ES2195374T3 - Derivados de tiadiazolil-piridazina que impiden la angiogenesis. - Google Patents

Derivados de tiadiazolil-piridazina que impiden la angiogenesis.

Info

Publication number
ES2195374T3
ES2195374T3 ES98940098T ES98940098T ES2195374T3 ES 2195374 T3 ES2195374 T3 ES 2195374T3 ES 98940098 T ES98940098 T ES 98940098T ES 98940098 T ES98940098 T ES 98940098T ES 2195374 T3 ES2195374 T3 ES 2195374T3
Authority
ES
Spain
Prior art keywords
sup
sub
alk
alkyl
formula
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
ES98940098T
Other languages
English (en)
Inventor
Raymond Antoine Stokbroekx
Marc Andre Ceusters
Der Aa Marcel Jozef Maria Van
Marcel Gerebernus Maria Luyckx
Marc Willems
Robert W Tuman
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.)
Janssen Pharmaceutica NV
Original Assignee
Janssen Pharmaceutica NV
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 Janssen Pharmaceutica NV filed Critical Janssen Pharmaceutica NV
Application granted granted Critical
Publication of ES2195374T3 publication Critical patent/ES2195374T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/433—Thidiazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/06—Antipsoriatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • 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
    • A61P35/00—Antineoplastic agents
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/83—Thioacids; Thioesters; Thioamides; Thioimides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
    • C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D241/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms
    • C07D241/28—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms in which said hetero-bound carbon atoms have double bonds to oxygen, sulfur or nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01—Five-membered rings
    • C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/08—1,2,4-Thiadiazoles; Hydrogenated 1,2,4-thiadiazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01—Five-membered rings
    • C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
    • C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
    • C07D285/135—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic 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
    • C07D295/04—Heterocyclic 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 with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14—Heterocyclic 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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/155—Heterocyclic 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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Cardiology (AREA)
  • Dermatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Lubricants (AREA)
  • Paper (AREA)
  • Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)

Abstract

La invención se refiere a compuestos de fórmula (I), a las formas N-óxido, las sales de adición de ácido farmacéuticamente aceptables y las formas etereoquímicamente isoméricas de éstos, en la fórmula (I) R{sup,1} es H, alquilo C{sub,1-6}, alcoxi C{sub,1-6}, alquiltio C{sub,1-6}, amino, mono- o diamino-(alquilo C{sub,1-6}), Ar{sup,1}, Ar{sup,1}-NH-, cicloalquilo C{sub,3-6}, hidroximetilo o benciloximetilo; R{sup,2} y R{sup,3} son H o juntos pueden formar un radical bivalente de fórmula -CH=CH-CH=CH-; R{sup,4}, R{sup,5} y R{sup,6} se seleccionan cada uno independientemente entre H, halo, alquilo C{sub,1-6}, alcoxilo C{sub,1-6}, trifluorometilo, nitro, amino, ciano, azido, alcoxi C{sub,1-6} alquilo C{sub,1-6}, alquiltio C{sub,1-6}, alcoxicarbonilo C{sub,1-6} o Het{sup,1}; o cuando R{sup,4} y R{sup,5} están juntos uno al otro, se pueden unir para formar un radical de fórmula -CH=CH-CH=CH-, A es un radical bivalente de fórmula NR{sup,7}, NR{sup,7}-Alk-X-, NR{sup,7}-Alk-X-Alk{sup,2}-, O-Alk{sup,1}-X-O-Alk{sup,1}-X-Alk{sup,2}- o bien S-Alk{sup,1}-X-; en los que X es un enlace directo, -O-, -S-, C=O, -NR{sup,8}- o bien Het{sup,2}; R{sup,7} es H, alquilo C{sub,1-6} o Ar{sup,2}metilo; R{sup,8} es H, alquilo C{sub,1-6} o Ar{sup,2} metilo; Alk{sup,1} es alcanedilo C{sub,1-6}; Alk{sup,2} es alcanedilo C{sub,1-4}; Ar{sup,1} y Ar{sup,2} son fenilos opcionalmente sustituidos; fenilo; Het{sup,1} y Het{sup,2} son heterociclos opcionalmente sustituidos, que tienen actividad inhibidora de la angiogénesis, su preparación, los compuestos que los contiene y su empleo como medicamentos.
ES98940098T 1997-06-24 1998-06-22 Derivados de tiadiazolil-piridazina que impiden la angiogenesis. Expired - Lifetime ES2195374T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP97201930 1997-06-24
US5219497P 1997-07-10 1997-07-10

Publications (1)

Publication Number Publication Date
ES2195374T3 true ES2195374T3 (es) 2003-12-01

Family

ID=8228477

Family Applications (1)

Application Number Title Priority Date Filing Date
ES98940098T Expired - Lifetime ES2195374T3 (es) 1997-06-24 1998-06-22 Derivados de tiadiazolil-piridazina que impiden la angiogenesis.

Country Status (24)

Country Link
EP (1) EP0991649B1 (es)
JP (1) JP2002512630A (es)
CN (1) CN1198822C (es)
AT (1) ATE235489T1 (es)
AU (1) AU732129B2 (es)
BR (1) BR9810321A (es)
CA (1) CA2294551A1 (es)
CZ (1) CZ296000B6 (es)
DE (1) DE69812623T2 (es)
DK (1) DK0991649T3 (es)
EE (1) EE03828B1 (es)
ES (1) ES2195374T3 (es)
HU (1) HU225154B1 (es)
ID (1) ID23443A (es)
IL (1) IL133652A (es)
MY (1) MY120046A (es)
NZ (1) NZ501649A (es)
PL (1) PL191409B1 (es)
PT (1) PT991649E (es)
RU (1) RU2194049C2 (es)
SK (1) SK283705B6 (es)
TR (1) TR199902955T2 (es)
WO (1) WO1998058929A1 (es)
ZA (1) ZA985467B (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6689883B1 (en) 1999-09-28 2004-02-10 Bayer Pharmaceuticals Corporation Substituted pyridines and pyridazines with angiogenesis inhibiting activity
US7977333B2 (en) 2000-04-20 2011-07-12 Bayer Healthcare Llc Substituted pyridines and pyridazines with angiogenesis inhibiting activity
US6903101B1 (en) 2000-08-10 2005-06-07 Bayer Pharmaceuticals Corporation Substituted pyridazines and fused pyridazines with angiogenesis inhibiting activity
EP2148878A4 (en) * 2007-04-20 2011-08-10 Merck Canada Inc NEW HETEROAROMATIC COMPOUNDS AS INHIBITORS OF STEAROYL-COENZYME-A-DELTA-9-DESATURASE
US9102669B2 (en) 2011-12-06 2015-08-11 Janssen Pharmaceutica Nv Substituted piperidinyl-pyridazinyl derivatives useful as SCD 1 inhibitors
US9238658B2 (en) 2011-12-06 2016-01-19 Janssen Pharmaceutica Nv Substituted piperidinyl-carboxamide derivatives useful as SCD 1 inhibitors
GB201309508D0 (en) * 2013-05-28 2013-07-10 Redx Pharma Ltd Compounds
GB201311953D0 (en) * 2013-07-03 2013-08-14 Redx Pharma Ltd Compounds

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6339868A (ja) * 1986-08-04 1988-02-20 Otsuka Pharmaceut Factory Inc ジ低級アルキルフエノ−ル誘導体
NZ326354A (en) * 1996-01-15 1999-05-28 Janssen Pharmaceutica Nv 3-(substituted-1-piperazinyl)-6-(substituted-1,2,4-thiadiazol-5 -yl)-pyridazine derivatives and medicaments

Also Published As

Publication number Publication date
IL133652A (en) 2003-04-10
SK176999A3 (en) 2000-09-12
DE69812623T2 (de) 2004-02-19
AU8853798A (en) 1999-01-04
IL133652A0 (en) 2001-04-30
JP2002512630A (ja) 2002-04-23
TR199902955T2 (xx) 2000-06-21
EP0991649B1 (en) 2003-03-26
NZ501649A (en) 2001-10-26
EP0991649A1 (en) 2000-04-12
ZA985467B (en) 1999-12-23
CZ450899A3 (cs) 2000-08-16
MY120046A (en) 2005-08-30
CN1198822C (zh) 2005-04-27
RU2194049C2 (ru) 2002-12-10
PT991649E (pt) 2003-08-29
ATE235489T1 (de) 2003-04-15
DK0991649T3 (da) 2003-07-21
SK283705B6 (sk) 2003-12-02
CN1261364A (zh) 2000-07-26
AU732129B2 (en) 2001-04-12
DE69812623D1 (de) 2003-04-30
WO1998058929A1 (en) 1998-12-30
ID23443A (id) 2000-04-20
BR9810321A (pt) 2000-09-05
PL191409B1 (pl) 2006-05-31
HUP0004457A2 (hu) 2002-02-28
HU225154B1 (en) 2006-07-28
HUP0004457A3 (en) 2002-03-28
EE9900591A (et) 2000-08-15
CZ296000B6 (cs) 2005-12-14
EE03828B1 (et) 2002-08-15
CA2294551A1 (en) 1998-12-30
PL337657A1 (en) 2000-08-28

Similar Documents

Publication Publication Date Title
AR049956A1 (es) DERIVADOS DE 1,3 - OXAZOLIDIN - 2 - ONA COMO INHIBIDORES DE CETP Y ELEVADORES DEL NIVEL DE LAD-C; COMPOSICIONES FARMACÉUTICAS QUE LOS CONTIENEN Y SU USO EN LA FABRICACIoN DE UN MEDICAMENTO PARA EL TRATAMIENTO DE LA ATEROSCLEROSIS.
CO5231142A1 (es) TIADIAZOLA COMO INGREDIENTE ACTIVO, EN COMBINACIàN CON AL ME NOS UN FUNGICIDA SELECCIONADO DE LOS COMPONENTES QUE TIENE UNA ACTIVIDAD FUNGICIDA CONTRA LAS ENFERMEDADES DE LAS PLAN- TAS Y UN METODO PARA EL USO DEL MISMO
PL410411A1 (pl) Pochodna 2-pirydyloetylobenzamidu
BRPI0509124A (pt) misturas fungicidas, agentes, processo para combater fungos nocivos, semente, e, uso de um composto
MX9700130A (es) 2-(1',2',4',-triazol-3'-iloximetilen)-anilidas y uso como agentes de control de plagas.
ES2195374T3 (es) Derivados de tiadiazolil-piridazina que impiden la angiogenesis.
BRPI0412596A (pt) derivados de triazolopirimidina como inibores de glicogênio sintase cinase 3
ES2095662T3 (es) Derivados de imidazol con actividad antagonista de la angiotensina ii.
AR044830A1 (es) Derivados de 4,5 diaril -3-heterociclilpirazin- 2- ester
BR0107884A (pt) Derivados de imida substituìdos
AR003412A1 (es) Derivados de 1,3-dihidro-1-(fenilalquenil)-2h-imidazol-2-ona, procedimiento para su preparacion, composicion que los comprenden, procedimiento para obtenerdicha composicion y uso de dichos compuestos para preparar medicamentos.
CO4990949A1 (es) Derivados de imidazol y su preparacion .
AR038156A1 (es) Compuestos de amidoacetonitrilo, proceso para su preparacion, composicion para controlar los parasitos, y uso de estos compuestos para preparar una composicion farmaceutica
ES2063273T3 (es) Nuevos compuestos de halo propargilo, y usos y procedimientos para su preparacion.
DE69911557D1 (de) Imidazoline Derivate,ihre Herstellung und pharmazeutische Zusammensetzungen die sie enthalten
BR0316254A (pt) Misturas e agentes fungicidas, processo para combater fungos nocivos fitopatogênicos, e, uso dos compostos
BR0116240A (pt) Mistura fungicida, método para controlar fungos nocivos, e, usos dos compostos de amida e dos derivados de imidazol
BR0312287A (pt) Derivados de 4-(3,3-dihalo-alilóxi) fenóxi alquila
SE8303117D0 (sv) Alfa-(1-triazolyl)-keto-derivat med fungicid aktivitet
AR013124A1 (es) Derivados de tiadiazolil piridacina inhibidores de angiogenesis, procedimiento para su preparacion, su uso para la manufactura de un medicamento, composicion farmaceutca que los comprende y procedimiento para preparar dicha composicion.
NZ501982A (en) N-oxide forms of 2,4,4-trisubstituted-1,3-dioxolane as anti-fungal agents
WO2002054870A3 (de) Fungizide mischungen auf der basis von imidazolderivaten
ATE83661T1 (de) Wasserloesliche zubereitungen von coccidiostatica.
FR2787450B1 (fr) Nouveaux derives spiroimidazoliniques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
AR007522A1 (es) Proceso para la preparacion de 5-(alcoximetil)-2,3-piridinodicarboximida, compuesto para su exclusivo uso en dicho procedimiento y procedimiento parapreparar compuestos herbicidas de imidazolinona.