ES2175834T3 - Nuevos analogos tretaciclicos de camptotecinam, sus procedimientos de preparacion, su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen. - Google Patents

Nuevos analogos tretaciclicos de camptotecinam, sus procedimientos de preparacion, su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen.

Info

Publication number
ES2175834T3
ES2175834T3 ES98962480T ES98962480T ES2175834T3 ES 2175834 T3 ES2175834 T3 ES 2175834T3 ES 98962480 T ES98962480 T ES 98962480T ES 98962480 T ES98962480 T ES 98962480T ES 2175834 T3 ES2175834 T3 ES 2175834T3
Authority
ES
Spain
Prior art keywords
alkyl
haloalkyl
radical
hydroxyalkyl
naphthyl
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
ES98962480T
Other languages
English (en)
Inventor
Dennis Bigg
Olivier Lavergne
Alain Rolland
Christophe Lanco
Gerard Ulibarri
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.)
Ipsen Pharma SAS
Original Assignee
Societe de Conseils de Recherches et dApplications Scientifiques SCRAS SAS
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 Societe de Conseils de Recherches et dApplications Scientifiques SCRAS SAS filed Critical Societe de Conseils de Recherches et dApplications Scientifiques SCRAS SAS
Application granted granted Critical
Publication of ES2175834T3 publication Critical patent/ES2175834T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)

Abstract

Un compuesto, caracterizado porque dicho compuesto es de fórmula (I), **fórmula** en la forma racémica, enantiómera o cualquier combinación de estas formas, en la cual R1 representa un radical alquilo, alquenilo, alquinilo, haloalquilo, alcoxialquilo o alquiltioalquilo; R2, R3 y R4 representan independientemente un radical H, hidroxi, alcoxi, arilalcoxi, halo, haloalquilo, alquilo, alquenilo, ciano, cianoalquilo, nitro, nitroalquilo, amido, amidoalquilo, (CH2)mNR6R7, (CH2)mOR6, (CH2)mSR6, (CH2)mCO2R6, (CH2)mNR6C(O)R8, (CH2)mC(O)R8, (CH2)mOC(O)R8, O(CH2)mNR6R7, OC(O)NR6R7, OC(O)(CH2)mCO2R6, o uno de los radicales fenilo, naftilo, antracilo, bifenilo, indenilo, fenilalquilo, naftilalquilo, antracilalquilo, bifenilalquilo o indenilaquilo eventualmente sustituidos de una a cuatro veces en el núcleo de fenilo, naftilo, antracilo, bifenilo o indenilo con uno o unos radicales escogidos entre un radical alquilo, halo, nitro, amino, alquilamino, haloalquilo, hidroxialquilo, alcoxi o alcoxialquilo, oR2 y R3, oR3 y R4, oR4 y R5, forman independientemente de forma conjunta una cadena de 3 ó 4 eslabones, en la que los elementos de la cadena se seleccionan entre el grupo constituido por CH, CH2, O,S, NoNR9; R5 representa un radical H, halo, haloalquilo, alquilo, alcoxi, alcoxialquilo, alquiltioalquilo, cicloalquilo, cicloalquilalquilo, ciano, cianoalquilo, alcanosulfonilalquilo, hidroxialquilo, nitro, (CH2)mC(O)R8, (CH2)mNR6C(O)R8, (CH2)mNR6R7, (CH2)mN(CH3)(CH2)nNR6R7, (CH2)mOC(O)R8, (CH2)mOC(O)NR6R7 o uno de los radicales fenilo, naftilo, antracilo, bifenilo, indenilo, fenilalquilo, naftilalquilo, antracilalquilo, bifenilalquilo o indenilaquilo eventualmente sustituidos de una a cuatro veces en el núcleo de fenilo, naftilo, antracilo, bifenilo o indenilo con uno o unos radicales escogidos entre un radical alquilo, halo, nitro, amino, alquilamino, haloalquilo, hidroxialquilo, alcoxi o alcoxialquilo; R6 y R7 representan, independientemente, H, un radical alquilo, hidroxialquilo, alquilaminoalquilo, aminoalquilo, cicloalquilo, cicloalquilalquilo, alquenilo, alcoxialquilo, haloalquilo, uno de los radicales fenilo, naftilo, antracilo, bifenilo, indenilo, fenilalquilo, naftilalquilo, antracilalquilo, bifenilalquilo o indenilaquilo eventualmente sustituidos de una a cuatro veces en el núcleo de fenilo, naftilo, antracilo, bifenilo o indenilo con uno o unos radicales escogidos entre un radical alquilo, halo, nitro, amino, alquilamino, haloalquilo, hidroxialquilo, alcoxi o alcoxialquilo, o bien, cuando las cadenas R6 y R7 están unidas a un mismo átomo de nitrógeno, R6 y R7 forman eventualmente de forma conjunta un grupo morfolino, piperazino o piperidino, estando eventualmente sustituido dicho grupo con uno o varios grupos escogidos entre radicales alquilo, fenilo, naftilo, antracilo, bifenilo, indenilo, fenilalquilo, naftilalquilo, antracilalquilo, bifenilalquilo o indenilaquilo, halo, nitro, amino, alquilamino, haloalquilo, hidroxialquilo, alcoxi o alcoxialquilo; R8 representa unradical H, alquilo, hidroxialquilo, amino, alquilamino, alquilaminoalquilo, aminoalquilo, cicloalquilo, cicloalquilalquilo, alquenilo, alcoxi, alcoxialquilo, haloalquilo o uno de los radicales fenilo, naftilo, antracilo, bifenilo, indenilo, fenilalquilo, naftilalquilo, antracilalquilo, bifenilalquilo o indenilaquilo eventualmente sustituidos de una a cuatro veces en el núcleo de fenilo, naftilo, antracilo, bifenilo o indenilo con uno o unos radicales escogidos entre un radical alquilo, halo, nitro, amino, alquilamino, haloalquilo, hidroxialquilo, alcoxi o alcoxialquilo; R9 representa un radical H, alquilo, haloalquilo, o uno de los radicales fenilo, naftilo, antracilo, bifenilo, indenilo, fenilalquilo, naftilalquilo, antracilalquilo, bifenilalquilo o indenilaquilo eventualmente sustituidos con uno de los grupos escogidos entre el radical alquilo, halo, nitro, amino, alquilamino, haloalquilo, hidroxialquilo, alcoxi o alcoxialquilo; R10 representa un radical ciano, C(O)OR11, 1H-1,2,3,4-tetrazo-5-ilo o 1-alquil-1,2,3,4-tetrazo-5-ilo; R11 representa un radical H, alquilo, haloalquilo, hidroxialquilo, alquilcarboniloxialquilo, (CH2)P NR6R7, o uno de los radicales fenilo, naftilo, antracilo, bifenilo, indenilo, fenilalquilo, naftilalquilo, antracilalquilo, bifenilalquilo o indenilaquilo eventualmente sustituidos en el ciclo aromático con uno o varios grupos escogidos entre el radical alquilo, halo, nitro, amino, alquilamino, haloalquilo, hidroxialquilo, alcoxi o alcoxialquilo; m es un número entero comprendido entre 0 y 6; n es un número entero comprendido entre 1 y 4; p es un número entero comprendido entre 2 y 6; debiendo entenderse que: cada uno de los grupos alquilo que entran en las definiciones de los radicales anteriores es lineal o ramicado y comprende de 1 a 6 átomos de carbono; cada uno de los grupos alquenilo o alquinilo que entran en las definiciones de los radicales anteriores es lineal o ramificado y comprende de 2 a 6 átomos de carbono; y cada uno de los grupos cicloalquilo que entran en las definiciones de los radicales anteriores comprende de 3 a 7 átomos de carbono; o una sal farmacéuticamente aceptable de este último.
ES98962480T 1997-12-24 1998-12-16 Nuevos analogos tretaciclicos de camptotecinam, sus procedimientos de preparacion, su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen. Expired - Lifetime ES2175834T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9716461A FR2772763B1 (fr) 1997-12-24 1997-12-24 Nouveaux analogues tetracycliques de camptothecines, leurs procedes de preparation, leur application comme medicaments et les compositions pharmaceutiques les contenant

Publications (1)

Publication Number Publication Date
ES2175834T3 true ES2175834T3 (es) 2002-11-16

Family

ID=9515095

Family Applications (1)

Application Number Title Priority Date Filing Date
ES98962480T Expired - Lifetime ES2175834T3 (es) 1997-12-24 1998-12-16 Nuevos analogos tretaciclicos de camptotecinam, sus procedimientos de preparacion, su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen.

Country Status (22)

Country Link
US (2) US6436951B1 (es)
EP (1) EP1042323B1 (es)
JP (1) JP2001527075A (es)
AR (1) AR016440A1 (es)
AT (1) ATE215951T1 (es)
AU (1) AU749224B2 (es)
CA (1) CA2315897C (es)
DE (1) DE69804856T2 (es)
DK (1) DK1042323T3 (es)
ES (1) ES2175834T3 (es)
FR (1) FR2772763B1 (es)
HU (1) HUP0004628A3 (es)
IL (1) IL136732A0 (es)
MY (1) MY117585A (es)
NO (1) NO316676B1 (es)
NZ (1) NZ505339A (es)
PL (1) PL193468B1 (es)
PT (1) PT1042323E (es)
RU (1) RU2220144C2 (es)
TW (1) TW513429B (es)
WO (1) WO1999033829A1 (es)
ZA (1) ZA9811796B (es)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003074524A2 (en) * 2002-03-01 2003-09-12 University Of Pittsburgh Mappicine analogs, intermediates in the synthesis of mappicine analogs and methods of synthesis of mappicine analogs
RS84904A (en) * 2002-03-26 2006-12-15 Bany Pharmaceutical Co.Ltd. Combined use of antitumor indolopyrrolocarbazole derivative and other antitumor agent
US20080003455A1 (en) * 2004-12-08 2008-01-03 Fuji Electric Holdings Co., Ltd. Organic El Device
AR059898A1 (es) 2006-03-15 2008-05-07 Janssen Pharmaceutica Nv Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2
TW200845978A (en) 2007-03-07 2008-12-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives
TW200900065A (en) 2007-03-07 2009-01-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives
JP5126707B2 (ja) * 2007-04-23 2013-01-23 有機合成薬品工業株式会社 α−ヒドロキシアシルピリジンの製造方法
PT2203439E (pt) 2007-09-14 2011-02-11 Ortho Mcneil Janssen Pharm 4-fenil-3,4,5,6-tetra-hidro-2h,1'h-[1,4']bipiridinil-2'- onas 1',3'-dissubstituídas
BRPI0918055A2 (pt) 2008-09-02 2015-12-01 Addex Pharmaceuticals Sa derivados de 3-azabiciclo[3,1,0]hexila como moduladores de receptores metabotrópicos de glutamato.
JP5690277B2 (ja) 2008-11-28 2015-03-25 ジャンセン ファーマシューティカルズ， インコーポレイテッド． 代謝型グルタミン酸受容体の調節因子としてのインドールおよびベンゾオキサジン誘導体
CN102439015B (zh) 2009-05-12 2015-05-13 杨森制药有限公司 1,2,4-三唑并[4,3-a]吡啶衍生物和其作为mGluR2受体的正向变构调节剂的用途
NZ596078A (en) 2009-05-12 2013-06-28 Janssen Pharmaceuticals Inc 1,2,4-TRIAZOLO [4,3-a] PYRIDINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OR PREVENTION OF NEUROLOGICAL AND PSYCHIATRIC DISORDERS
MY153913A (en) 2009-05-12 2015-04-15 Janssen Pharmaceuticals Inc 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
CA2814998C (en) 2010-11-08 2019-10-29 Janssen Pharmaceuticals, Inc. 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
US9271967B2 (en) 2010-11-08 2016-03-01 Janssen Pharmaceuticals, Inc. 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors
US8993591B2 (en) 2010-11-08 2015-03-31 Janssen Pharmaceuticals, Inc. 1,2,4-triazolo[4,3-a] pyridine derivatives and their use as positive allosteric modulators of MGLUR2 receptors
WO2014127214A1 (en) 2013-02-15 2014-08-21 Kala Pharmaceuticals, Inc. Therapeutic compounds and uses thereof
US9688688B2 (en) 2013-02-20 2017-06-27 Kala Pharmaceuticals, Inc. Crystalline forms of 4-((4-((4-fluoro-2-methyl-1H-indol-5-yl)oxy)-6-methoxyquinazolin-7-yl)oxy)-1-(2-oxa-7-azaspiro[3.5]nonan-7-yl)butan-1-one and uses thereof
JP2016510000A (ja) 2013-02-20 2016-04-04 カラ ファーマシューティカルズ インコーポレイテッド 治療用化合物およびその使用
JO3368B1 (ar) 2013-06-04 2019-03-13 Janssen Pharmaceutica Nv مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2
JO3367B1 (ar) 2013-09-06 2019-03-13 Janssen Pharmaceutica Nv مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2
CA2928658A1 (en) 2013-11-01 2015-05-07 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
US9890173B2 (en) 2013-11-01 2018-02-13 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
CN103588660B (zh) * 2013-11-18 2016-06-01 中国医学科学院生物医学工程研究所 一种新型的酰基苯胺化合物及用途
JP6219523B2 (ja) 2013-12-13 2017-10-25 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ ブルトンチロシンキナーゼの阻害剤
SI3096790T1 (sl) 2014-01-21 2019-11-29 Janssen Pharmaceutica Nv Kombinacije, ki vsebujejo pozitivne aleostrične modulatorje ali ortosterične agoniste metabotropnega glutamatergičnega receptorja podtipa 2 in njihova uporaba
ME03518B (me) 2014-01-21 2020-04-20 Janssen Pharmaceutica Nv Kombinacije koje obuhvataju pozitivne alosterične modulatore ili ortosterične agoniste metabotropnog glutamatergičnog receptora podtipa 2 i njihova primjena
AU2017324251A1 (en) 2016-09-08 2019-03-21 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
US10253036B2 (en) 2016-09-08 2019-04-09 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof
US10392399B2 (en) 2016-09-08 2019-08-27 Kala Pharmaceuticals, Inc. Crystalline forms of therapeutic compounds and uses thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK1251125T3 (da) * 1995-06-21 2006-04-18 Sod Conseils Rech Applic Hidtil ukendte camptothecin-analoger, fremgangsmåde til fremstilling heraf, anvendelse heraf som lægemidler og farmaceutiske præparater indeholdende disse
GB9624482D0 (en) * 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds

Also Published As

Publication number Publication date
PT1042323E (pt) 2002-09-30
NZ505339A (en) 2003-01-31
HUP0004628A3 (en) 2001-11-28
AU749224B2 (en) 2002-06-20
EP1042323A1 (fr) 2000-10-11
ATE215951T1 (de) 2002-04-15
AR016440A1 (es) 2001-07-04
DK1042323T3 (da) 2002-08-05
FR2772763B1 (fr) 2004-01-23
US6632946B2 (en) 2003-10-14
NO316676B1 (no) 2004-03-29
CA2315897C (fr) 2010-01-19
ZA9811796B (en) 1999-06-29
WO1999033829A1 (fr) 1999-07-08
JP2001527075A (ja) 2001-12-25
TW513429B (en) 2002-12-11
NO20003314L (no) 2000-06-30
PL341288A1 (en) 2001-04-09
US6436951B1 (en) 2002-08-20
IL136732A0 (en) 2001-06-14
DE69804856D1 (de) 2002-05-16
AU1764599A (en) 1999-07-19
NO20003314D0 (no) 2000-06-23
EP1042323B1 (fr) 2002-04-10
CA2315897A1 (fr) 1999-07-08
FR2772763A1 (fr) 1999-06-25
US20010000521A1 (en) 2001-04-26
RU2220144C2 (ru) 2003-12-27
DE69804856T2 (de) 2002-11-07
HUP0004628A1 (hu) 2001-05-28
MY117585A (en) 2004-07-31
PL193468B1 (pl) 2007-02-28

Similar Documents

Publication Publication Date Title
ES2175834T3 (es) Nuevos analogos tretaciclicos de camptotecinam, sus procedimientos de preparacion, su aplicacion como medicamentos y las composiciones farmaceuticas que los contienen.
ATE44383T1 (de) Bisacylphosphinoxide, ihre herstellung und verwendung.
CO4700576A1 (es) Nuevos taxoides, su preparacion y las composiciones farmaceuticas que los contienen
CO4970713A1 (es) Derivados de carboxamidotiazoles, su preparacion, composiciones farmaceuticas que los contienen
AR004195A1 (es) Nuevos derivados de la 5-0 desosaminil-6-0-metil-eritronolida a, su procedimiento de preparacion, compuestos intermediarios, metodo de aplicacionde los mismos para la preparacion de productos biologicamente activos.
ES2199696B1 (es) Mezclas de estabilizantes.
DK1204662T3 (da) Azaindoler med serotoninreceptoraffinitet
HUP0004588A2 (hu) Szubsztituált 1,2,3,4,5,6-hexahidro-2,6-metano-3-benzazocin-10-ol-származékok, eljárás előállításukra és alkalmazásuk gyógyszerként, valamint a vegyületeket tartalmazó gyógyszerkészítmények
EA200000948A1 (ru) Новые полициклические азаиндолы, способ их получения и фармацевтические композиции, содержащие их
ES8503333A1 (es) Un metodo de preparar derivados de 4-quinolona
DK0664287T3 (da) Vitamin D-forbindelser og fremgangsmåde til fremstilling af disse
AR041720A1 (es) Derivados de n- benzodioxolilo, n- benzodioxanilo y n- benzodioxepinilarilcarboxamida que pueden usarse para el tratamiento de dislipidemia, y composiciones farmaceuticas que los contienen
CO5011097A1 (es) Derivados de 8-azabiciclo [3.2.1]octan-3-metanamina .
EA200300458A1 (ru) Новые соединения аминотриазолона, способ их получения и фармацевтические композиции, содержащие их
IL74324A0 (en) New 3-phenyl-2-propeneamine derivatives,their preparation and compositions containing them
ES8702380A1 (es) Procedimiento para preparar un derivado de (imina ciclica)- difenil-eter
DE3464243D1 (de) Esters of 2-adamantanone oxime
BG102429A (en) Derivatives of 5-naphthalen-1-yl-1,3-dioxan, their preparation and usage as therapeutical means
ES2115855T3 (es) Nuevos derivados de 17-iminometilalquenil-5-beta-14-beta-androstanos y 17-iminoalquil-5-beta,14-beta-androstanos, un procedimiento para su produccion y las composiciones farmaceuticas que los incluyen.
MX9304249A (es) Derivados de n-acildihidroquinolina, metodo para su produccion y composiciones herbicidas que los contienen.
CO4940468A1 (es) Nuevos derivados de naftilpiperacina
ATE136036T1 (de) Androst-4-en(4,5-b>-pyrrol-derivate und ein verfahren zu ihrer herstellung
TW349935B (en) Oxime ether compounds, their intermediates and their use as pesticides
DE3361834D1 (en) Dithiino (1,4) (2,3-c) pyrrole derivatives, their preparation and pharmaceutical compositions containing them

Legal Events

Date Code Title Description
FG2A Definitive protection

Ref document number: 1042323

Country of ref document: ES