LTIP227A - New pharmacologically active catechol derivatives - Google Patents

New pharmacologically active catechol derivatives

Info

Publication number
LTIP227A
LTIP227A LTIP227A LTIP227A LTIP227A LT IP227 A LTIP227 A LT IP227A LT IP227 A LTIP227 A LT IP227A LT IP227 A LTIP227 A LT IP227A LT IP227 A LTIP227 A LT IP227A
Authority
LT
Lithuania
Prior art keywords
pharmacologically active
catechol derivatives
new pharmacologically
active catechol
new
Prior art date
Application number
LTIP227A
Other languages
Lithuanian (lt)
Inventor
Johannes Reijo Backstrom
Erkki Honkanen
Britt Inge LINDEN
Aarne Olavi Erkki NISSINEN
Aino Pippuri
Pentti Pohto
Tapio Korkolainen
Original Assignee
Orion-Yhtymae Oy
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
Priority claimed from GB909009565A external-priority patent/GB9009565D0/en
Priority claimed from GB919101563A external-priority patent/GB9101563D0/en
Application filed by Orion-Yhtymae Oy filed Critical Orion-Yhtymae Oy
Publication of LTIP227A publication Critical patent/LTIP227A/en
Publication of LT3137B publication Critical patent/LT3137B/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52—Two oxygen atoms
    • C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
    • 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
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00—General protective or antinoxious agents
    • A61P39/06—Free radical scavengers or antioxidants
    • 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
    • A61P9/08—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
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/96—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • C07D239/38—One sulfur atom
    • C07D239/40—One sulfur atom as doubly bound sulfur atom or as unsubstituted mercapto radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/60—Three or more oxygen or sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/60—Three or more oxygen or sulfur atoms
    • C07D239/62—Barbituric acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
    • C07D263/46—Sulfur atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Toxicology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Transplantation (AREA)
  • Biochemistry (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Steroid Compounds (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

Formulę (1) atitinkantys katecholio junginiai, kurioje R1 reiškia tokį elektriškai neigiamą pakaitą, kaip nitro-, halogeno ar ciano-grupė, o R2 yra grupė, pasirinkta iš (1a) ir (1b), kur R reiškia vandenilį arba alkilo, cikloalkilo ar arilo grupę, kurioje X1, X2, Y ir Z nepriklausomai reiškia deguonį ar sierą, priklausančius NR, kur R gali turėti aukščiau nurodytas reikšmes ir farmaciškai priimtinos jų druskos bei esterai, naudingi dėl lipidų peroksidacijos atsiradusio audinių pakenkimo profilaktikai ir gydymui.The catechol compounds of formula (1) wherein R 1 represents an electrically negative substituent such as nitro, halogen or cyano, and R 2 is a group selected from (1a) and (1b) wherein R represents hydrogen or alkyl, cycloalkyl or an aryl group wherein X 1, X 2, Y and Z independently represent oxygen or sulfur, which are NR, wherein R may have the above values and pharmaceutically acceptable salts and esters thereof useful for prophylaxis and treatment of tissue damage resulting from lipid peroxidation.

LTIP227A 1990-04-27 1992-11-17 New pharmacologically active catechol derivatives LT3137B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB909009565A GB9009565D0 (en) 1990-04-27 1990-04-27 New pharmacologically active catechol derivatives
GB919101563A GB9101563D0 (en) 1991-01-24 1991-01-24 New pharmacologically active catechol derivatives
PCT/FI1991/000124 WO1991017151A1 (en) 1990-04-27 1991-04-26 New pharmacologically active catechol derivatives

Publications (2)

Publication Number Publication Date
LTIP227A true LTIP227A (en) 1994-08-25
LT3137B LT3137B (en) 1995-01-31

Family

ID=26297011

Family Applications (1)

Application Number Title Priority Date Filing Date
LTIP227A LT3137B (en) 1990-04-27 1992-11-17 New pharmacologically active catechol derivatives

Country Status (17)

Country Link
US (3) US5362733A (en)
EP (1) EP0526598B1 (en)
JP (1) JP2972377B2 (en)
KR (1) KR100207144B1 (en)
AT (1) ATE146462T1 (en)
AU (1) AU646464B2 (en)
CA (1) CA2080917C (en)
DE (1) DE69123738T2 (en)
FI (1) FI95129C (en)
HU (1) HU214872B (en)
IE (1) IE911430A1 (en)
LT (1) LT3137B (en)
LV (1) LV10097B (en)
NO (1) NO301928B1 (en)
PL (1) PL166269B1 (en)
PT (1) PT97507B (en)
WO (1) WO1991017151A1 (en)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0722729A3 (en) * 1995-01-23 1997-11-26 Eli Lilly And Company Aryl-substituted rhodanines for treating multiple sclerosis
WO1998033777A1 (en) * 1997-01-31 1998-08-06 Shionogi & Co., Ltd. Compounds having metalloprotease inhibitory activity
JP2001514663A (en) * 1997-03-12 2001-09-11 エスモンド，ロバート ダブリュー． Methods for treating or preventing Alzheimer's disease
US20040058873A1 (en) * 1998-03-12 2004-03-25 Esmond Robert W. Method for treating or preventing Alzheimer's disease
US6191154B1 (en) 1998-11-27 2001-02-20 Case Western Reserve University Compositions and methods for the treatment of Alzheimer's disease, central nervous system injury, and inflammatory diseases
AU7961800A (en) * 1999-10-28 2001-05-08 Kyowa Hakko Kogyo Co. Ltd. Thiazolidinedione derivatives
WO2002053155A1 (en) * 2000-12-30 2002-07-11 Geron Corporation Telomerase inhibitor
WO2003009807A2 (en) * 2001-07-23 2003-02-06 Galileo Laboratories, Inc. Cytoprotective compounds, pharmaceutical and cosmetic formulations, and methods
US6679051B1 (en) * 2002-07-31 2004-01-20 Ford Global Technologies, Llc Diesel engine system for use with emission control device
BRPI0416752B8 (en) 2003-11-21 2021-05-25 Actelion Pharmaceuticals Ltd pharmaceutical composition, use of one or more compounds, and compounds
USRE43833E1 (en) 2003-11-21 2012-11-27 Actelion Pharmaceuticals Ltd. Thiazolidin-4-one derivatives
US7872027B2 (en) * 2006-02-17 2011-01-18 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Low molecular weight Myc-max inhibitors
DK2094676T3 (en) * 2006-11-23 2013-06-10 Actelion Pharmaceuticals Ltd NEW PROCEDURE FOR THE PREPARATION OF 2-IMINOTHIAZOLIDIN-4-ON DERIVATIVES
US8912340B2 (en) 2006-11-23 2014-12-16 Actelion Pharmaceuticals Ltd. Process for the preparation of 2-imino-thiazolidin-4-one derivatives
FR2919608B1 (en) * 2007-08-01 2012-10-05 Univ Rennes IMIDAZOLON DERIVATIVES, PREPARATION METHOD AND BIOLOGICAL APPLICATIONS
AU2009274571A1 (en) * 2008-07-23 2010-01-28 Massachusetts Institute Of Technology Activation of histone deacetylase 1 (HDAC1) protects against DNA damage and increases neuronal survival
KR101411838B1 (en) * 2011-02-09 2014-06-27 부산대학교 산학협력단 New compounds having skin whitening, antioxidant and PPAR activity, and medical use thereof
PT2734510T (en) 2011-07-22 2019-02-13 Massachusetts Inst Technology Activators of class i histone deacetlyases (hdacs) and uses thereof
HUE050733T2 (en) 2012-08-17 2021-01-28 Actelion Pharmaceuticals Ltd Process (2Z, 5Z) -5- (3-chloro-4 - ((R) -2,3-dihydroxypropoxy) benzylidene) -2- (propylimino) -3- (O-tolyl) thiazolidin-4-one and an intermediate used in this process
DK3439667T3 (en) 2016-04-05 2024-04-02 Immune Sensor Llc CGAS ANTAGONIST COMPOUNDS
JPWO2022163843A1 (en) * 2021-02-01 2022-08-04

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1038050B (en) * 1955-11-17 1958-09-04 Farmaceutici Italia S A Soc Process for the preparation of 5- (3 ', 4'-dioxybenzylidene) derivatives of heterocyclic compounds
US4013770A (en) * 1972-06-16 1977-03-22 Canada Packers Limited Antiviral 5-(substituted benzal) hydantoins
US4264617A (en) * 1972-06-16 1981-04-28 Canada Packers, Limited Antiviral 5-(substituted benzal) hydantoins
GB1439318A (en) * 1972-06-16 1976-06-16 Canada Packers Ltd 5-substituted benzal- hydantoins derivatives
GB1601310A (en) * 1978-05-23 1981-10-28 Lilly Industries Ltd Aryl hydantoins
JPS5697277A (en) * 1980-01-07 1981-08-05 Takeda Chem Ind Ltd Thiazolidine derivative
DE3013647C2 (en) * 1980-04-09 1985-07-11 Degussa Ag, 6000 Frankfurt Process for the preparation of 5-arylidene hydantoins (B)
DE3013626C2 (en) * 1980-04-09 1985-06-27 Degussa Ag, 6000 Frankfurt Process for the preparation of 5-arylidene hydantoins (A)
JPS60233063A (en) * 1984-05-02 1985-11-19 Showa Denko Kk Production of 5-benzylidenehydantoin
US4650876A (en) * 1984-08-17 1987-03-17 Stauffer Chemical Company Hydrogenation of substituted, unsaturated hydantoins to substituted, saturated hydantoins
US4582903A (en) * 1984-08-17 1986-04-15 Stauffer Chemical Company Synthesis of unsaturated hydantoins with an inexpensive catalyst
PT83152B (en) * 1985-08-09 1989-03-30 Lilly Co Eli PROCESS FOR THE PREPARATION OF DI-T-BUTYLPHENOIC COMPOUNDS
US5208250A (en) * 1988-05-25 1993-05-04 Warner-Lambert Company Known and selected novel arylmethylenyl derivatives of thiazolidinones, imidazolidinones and oxazolidinones useful as antiallergy agents and anti-inflammatory agents
US5306822A (en) * 1988-05-25 1994-04-26 Warner-Lambert Company Arylmethylenyl derivatives of oxazolidinone
IE940525L (en) * 1988-05-25 1989-11-25 Warner Lambert Co Known and selected novel arylmethylenyl derivatives of¹thiazolidinones, imidazolidinones and oxazolidinones useful¹as antiallergy agents and antiinflammatory agents
GB8911073D0 (en) * 1989-05-15 1989-06-28 Fujisawa Pharmaceutical Co New benzofuran derivatives,a process for the preparation thereof and pharmaceutical composition comprising the same
JPH1052765A (en) 1996-08-09 1998-02-24 Sukematsu Iwashita Reinforcing material pressure welding device

Also Published As

Publication number Publication date
HU214872B (en) 1998-07-28
PL166269B1 (en) 1995-04-28
NO301928B1 (en) 1997-12-29
KR100207144B1 (en) 1999-07-15
ATE146462T1 (en) 1997-01-15
US5362733A (en) 1994-11-08
FI924838A0 (en) 1992-10-23
DE69123738D1 (en) 1997-01-30
PT97507A (en) 1992-01-31
IE911430A1 (en) 1991-11-06
FI95129B (en) 1995-09-15
FI95129C (en) 1995-12-27
FI924838A7 (en) 1992-10-23
HU9203369D0 (en) 1993-01-28
NO924132L (en) 1992-12-23
KR930700468A (en) 1993-03-15
CA2080917A1 (en) 1991-10-28
NO924132D0 (en) 1992-10-26
LV10097B (en) 1995-02-20
DE69123738T2 (en) 1997-07-03
AU646464B2 (en) 1994-02-24
EP0526598A1 (en) 1993-02-10
CA2080917C (en) 2001-06-12
JP2972377B2 (en) 1999-11-08
US5614541A (en) 1997-03-25
US5889037A (en) 1999-03-30
JPH05331148A (en) 1993-12-14
EP0526598B1 (en) 1996-12-18
LV10097A (en) 1994-05-10
AU7761891A (en) 1991-11-27
HUT65662A (en) 1994-07-28
PT97507B (en) 1998-08-31
WO1991017151A1 (en) 1991-11-14
LT3137B (en) 1995-01-31

Similar Documents

Publication Publication Date Title
CA2080917A1 (en) New pharmacologically active catechol derivatives
DE69433353D1 (en) BICYCLIC, HETEROCYCLIC SULFONAMIDES AND SULFONIC ACID ESTERS
ES2194986T3 (en) CARBONIL-PIPERAZINYL AND PIPERIDINYL COMPOUNDS THAT INHIBIT THE FARNESIL-PROTEIN-TRANSFERASA.
NO171785C (en) ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY EFFECTIVE CHINAZOLINE DERIVATIVES
DE68924681D1 (en) Heterocyclic bisphosphonic acid derivatives.
AU647904B2 (en) Novel nonsedative antihistaminics derived from benzimidazoles
RU95110762A (en) Derivatives of 5-hydrazine quinolone, composition for treatment or prophylaxis of infection diseases, method for treatment or prophylaxis
DE69624143D1 (en) PHOSPHONSAUREDIESTER DERIVATIVES
NO862621L (en) PROCEDURE FOR PREPARING PYRIDON CARBOXYLIC ACID DERIVATIVES.
FI914187A0 (en) The process is prepared from a 1-methylcarbapenem derivative of formula (I)
ATE252074T1 (en) PHENYLALKYLCARBOXIC ACID DERIVATIVES
ATE267826T1 (en) PHARMACEUTICALLY ACTIVE SULFONYL HYDRAZIDE DERIVATIVES
IE821434L (en) Arylsulphonamides.
NO168243C (en) ANALOGUE PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVE ALKANSULPHONANILIDE DERIVATIVES.
IS3828A (en) Similar method for preparing new derivatives of thiazolidinone and oxazolidinone useful for vasodilatation
AU6731100A (en) Integrase inhibitors containing aromatic heterocycle derivatives
AU7587096A (en) Inhibitor of Kainic acid neurotoxicity and pyridothiazine derivative
AU692334B2 (en) Thiazolidinone compounds or angina pectoris remedy or preventive containing the same as active ingredient
ES2158290T3 (en) OPTICALLY ACTIVE THIAZOLIDINONE DERIVATIVES.
DK0688218T3 (en) Interleukin-1 inhibitor
EP1197211A4 (en) Preventive and therapeutic agents for cancer
DE59006477D1 (en) Five-ring heterocyclically fused quinoline derivatives.
AU553765B2 (en) Biologically active heterocyclic hydroximidates and thiolhydroximidates and carbamate ester derivatives thereof
EP0314432A3 (en) Fungicidal pyridyl sulphenyl carbamates
NO20004679L (en) Pharmaceutical composition containing a cysteine protease inhibitor for prevention and therapy of brain tissue deterioration

Legal Events

Date Code Title Description
MM9A Lapsed patents

Effective date: 20021117