HK (1) | HK1163064A1 (es) |
HR (1) | HRP20150096T1 (es) |
IL (1) | IL214033A0 (es) |
MA (1) | MA33239B1 (es) |
ME (1) | ME02117B (es) |
MX (1) | MX2011008948A (es) |
MY (1) | MY161092A (es) |
NZ (1) | NZ594589A (es) |
PE (1) | PE20120589A1 (es) |
PL (1) | PL2403852T3 (es) |
PT (1) | PT2403852E (es) |
RS (1) | RS53757B1 (es) |
SG (1) | SG174250A1 (es) |
SI (1) | SI2403852T1 (es) |
SM (1) | SMT201500053B (es) |
TN (1) | TN2011000446A1 (es) |
TW (1) | TWI466869B (es) |
UY (1) | UY32470A (es) |
WO (1) | WO2010100249A1 (es) |
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UY32470A (es) | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
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TW201305178A (zh) | 2010-10-29 | 2013-02-01 | Glenmark Pharmaceuticals Sa | 作為mPGES-1抑制物的三環化合物 |
US8486968B2 (en) | 2010-12-10 | 2013-07-16 | Boehringer Ingelheim International Gmbh | Compounds |
US8466186B2 (en) * | 2010-12-10 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Compounds |
UY33779A (es) | 2010-12-10 | 2012-07-31 | Boehringer Ingelheim Int | ?2-(fenilamino)-1H-bencimidazol-5-carboxamidas novedosas? |
AR084174A1 (es) | 2010-12-21 | 2013-04-24 | Lilly Co Eli | Compuestos de imidazol-2-benzamida utiles para el tratamiento de osteoartritis y una composicion farmaceutica |
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WO2013038308A1 (en) | 2011-09-15 | 2013-03-21 | Glenmark Pharmaceuticals S.A. | SUBSTITUTED BICYCLIC HETEROARYL COMPOUNDS AS mPGES-1 INHIBITORS |
PL2766359T3 (pl) * | 2011-10-14 | 2016-11-30 | Związki heterocykliczne i ich zastosowanie jako modulatorów receptorowych kinaz tyrozynowych typu iii | |
WO2013072825A1 (en) | 2011-11-16 | 2013-05-23 | Glenmark Pharmaceuticals S.A. | Phtalazinone derivatives as mpegs -1 inhibitors |
WO2013118071A1 (en) | 2012-02-09 | 2013-08-15 | Glenmark Pharmaceuticals S.A. | BICYCLIC COMPOUNDS AS mPGES-1 INHIBITORS |
WO2013152039A1 (en) | 2012-04-02 | 2013-10-10 | The Trustees Of Columbia University In The City Of New York | Compounds, compositions, and methods for modulating ferroptosis and treating excitotoxic disorders |
WO2013153535A1 (en) | 2012-04-13 | 2013-10-17 | Glenmark Pharmaceuticals S.A. | TRICYCLIC COMPOUNDS AS mPGES-1 INHIBITORS |
CN103450329B (zh) * | 2012-05-29 | 2015-05-27 | 首都医科大学 | 3h-咪唑并吡啶-6-甲酰氨基酸苄酯、其合成、抗肿瘤活性和应用 |
TWI568722B (zh) | 2012-06-15 | 2017-02-01 | 葛蘭馬克製藥公司 | 作爲mPGES-1抑制劑之三唑酮化合物 |
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JP2016522252A (ja) * | 2013-06-20 | 2016-07-28 | ノヴァサイド・アクチボラグ | Mpges−1阻害剤としての新規なピペリジニルベンゾイミダゾール誘導体 |
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