ES2180664T3 - Derivados de aril- y heteroarilsulfonamida, obtencion y uso de los mismos en calidad de antagonistas de endotelina. - Google Patents

Derivados de aril- y heteroarilsulfonamida, obtencion y uso de los mismos en calidad de antagonistas de endotelina.

Info

Publication number
ES2180664T3
ES2180664T3 ES95941660T ES95941660T ES2180664T3 ES 2180664 T3 ES2180664 T3 ES 2180664T3 ES 95941660 T ES95941660 T ES 95941660T ES 95941660 T ES95941660 T ES 95941660T ES 2180664 T3 ES2180664 T3 ES 2180664T3
Authority
ES
Spain
Prior art keywords
signifies
alkyl
phenyl
heterocyclyl
substituted phenyl
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
Application number
ES95941660T
Other languages
English (en)
Inventor
Volker Breu
Kaspar Burri
Jean-Marie Cassal
Martine Clozel
Georges Hirth
Bernd-Michael Loffler
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche 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 F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Application granted granted Critical
Publication of ES2180664T3 publication Critical patent/ES2180664T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72Nitrogen atoms
    • C07D213/76Nitrogen atoms to which a second hetero atom is attached
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/22Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/29Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/64Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
    • C07C323/67Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton containing sulfur atoms of sulfonamide groups, bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182Radicals derived from carboxylic acids
    • C07D295/192Radicals derived from carboxylic acids from aromatic carboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Steroid Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

COMPUESTOS DE FORMULA (I) DONDE R 1 SIGNIFICA FENILO, FENILO SUSTITUIDO O HETEROCICLO; R{SUP,2} SIGNIFICA FENILO O FENILO SUSTITUIDO; R{SUP,3} SIGNIFICA HIDROGENO, ALQUILO DE BAJO PESO MOLECULAR, CIANO, CARBOXI, CARBOXI ESTERIFICADO, FENILO, FENILO SUSTITUIDO, HETEROCICLO O UN RESIDUO - CONR{SUP,5}R{SUP,6} O - NR{SUP,5}COR{SUP,7}; R{SUP,4} SIGNIFICA HIDROGENO O ALQUILO DE BAJO PESO MOLECULAR; R{SUP,5} SIGNIFICA HIDROGENO O UN RESIDUO R{SUP,7}, Y R{SUP,6} SIGNIFICA - (CH{SUB,2}){SUB,M}R{SUP,7}; O R{SUP,5} Y R{SUP,6} JUNTO AL ATOMO DE N ASOCIADO A ELLOS SIGNIFICA UN RESTO HETEROCICLO; R{SUP,7} SIGNIFICA FENILO, FENILO SUSTITUIDO, CICLOALQUILO, HETEROCICLO, ALQUILO DE BAJO PESO MOLECULAR, CIANOALQUILO DE BAJO PESO MOLECULAR, HIDROXIALQUILO DE BAJO PESO MOLECULAR, DI - ALQUILAMINO DE BAJO PESO MOLECULAR ALQUILO DE BAJO PESO MOLECULAR, CARBOXIALQUILO DE BAJO PESO MOLECULAR, ALCOXICARBONILO DE BAJO PESO MOLECULAR - ALQUILO DE BAJO PESO MOLECULAR, ALCOXICARBONILAMINO DE BAJO PESO MOLECULAR ALQUILODE BAJO PESO MOLECULAR O FENILO - ALCOXICARBONILO DE BAJO PESO MOLECULAR; R{SUP,A} SIGNIFICA HIDROGENO, ALQUILO DE BAJO PESO MOLECULAR O HIDROXI; R{SUP,B} SIGNIFICA HIDROGENO O ALQUILO DE BAJO PESO MOLECULAR; Z SIGNIFICA HIDROXI, AMINO O UN RESIDUO - OR{SUP,8}, - OC(O)NHR{SUP,8}, - OC(O)OR{SUP,8}, NHC(O)NHR{SUP,8} O - NHC(O)OR{SUP,8}; R{SUP,8} SIGNIFICA HETEROCICLO, FENILO, FENILO SUSTITUIDO O ALQUILO DE BAJO PESO MOLECULAR; A E Y SIGNIFICAN INDEPENDIENTEMENTE OXIGENO O AZUFRE; X SIGNIFICA NITROGENO O CH; M SIGNIFICA 0, 1 O 2; Y N SIGNIFICA 0, 1 O 2; Y SALES UTILES FARMACEUTICAMENTE; SON INHIBIDORES DE LOS RECEPTORES DE ENDOTELINA. POR TANTO PUEDEN UTILIZARSE PARA EL TRATAMIENTO DE ALTERACIONES ASOCIADAS A LAS ACTIVIDADES DE ENDOTELINA, ESPECIALMENTE TRASTORNOS CIRCULATORIOS COMO HIPERTENSION, ISQUEMIA, VASOESPASMO Y ANGINA DE PECHO.
ES95941660T 1994-12-20 1995-12-04 Derivados de aril- y heteroarilsulfonamida, obtencion y uso de los mismos en calidad de antagonistas de endotelina. Expired - Lifetime ES2180664T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH383894 1994-12-20
CH307995 1995-10-31

Publications (1)

Publication Number Publication Date
ES2180664T3 true ES2180664T3 (es) 2003-02-16

Family

ID=31189207

Family Applications (1)

Application Number Title Priority Date Filing Date
ES95941660T Expired - Lifetime ES2180664T3 (es) 1994-12-20 1995-12-04 Derivados de aril- y heteroarilsulfonamida, obtencion y uso de los mismos en calidad de antagonistas de endotelina.

Country Status (25)

Country Link
US (2) US5962682A (es)
EP (1) EP0799206B1 (es)
JP (1) JP2930731B2 (es)
KR (1) KR100432843B1 (es)
CN (1) CN1136192C (es)
AT (1) ATE223899T1 (es)
AU (1) AU695255B2 (es)
BR (1) BR9510533A (es)
CA (1) CA2208011A1 (es)
CZ (1) CZ289090B6 (es)
DE (1) DE69528198T2 (es)
DK (1) DK0799206T3 (es)
ES (1) ES2180664T3 (es)
FI (1) FI116622B (es)
HU (1) HUT77307A (es)
IL (1) IL116410A (es)
MA (1) MA23745A1 (es)
MX (1) MX9704588A (es)
MY (1) MY113214A (es)
NO (1) NO308297B1 (es)
NZ (1) NZ297774A (es)
PT (1) PT799206E (es)
RU (1) RU2163598C2 (es)
TW (1) TW474920B (es)
WO (1) WO1996019455A1 (es)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5962490A (en) 1987-09-25 1999-10-05 Texas Biotechnology Corporation Thienyl-, furyl- and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin
US6613804B2 (en) 1993-05-20 2003-09-02 Encysive Pharmaceuticals, Inc. Biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin
US6541498B2 (en) 1993-05-20 2003-04-01 Texas Biotechnology Benzenesulfonamides and the use thereof to modulate the activity of endothelin
US6342610B2 (en) 1993-05-20 2002-01-29 Texas Biotechnology Corp. N-aryl thienyl-, furyl-, and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin
US6376523B1 (en) 1994-05-20 2002-04-23 Texas Biotechnology Corporation Benzenesulfonamides and the use thereof to modulate the activity of endothelin
DK0799206T3 (da) * 1994-12-20 2003-01-27 Hoffmann La Roche Aryl- og heteroaryl-sulfonamidderivater, fremstillingen deraf og anvendelsen deraf som endothelinantagonister
US5977117A (en) 1996-01-05 1999-11-02 Texas Biotechnology Corporation Substituted phenyl compounds and derivatives thereof that modulate the activity of endothelin
US5804585A (en) 1996-04-15 1998-09-08 Texas Biotechnology Corporation Thieno-pyridine sulfonamides derivatives thereof and related compounds that modulate the activity of endothelin
US6653331B2 (en) * 1996-07-03 2003-11-25 Pharmacia & Upjohn Company Targeted drug delivery using sulfonamide derivatives
HU227183B1 (en) 1997-04-28 2010-09-28 Encysive Pharmaceuticals Inc Sulfonamide derivatives and pharmaceutical compositions containing them for the treatment of endothelin-mediated disorders
US5783705A (en) 1997-04-28 1998-07-21 Texas Biotechnology Corporation Process of preparing alkali metal salys of hydrophobic sulfonamides
US6191170B1 (en) * 1998-01-13 2001-02-20 Tularik Inc. Benzenesulfonamides and benzamides as therapeutic agents
CA2315614C (en) 1999-07-29 2004-11-02 Pfizer Inc. Pyrazoles
CN1407973A (zh) * 1999-12-22 2003-04-02 埃科特莱茵药品有限公司 丁炔二醇衍生物
CA2395684C (en) 1999-12-31 2012-01-03 Texas Biotechnology Corporation Sulfonamides and derivatives thereof that modulate the activity of endothelin
US6387915B2 (en) 2000-05-31 2002-05-14 Pfizer Inc. Isoxazole-sulfonamide endothelin antagonists
US6670362B2 (en) 2000-09-20 2003-12-30 Pfizer Inc. Pyridazine endothelin antagonists
SE0102764D0 (sv) 2001-08-17 2001-08-17 Astrazeneca Ab Compounds
NZ541234A (en) 2002-12-20 2008-06-30 Amgen Inc Asthma and allergic inflammation modulators
WO2004074438A2 (en) * 2003-02-14 2004-09-02 Smithkline Beecham Corporation Ccr8 antagonists
WO2004073619A2 (en) * 2003-02-14 2004-09-02 Smithkline Beecham Corporation Ccr8 antagonists
CA2707789A1 (en) 2007-12-19 2009-07-09 Amgen Inc. Phenyl acetic acid derivatives as inflammation modulators
WO2010015623A1 (en) * 2008-08-05 2010-02-11 Farmaprojects, S. A. Process for the preparation of endothelin receptor antagonists
AR076221A1 (es) 2009-04-09 2011-05-26 Astrazeneca Ab Derivado de pirazol [4,5-e] pirimidina y su uso para tratar diabetes y obesidad
CN110092743B (zh) * 2018-01-30 2022-03-15 中国医学科学院药物研究所 苯甲酰胺类化合物及其制备方法、用途和药物组合物

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1521932A (en) * 1976-03-08 1978-08-16 Labaz Sulphonamide derivatives and process for preparing the same
GB8708233D0 (en) * 1987-04-07 1987-05-13 Smith Kline French Lab Pharmaceutically active compounds
EP0472053B1 (en) * 1990-08-20 1998-06-17 Eisai Co., Ltd. Sulfonamide derivatives
TW270116B (es) * 1991-04-25 1996-02-11 Hoffmann La Roche
RU2086544C1 (ru) * 1991-06-13 1997-08-10 Хоффманн-Ля Рош АГ Бензолсульфонамидные производные пиримидина или их соли, фармацевтическая композиция для лечения заболеваний, связанных с активностью эндотелина
NZ247440A (en) * 1992-05-06 1995-04-27 Squibb & Sons Inc Phenyl sulphonamide derivatives, preparation and pharmaceutical compositions thereof
TW287160B (es) * 1992-12-10 1996-10-01 Hoffmann La Roche
IL111959A (en) * 1993-12-17 2000-07-16 Tanabe Seiyaku Co N-(polysubstituted pyrimidin-4-yl) benzenesulfonamide derivatives their preparation and pharmaceutical compositions containing them
GB9504854D0 (en) * 1994-03-31 1995-04-26 Zeneca Ltd Nitrogen derivatives
DK0799206T3 (da) * 1994-12-20 2003-01-27 Hoffmann La Roche Aryl- og heteroaryl-sulfonamidderivater, fremstillingen deraf og anvendelsen deraf som endothelinantagonister

Also Published As

Publication number Publication date
FI116622B (fi) 2006-01-13
MA23745A1 (fr) 1996-07-01
AU4301696A (en) 1996-07-10
FI972629A (fi) 1997-06-18
CZ289090B6 (cs) 2001-10-17
CZ187397A3 (en) 1997-09-17
KR100432843B1 (ko) 2004-10-14
JP2930731B2 (ja) 1999-08-03
US5962682A (en) 1999-10-05
DK0799206T3 (da) 2003-01-27
AU695255B2 (en) 1998-08-13
NO308297B1 (no) 2000-08-28
FI972629A0 (fi) 1997-06-18
CN1136192C (zh) 2004-01-28
PT799206E (pt) 2003-01-31
RU2163598C2 (ru) 2001-02-27
MX9704588A (es) 1998-07-31
US6133442A (en) 2000-10-17
EP0799206B1 (en) 2002-09-11
IL116410A (en) 2000-08-13
WO1996019455A1 (en) 1996-06-27
DE69528198D1 (de) 2002-10-17
NO972841L (no) 1997-08-18
CN1170405A (zh) 1998-01-14
HUT77307A (hu) 1998-03-30
TW474920B (en) 2002-02-01
BR9510533A (pt) 1998-07-14
IL116410A0 (en) 1996-03-31
EP0799206A1 (en) 1997-10-08
NO972841D0 (no) 1997-06-19
ATE223899T1 (de) 2002-09-15
NZ297774A (en) 1998-10-28
DE69528198T2 (de) 2003-07-31
JPH10500997A (ja) 1998-01-27
MY113214A (en) 2001-12-31
CA2208011A1 (en) 1996-06-27

Similar Documents

Publication Publication Date Title
ES2180664T3 (es) Derivados de aril- y heteroarilsulfonamida, obtencion y uso de los mismos en calidad de antagonistas de endotelina.
TR199802269T2 (xx) Endotelin resept�r antagonistleri olarak faydal� indol t�revleri.
ES2159749T3 (es) Derivados de bencilamino-2-metil-propanamidas 2-(4-sustituidas).
LV11617A (lv) Morfolins un tiomorfolins ar tahikinina receptoru antagonistu ipasibam
SE9702773D0 (sv) Novel compounds
DE69903333D1 (de) Crf rezeptor-antagonisten und darauf bezogene methoden
TR199801734T2 (xx) Yeni arilglisinamid t�revleri, �retim y�ntemleri.
TR200103183T2 (tr) Amin türevi bileşimler
AU9281198A (en) Benzofuran derivatives
DE3575140D1 (de) Dreizyklische oxindole als antientzuendungsmittel.
ES2099800T3 (es) Dihidropiridinas utilizables en la terapia antitumoral.
MY131762A (en) Pharmaceutical compounds
PE17098A1 (es) Nuevas sulfonamidas
DE69423055T2 (de) Indol Derivate als Glutamat Antagonisten
EA199900684A1 (ru) Производные иминоазаантрациклинона для лечения амилоидоза
ATE229997T1 (de) Mischungen von faserreaktiven farbstoffen und deren verwendung
DK0782574T3 (da) Bicycliske carboxiamider som 5-HT1A-receptorligander
ATE119523T1 (de) Isochinolinderivate und ihre salze als proteasehemmer.
ES8506032A1 (es) Un procedimiento para la preparacion de un derivado de ergolina
CO4130164A1 (es) Compuestos y composiciones insecticidas a base de diamino- quinazolinas y metodos de utilizacion