ES2092835T3 - N-ciano-n'-piridilguanidinas como antagonistas de la serotonina. - Google Patents

N-ciano-n'-piridilguanidinas como antagonistas de la serotonina.

Info

Publication number
ES2092835T3
ES2092835T3 ES93919045T ES93919045T ES2092835T3 ES 2092835 T3 ES2092835 T3 ES 2092835T3 ES 93919045 T ES93919045 T ES 93919045T ES 93919045 T ES93919045 T ES 93919045T ES 2092835 T3 ES2092835 T3 ES 2092835T3
Authority
ES
Spain
Prior art keywords
nitro
halogen
ciano
alkyl
hydrogen
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
ES93919045T
Other languages
English (en)
Inventor
Erik Bramm
Hans Jorgen Petersen
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.)
Leo Pharma AS
Original Assignee
Leo Pharmaceutical Products Ltd AS
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 Leo Pharmaceutical Products Ltd AS filed Critical Leo Pharmaceutical Products Ltd AS
Application granted granted Critical
Publication of ES2092835T3 publication Critical patent/ES2092835T3/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
    • C07D213/75Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Psychiatry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

LA PRESENTE INVENCION ES RELATIVA A COMPUESTOS DESCONOCIDOS HASTA AHORA DE FORMULA (I) O SUS FORMAS TAUTOMERAS, ESTANDO LA CONEXION AL ANILLO DE PIRIDINA EN LA POSICION 3- O 4-, EN LA QUE R'', R'''' SON IGUALES O DIFERENTES Y REPRESENTAN HIDROGENO, HALOGENO, TRIFLUOROMETILO, HIDROXI, ALQUILO C1-C4, GRUPOS NITRO O CIANO. ALQUILENO REPRESENTA UNA CADENA DE CARBONO LINEAL O RAMIFICADA DE C1 A C8, QUE PUEDE SER SUSTITUIDO POR HIDROXI O HALOGENO, GRUPOS NITRO O CIANO. X REPRESENTA OXIGENO, -S(O)NDONDE N REPRESENTA UN ENTERO DE 0 A 2, O =NR1 DONDE R1 ES HIDROGENO O ALQUILO C1-C4. R REPRESENTA HIDROGENO O UNO O MAS RADICALES ALQUILO C1-C4 O ALCOXILO, HIDROXILO, HALOGENO, TRIFLUOROMETILO, CIANO, CARBOXAMIDO, SULFAMOILO O NITRO. LOS COMPUESTOS PRESENTADOS SON VALIOSOS EN LA PRACTICA HUMANA Y VETERINARIA COMO ANTAGONISTAS DE RECEPTOR DE SEROTONINA SELECTIVA.
ES93919045T 1992-09-15 1993-09-13 N-ciano-n'-piridilguanidinas como antagonistas de la serotonina. Expired - Lifetime ES2092835T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB929219472A GB9219472D0 (en) 1992-09-15 1992-09-15 Chemical compounds

Publications (1)

Publication Number Publication Date
ES2092835T3 true ES2092835T3 (es) 1996-12-01

Family

ID=10721912

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93919045T Expired - Lifetime ES2092835T3 (es) 1992-09-15 1993-09-13 N-ciano-n'-piridilguanidinas como antagonistas de la serotonina.

Country Status (16)

Country Link
US (1) US5563160A (es)
EP (1) EP0660823B1 (es)
JP (1) JP3485567B2 (es)
KR (1) KR100292592B1 (es)
AT (1) ATE141262T1 (es)
AU (1) AU670816B2 (es)
CA (1) CA2143756C (es)
DE (1) DE69304076T2 (es)
DK (1) DK0660823T3 (es)
ES (1) ES2092835T3 (es)
FI (1) FI109118B (es)
GB (1) GB9219472D0 (es)
GR (1) GR3021015T3 (es)
NZ (1) NZ255330A (es)
RU (1) RU2141951C1 (es)
WO (1) WO1994006770A1 (es)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5696140A (en) * 1992-09-15 1997-12-09 Leo Pharmaceutical Products Ltd. N-cyano-N'-pyridylguanidines as serotonin antagonists
EP0795328A1 (en) * 1996-03-15 1997-09-17 Pfizer Inc. Use of naphthalene derivatives in treating lung carcinoma
US5869497A (en) * 1996-03-15 1999-02-09 Eli Lilly And Company Method of treating or ameliorating the symptoms of common cold or allergic rhinitis
GB9711125D0 (en) * 1997-05-29 1997-07-23 Leo Pharm Prod Ltd Novel cyanoguanidines
GB9711123D0 (en) * 1997-05-29 1997-07-23 Leo Pharm Prod Ltd Novel cyanoguanidines
GB9711122D0 (en) * 1997-05-29 1997-07-23 Leo Pharm Prod Ltd Novel cyanoguanidines
GB9711127D0 (en) * 1997-05-29 1997-07-23 Leo Pharm Prod Ltd Novel cyanoguanidines
GB9711126D0 (en) * 1997-05-29 1997-07-23 Leo Pharm Prod Ltd Cyanoamidines
GB9711119D0 (en) * 1997-05-29 1997-07-23 Leo Pharm Prod Ltd Novel cyanoguanidines
GB9711124D0 (en) 1997-05-29 1997-07-23 Leo Pharm Prod Ltd Novel cyanoguanidines
AU762615B2 (en) * 1998-06-15 2003-07-03 Arch Development Corporation Combination of radiotherapy and anti-angiogenic factors
WO2000061561A1 (en) * 1999-04-09 2000-10-19 Shionogi Bioresearch Corp. Cyanoguanidine compounds
US6417207B1 (en) 1999-05-12 2002-07-09 Nitromed, Inc. Nitrosated and nitrosylated potassium channel activators, compositions and methods of use
AU1494702A (en) 2000-11-21 2002-06-03 Leo Pharma As Cyanoguanidine prodrugs
ATE442362T1 (de) * 2001-05-24 2009-09-15 Leo Pharma As Pyridylcyanoguanidin verbindungen
US20030045515A1 (en) * 2001-05-24 2003-03-06 Lise Binderup Combination medicament for treatment of neoplastic diseases
GB0217920D0 (en) * 2002-04-23 2002-09-11 Aventis Pharm Prod Inc Interleukin-4 Gene Expression inhibitors
CA2485351C (en) * 2002-05-17 2011-12-06 Leo Pharma A/S Cyanoguanidine prodrugs
US7253193B2 (en) 2002-05-17 2007-08-07 Leo Pharma A/S Cyanoguanidine prodrugs
JP4935073B2 (ja) * 2003-10-14 2012-05-23 味の素株式会社 エーテル誘導体
DE102004008141A1 (de) * 2004-02-19 2005-09-01 Abbott Gmbh & Co. Kg Guanidinverbindungen und ihre Verwendung als Bindungspartner für 5-HT5-Rezeptoren
ES2572777T3 (es) 2004-12-22 2016-06-02 Leo Pharma A/S Compuestos novedosos de cianoguanidina
EP1917244A2 (de) 2005-08-24 2008-05-07 Abbott GmbH & Co. KG Hetaryl substituierte guanidinverbindungen und ihre verwendung als bindungspartner für 5-ht5-rezeptoren
WO2009072004A2 (en) * 2007-09-26 2009-06-11 Gemin X Pharmaceuticals Canada, Inc. Compositions and methods for effecting nad+ levels using a nicotinamide phosphoribosyl transferase inhibitor
US8173677B2 (en) 2007-09-26 2012-05-08 Gemin X Pharmaceuticals Canada Inc. Compositions and methods for effecting NAD+ levels using a nicotinamide phosphoribosyl transferase inhibitor
CA2751495C (en) 2009-02-06 2013-08-20 Tianjin Hemay Bio-Tech Co., Ltd. Pharmaceutical compositions comprising a pyridyl cyanoguanidine and cyclodextrin and/or derivatives thereof
US8912184B1 (en) 2010-03-01 2014-12-16 Alzheimer's Institute Of America, Inc. Therapeutic and diagnostic methods
JP2013540781A (ja) 2010-10-26 2013-11-07 ティエンジン ホーメイ バイオ−テック カンパニー, リミテッド N−(6−(4−クロロフェノキシ)ヘキシル)−n’−シアノ−n’’−(4−ピリジル)グアニジンの結晶多形とその製造及び使用

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1489879A (en) * 1974-12-20 1977-10-26 Leo Pharm Prod Ltd N'-cyano-n'-3-pyridylguanidines
CA2009074C (en) * 1989-02-03 1999-07-27 David Wayne Robertson Improvements in and relating to guanidine derivatives
GB2242628A (en) * 1990-04-06 1991-10-09 Sandoz Ltd Asthma prophylactic use of K+ channel activators

Also Published As

Publication number Publication date
CA2143756A1 (en) 1994-03-31
US5563160A (en) 1996-10-08
NZ255330A (en) 1997-06-24
CA2143756C (en) 2003-11-11
DE69304076D1 (de) 1996-09-19
RU2141951C1 (ru) 1999-11-27
AU4945693A (en) 1994-04-12
WO1994006770A1 (en) 1994-03-31
DE69304076T2 (de) 1997-04-03
GB9219472D0 (en) 1992-10-28
FI951189L (fi) 1995-03-14
FI951189A0 (fi) 1995-03-14
KR100292592B1 (ko) 2001-09-17
ATE141262T1 (de) 1996-08-15
AU670816B2 (en) 1996-08-01
GR3021015T3 (en) 1996-12-31
EP0660823B1 (en) 1996-08-14
JPH08501539A (ja) 1996-02-20
DK0660823T3 (da) 1996-09-23
EP0660823A1 (en) 1995-07-05
KR950702964A (ko) 1995-08-23
FI109118B (fi) 2002-05-31
RU95105437A (ru) 1996-10-27
JP3485567B2 (ja) 2004-01-13

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