[go: up one dir, main page]

PE20001403A1 - Derivados de pirrolidina como antagonistas del receptor ccr-3 - Google Patents

Derivados de pirrolidina como antagonistas del receptor ccr-3

Info

Publication number
PE20001403A1
PE20001403A1 PE1999001161A PE00116199A PE20001403A1 PE 20001403 A1 PE20001403 A1 PE 20001403A1 PE 1999001161 A PE1999001161 A PE 1999001161A PE 00116199 A PE00116199 A PE 00116199A PE 20001403 A1 PE20001403 A1 PE 20001403A1
Authority
PE
Peru
Prior art keywords
alkyl
alkylene
pyrrolidine derivatives
haloalkyl
ccr
Prior art date
Application number
PE1999001161A
Other languages
English (en)
Inventor
Daniel Harry Rogers
John Saunders
John Patrick Williams
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20001403A1 publication Critical patent/PE20001403A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • C07D207/09Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

SE REFIERE A DERIVADOS DE PIRROLIDINA DE FORMULA I DONDE Z ES N, (N+R)-X(-); R ES ALQUILO, HALOALQUILO, ARALQUILO, HIDROXIALQUILO, CARBOXIALQUILO, ALCOXICARBONILALQUILO, CIANOALQUILO; X ES UN ION; Ar1 Y Ar2 SON ARILO, HETEROARILO; Q ES ALQUILENO C1-C3; R1 ES H, ALQUILO; A ES i)NR2CO, CUANDO B ES a)ALQUILENO C1-C4 OPCIONALMENTE REEMPLAZADO CON CO, N(R4), O, S(O)n, NR5C(O), NR6SO2; n ES 0-2; b)ALQUINILENO; R2 ES H, ALQUILO, HETEROCICLILALQUILO, (ALQUILENO)-C(O)-Z`; Z' ES ALQUILO, HALOALQUILO, HIDROXI, AMINO; R4, R5, R6 SON H, ALQUILO, ACILO, HALOALQUILO, HETEROALQUILO, HETEROCICLILALQUILO, (ALQUILENO)-C(O)-Z'; ii)NR2CS, NR2CONR3, NR2CSNR3, ENTRE OTROS; B ES UN ENLACE, ALQUILENO, ALQUENILENO, ALQUINILENO; R3 ES H, ALQUILO, ARILO, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCESO PARA LA PREPARACION. LOS DERIVADOS DE PIRROLIDINA SON ANTAGONISTAS DEL RECEPTOR DE QUIMIOCINAS CCR-3 POR LO QUE PUEDEN SER UTILES PARA EL TRATAMIENTO DE ENFERMEDADES INFLAMATORIAS MEDIADAS POR EOSINOFILOS TAL COMO ASMA
PE1999001161A 1998-11-20 1999-11-16 Derivados de pirrolidina como antagonistas del receptor ccr-3 PE20001403A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10929798P 1998-11-20 1998-11-20

Publications (1)

Publication Number Publication Date
PE20001403A1 true PE20001403A1 (es) 2000-12-15

Family

ID=22326918

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1999001161A PE20001403A1 (es) 1998-11-20 1999-11-16 Derivados de pirrolidina como antagonistas del receptor ccr-3

Country Status (27)

Country Link
US (1) US6166015A (es)
EP (1) EP1131288A1 (es)
JP (1) JP3593037B2 (es)
KR (1) KR20010086045A (es)
CN (1) CN1158256C (es)
AR (1) AR023707A1 (es)
AU (1) AU763960B2 (es)
BR (1) BR9915520A (es)
CA (1) CA2350903A1 (es)
CO (1) CO5140119A1 (es)
CZ (1) CZ20011760A3 (es)
DE (1) DE19955794A1 (es)
ES (1) ES2158814B1 (es)
FR (1) FR2786185A1 (es)
GB (1) GB2343893B (es)
HU (1) HUP0104364A2 (es)
ID (1) ID29067A (es)
IL (1) IL143226A0 (es)
IT (1) IT1307900B1 (es)
MA (1) MA26762A1 (es)
NO (1) NO20012411L (es)
PE (1) PE20001403A1 (es)
PL (1) PL348375A1 (es)
TR (1) TR200101398T2 (es)
UY (1) UY25811A1 (es)
WO (1) WO2000031032A1 (es)
ZA (1) ZA200103942B (es)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6339087B1 (en) 1997-08-18 2002-01-15 Syntex (U.S.A.) Llc Cyclic amine derivatives-CCR-3 receptor antagonists
IL125658A0 (en) 1997-08-18 1999-04-11 Hoffmann La Roche Ccr-3 receptor antagonists
US6316623B1 (en) * 1998-08-21 2001-11-13 Isis Pharmaceuticals, Inc. Ethylenediamine compound libraries
AU1774600A (en) 1998-11-20 2000-06-13 F. Hoffmann-La Roche Ag Piperidine ccr-3 receptor antagonists
EP1179341B1 (en) 1999-05-18 2005-11-09 Teijin Limited Remedies or preventives for diseases in association with chemokines
KR100667645B1 (ko) * 1999-08-04 2007-02-28 데이진 가부시키가이샤 환상 아민 ccr3 길항제
ATE346042T1 (de) * 1999-12-08 2006-12-15 Teijin Ltd Zyklische aminverbindungen als ccr5-rezeptor antagonisten
ES2527688T3 (es) 2000-09-29 2015-01-28 Glaxo Group Limited Derivados de morfolin-acetamida para el tratamiento de enfermedades inflamatorias
CN1478084A (zh) 2000-09-29 2004-02-25 用于治疗炎性疾病的化合物
WO2002050064A1 (en) * 2000-12-19 2002-06-27 F. Hoffmann-La Roche Ag Substituted pyrrolidines as ccr-3 receptor antagonists
FR2821356A1 (fr) 2001-02-23 2002-08-30 Cerep Nouveaux derives d'arylcarbamates et d'arylurees, preparations et utilisations
GB0117387D0 (en) * 2001-07-17 2001-09-05 Novartis Ag Organic compounds
KR100652451B1 (ko) * 2001-09-13 2006-12-01 에프. 호프만-라 로슈 아게 Ccr-3 수용체 길항제 v
US7067549B2 (en) * 2001-12-31 2006-06-27 Actelion Pharmaceuticals Ag Pyrrolidone carboxamides
GB0207432D0 (en) * 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0207436D0 (en) * 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0207439D0 (en) * 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0207443D0 (en) * 2002-03-28 2002-05-08 Glaxo Group Ltd Novel compounds
GB0212355D0 (en) * 2002-05-29 2002-07-10 Glaxo Group Ltd Novel compounds
US7842693B2 (en) 2002-06-12 2010-11-30 Chemocentryx, Inc. Substituted piperazines
US7589199B2 (en) 2002-06-12 2009-09-15 Chemocentryx, Inc. Substituted piperazines
ATE438401T1 (de) 2002-06-12 2009-08-15 Chemocentryx Inc 1-aryl-4-substituierte piperazin-derivate zur verwendung als ccr1-antagonisten zur behandlung von entzündungen und immunerkrankungen
CA2490148A1 (en) 2002-07-02 2004-01-15 F. Hoffmann-La Roche Ag 2, 5-substituted pyrimidine derivatives as ccr-3 receptor antagonists ix
US6919356B2 (en) * 2002-09-26 2005-07-19 Bristol Myers Squibb Company N-substituted heterocyclic amines as modulators of chemokine receptor activity
DE602004022783D1 (de) 2003-03-06 2009-10-08 Glaxo Group Ltd Heterozyklische harnstoff-derivate für die behandlung von schmerzen.
JP2006519806A (ja) 2003-03-07 2006-08-31 グラクソ グループ リミテッド 尿素誘導体および疼痛治療におけるバニロイド受容体拮抗剤としてのそれらの使用。
GB0305426D0 (en) * 2003-03-08 2003-04-16 Glaxo Group Ltd Novel compounds
NZ542304A (en) 2003-03-14 2009-07-31 Ono Pharmaceutical Co Nitrogen-containing heterocyclic derivatives and drugs containing the same as the active ingredient
US7498323B2 (en) 2003-04-18 2009-03-03 Ono Pharmaceuticals Co., Ltd. Spiro-piperidine compounds and medicinal use thereof
SG131946A1 (en) * 2003-10-24 2007-05-28 Hoffmann La Roche Ccr3 receptor antagonists
JP4845873B2 (ja) 2004-03-03 2011-12-28 ケモセントリックス インコーポレーティッド 二環式および架橋した窒素複素環
US7435831B2 (en) 2004-03-03 2008-10-14 Chemocentryx, Inc. Bicyclic and bridged nitrogen heterocycles
RU2530889C2 (ru) * 2004-05-14 2014-10-20 Эмисфире Текнолоджис, Инк. Соединения и составы для доставки активных веществ
NZ551196A (en) * 2004-05-14 2010-08-27 Emisphere Tech Inc Compounds and compositions for delivering active agents
ES2457041T3 (es) 2004-09-13 2014-04-24 Ono Pharmaceutical Co., Ltd. Derivados de N-4-piperidilurea y medicamentos que los contienen como principio activo
WO2006088541A2 (en) * 2005-02-17 2006-08-24 State Of Oregon Acting By & Through The State Board Of Higher Edu. On Behalf Of Portland State Unv. Quinoline derivatives and uses thereof
US20110052612A1 (en) 2005-05-31 2011-03-03 Ono Pharmaceutical Co., Ltd. Spiropiperidine compound and medicinal use thereof
JP2009501792A (ja) * 2005-07-21 2009-01-22 アストラゼネカ・アクチエボラーグ ケモカイン受容体のモジュレーターとしてのn−ベンジル−モルホリン誘導体
KR100743617B1 (ko) * 2005-08-25 2007-07-27 주식회사 알에스텍 고광학순도를 갖는 키랄 3-히드록시 피롤리딘 및 그유도체를 제조하는 방법
HUP0500879A2 (en) * 2005-09-22 2007-05-29 Sanofi Aventis Amide derivatives as ccr3 receptor ligands, process for producing them, pharmaceutical compositions containing them and their use and intermediates
JP2009508929A (ja) * 2005-09-22 2009-03-05 サノフイ−アベンテイス Ccr3受容体リガンドとしてのアミノ−アルキル−アミド誘導体
HUP0500877A2 (en) * 2005-09-22 2007-05-29 Sanofi Aventis Amide derivatives as ccr3 receptor ligands, process for producing them, pharmaceutical compositions containing them and their use and intermediates
HUP0500886A2 (en) * 2005-09-23 2007-05-29 Sanofi Aventis Amide derivatives as ccr3 receptor ligands, process for producing them, pharmaceutical compositions containing them and their use
PL1942108T3 (pl) 2005-10-28 2014-03-31 Ono Pharmaceutical Co Związek zawierający grupę zasadową i jego zastosowanie
DK1961744T3 (da) 2005-11-18 2013-07-15 Ono Pharmaceutical Co Forbindelse indeholdende basiske grupper samt anvendelse deraf
BRPI0708731A2 (pt) 2006-03-10 2011-06-07 Ono Pharmaceutical Co derivado heterocìclico nitrogenado, e agente farmacêutico compreendendo o derivado como ingrediente ativo
JP5257068B2 (ja) 2006-05-16 2013-08-07 小野薬品工業株式会社 保護されていてもよい酸性基を含有する化合物およびその用途
US20090325992A1 (en) 2006-07-31 2009-12-31 Ono Pharmaceutical Co., Ltd. Compound having cyclic group bound thereto through spiro binding and use thereof
WO2010129351A1 (en) 2009-04-28 2010-11-11 Schepens Eye Research Institute Method to identify and treat age-related macular degeneration
CN101906060B (zh) * 2010-05-06 2012-07-04 爱斯医药科技(南京)有限公司 N-取代的3-氨甲基吡咯烷的制备方法

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3459757A (en) * 1965-10-22 1969-08-05 American Cyanamid Co Imidazolidines
NZ186175A (en) * 1977-01-27 1980-03-05 Shionogi & Co Meta-sulphonamidobenzamide derivatives
JPS59186969A (ja) * 1983-04-08 1984-10-23 Yoshitomi Pharmaceut Ind Ltd ベンゾフラン−およびベンゾピランカルボキサミド誘導体
FI95572C (fi) * 1987-06-22 1996-02-26 Eisai Co Ltd Menetelmä lääkeaineena käyttökelpoisen piperidiinijohdannaisten tai sen farmaseuttisen suolan valmistamiseksi
JPH01117860A (ja) * 1987-10-30 1989-05-10 Dainippon Pharmaceut Co Ltd 安息香酸アミド誘導体
JPH02104572A (ja) * 1988-10-13 1990-04-17 Dainippon Pharmaceut Co Ltd 安息香酸アミド誘導体
FR2662162B1 (fr) * 1990-05-18 1995-01-20 Adir Nouveaux derives de l'amino piperidine, de l'amino pyrrolidine et de l'amino perhydroazepine, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent.
US5214055A (en) * 1990-05-18 1993-05-25 Adir Et Compagnie Aminopiperidine 4-oxo-4H-chromen-2-yl compounds
US5254569A (en) * 1991-01-14 1993-10-19 The Du Pont Merck Pharmaceutical Company (Amidomethyl)nitrogen heterocyclic analgesics
GB9113031D0 (en) * 1991-06-17 1991-08-07 Smithkline Beecham Plc Compounds
FR2679906B1 (fr) * 1991-07-31 1995-01-20 Adir Nouvelles (isoquinolein-5 yl) sulfonamides, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
PT100785A (pt) * 1991-08-20 1994-04-29 Smithkline Beecham Plc Utilizacao de compostos, por exemplo indole-3-carboxilatos, para a producao de medicamentos, compostos ai utilizados e composicoes farmaceuticas que os contem.
JPH06212757A (ja) * 1993-01-19 1994-08-02 Ribaa Kentetsu Kk ソリ型運搬治具による折板屋根葺き工法
EP0742208A1 (en) * 1995-05-05 1996-11-13 Grelan Pharmaceutical Co., Ltd. 2-Ureido-benzamide derivatives
US5827875A (en) * 1996-05-10 1998-10-27 Bristol-Myers Squibb Company Inhibitors of microsomal triglyceride transfer protein and method
CA2261633A1 (en) * 1996-07-29 1998-02-05 Banyu Pharmaceutical Co., Ltd. Chemokine receptor antagonists
IL125658A0 (en) * 1997-08-18 1999-04-11 Hoffmann La Roche Ccr-3 receptor antagonists
JPH11140276A (ja) * 1997-11-11 1999-05-25 Sumitomo Chem Co Ltd 多官能シアン酸エステル樹脂組成物および樹脂封止型半導体装置
BR9814645A (pt) * 1997-11-18 2001-07-31 Teijin Ltd Derivados de amina cìclica e seu uso como medicamentos

Also Published As

Publication number Publication date
NO20012411D0 (no) 2001-05-16
TR200101398T2 (tr) 2001-09-21
CO5140119A1 (es) 2002-03-22
NO20012411L (no) 2001-05-16
ES2158814A1 (es) 2001-09-01
ZA200103942B (en) 2002-08-15
GB9927227D0 (en) 2000-01-12
IL143226A0 (en) 2002-04-21
HUP0104364A2 (hu) 2002-04-29
FR2786185A1 (fr) 2000-05-26
BR9915520A (pt) 2001-07-17
GB2343893A (en) 2000-05-24
EP1131288A1 (en) 2001-09-12
ID29067A (id) 2001-07-26
UY25811A1 (es) 2001-07-31
JP3593037B2 (ja) 2004-11-24
CN1158256C (zh) 2004-07-21
CN1331677A (zh) 2002-01-16
AU763960B2 (en) 2003-08-07
MA26762A1 (fr) 2004-12-20
ES2158814B1 (es) 2002-03-16
CZ20011760A3 (cs) 2001-12-12
ITTO991009A0 (it) 1999-11-19
JP2002530374A (ja) 2002-09-17
PL348375A1 (en) 2002-05-20
KR20010086045A (ko) 2001-09-07
US6166015A (en) 2000-12-26
WO2000031032A1 (en) 2000-06-02
ITTO991009A1 (it) 2001-05-19
AU1382500A (en) 2000-06-13
IT1307900B1 (it) 2001-11-19
DE19955794A1 (de) 2000-05-31
CA2350903A1 (en) 2000-06-02
GB2343893B (en) 2002-01-09
AR023707A1 (es) 2002-09-04

Similar Documents

Publication Publication Date Title
PE20001403A1 (es) Derivados de pirrolidina como antagonistas del receptor ccr-3
HUP0303037A2 (hu) Alzheimer-kór kezelésére alkalmas vegyületek és ezeket tartalmazó gyógyszerkészítmények
YU29503A (sh) Novi antiholinergici koji se mogu primeniti kao lekovi, kao i postupak za njihovo dobijanje
PE20001401A1 (es) Sales cuaternarias de piperidina como antagonistas del receptor ccr-3
ATE249213T1 (de) Pentafluorobenzensulfonamiden und analoge
ES8700252A1 (es) Procedimiento para preparar nuevos compuestos indolicos
YU40997A (sh) Novi oksadiazoli, postupci za njihovo pripremanje
DE60236600D1 (de) Substituierte 1h-dihydropyrazole, ihre herstellung und verwendung
CY1106982T1 (el) 4-διαρυλυλο-1-φαινυλαζετιδιν-2-ονες
BRPI0312882B8 (pt) derivados de pleuromutilina e composição farmacêutica
EA200100983A1 (ru) Производные 13-метилэритромицина
SE9703414D0 (sv) New compounds
ES2174298T3 (es) Derivados de aminotiazol, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen.
ATE73790T1 (de) Amino 5,6,7,8tetrahydronaphtho(2,3b>furanderivate, verfahren zu ihrer herstellung und diese enthaltende arzneimittel.
ES2110260T3 (es) Androstenonas.
TR199802384T2 (xx) N�rodejeneratif hastal�klar�n tedavisinde yararl� farmas�tik bile�imlerin haz�rlanmas� i�in P-Aminofenol t�revlerinin kullan�m�.
TR200200125T2 (tr) Yeni aminotiyazol türevleri, bunların hazırlanması ve bunları içeren farmasötik kompozisyonlar.
AP2001002188A0 (en) 5HT1 antagonists for antidepressant therapy.
MX9700807A (es) Derivados de 3-azabiciclo (3.2.0)heptano n-sustituidos utiles como neurolepticos.
PT86656A (pt) 5-(3-alkyl-5-tert.butyl-4-hydroxyphenyl)-2-amino-6h-1,3,4-thadiazine verfahren zu ihrer herstellung die sie enthaltenden arzneimittel und ihre verwendung
DE60105028D1 (de) Ruthenium (ii) verbindungen in der krebsbehandlung
TR200100475T2 (tr) N-İkameli azabisikloheptan türevlerinin üretimleri ve kullanımları.
EA200001157A3 (ru) Новые замещенные производные (дигидро)бензоксазина и (дигидро)бензотиазина, способ их получения и содержащие их фармацевтические композиции
MX9102326A (es) 3-(2-cloro-4-(trifluorometil)fenoxi)-1-acetidina carboxamidas y composicion farmaceutica que las contiene.
DK0871611T3 (da) Hidtil ukendte glycylanilidderivater, deres fremstilling og deres terapeutiske anvendelse

Legal Events

Date Code Title Description
FC Refusal