ZA9311B - Novel pharmaceutically active 1,2,4,-triaminobenzene derivatives, processes for their preparation and pharmacuetical compositions containing them - Google Patents

Novel pharmaceutically active 1,2,4,-triaminobenzene derivatives, processes for their preparation and pharmacuetical compositions containing them

Info

Publication number
ZA9311B
ZA9311B ZA9311A ZA9311A ZA9311B ZA 9311 B ZA9311 B ZA 9311B ZA 9311 A ZA9311 A ZA 9311A ZA 9311 A ZA9311 A ZA 9311A ZA 9311 B ZA9311 B ZA 9311B
Authority
ZA
South Africa
Prior art keywords
alkyl
radical
nhco
alkoxy
hydrogen
Prior art date
Application number
ZA9311A
Other languages
English (en)
Inventor
Hans-Reinhold Dieter
Jurgen Engel
Bernbard Kutscher
Emmanuel Polymeropoulos
Stefan Szelenyi
Bernd Nickel
Original Assignee
Asta Medica Ag
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Asta Medica Ag filed Critical Asta Medica Ag
Publication of ZA9311B publication Critical patent/ZA9311B/xx

Links

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)
ZA9311A 1992-01-08 1993-01-04 Novel pharmaceutically active 1,2,4,-triaminobenzene derivatives, processes for their preparation and pharmacuetical compositions containing them ZA9311B (en)

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
ZA9311B true ZA9311B (en) 1993-08-05

Family

ID=6449201

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA9311A ZA9311B (en) 1992-01-08 1993-01-04 Novel pharmaceutically active 1,2,4,-triaminobenzene derivatives, processes for their preparation and pharmacuetical compositions containing them

Country Status (13)

Country Link
US (1) US5384330A (fr)
EP (1) EP0554543B1 (fr)
JP (1) JP3145220B2 (fr)
AT (1) ATE134611T1 (fr)
CA (1) CA2086654C (fr)
DE (3) DE4200259A1 (fr)
DK (1) DK0554543T3 (fr)
ES (1) ES2084914T3 (fr)
GR (1) GR3019653T3 (fr)
LU (1) LU91869I2 (fr)
MX (1) MX9300014A (fr)
SG (1) SG48046A1 (fr)
ZA (1) ZA9311B (fr)

Families Citing this family (87)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996025157A1 (fr) 1995-02-17 1996-08-22 Smithkline Beecham Corporation Antagonistes des recepteurs d'il-8
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
US6211373B1 (en) 1996-03-20 2001-04-03 Smithkline Beecham Corporation Phenyl urea antagonists of the IL-8 receptor
US6262113B1 (en) 1996-03-20 2001-07-17 Smithkline Beecham Corporation IL-8 receptor antagonists
AU3409197A (en) * 1996-06-27 1998-01-14 Smithkline Beecham Corporation Il-8 receptor antagonists
EP0915651A4 (fr) 1996-06-27 2001-10-24 Smithkline Beecham Corp Antagonistes des recepteurs d'il-8
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
US20020183395A1 (en) * 2001-04-04 2002-12-05 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
US7368472B2 (en) * 2002-12-27 2008-05-06 H. Lundbeck A/S 1,2,4-Triaminobenzene derivatives useful for treating disorders of the central nervous system
US7906537B2 (en) 2003-03-21 2011-03-15 H. Lundbeck A/S Substituted p-diaminobenzene derivatives
AU2004233941A1 (en) * 2003-04-25 2004-11-11 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
TWI349666B (en) 2004-03-12 2011-10-01 Lundbeck & Co As H Substituted morpholine and thiomorpholine derivatives
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
US7812020B2 (en) 2005-03-03 2010-10-12 H. Lundbeck A/S Substituted pyridine derivatives
MX2007013179A (es) * 2005-04-22 2008-01-16 Wyeth Corp Formas cristalinas de clorhidrato de {[(2r)-7-(diclorofenil)-5- fluoro-2,3-dihidro-1-benzofurano-2-il]metil}amina.
BRPI0610037A2 (pt) * 2005-04-22 2010-05-25 Wyeth Corp derivados de dihidrobenzofurano e uso dos mesmos
WO2006116150A1 (fr) * 2005-04-22 2006-11-02 Wyeth Derives de dihydrobenzofurane et utilisations associees
EP1871358A1 (fr) * 2005-04-22 2008-01-02 Wyeth Derives d'alcanamine de benzofuranyle et leurs utilisations comme agonistes 5-ht2c
AU2006239941A1 (en) * 2005-04-24 2006-11-02 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
MX2008009655A (es) 2006-02-07 2008-09-03 Lundbeck & Co As H Metodo para tratar o reducir los sintomas de la esquizofrenia.
EP1998773A2 (fr) * 2006-03-24 2008-12-10 Wyeth a Corporation of the State of Delaware Nouvelles combinaisons thérapeutiques pour le traitement de la dépression
EP1998781A2 (fr) * 2006-03-24 2008-12-10 Wyeth a Corporation of the State of Delaware Traitement de la douleur
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
AU2007288253B2 (en) * 2006-08-23 2013-05-02 Xenon Pharmaceuticals Inc. Derivatives of 4-(N-azacycloalkyl) anilides 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
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
KR20090083479A (ko) * 2006-11-28 2009-08-03 밸리언트 파마슈티컬즈 인터내셔널 칼륨 채널 조절제로서의 1,4 디아미노 이환 레티가빈 유사체
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
CN101868443A (zh) 2007-09-20 2010-10-20 特拉维夫大学拉莫特有限公司 N-苯基邻氨基苯甲酸衍生物及其用途
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
JP2011528666A (ja) * 2008-07-18 2011-11-24 バレアント プハルマセウトイカルス インターナショナル 放出調節製剤及びその使用方法
US20100323016A1 (en) * 2008-07-18 2010-12-23 Biljana Nadjsombati Modified release formulation and methods of use
US20100323015A1 (en) * 2008-07-18 2010-12-23 Biljana Nadjsombati Modified release formulation and methods of use
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
DE102009013613A1 (de) 2009-03-17 2010-09-23 Ratiopharm Gmbh Trockenverarbeitung von Retigabin
WO2011012659A2 (fr) 2009-07-28 2011-02-03 Medichem S.A. 4-(4-fluorobenzylamino)-1,2-phénylèridicarbonate de diéthyle et ses sels
WO2011039369A2 (fr) 2009-10-02 2011-04-07 Medichem S.A. Formes amorphes d'un dérivé de 2-amino-4-(4-fluorobenzylamino)phénylcarbamate
BR112012017691A2 (pt) 2010-01-20 2016-04-05 Glaxo Group Ltd nova composição
EP2536394A2 (fr) 2010-02-19 2012-12-26 Medichem S.A. Dérivé de phénylcarbamate stabilisé à l'état solide
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 (fr) 2011-07-21 2013-01-24 Arch Pharmalabs Limited Procédé de préparation de rétigabine de formule i et de ses sels pharmaceutiquement acceptables
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
JP6195906B2 (ja) 2012-04-30 2017-09-13 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２−アミノ−４−（ベンジルアミノ）フェニルカルバメート誘導体
WO2014023270A1 (fr) 2012-08-09 2014-02-13 Zentiva, K.S. Sels ou co-cristaux de n-[2-amino-4-[(4-fluorophényl)méthylamino]-phényl]carbamate d'éthyle
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 (fr) * 2014-11-13 2016-05-19 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Carbamates (2-amino-4(arylamino)phényl)
CA3023340A1 (fr) 2016-06-10 2017-12-14 Scifluor Life Sciences, Inc. Derives fluores 2-amino-4-(amino substitue)phenyl carbamate
PT3554490T (pt) 2016-12-16 2022-03-17 Idorsia Pharmaceuticals Ltd Combinação farmacêutica compreendendo um bloqueador de canais de cálcio de tipo t
US11369593B2 (en) 2017-07-14 2022-06-28 Texas Tech University System Functionalized pyridine carbamates with enhanced neuroprotective activity
EP3724163A4 (fr) 2017-12-13 2021-07-28 SciFluor Life Sciences, Inc. Dérivés fluorés 4-(amino substitué)phényl carbamate
US11358930B2 (en) 2018-04-20 2022-06-14 University of Pittsburgh—of the Commonwealth System of Higher Education Selective potassium channel agonists
WO2020157126A1 (fr) 2019-01-29 2020-08-06 Università degli Studi di Salerno Modulateurs de canaux ioniques potassiques et leurs utilisations
CA3162907A1 (fr) 2019-12-02 2021-06-10 Xenon Pharmaceuticals Inc. Formulation pediatrique a liberation immediate d'ezogabine a ouverture des canaux potassiques
MX2023010978A (es) * 2021-03-19 2023-12-07 Xyzagen Inc Profármacos de abridores de canales kv7.
WO2023091461A1 (fr) 2021-11-19 2023-05-25 Icagen, Llc Composés de pyridine comme séquence activatrice de kv7.2
WO2023091554A1 (fr) 2021-11-19 2023-05-25 Icagen, Llc Nouveaux composés hétéroaryle-urée utilisés en tant qu'inhibiteurs de kv7.2
WO2023121992A1 (fr) 2021-12-22 2023-06-29 Icagen, Llc Composés cyclopropyles
WO2023158584A1 (fr) 2022-02-15 2023-08-24 Icagen, Llc Nouveaux dérivés de bicyclopentane

Family Cites Families (5)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
LU91869I2 (fr) 2011-11-14
EP0554543A2 (fr) 1993-08-11
DE4200259A1 (de) 1993-07-15
US5384330A (en) 1995-01-24
GR3019653T3 (en) 1996-07-31
CA2086654C (fr) 2003-09-23
DE59205496D1 (de) 1996-04-04
ES2084914T3 (es) 1996-05-16
EP0554543B1 (fr) 1996-02-28
ATE134611T1 (de) 1996-03-15
MX9300014A (es) 1993-07-01
JP3145220B2 (ja) 2001-03-12
CA2086654A1 (fr) 1993-07-09
EP0554543A3 (en) 1993-10-27
SG48046A1 (en) 1998-04-17
JPH05345752A (ja) 1993-12-27
DE122011100044I1 (de) 2012-01-19
DK0554543T3 (da) 1996-03-18

Similar Documents

Publication Publication Date Title
ZA9311B (en) Novel pharmaceutically active 1,2,4,-triaminobenzene derivatives, processes for their preparation and pharmacuetical compositions containing them
IL110216A0 (en) Valproic acid amide and 2-valproenoic acid amide derivatives, their preparation and pharmaceutical compositions containing them
CA2230082A1 (fr) Composes amide et leur utilisation
GR3018819T3 (en) Novel arylethylamin derivatives, processes for their preparation and pharmaceutical compositions containing them.
HUP0105190A2 (hu) Ketolid antibiotikumok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk
ATE2958T1 (de) Muramyldipeptid-derivate, verfahren zur herstellung dieser verbindungen und diese enthaltende pharmazeutische zusammensetzungen.
AU2505297A (en) Acylated N-hydroxymethyl thalidomide prodrugs having an immunomodulatory effect
HUT65188A (en) Process for preparing cyclopentane and cyclopentene-beta-aminoacids and pharmaceutical compositions containing them as active agent
ZA93494B (en) Napthalene amides and sulphonamides, processes for their preparation and pharmaceutical compositions containing them
AU558261B2 (en) Dialkylaminoalkyoxybenzylalcohol derivatives
ZA944727B (en) Phosphonic acid compounds processes for preparing them and pharmaceutical compositions containing them
ATE161178T1 (de) Pyrazolpyridine für die behandlung der anämie
IL108856A0 (en) Hydroxymethyl-furazancarboxylic acid derivatives, their preparation and pharmaceutical compositions containing them
IL80866A0 (en) Alpha-hydroxy thioethers,their preparation and pharmaceutical compositions containing them
DE69412980D1 (de) Eburnan-Derivate, Verfahren zur ihrer Herstellung und diese enthaltende pharmazeutische Zusammensetzungen
SE9202218D0 (sv) Pharmacologically active alfa-(tertiary-aminomethyl)-benzenemethanol derivatives, pharmaceutical composition containing them, therapeutical use thereof and processes for their preparation
HK1068347A1 (en) Dimeric compounds and their use as anti-viral agents
DE69300197D1 (de) Aminoalkylchromone, Verfahren zu ihrer Herstellung und diese enthaltende Zusammensetzungen.
JPS6354322A (ja) 副作用の軽減されたペネム型またはカルバペネム型抗生物質製剤
EP0331756A4 (en) Agents for prophylaxis and treatment of thrombopenia
DE3885978D1 (de) Cephemverbindungen und Verfahren zu ihrer Herstellung.
ZA933942B (en) Pyrrolothienopyrazine compounds, processes for the preparation thereof and pharmaceutical compositions containing them