FI121708B - Substituoidut 1,3,4-oksadiatsolit - Google Patents

Substituoidut 1,3,4-oksadiatsolit Download PDF

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Publication number
FI121708B
FI121708B FI20021192A FI20021192A FI121708B FI 121708 B FI121708 B FI 121708B FI 20021192 A FI20021192 A FI 20021192A FI 20021192 A FI20021192 A FI 20021192A FI 121708 B FI121708 B FI 121708B
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FI
Finland
Prior art keywords
ethyl
carbon atoms
methoxyphenyl
compound
hydrogen
Prior art date
Application number
FI20021192A
Other languages
English (en)
Finnish (fi)
Swedish (sv)
Other versions
FI20021192A (fi
FI20021192A0 (fi
Inventor
Hon-Wah Man
George Muller
Original Assignee
Celgene Corp
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Filing date
Publication date
Application filed by Celgene Corp filed Critical Celgene Corp
Publication of FI20021192A0 publication Critical patent/FI20021192A0/fi
Publication of FI20021192A publication Critical patent/FI20021192A/fi
Application granted granted Critical
Publication of FI121708B publication Critical patent/FI121708B/fi

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • 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
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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 two hetero rings
    • C07D471/04Ortho-condensed systems
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Virology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Neurosurgery (AREA)
  • Transplantation (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • AIDS & HIV (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Molecular Biology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
  • Paper (AREA)
FI20021192A 1999-12-21 2002-06-19 Substituoidut 1,3,4-oksadiatsolit FI121708B (fi)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US47020399 1999-12-21
US09/470,203 US6326388B1 (en) 1999-12-21 1999-12-21 Substituted 1,3,4-oxadiazoles and a method of reducing TNF-alpha level
US0034457 2000-12-19
PCT/US2000/034457 WO2001046183A1 (fr) 1999-12-21 2000-12-19 1,3,4-OXADIAZOLES SUBSTITUES ET METHODE DE REDUCTION DES TAUX DE TNF-$g(a)

Publications (3)

Publication Number Publication Date
FI20021192A0 FI20021192A0 (fi) 2002-06-19
FI20021192A FI20021192A (fi) 2002-08-21
FI121708B true FI121708B (fi) 2011-03-15

Family

ID=23866662

Family Applications (1)

Application Number Title Priority Date Filing Date
FI20021192A FI121708B (fi) 1999-12-21 2002-06-19 Substituoidut 1,3,4-oksadiatsolit

Country Status (18)

Country Link
US (1) US6326388B1 (fr)
EP (3) EP1462449B9 (fr)
JP (1) JP4806151B2 (fr)
KR (2) KR100832499B1 (fr)
CN (1) CN1413211A (fr)
AT (3) ATE441644T1 (fr)
AU (1) AU782168B2 (fr)
CA (1) CA2394615C (fr)
DE (3) DE60016029T2 (fr)
ES (3) ES2356238T3 (fr)
FI (1) FI121708B (fr)
HK (3) HK1050522B (fr)
MX (1) MXPA02006084A (fr)
NO (1) NO323449B1 (fr)
NZ (1) NZ529009A (fr)
PT (1) PT1242413E (fr)
TW (2) TWI280961B (fr)
WO (1) WO2001046183A1 (fr)

Families Citing this family (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6429221B1 (en) * 1994-12-30 2002-08-06 Celgene Corporation Substituted imides
KR100539030B1 (ko) * 1996-08-12 2005-12-27 셀진 코포레이션 면역치료제 및 이를 이용하여 사이토카인 농도를 감소시키는 방법
US7812169B2 (en) 2000-11-30 2010-10-12 The Children's Medical Center Corporation Method of synthesis of 4-amino-thalidomide enantiomers
US7393862B2 (en) 2002-05-17 2008-07-01 Celgene Corporation Method using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for treatment of certain leukemias
USRE48890E1 (en) 2002-05-17 2022-01-11 Celgene Corporation Methods for treating multiple myeloma with 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione after stem cell transplantation
US7323479B2 (en) * 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
EP1556033A4 (fr) 2002-05-17 2006-05-31 Celgene Corp Methodes et compositions mettant en oeuvre des medicaments selectifs inhibiteurs des cytokines pour le traitement et la prise en charge des cancers et autres maladies
US7968569B2 (en) * 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
EP1539174A4 (fr) * 2002-09-16 2006-10-25 Alcon Mfg Ltd Utilisation d'inhibiteurs de pde iv pour le traitement de l'angiogenese
CN1713905A (zh) * 2002-10-15 2005-12-28 细胞基因公司 用于治疗骨髓增生异常综合征的选择性细胞因子抑制药
US20040087558A1 (en) * 2002-10-24 2004-05-06 Zeldis Jerome B. Methods of using and compositions comprising selective cytokine inhibitory drugs for treatment, modification and management of pain
US7776907B2 (en) * 2002-10-31 2010-08-17 Celgene Corporation Methods for the treatment and management of macular degeneration using cyclopropyl-N-{2-[(1S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl]-3-oxoisoindoline-4-yl}carboxamide
NZ540383A (en) 2002-11-06 2008-03-28 Celgene Corp Methods and compositions using selective cytokine inhibitory drugs for treatment and management of chronic uveitis
MXPA05004777A (es) * 2002-11-06 2005-07-22 Celgene Corp Metodos de uso y composiciones que comprenden farmacos inhibidores selectivos de citocina para el tratamiento y el manejo de padecimientos mieloproliferativos.
CN1738614A (zh) * 2002-11-18 2006-02-22 细胞基因公司 包含(-)-3-(3,4-二甲氧基-苯基)-3-(1-氧代-1,3-二氢-异吲哚-2-基)-丙酰胺的组合物及其使用方法
CA2506232A1 (fr) * 2002-11-18 2004-06-03 Celgene Corporation Compositions comprenant un (+)-3-(3,4-dimethoxy-phenyl)-3-(1-oxo-1,3-dihydro-isoindol-2-yl)-propionamide et methodes d'utilisation de ces compositions
CA2511843C (fr) * 2002-12-30 2012-04-24 Celgene Corporation Composes 1, 3-dihydro-isoindolyle a substitution fluoroalcoxy et leurs utilisations pharmaceutiques
US20040175382A1 (en) * 2003-03-06 2004-09-09 Schafer Peter H. Methods of using and compositions comprising selective cytokine inhibitory drugs for the treatment and management of disorders of the central nervous system
UA83504C2 (en) 2003-09-04 2008-07-25 Селджин Корпорейшн Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione
US20070208057A1 (en) * 2003-11-06 2007-09-06 Zeldis Jerome B Methods And Compositions Using Thalidomide For The Treatment And Management Of Cancers And Other Diseases
US20050142104A1 (en) * 2003-11-06 2005-06-30 Zeldis Jerome B. Methods of using and compositions comprising PDE4 modulators for the treatment and management of asbestos-related diseases and disorders
CA2546493A1 (fr) 2003-11-19 2005-06-09 Signal Pharmaceuticals, Llc Composes d'indazole et leurs procedes d'utilisation en tant qu'inhibiteurs de la proteine kinase
CA2563207A1 (fr) * 2004-04-14 2005-11-24 Celgene Corporation Procedes d'utilisation et compositions comprenant des medicaments d'inhibition selective de cytokine, pour traiter et controler des syndromes myelodysplasiques
WO2005102317A1 (fr) * 2004-04-23 2005-11-03 Celgene Corporation Procede d'utilisation de modulateurs de pde4 et compositions les renfermant pour le traitement et la gestion de l'hypertension pulmonaire
US7405237B2 (en) * 2004-07-28 2008-07-29 Celgene Corporation Isoindoline compounds and methods of their use
US20070190070A1 (en) * 2004-09-03 2007-08-16 Zeldis Jerome B Methods of using and compositions comprising selective cytokine inhibitory drugs for the treatment and management of disorders of the central nervous system
CN101309585A (zh) * 2004-10-28 2008-11-19 细胞基因公司 使用pde4调节剂治疗和控制中枢神经系统损伤的方法和组合物
US20060270707A1 (en) * 2005-05-24 2006-11-30 Zeldis Jerome B Methods and compositions using 4-[(cyclopropanecarbonylamino)methyl]-2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione for the treatment or prevention of cutaneous lupus
CL2007002218A1 (es) * 2006-08-03 2008-03-14 Celgene Corp Soc Organizada Ba Uso de 3-(4-amino-1-oxo-1,3-dihidro-isoindol-2-il)-piperidina 2,6-diona para la preparacion de un medicamento util para el tratamiento de linfoma de celula de capa.
WO2009020590A1 (fr) * 2007-08-07 2009-02-12 Celgene Corporation Procédés de traitement de lymphomes chez certaines populations de patients et criblage de patients pour ladite thérapie
WO2009149191A2 (fr) 2008-06-03 2009-12-10 University Of Rochester Procédés de traitement de maladie intestinale inflammatoire et gestion des symptômes de celle-ci
WO2010039538A2 (fr) 2008-09-23 2010-04-08 Georgetown University Inhibiteur de flavivirus et procédés d'utilisation de ceux-ci
EP2344479B1 (fr) 2008-09-23 2015-04-08 Georgetown University Dérivés de 1,2-benzisothiazolinone et d'isoindolinone
AU2010213936B2 (en) 2009-02-10 2014-07-31 Celgene Corporation Methods of using and compositions comprising PDE4 modulators for treatment, prevention and management of tuberculosis
US8846000B2 (en) * 2009-05-29 2014-09-30 Merck Sharp & Dohme Corp. Radiolabeled PDE10 inhibitors
US9408831B2 (en) 2010-04-07 2016-08-09 Celgene Corporation Methods for treating respiratory viral infection
JP2013531499A (ja) 2010-06-15 2013-08-08 セルジーン コーポレイション 乾癬の治療のためのバイオマーカー
WO2013025897A1 (fr) 2011-08-16 2013-02-21 Georgetown University Méthodes de traitement d'infections bactériennes au moyen de dérivés de 1,2-benzisothiazolinone et d'isoindolinone
WO2015175956A1 (fr) 2014-05-16 2015-11-19 Celgene Corporation Compositions et procédés de traitement de maladies cardiovasculaires athérosclérotiques à l'aide de modulateurs de pde4
EP3182996B1 (fr) 2014-08-22 2022-12-28 Celgene Corporation Méthodes de traitement du myélome multiple avec des composés immunomodulateurs en combinaison avec des anticorps
JP2018527302A (ja) 2015-06-26 2018-09-20 セルジーン コーポレイション 免疫調節化合物を用いたカポジ肉腫またはkshv誘発性リンパ腫の治療方法、及びバイオマーカーの使用
US10682336B2 (en) 2015-10-21 2020-06-16 Amgen Inc. PDE4 modulators for treating and preventing immune reconstitution inflammatory syndrome (IRIS)
CN107698484B (zh) * 2017-11-13 2020-05-19 广东中科药物研究有限公司 一种来那度胺的衍生物的制备方法与应用
CN110386893A (zh) 2018-04-17 2019-10-29 天津合美医药科技有限公司 异吲哚衍生物
WO2020060963A1 (fr) * 2018-09-18 2020-03-26 Alxerion Biotech Corp. Dérivés de 1, 3, 4-oxadiazole et leurs utilisations

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4173652A (en) 1976-12-18 1979-11-06 Akzona Incorporated Pharmaceutical hydroxamic acid compositions and uses thereof
SE434638B (sv) 1980-06-06 1984-08-06 Lekemedelsfabriken Medica Ab Nya terapeutiska verdefulla taurinderivat och deras framstellning
US4820828A (en) 1987-03-04 1989-04-11 Ortho Pharmaceutical Corporation Cinnamohydroxamic acids
BR9306201A (pt) * 1992-04-07 1998-06-23 Pfizer Derivados de indol como agonistas 5-ht1
US5605914A (en) 1993-07-02 1997-02-25 Celgene Corporation Imides
US5698579A (en) 1993-07-02 1997-12-16 Celgene Corporation Cyclic amides
US5463063A (en) * 1993-07-02 1995-10-31 Celgene Corporation Ring closure of N-phthaloylglutamines
FR2712886B1 (fr) * 1993-11-26 1996-01-05 Synthelabo Dérivés de 1,3,4-oxadiazol-2(3H)-one, leur préparation et leur application en thérapeutique.
JPH07278125A (ja) * 1994-03-31 1995-10-24 Nippon Chemiphar Co Ltd アルキレンジアミン誘導体
US5703098A (en) 1994-12-30 1997-12-30 Celgene Corporation Immunotherapeutic imides/amides
US6429221B1 (en) * 1994-12-30 2002-08-06 Celgene Corporation Substituted imides
US5801195A (en) 1994-12-30 1998-09-01 Celgene Corporation Immunotherapeutic aryl amides
NZ305940A (en) 1995-07-26 1999-05-28 Pfizer N-(aroyl)glycine hydroxamic acid derivatives and related compounds that inhibit the production of tnf and are useful in treating asthma
US5728845A (en) 1995-08-29 1998-03-17 Celgene Corporation Immunotherapeutic nitriles
US5728844A (en) 1995-08-29 1998-03-17 Celgene Corporation Immunotherapeutic agents
US5658940A (en) 1995-10-06 1997-08-19 Celgene Corporation Succinimide and maleimide cytokine inhibitors
US5670526A (en) * 1995-12-21 1997-09-23 Otsuka Pharmaceutical Co., Ltd. 1,3,4-oxadiazoles
PT871439E (pt) 1996-01-02 2004-08-31 Aventis Pharma Inc Compostos do acido hidroxamico substituidos (arilo heteroarilo arilmetilo ou heteroarilmetilo)
KR100539030B1 (ko) 1996-08-12 2005-12-27 셀진 코포레이션 면역치료제 및 이를 이용하여 사이토카인 농도를 감소시키는 방법
JP2921760B2 (ja) * 1997-05-21 1999-07-19 日本たばこ産業株式会社 フタルイミド誘導体及びそれら誘導体を含んでなる医薬
CA2309204A1 (fr) * 1997-11-26 1999-06-03 Dupont Pharmaceuticals Company 1,3,4-thiadiazoles et 1,3,4-oxadiazoles utilises comme antagonistes de .alpha.v.beta.3
JP2002527352A (ja) * 1998-01-29 2002-08-27 ブリストル−マイヤーズ スクイブ カンパニー 1,3,4−オキサジアゾロン誘導体
US6020358A (en) 1998-10-30 2000-02-01 Celgene Corporation Substituted phenethylsulfones and method of reducing TNFα levels

Also Published As

Publication number Publication date
FI20021192A (fi) 2002-08-21
ES2333011T3 (es) 2010-02-16
ATE282612T1 (de) 2004-12-15
EP1462449A1 (fr) 2004-09-29
HK1050522B (zh) 2005-09-02
CN1413211A (zh) 2003-04-23
WO2001046183A1 (fr) 2001-06-28
HK1069581A1 (en) 2005-05-27
EP1242413A4 (fr) 2003-04-23
MXPA02006084A (es) 2004-10-14
KR20020072283A (ko) 2002-09-14
US6326388B1 (en) 2001-12-04
TW200733960A (en) 2007-09-16
NO323449B1 (no) 2007-05-14
EP1462449B1 (fr) 2009-09-02
EP1510518A3 (fr) 2006-11-22
KR20070049688A (ko) 2007-05-11
CA2394615C (fr) 2010-03-02
EP1462449B9 (fr) 2010-03-10
NZ529009A (en) 2006-02-24
TWI280961B (en) 2007-05-11
FI20021192A0 (fi) 2002-06-19
PT1242413E (pt) 2005-03-31
JP4806151B2 (ja) 2011-11-02
EP1242413A1 (fr) 2002-09-25
AU782168B2 (en) 2005-07-07
DE60016029D1 (de) 2004-12-23
ES2356238T3 (es) 2011-04-06
NO20022937L (no) 2002-08-15
CA2394615A1 (fr) 2001-06-28
ATE441644T1 (de) 2009-09-15
ATE489996T1 (de) 2010-12-15
HK1075890A1 (en) 2005-12-30
DE60045320D1 (de) 2011-01-13
DE60016029T2 (de) 2005-10-20
ES2233488T3 (es) 2005-06-16
HK1050522A1 (en) 2003-06-27
JP2003518115A (ja) 2003-06-03
DE60042902D1 (de) 2009-10-15
EP1242413B1 (fr) 2004-11-17
EP1510518A2 (fr) 2005-03-02
NO20022937D0 (no) 2002-06-18
EP1510518B1 (fr) 2010-12-01
AU2278501A (en) 2001-07-03
KR100832499B1 (ko) 2008-05-26

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