AR004493A1 - Derivados de oxindol 3- sustituido util como moduladores de canales de potasio y composiciones farmaceuticas que lo contienen. - Google Patents
Derivados de oxindol 3- sustituido util como moduladores de canales de potasio y composiciones farmaceuticas que lo contienen.Info
- Publication number
- AR004493A1 AR004493A1 ARP960102970A AR10297096A AR004493A1 AR 004493 A1 AR004493 A1 AR 004493A1 AR P960102970 A ARP960102970 A AR P960102970A AR 10297096 A AR10297096 A AR 10297096A AR 004493 A1 AR004493 A1 AR 004493A1
- Authority
- AR
- Argentina
- Prior art keywords
- potassium channel
- derivatives
- channel modulators
- oxindol
- contain
- Prior art date
Links
Classifications
-
- 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
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/34—Oxygen atoms in position 2
-
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
- A61P25/08—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
- A61P25/28—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
- 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
- A61P9/08—Vasodilators for multiple indications
-
- 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
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/32—Oxygen atoms
- C07D209/38—Oxygen atoms in positions 2 and 3, e.g. isatin
-
- 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
- C07D209/56—Ring systems containing three or more rings
- C07D209/58—[b]- or [c]-condensed
- C07D209/60—Naphtho [b] pyrroles; Hydrogenated naphtho [b] pyrroles
Abstract
Derivados de oxindol 3-sustituido, útil como moduladores de canales de potasio, caracterizado por la fórmula (I), en donde: R es hidrógeno, hidroxi ofluoro, R1, R2, R3 y R4 son cada uno independientemente hidrógeno, alquilo de 1 a 4 átomos de carbono, halógeno, trifluormetilo, fenilo, p-metilfenilo ó p-trifluorometilfenilo, ó R1 y R2, R2 y R3, ó R3 y R4 están unidos uno con otro, para formar un anillo benzofusionado. R5 es hidrógeno o alquilo de 1 a 4 átomosde carbono y R6 es cloro o trifluorometilo, o una sal, solvato o hidrato de los mismos no tóxico, farmacéuticamente aceptable del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/477,047 US5565483A (en) | 1995-06-07 | 1995-06-07 | 3-substituted oxindole derivatives as potassium channel modulators |
Publications (1)
Publication Number | Publication Date |
---|---|
AR004493A1 true AR004493A1 (es) | 1998-12-16 |
Family
ID=23894292
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP960102970A AR004493A1 (es) | 1995-06-07 | 1996-06-06 | Derivados de oxindol 3- sustituido util como moduladores de canales de potasio y composiciones farmaceuticas que lo contienen. |
Country Status (26)
Country | Link |
---|---|
US (2) | US5565483A (es) |
EP (1) | EP0747354B1 (es) |
JP (1) | JP4011135B2 (es) |
KR (1) | KR100432157B1 (es) |
CN (1) | CN1076348C (es) |
AR (1) | AR004493A1 (es) |
AT (1) | ATE195515T1 (es) |
AU (1) | AU707760B2 (es) |
BR (1) | BR1100180A (es) |
CA (1) | CA2176183C (es) |
CZ (1) | CZ289248B6 (es) |
DE (1) | DE69609772T2 (es) |
DK (1) | DK0747354T3 (es) |
ES (1) | ES2148685T3 (es) |
GR (1) | GR3034523T3 (es) |
HK (1) | HK1003301A1 (es) |
HU (1) | HU222046B1 (es) |
IL (1) | IL118349A (es) |
NO (1) | NO304829B1 (es) |
NZ (1) | NZ286748A (es) |
PL (1) | PL184660B1 (es) |
PT (1) | PT747354E (es) |
RU (1) | RU2165925C2 (es) |
SG (1) | SG70572A1 (es) |
TW (1) | TW384284B (es) |
ZA (1) | ZA964327B (es) |
Families Citing this family (69)
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TW504504B (en) * | 1996-11-26 | 2002-10-01 | Bristol Myers Squibb Co | 4-aryl-3-hydroxyquinolin-2-one derivatives as ion channel modulators |
US5808095A (en) * | 1997-05-30 | 1998-09-15 | Bristol-Myers Squibb Company | Preparation of 3-fluoro oxindole derivatives |
US5893085A (en) * | 1997-06-10 | 1999-04-06 | Phillips; Ronald W. | Dynamic fuzzy logic process for identifying objects in three-dimensional data |
US5972894A (en) * | 1997-08-07 | 1999-10-26 | Cytran, Inc. | Peptides having potassium channel opener activity |
WO1999009983A1 (en) * | 1997-08-28 | 1999-03-04 | Bristol-Myers Squibb Company | 4-aryl-3-aminoquinoline-2-one derivatives as potassium channel modulators |
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WO2000033834A1 (en) * | 1998-12-04 | 2000-06-15 | Neurosearch A/S | Use of isatin derivatives as ion channel activating agents |
US6391907B1 (en) * | 1999-05-04 | 2002-05-21 | American Home Products Corporation | Indoline derivatives |
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US6355648B1 (en) * | 1999-05-04 | 2002-03-12 | American Home Products Corporation | Thio-oxindole derivatives |
CA2378936A1 (en) * | 1999-08-03 | 2001-02-08 | Abbott Laboratories | Potassium channel openers |
ATE343562T1 (de) | 2000-03-23 | 2006-11-15 | Elan Pharm Inc | Verbindungen und verfahren zur behandlung der alzheimerschen krankheit |
US6992081B2 (en) | 2000-03-23 | 2006-01-31 | Elan Pharmaceuticals, Inc. | Compounds to treat Alzheimer's disease |
CA2412208C (en) * | 2000-06-29 | 2009-08-18 | Neurosearch A/S | Use of 3-substituted oxindole derivatives as kcnq potassium channel modulators |
PE20020276A1 (es) | 2000-06-30 | 2002-04-06 | Elan Pharm Inc | COMPUESTOS DE AMINA SUSTITUIDA COMO INHIBIDORES DE ß-SECRETASA PARA EL TRATAMIENTO DE ALZHEIMER |
CN1217920C (zh) | 2000-06-30 | 2005-09-07 | 艾兰制药公司 | 治疗早老性痴呆的化合物 |
US20030096864A1 (en) * | 2000-06-30 | 2003-05-22 | Fang Lawrence Y. | Compounds to treat alzheimer's disease |
US6846813B2 (en) * | 2000-06-30 | 2005-01-25 | Pharmacia & Upjohn Company | Compounds to treat alzheimer's disease |
EP1330426A4 (en) * | 2000-10-13 | 2005-09-14 | Bristol Myers Squibb Co | SELECTIVE MAXI-K CALIUM CHANNEL OPENING OPERATORS UNDER CONDITIONS OF HIGH INTRA-CELLULAR CALCIUM CONCENTRATIONS, METHOD AND THEIR USE |
US6348486B1 (en) | 2000-10-17 | 2002-02-19 | American Home Products Corporation | Methods for modulating bladder function |
EP1363624A2 (en) * | 2001-02-20 | 2003-11-26 | Bristol-Myers Squibb Company | Fluoro oxindole derivatives as modulators of kcnq potassium channels |
CA2438868A1 (en) | 2001-02-20 | 2002-09-19 | Valentin K. Gribkoff | Modulators of kcnq potassium channels and use thereof in treating migraine and mechanistically related diseases |
US6469042B1 (en) * | 2001-02-20 | 2002-10-22 | Bristol-Myers Squibb Company | Fluoro oxindole derivatives as modulators if KCNQ potassium channels |
US20020183395A1 (en) * | 2001-04-04 | 2002-12-05 | Wyeth | Methods for treating hyperactive gastric motility |
MXPA04000140A (es) * | 2001-06-27 | 2004-06-03 | Elan Pharm Inc | Derivados de beta-hidroxiamina utiles en el tratamiento de enfermedad de alzheimer. |
GEP20074230B (en) * | 2002-03-20 | 2007-11-12 | Bristol Myers Squibb Co | Phosphate prodrugs of fluorooxindoles |
AU2003240427A1 (en) | 2002-06-26 | 2004-01-19 | Poseidon Pharmaceuticals A/S | Novel benzimidazol-2-one derivatives and their use |
TWI271402B (en) * | 2002-10-15 | 2007-01-21 | Tanabe Seiyaku Co | Large conductance calcium-activated K channel opener |
US7632866B2 (en) | 2002-10-21 | 2009-12-15 | Ramot At Tel Aviv University | Derivatives of N-phenylanthranilic acid and 2-benzimidazolone as potassium channel and/or neuron activity modulators |
KR20050074493A (ko) * | 2002-10-21 | 2005-07-18 | 라모트 앳 텔-아비브 유니버시티 리미티드 | 칼륨 채널 및/또는 피질 뉴우런 작용 조절제로서 유용한n-페닐안트라닐산 및/또는 2-벤즈이미다졸론의 유도체 |
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HUP0500167A2 (en) * | 2005-02-02 | 2007-03-28 | Sanofi Aventis | Optically active 4-chloro-3-(5-chloro-3-alkyl-2-oxo-2,3-dihydro-1h-indol-3-yl)benzoic acid derivatives and process for producing them |
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US7576082B2 (en) * | 2005-06-24 | 2009-08-18 | Hoffman-La Roche Inc. | Oxindole derivatives |
AR054849A1 (es) * | 2005-07-26 | 2007-07-18 | Wyeth Corp | Diazepinoquinolinas, sintesis de las mismas, e intermediarios para obtenerlas |
TW200734334A (en) * | 2006-01-13 | 2007-09-16 | Wyeth Corp | Treatment of substance abuse |
BRPI0709163A2 (pt) * | 2006-03-24 | 2011-06-28 | Wyeth Corp | tratamento da dor |
JP2009531435A (ja) * | 2006-03-24 | 2009-09-03 | ワイス | うつ病の治療用の新規な治療組み合わせ |
CL2007000773A1 (es) * | 2006-03-24 | 2008-01-25 | Wyeth Corp | Uso de compuestos derivados de diazepina condensada para el tratamiento de un desorden cognitivo como add o adhd;o su uso para tratar spm o pmdd. |
WO2008016709A2 (en) * | 2006-08-04 | 2008-02-07 | California Institute Of Technology | Methods and systems for selective fluorination of organic molecules |
US8252559B2 (en) * | 2006-08-04 | 2012-08-28 | The California Institute Of Technology | Methods and systems for selective fluorination of organic molecules |
US8802401B2 (en) * | 2007-06-18 | 2014-08-12 | The California Institute Of Technology | Methods and compositions for preparation of selectively protected carbohydrates |
WO2009037707A2 (en) | 2007-09-20 | 2009-03-26 | Ramot At Tel Aviv University Ltd. | N-phenyl anthranilic acid derivatives and uses thereof |
CL2008002777A1 (es) * | 2007-09-21 | 2010-01-22 | Wyeth Corp | Metodo de preparacion de compuestos diazepinoquinolinicos quirales por recristalizacion en un sistema de solvente ternario. |
EP2205079A4 (en) * | 2007-10-04 | 2010-10-27 | Merck Sharp & Dohme | N-SUBSTITUTED OXINDOLINE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS |
KR100985286B1 (ko) * | 2007-12-28 | 2010-10-04 | 주식회사 포스코 | 내지연파괴 특성이 우수한 고강도 고망간강 및 제조방법 |
EP2540295A1 (en) | 2011-06-27 | 2013-01-02 | Centre national de la recherche scientifique | Compositions for the treatment of Fragile X syndrome |
MX2017013886A (es) | 2015-04-29 | 2018-03-12 | Janssen Pharmaceutica Nv | Azabenzimidazoles y su uso como moduladores del receptor ampa. |
ES2767707T3 (es) * | 2015-04-29 | 2020-06-18 | Janssen Pharmaceutica Nv | Compuestos de indolona y su uso como moduladores de receptor AMPA |
AU2018225758A1 (en) | 2017-02-24 | 2019-09-05 | Ovid Therapeutics Inc. | Methods of treating seizure disorders |
US11819909B2 (en) * | 2019-01-25 | 2023-11-21 | Jfe Steel Corporation | Method for manufacturing high-manganese steel cast slab and method for manufacturing high-manganese steel slab or steel sheet |
CN110240558B (zh) * | 2019-07-10 | 2022-05-27 | 上海华理生物医药股份有限公司 | 一种Flindokalner消旋体的新合成方法 |
KR102209406B1 (ko) * | 2019-11-21 | 2021-01-29 | 주식회사 포스코 | 미세한 주조조직을 갖는 고망간강 및 그 제조방법과 이를 이용한 고망간 강판 |
EP3912625A1 (en) | 2020-05-20 | 2021-11-24 | Kaerus Bioscience Limited | Novel maxi-k potassium channel openers for the treatment of fragile x associated disorders |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3114351A1 (de) * | 1981-04-09 | 1982-11-04 | Hoechst Ag, 6000 Frankfurt | "oxindol-derivate, verfahren zu ihrer herstellung und sie enthaltende arzneimittel mit neuroanaboler wirkung" |
DE3803775A1 (de) * | 1988-02-09 | 1989-08-17 | Boehringer Mannheim Gmbh | Neue substituierte lactame, verfahren zu ihrer herstellung und arzneimittel, die diese verbindungen enthalten |
NZ239540A (en) * | 1990-09-24 | 1993-11-25 | Neurosearch As | 1-phenyl benzimidazole derivatives and medicaments |
US5200422A (en) * | 1990-09-24 | 1993-04-06 | Neurosearch A/S | Benzimidazole derivatives, their preparation and use |
SK278514B6 (en) * | 1990-09-25 | 1997-08-06 | Andreas Kiener | Rhodococcus erythropolis microorganism and a method for producing hydroxylated pyrazines and quinoxalines |
US5234947A (en) * | 1991-11-07 | 1993-08-10 | New York University | Potassium channel activating compounds and methods of use thereof |
FR2714378B1 (fr) * | 1993-12-24 | 1996-03-15 | Sanofi Sa | Dérivés de l'indol-2-one substitués en 3 par un groupe azoté, leur préparation, les compositions pharmaceutiques en contenant. |
-
1995
- 1995-06-07 US US08/477,047 patent/US5565483A/en not_active Expired - Lifetime
-
1996
- 1996-04-19 US US08/635,316 patent/US5602169A/en not_active Expired - Lifetime
- 1996-05-09 CA CA2176183A patent/CA2176183C/en not_active Expired - Fee Related
- 1996-05-18 TW TW085105918A patent/TW384284B/zh not_active IP Right Cessation
- 1996-05-21 IL IL11834996A patent/IL118349A/xx not_active IP Right Cessation
- 1996-05-28 ZA ZA9604327A patent/ZA964327B/xx unknown
- 1996-05-31 NO NO962232A patent/NO304829B1/no not_active IP Right Cessation
- 1996-06-04 CZ CZ19961618A patent/CZ289248B6/cs not_active IP Right Cessation
- 1996-06-05 NZ NZ286748A patent/NZ286748A/en not_active IP Right Cessation
- 1996-06-06 DK DK96304188T patent/DK0747354T3/da active
- 1996-06-06 AT AT96304188T patent/ATE195515T1/de not_active IP Right Cessation
- 1996-06-06 HU HU9601547A patent/HU222046B1/hu not_active IP Right Cessation
- 1996-06-06 RU RU96111002/04A patent/RU2165925C2/ru not_active IP Right Cessation
- 1996-06-06 AU AU54757/96A patent/AU707760B2/en not_active Ceased
- 1996-06-06 ES ES96304188T patent/ES2148685T3/es not_active Expired - Lifetime
- 1996-06-06 DE DE69609772T patent/DE69609772T2/de not_active Expired - Lifetime
- 1996-06-06 PT PT96304188T patent/PT747354E/pt unknown
- 1996-06-06 EP EP96304188A patent/EP0747354B1/en not_active Expired - Lifetime
- 1996-06-06 AR ARP960102970A patent/AR004493A1/es unknown
- 1996-06-07 CN CN96106834A patent/CN1076348C/zh not_active Expired - Fee Related
- 1996-06-07 SG SG1996010008A patent/SG70572A1/en unknown
- 1996-06-07 JP JP14526396A patent/JP4011135B2/ja not_active Expired - Fee Related
- 1996-06-07 PL PL96314672A patent/PL184660B1/pl not_active IP Right Cessation
- 1996-06-07 KR KR1019960020225A patent/KR100432157B1/ko not_active IP Right Cessation
-
1997
- 1997-03-20 BR BR1100180-1A patent/BR1100180A/pt active IP Right Grant
-
1998
- 1998-03-23 HK HK98102434A patent/HK1003301A1/xx not_active IP Right Cessation
-
2000
- 2000-09-29 GR GR20000402213T patent/GR3034523T3/el unknown
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