ES2422603T3 - Compuestos oxiimino y el uso de estos - Google Patents
Compuestos oxiimino y el uso de estosInfo
- Publication number
- ES2422603T3 ES2422603T3 ES08767992T ES08767992T ES2422603T3 ES 2422603 T3 ES2422603 T3 ES 2422603T3 ES 08767992 T ES08767992 T ES 08767992T ES 08767992 T ES08767992 T ES 08767992T ES 2422603 T3 ES2422603 T3 ES 2422603T3
- Authority
- ES
- Spain
- Prior art keywords
- optionally substituted
- substituted lower
- heterocyclyl
- cycloalkenyl
- cycloalkyl
- 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.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
- C07D211/96—Sulfur atom
-
- 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
- A61P25/04—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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
-
- 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
- A61P9/12—Antihypertensives
Abstract
Un compuesto que tiene la Fórmula I: **Fórmula** una sal o solvato farmacéuticamente aceptable de este, donde: Y es CO o SOm; Z es hidrógeno, alquilo inferior opcionalmente sustituido, alquenilo inferior opcionalmente sustituido, alquiniloinferior opcionalmente sustituido, cicloalquilo opcionalmente sustituido, bicicloalquilo opcionalmente sustituido,cicloalquenilo opcionalmente sustituido, arilo opcionalmente sustituido, heterociclilo opcionalmente sustituido,NR5R6, OR5, SR5, COR5 o CONR5R6; R1 y R2 son cada uno independientemente hidrógeno, alquilo inferior opcionalmente sustituido, alquenilo inferioropcionalmente sustituido, alquinilo inferior opcionalmente sustituido, cicloalquilo opcionalmente sustituido,cicloalquenilo opcionalmente sustituido, arilo opcionalmente sustituido, heterociclilo opcionalmente sustituido,ciano, COR5 o CONR5R6, o R1 y R2, considerados conjuntamente con el átomo al que están unidos, forman un cicloalquilo opcionalmentesustituido, bicicloalquilo opcionalmente sustituido, cicloalquenilo opcionalmente sustituido o heterocicliloopcionalmente sustituido; R5 y R6 son cada uno independientemente hidrógeno, alquilo inferior opcionalmente sustituido, alquenilo inferioropcionalmente sustituido, alquinilo inferior opcionalmente sustituido, cicloalquilo opcionalmente sustituido,bicicloalquilo opcionalmente sustituido, cicloalquenilo opcionalmente sustituido, arilo opcionalmente sustituido oheterociclilo opcionalmente sustituido; cada X es independientemente >=O, alquilo inferior opcionalmente sustituido, alquenilo inferior opcionalmentesustituido, alquinilo inferior opcionalmente sustituido, halógeno, ciano, nitro, NR5R6, OR5, SR5, COR5, COOR5,CONR5R6, NR5COR5, OCOR5, SOR5, SO2R5, SO3R5, SONR5R6, SO2NR5R6, NR5SOR5 o NR5SO2R5;m es 1 o 2. p es 0, 1 o 2; y q es 0 o 1.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US92480807P | 2007-05-31 | 2007-05-31 | |
PCT/US2008/006888 WO2008150470A1 (en) | 2007-05-31 | 2008-05-30 | Oxyimino compounds and the use thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2422603T3 true ES2422603T3 (es) | 2013-09-12 |
Family
ID=40094014
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES08767992T Active ES2422603T3 (es) | 2007-05-31 | 2008-05-30 | Compuestos oxiimino y el uso de estos |
Country Status (5)
Country | Link |
---|---|
US (1) | US8563732B2 (es) |
EP (1) | EP2164325B1 (es) |
JP (1) | JP5323063B2 (es) |
ES (1) | ES2422603T3 (es) |
WO (1) | WO2008150470A1 (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8563732B2 (en) | 2007-05-31 | 2013-10-22 | Shionogi & Co., Ltd. | Oxyimino compounds and the use thereof |
JP5380435B2 (ja) * | 2007-05-31 | 2014-01-08 | ユーロ−セルティーク ソシエテ アノニム | アミド化合物およびその使用 |
ES2408159T3 (es) | 2008-06-11 | 2013-06-18 | Shionogi & Co., Ltd. | Compuestos de oxicarbamoilo y su utilización |
GB0813144D0 (en) | 2008-07-17 | 2008-08-27 | Glaxo Group Ltd | Novel compounds |
GB0813142D0 (en) | 2008-07-17 | 2008-08-27 | Glaxo Group Ltd | Novel compounds |
ES2436566T3 (es) | 2009-04-02 | 2014-01-03 | Shionogi & Co., Ltd. | Compuestos de acrilamida y utilización de los mismos |
WO2012125521A1 (en) | 2011-03-14 | 2012-09-20 | Eternity Bioscience Inc. | Quinazolinediones and their use |
TWI527800B (zh) | 2011-04-01 | 2016-04-01 | 南京英派藥業有限公司 | 作為聚(二磷酸腺苷酸-核醣)聚合酶(parp)之抑制劑之1-(芳基甲基)喹唑啉-2,4(1h,3h)-二酮及其應用 |
Family Cites Families (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3577441A (en) | 1967-03-07 | 1971-05-04 | Warner Lambert Pharmaceutical | Nitro substituted benzofurans |
HU167365B (es) | 1973-11-29 | 1975-09-27 | ||
MX6634E (es) | 1979-01-09 | 1985-09-12 | Robins Co Inc A H | Procedimiento para preparar el isomero trans de 3-ariloxi-4-hidroxipirrolidinas |
US4585785A (en) | 1979-01-09 | 1986-04-29 | A. H. Robins Company, Inc. | Cis and trans-3-aryloxy-4-hydroxypyrrolidines used as anti-arrhythmics |
GB8518869D0 (en) * | 1985-07-25 | 1985-08-29 | Beecham Group Plc | Compounds |
EP0210815A3 (en) * | 1985-07-25 | 1988-04-20 | Beecham Group Plc | 6-beta-(alpha-etherified oxyimino)-acylamino penicillanic-acid derivatives, their preparation and use |
GB8908529D0 (en) | 1989-04-14 | 1989-06-01 | Merck Sharp & Dohme | Therapeutic agents |
ATE301457T1 (de) | 1995-06-12 | 2005-08-15 | Searle & Co | Mittel, enthaltend einen cyclooxygenase-2 inhibitor und einen 5-lipoxygenase inhibitor |
US5880138A (en) | 1996-10-01 | 1999-03-09 | Eli Lilly And Company | NMDA receptor selective antagonists |
AR011913A1 (es) | 1997-03-06 | 2000-09-13 | Yamano Masaki | Derivados de 4,4-difluoro-2,3,4,5-tetrahidro-1h-1-benzoazepina y composiciones farmaceuticas de los mismos. |
ATE231837T1 (de) | 1997-11-12 | 2003-02-15 | Darwin Discovery Ltd | Hydroxamsäure- und carbonsäurederivate mit mmp und tnf hemmender wirkung |
AU751412B2 (en) | 1997-11-26 | 2002-08-15 | 3-Dimensional Pharmaceuticals, Inc. | Heteroaryl aminoguanidines and alkoxyguanidines and their use as protease inhibitors |
US6492375B2 (en) | 1998-06-30 | 2002-12-10 | Neuromed Technologies, Inc. | Partially saturated calcium channel blockers |
US6310059B1 (en) * | 1998-06-30 | 2001-10-30 | Neuromed Technologies, Inc. | Fused ring calcium channel blockers |
US6011035A (en) | 1998-06-30 | 2000-01-04 | Neuromed Technologies Inc. | Calcium channel blockers |
TR200102533T2 (tr) | 1998-12-18 | 2006-06-21 | Axys Pharmaceuticals, Inc. | Proteaz inhibitörleri |
FR2812635B1 (fr) | 2000-08-01 | 2002-10-11 | Aventis Pharma Sa | Nouveaux composes heterocycliques, preparation et utilisation comme medicaments notamment comme anti- bacteriens |
WO2002057241A1 (en) * | 2000-12-22 | 2002-07-25 | Bayer Pharmaceuticals Corporation | 8-(AMINOALKOXYMINO)-8H-DIBENZO[a,e]TRIAZOLO[4,5-c]CYCLOHEPTENES AS GROWTH HORMONE SECRETAGOGUES |
EP1390347B1 (en) | 2001-03-20 | 2008-05-07 | Laboratoires Serono SA | Pyrrolidine ester derivatives with oxytocin modulating activity |
FR2835186B1 (fr) | 2002-01-28 | 2006-10-20 | Aventis Pharma Sa | Nouveaux composes heterocycliques, actifs comme inhibiteurs de beta-lactamases |
AU2003261756A1 (en) | 2002-08-28 | 2004-03-29 | Toray Industries, Inc. | Acrylamide derivatives |
US20040204404A1 (en) | 2002-09-30 | 2004-10-14 | Robert Zelle | Human N-type calcium channel blockers |
TW200505834A (en) | 2003-03-18 | 2005-02-16 | Sankyo Co | Sulfamide derivative and the pharmaceutical composition thereof |
EP1633343A1 (en) * | 2003-05-30 | 2006-03-15 | Neuromed Technologies, Inc. | 3-aminomethyl-pyrrolidines as n-type calcium channel blockers |
EP1664010A1 (en) * | 2003-08-29 | 2006-06-07 | Vernalis (R&D) Limited | Sulfonamides antagonising n-type calcium channels |
CA2545774A1 (en) | 2003-11-14 | 2005-06-02 | 3M Innovative Properties Company | Oxime substituted imidazo ring compounds |
EP1732566A4 (en) | 2004-04-05 | 2010-01-13 | Takeda Pharmaceutical | 6-azaindole COMPOUND |
EP1741702A1 (en) | 2004-04-28 | 2007-01-10 | Ono Pharmaceutical Co., Ltd. | Nitrogen-containing heterocyclic compounds and medicinal use thereof |
TW200630337A (en) * | 2004-10-14 | 2006-09-01 | Euro Celtique Sa | Piperidinyl compounds and the use thereof |
KR20080015102A (ko) * | 2005-05-10 | 2008-02-18 | 버텍스 파마슈티칼스 인코포레이티드 | 이온 채널 조절인자로서의 바이사이클릭 유도체 |
TWI359149B (en) * | 2005-07-11 | 2012-03-01 | Mitsubishi Tanabe Pharma Corp | An oxime derivative and preparations thereof |
JP2009507800A (ja) | 2005-09-09 | 2009-02-26 | ユーロ−セルティーク エス.エイ. | 縮合およびスピロ環化合物ならびにその使用 |
EP1987009A1 (en) | 2006-01-30 | 2008-11-05 | Euro-Celtique S.A. | Cyclourea compounds as calcium channel blockers |
US8247442B2 (en) | 2006-03-29 | 2012-08-21 | Purdue Pharma L.P. | Benzenesulfonamide compounds and their use |
WO2007118854A1 (en) | 2006-04-13 | 2007-10-25 | Euro-Celtique S.A. | Benzenesulfonamide compounds and the use thereof |
WO2007118853A1 (en) | 2006-04-13 | 2007-10-25 | Euro-Celtique S.A. | Benzenesulfonamide compounds and their use as blockers of calcium channels |
CN1850823A (zh) | 2006-05-19 | 2006-10-25 | 中国科学院上海药物研究所 | 一类含有肟基的喹诺酮类化合物及其制备方法和用途 |
TWI372762B (en) * | 2006-06-23 | 2012-09-21 | Sigma Tau Ind Farmaceuti | Amino derivatives of b-homoandrostanes and b-heteroandrostanes |
JP5539717B2 (ja) | 2006-07-14 | 2014-07-02 | 塩野義製薬株式会社 | オキシム化合物およびその使用 |
US8399486B2 (en) | 2007-04-09 | 2013-03-19 | Purdue Pharma L.P. | Benzenesulfonyl compounds and the use thereof |
JP5380435B2 (ja) | 2007-05-31 | 2014-01-08 | ユーロ−セルティーク ソシエテ アノニム | アミド化合物およびその使用 |
US8563732B2 (en) | 2007-05-31 | 2013-10-22 | Shionogi & Co., Ltd. | Oxyimino compounds and the use thereof |
WO2009040659A2 (en) | 2007-09-28 | 2009-04-02 | Purdue Pharma L.P. | Benzenesulfonamide compounds and the use thereof |
ES2408159T3 (es) | 2008-06-11 | 2013-06-18 | Shionogi & Co., Ltd. | Compuestos de oxicarbamoilo y su utilización |
EP2331522B1 (en) | 2008-08-01 | 2013-09-18 | Purdue Pharma LP | Tetrahydropyridinyl and dihydropyrrolyl compounds and the use thereof |
-
2008
- 2008-05-30 US US12/602,441 patent/US8563732B2/en active Active
- 2008-05-30 ES ES08767992T patent/ES2422603T3/es active Active
- 2008-05-30 EP EP08767992.4A patent/EP2164325B1/en not_active Not-in-force
- 2008-05-30 JP JP2010510361A patent/JP5323063B2/ja not_active Expired - Fee Related
- 2008-05-30 WO PCT/US2008/006888 patent/WO2008150470A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
JP5323063B2 (ja) | 2013-10-23 |
US20100240703A1 (en) | 2010-09-23 |
US8563732B2 (en) | 2013-10-22 |
WO2008150470A1 (en) | 2008-12-11 |
EP2164325A4 (en) | 2011-09-14 |
EP2164325A1 (en) | 2010-03-24 |
JP2010529020A (ja) | 2010-08-26 |
EP2164325B1 (en) | 2013-04-24 |
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