ES2084914T3 - Nuevos derivados de 1,2,4-triaminobenceno y procedimiento para su preparacion. - Google Patents
Nuevos derivados de 1,2,4-triaminobenceno y procedimiento para su preparacion.Info
- Publication number
- ES2084914T3 ES2084914T3 ES92121028T ES92121028T ES2084914T3 ES 2084914 T3 ES2084914 T3 ES 2084914T3 ES 92121028 T ES92121028 T ES 92121028T ES 92121028 T ES92121028 T ES 92121028T ES 2084914 T3 ES2084914 T3 ES 2084914T3
- Authority
- ES
- Spain
- Prior art keywords
- rest
- triaminobenzene
- procedure
- preparation
- hidroxi
- 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.)
- Expired - Lifetime
Links
- JSYBAZQQYCNZJE-UHFFFAOYSA-N benzene-1,2,4-triamine Chemical class NC1=CC=C(N)C(N)=C1 JSYBAZQQYCNZJE-UHFFFAOYSA-N 0.000 title abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000000144 pharmacologic effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/42—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
- C07C233/43—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- 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
- A61P25/08—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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
- C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/40—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Neurology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
Abstract
COMPUESTOS ACTIVOS FARMACOLOGICOS DERIVADOS 1,2,4 TRIAMINOBENZOL DE LA FORMULA GENERAL: DONDE LOS SIMBOLOS R1, R2, R3, R4, R5, AR TIENEN EL SIGUIENTE SIGNIFICADO: R1: HIDROGENO, C1 O C1 LAMINO, C1 DIO DEL RESTO AR, C1 ALQUINIL, EL RESTO AR O EL RESTO ARO-; R4: HIDROGENO, C1 ESTO AR; ALK: UN GRUPO ALQUILENO DE CADENA RECTA O RAMIFICADA CON 1 ES DEL RESTO AR; AR: RESTO FENIL, QUE ES SUSTITUIDO POR MEDIO DEL RESTO R6, R7 Y/O R8, DONDE LOS RESTOS R6, R7 Y R8 SON IGUALES O DIFERENTES Y SIGNIFICAN C1 OALQUIL, HIDROXI, C1 C6 ENO, HIDROXI, C1 -C6 HALOGENOALQUIL, UIL, ONH NH O2 SO2 ON ACIDA ACEPTABLES FARMACEUTICAMENTE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4200259A DE4200259A1 (de) | 1992-01-08 | 1992-01-08 | Neue 1,2,4-triaminobenzol-derivate und verfahren zu deren herstellung |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2084914T3 true ES2084914T3 (es) | 1996-05-16 |
Family
ID=6449201
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES92121028T Expired - Lifetime ES2084914T3 (es) | 1992-01-08 | 1992-12-10 | Nuevos derivados de 1,2,4-triaminobenceno y procedimiento para su preparacion. |
Country Status (13)
Country | Link |
---|---|
US (1) | US5384330A (es) |
EP (1) | EP0554543B1 (es) |
JP (1) | JP3145220B2 (es) |
AT (1) | ATE134611T1 (es) |
CA (1) | CA2086654C (es) |
DE (3) | DE4200259A1 (es) |
DK (1) | DK0554543T3 (es) |
ES (1) | ES2084914T3 (es) |
GR (1) | GR3019653T3 (es) |
LU (1) | LU91869I2 (es) |
MX (1) | MX9300014A (es) |
SG (1) | SG48046A1 (es) |
ZA (1) | ZA9311B (es) |
Families Citing this family (89)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11503110A (ja) | 1995-02-17 | 1999-03-23 | スミスクライン・ビーチャム・コーポレイション | Il−8受容体拮抗剤 |
US5780483A (en) * | 1995-02-17 | 1998-07-14 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
DE19539861A1 (de) * | 1995-10-26 | 1997-04-30 | Asta Medica Ag | Verwendung von 4-Amino-4-(4-fluorbenzylamino)-1-ethoxy-carbonylaminobenzen zur Prophylaxe und Behandlung der Folgen der akuten und chronischen zerebralen Minderdurchblutung sowie neurodegenerativer Erkrankungen |
US6005008A (en) * | 1996-02-16 | 1999-12-21 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
US6262113B1 (en) | 1996-03-20 | 2001-07-17 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
US6211373B1 (en) | 1996-03-20 | 2001-04-03 | Smithkline Beecham Corporation | Phenyl urea antagonists of the IL-8 receptor |
WO1997049286A1 (en) | 1996-06-27 | 1997-12-31 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
US6133319A (en) * | 1996-06-27 | 2000-10-17 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
DE19701694A1 (de) * | 1997-01-20 | 1998-07-23 | Asta Medica Ag | Neue Modifikationen des 2-Amino-4-(4-fluorbenzylamino)-l-ethoxycarbonyl-aminobenzen sowie Verfahren zu ihrer Herstellung |
DE19752748A1 (de) | 1997-11-28 | 1999-06-02 | Bayer Ag | Substituierte Phenyluracile |
GB9915414D0 (en) * | 1999-07-01 | 1999-09-01 | Glaxo Group Ltd | Medical use |
US6117900A (en) * | 1999-09-27 | 2000-09-12 | Asta Medica Aktiengesellschaft | Use of retigabine for the treatment of neuropathic pain |
US6378671B1 (en) | 2000-03-29 | 2002-04-30 | Lord Corporation | Magnetically actuated motion control device |
TWI287984B (en) | 2000-10-17 | 2007-10-11 | Wyeth Corp | Pharmaceutical composition for modulating bladder function |
US6589986B2 (en) * | 2000-12-20 | 2003-07-08 | Wyeth | Methods of treating anxiety disorders |
AU2002338333A1 (en) * | 2001-04-04 | 2002-10-21 | Wyeth | Methods for treating hyperactive gastric motility |
DE10136046A1 (de) * | 2001-07-25 | 2003-02-13 | Viatris Gmbh | Verfahren zur Herstellung von 1,2,4-Triaminobenzol-carbamidsäureestern |
US7205307B2 (en) | 2002-02-14 | 2007-04-17 | Icagen, Inc. | Pyrimidines as novel openers of potassium ion channels |
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 |
PL377221A1 (pl) * | 2002-12-27 | 2006-01-23 | H. Lundbeck A/S | Pochodne 1,2,4-triaminobenzenu |
DK1578740T3 (da) * | 2002-12-27 | 2007-07-30 | Lundbeck & Co As H | 1,2,4-triaminobenzenderivater, der er egnede til behandling af lidelser i centralnervesystemet |
US7906537B2 (en) | 2003-03-21 | 2011-03-15 | H. Lundbeck A/S | Substituted p-diaminobenzene derivatives |
EP1631546A1 (en) * | 2003-04-25 | 2006-03-08 | H. Lundbeck A/S | Sustituted indoline and indole derivatives |
US20050089559A1 (en) * | 2003-10-23 | 2005-04-28 | Istvan Szelenyi | Combinations of potassium channel openers and sodium channel inhibitors or sodium channel-influencing active compounds for treating pains |
TWI357901B (en) | 2004-03-12 | 2012-02-11 | Lundbeck & Co As H | Substituted morpholine and thiomorpholine derivati |
UA89503C2 (uk) * | 2004-09-13 | 2010-02-10 | Х. Луннбек А/С | Заміщені похідні аніліну |
GT200500317A (es) * | 2004-11-05 | 2006-10-27 | Proceso para preparar compuestos de quinolina y productos obtenidos de los mismos | |
AU2006220130B2 (en) | 2005-03-03 | 2011-07-28 | H. Lundbeck A/S | Substituted pyridine derivatives |
WO2006116151A1 (en) * | 2005-04-22 | 2006-11-02 | Wyeth | Benzofuranyl alkanamine derivatives and uses thereof as 5-ht2c agonists |
TW200716583A (en) * | 2005-04-22 | 2007-05-01 | Wyeth Corp | Crystal forms of {[(2R)-7-(2,6-dichlorophenyl)-5-fluoro-2,3-dihydro-1-benzofuran-2-yl]methyl}amine hydrochloride |
AR056980A1 (es) * | 2005-04-22 | 2007-11-07 | Wyeth Corp | Derivados de dihidrobenzofurano, composiciones farmaceuticas, y uso de los mismos |
AU2006239942A1 (en) * | 2005-04-22 | 2006-11-02 | Wyeth | Dihydrobenzofuran derivatives and uses thereof |
EP1874292A2 (en) * | 2005-04-24 | 2008-01-09 | Wyeth | Methods for modulating bladder function |
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 |
EP2554162A1 (en) * | 2006-02-07 | 2013-02-06 | H. Lundbeck A/S | Use of KCNQ-Openers for Treating or Reducing the Symptoms of Schizophrenia |
CN101410112A (zh) * | 2006-03-24 | 2009-04-15 | 惠氏公司 | 治疗抑郁症的新治疗组合 |
JP2009531434A (ja) * | 2006-03-24 | 2009-09-03 | ワイス | 痛みの治療 |
US7960436B2 (en) * | 2006-06-05 | 2011-06-14 | Valeant Pharmaceuticals International | Substituted arylamino-1,2,3,4-tetrahydro naphthalenes and-2,3-dihydro-1H-indenes as potassium channel modulators |
US20080045534A1 (en) * | 2006-08-18 | 2008-02-21 | Valeant Pharmaceuticals North America | Derivatives of 1,3-diamino benzene as potassium channel modulators |
US8993593B2 (en) * | 2006-08-23 | 2015-03-31 | Valeant Pharmaceuticals International | N-(4-(6-fluoro-3,4-dihydroisoquinolin-2(1H)-yl)-2,6-dimethylphenyl)-3,3-dimethylbutanamide as potassium channel modulators |
PT2061465E (pt) * | 2006-08-23 | 2013-07-15 | Valeant Pharmaceuticals Int | Derivados de 4-(n-azacicloalquil)anilidas como moduladores do canal de potássio |
US8722929B2 (en) * | 2006-10-10 | 2014-05-13 | Valeant Pharmaceuticals International | N-[2-amino-4-(phenylmethoxy)phenyl] amides and related compounds as potassium channel modulators |
US8030518B2 (en) * | 2006-11-28 | 2011-10-04 | Valeant Pharmaceuticals International | 1,4 diamino bicyclic retigabine analogues as potassium channel modulators |
US8367684B2 (en) * | 2007-06-13 | 2013-02-05 | Valeant Pharmaceuticals International | Derivatives of 4-(N-azacycloalkyl) anilides as potassium channel modulators |
US8563566B2 (en) | 2007-08-01 | 2013-10-22 | Valeant Pharmaceuticals International | Naphthyridine derivatives as potassium channel modulators |
US7786146B2 (en) | 2007-08-13 | 2010-08-31 | Valeant Pharmaceuticals International | Derivatives of 5-amino-4,6-disubstituted indole and 5-amino-4,6-disubstituted indoline as potassium channel modulators |
EP2203411B1 (en) | 2007-09-20 | 2016-01-06 | 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. |
GB0723794D0 (en) | 2007-12-05 | 2008-01-16 | Lectus Therapeutics Ltd | Potassium ion channel modulators and uses thereof |
WO2010009433A1 (en) * | 2008-07-18 | 2010-01-21 | Valeant Pharmaceuticals International | Modified release formulation and methods of use |
US20100323015A1 (en) * | 2008-07-18 | 2010-12-23 | Biljana Nadjsombati | Modified release formulation and methods of use |
US20100323016A1 (en) * | 2008-07-18 | 2010-12-23 | Biljana Nadjsombati | Modified release formulation and methods of use |
DE102009013613A1 (de) | 2009-03-17 | 2010-09-23 | Ratiopharm Gmbh | Trockenverarbeitung von Retigabin |
DE102009013612A1 (de) | 2009-03-17 | 2010-09-23 | Ratiopharm Gmbh | Retigabin-Tabletten, bevorzugt mit modifizierter Freisetzung |
DE102009013611A1 (de) | 2009-03-17 | 2010-09-23 | Ratiopharm Gmbh | Festes Retigabin in nicht-kristalliner Form |
WO2011012659A2 (en) | 2009-07-28 | 2011-02-03 | Medichem S.A. | Diethyl 4-(4-fluorobenzylamino)-1,2-phenylenedicarbamate, and salts thereof |
WO2011039369A2 (en) | 2009-10-02 | 2011-04-07 | Medichem S.A. | Amorphous forms of a 2-amino-4-(4-fluorobenzylamino)phenylcarbamate derivative |
KR20120118012A (ko) | 2010-01-20 | 2012-10-25 | 글락소 그룹 리미티드 | 신규의 레티가빈 조성물 |
EP2536394A2 (en) | 2010-02-19 | 2012-12-26 | Medichem S.A. | Stabilized phenylcarbamate derivative in solid state |
CN101921195A (zh) * | 2010-08-02 | 2010-12-22 | 北京德众万全医药科技有限公司 | 一种瑞替加滨中间体的简单合成方法 |
JP2014510714A (ja) * | 2011-01-18 | 2014-05-01 | グラクソ グループ リミテッド | レチガビンの製造方法 |
CN102241608A (zh) * | 2011-05-12 | 2011-11-16 | 天津市汉康医药生物技术有限公司 | 瑞替加滨化合物及其组合物 |
WO2013011518A1 (en) | 2011-07-21 | 2013-01-24 | Arch Pharmalabs Limited | Process for the preparation of retigabine of the formula i and pharmaceutically acceptable salts thereof |
CN103073455B (zh) | 2011-10-25 | 2015-08-19 | 中国科学院上海药物研究所 | 一类新型的kcnq钾通道激动剂、其制备方法和用途 |
CN102531966B (zh) * | 2011-12-23 | 2013-07-24 | 山东创新药物研发有限公司 | 瑞替加滨的晶型d及其制备方法 |
ITMI20120137A1 (it) * | 2012-02-02 | 2013-08-03 | Olon Spa | Procedimento ed intermedi per la preparazione di retigabina |
CN103373941B (zh) * | 2012-04-11 | 2016-08-17 | 浙江九洲药物科技有限公司 | 瑞替加滨及其中间体的制备方法 |
AU2013257209B2 (en) * | 2012-04-30 | 2016-05-19 | Scifluor Life Sciences, Inc | Fluorinated 2-amino-4-(benzylamino)phenylcarbamate derivatives |
WO2014023270A1 (en) | 2012-08-09 | 2014-02-13 | Zentiva, K.S. | Salts or co-crystals of ethyl n-[2-amino-4-[(4-fluorophenyl)methylamino]-phenyl]carbamate |
ITMI20121922A1 (it) * | 2012-11-12 | 2014-05-13 | Dipharma Francis Srl | Procedimento per la preparazione di un composto anticonvulsivante |
CN103193657B (zh) * | 2013-04-16 | 2015-08-05 | 石家庄度恩医药科技有限公司 | 一种合成依佐加滨中间体的方法 |
CN103664678B (zh) * | 2013-11-06 | 2015-10-28 | 河北科技大学 | 一种n1-(4-氟苄基)-4-硝基苯基-1,3-二胺的中间体及其制备方法 |
CN105017085B (zh) | 2014-04-28 | 2018-06-29 | 中国科学院上海药物研究所 | 一类kcnq钾通道激动剂、其制备方法和用途 |
WO2016077724A1 (en) * | 2014-11-13 | 2016-05-19 | University Of Pittsburgh - Of The Commonwealth System Of Higher Education | (2-amino-4(arylamino)phenyl) carbamates |
RU2018147263A (ru) | 2016-06-10 | 2020-07-10 | Сайфлуор Лайф Сайенсиз, Инк | Фторированные 2-амино-4-(замещенные амино)фенилкарбаматные производные |
TWI808952B (zh) | 2016-12-16 | 2023-07-21 | 瑞士商愛杜西亞製藥有限公司 | 包含t型鈣通道阻斷劑之醫藥組合 |
WO2019014547A1 (en) | 2017-07-14 | 2019-01-17 | Texas Tech University System | FUNCTIONALIZED PYRIDINE CARBAMATES HAVING ENHANCED NEUROPROTECTOR ACTIVITY |
EP3694833A4 (en) | 2017-10-09 | 2021-06-30 | Ramot at Tel-Aviv University Ltd. | TRPV1 AND POTASIC IONIC CHANNEL MODULATORS AND THEIR USES |
JP2021506810A (ja) | 2017-12-13 | 2021-02-22 | サイフルーア ライフ サイエンシズ インコーポレイテッド | フッ素化4−(置換アミノ)フェニルカルバメート誘導体 |
US11358930B2 (en) | 2018-04-20 | 2022-06-14 | University of Pittsburgh—of the Commonwealth System of Higher Education | Selective potassium channel agonists |
WO2020157126A1 (en) | 2019-01-29 | 2020-08-06 | Università degli Studi di Salerno | Modulators of potassium ion channels and uses thereof |
IL293352A (en) | 2019-12-02 | 2022-07-01 | Xenon Pharmaceuticals Inc | A pediatric immediate-release formulation of the potassium channel opener azogabine |
CA3214084A1 (en) * | 2021-03-19 | 2022-09-22 | Xyzagen, Inc. | Prodrugs of kv7 channel openers |
AU2022390453A1 (en) | 2021-11-19 | 2024-05-30 | F. Hoffmann-La Roche Ag | Novel heteroaryl-urea compounds as kv7.2 inhibitors |
CN118265710A (zh) | 2021-11-19 | 2024-06-28 | 伊卡根有限责任公司 | 吡啶化合物作为kv7.2增强剂 |
CN118510757A (zh) | 2021-12-22 | 2024-08-16 | 伊卡根有限责任公司 | 环丙基化合物 |
CN116478068A (zh) | 2022-01-14 | 2023-07-25 | 中国科学院上海药物研究所 | 一种高选择性kcnq4钾通道激动剂、其制备方法和用途 |
WO2023158584A1 (en) | 2022-02-15 | 2023-08-24 | Icagen, Llc | New bicyclopentane derivatives |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3337593A1 (de) * | 1982-10-27 | 1984-05-03 | Degussa Ag, 6000 Frankfurt | 2-amino-3-acylamino-6-benzylamino-pyridin-derivate mit antiepileptischer wirkung |
MC2029A1 (fr) * | 1988-05-16 | 1990-04-25 | Asta Pharma Ag | (n-heterocyclyl)-3 diamino-2,6 pyridines substituees et leurs n-oxydes,preparation de ces composes et leur application comme medicaments |
DE3917113A1 (de) * | 1989-05-26 | 1990-11-29 | Schwarzkopf Gmbh Hans | Verfahren zur selektiven herstellung von n(pfeil hoch)4(pfeil hoch)-substituierten 1,4-diamino-2-nitrobenzolen |
GB8921792D0 (en) * | 1989-09-27 | 1989-11-08 | May & Baker Ltd | New compositions of matter |
US5220059A (en) * | 1990-04-19 | 1993-06-15 | Abbott Laboratories | Lipoxygenase-inhibiting compounds derived from non-steroidal antiinflammatory carboxylic acids |
-
1992
- 1992-01-08 DE DE4200259A patent/DE4200259A1/de not_active Withdrawn
- 1992-12-10 ES ES92121028T patent/ES2084914T3/es not_active Expired - Lifetime
- 1992-12-10 AT AT92121028T patent/ATE134611T1/de active
- 1992-12-10 SG SG1996006604A patent/SG48046A1/en unknown
- 1992-12-10 DE DE59205496T patent/DE59205496D1/de not_active Expired - Lifetime
- 1992-12-10 EP EP92121028A patent/EP0554543B1/de not_active Expired - Lifetime
- 1992-12-10 DK DK92121028.2T patent/DK0554543T3/da active
-
1993
- 1993-01-04 ZA ZA9311A patent/ZA9311B/xx unknown
- 1993-01-04 CA CA002086654A patent/CA2086654C/en not_active Expired - Lifetime
- 1993-01-06 MX MX9300014A patent/MX9300014A/es unknown
- 1993-01-07 JP JP00105493A patent/JP3145220B2/ja not_active Expired - Fee Related
- 1993-01-08 US US08/002,458 patent/US5384330A/en not_active Expired - Lifetime
-
1996
- 1996-04-16 GR GR960401034T patent/GR3019653T3/el unknown
-
2011
- 2011-09-07 DE DE201112100044 patent/DE122011100044I1/de active Pending
- 2011-09-14 LU LU91869C patent/LU91869I2/fr unknown
Also Published As
Publication number | Publication date |
---|---|
DE59205496D1 (de) | 1996-04-04 |
DE4200259A1 (de) | 1993-07-15 |
JPH05345752A (ja) | 1993-12-27 |
DK0554543T3 (da) | 1996-03-18 |
US5384330A (en) | 1995-01-24 |
GR3019653T3 (en) | 1996-07-31 |
DE122011100044I1 (de) | 2012-01-19 |
MX9300014A (es) | 1993-07-01 |
CA2086654A1 (en) | 1993-07-09 |
EP0554543A3 (en) | 1993-10-27 |
SG48046A1 (en) | 1998-04-17 |
EP0554543A2 (de) | 1993-08-11 |
ZA9311B (en) | 1993-08-05 |
LU91869I2 (fr) | 2011-11-14 |
EP0554543B1 (de) | 1996-02-28 |
CA2086654C (en) | 2003-09-23 |
ATE134611T1 (de) | 1996-03-15 |
JP3145220B2 (ja) | 2001-03-12 |
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