Nothing Special   »   [go: up one dir, main page]

HUP0400467A2 - 2-Iminopirrolidin-származékok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk - Google Patents

2-Iminopirrolidin-származékok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk

Info

Publication number
HUP0400467A2
HUP0400467A2 HU0400467A HUP0400467A HUP0400467A2 HU P0400467 A2 HUP0400467 A2 HU P0400467A2 HU 0400467 A HU0400467 A HU 0400467A HU P0400467 A HUP0400467 A HU P0400467A HU P0400467 A2 HUP0400467 A2 HU P0400467A2
Authority
HU
Hungary
Prior art keywords
alkyl
hydrogen
compounds
pharmaceutical compositions
group
Prior art date
Application number
HU0400467A
Other languages
English (en)
Inventor
Shuichi Suzuki
Makoto Kotake
Mitsuaki Miyamoto
Tetsuya Kawahara
Akiharu Kajiwara
Ieharu Hishinuma
Kazuo Okano
Syuhei Miyazawa
Richard Clark
Fumihiro Ozaki
Nobuaki Sato
Masanobu Shinoda
Atsushi Kamada
Itaru Tsukada
Fumiyoshi Matsuura
Yoshimitsu Naoe
Taro Terauchi
Yoshiaki Oohashi
Osamu Ito
Hiroshi Tanaka
Takashi Musha
Motoji Kogushi
Tsutomu Kawata
Toshiyuki Matsuoka
Hiroko Kobayashi
Ken-Ichi Chiba
Akifumi Kimura
Naoto Ono
Original Assignee
Eisai Co., Ltd.
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 Eisai Co., Ltd. filed Critical Eisai Co., Ltd.
Publication of HUP0400467A2 publication Critical patent/HUP0400467A2/hu
Publication of HUP0400467A3 publication Critical patent/HUP0400467A3/hu

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • 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
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • 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
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • 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
    • 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
    • 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
    • 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
    • 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
    • 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
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Pulmonology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Vascular Medicine (AREA)
  • Immunology (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyrrole Compounds (AREA)
  • Indole Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Lubricants (AREA)

Abstract

A találmány tárgyát képezik az (I) általános képletű 2-iminopirrolidin-származékok, ahol a B jelentése benzolgyűrű,piridingyűrű és hasonlók; R101-R103 jelentése hidrogén-, halogénatom,1-6 szénatomos alkilcsoport és hasonlók; R5 jelentése hidrogénatom, 1-6 szénatomos alkil-, (1-6 szénatomos alkoxi)(1-6 szénatomos alkil)-csoport és hasonlók; R6 jelentése hidrogénatom, 1-6 szilárd anyagalkil-, 1-6 szénatomos alkoxikarbonil-csoport és hasonlók; Y1jelentése vegyértékkötés, -CH2- csoport és hasonlók, Y2 jelentésevegyértékkötés, -CO- csoport és hasonlók; és Ar jelentése hidrogénatomvagy egy (II) általános képletű csoport, ahol R10-R14 jelentésehidrogénatom, 1-6 szénatomos alkil-, hidroxil-, 1-6 szénatomosalkoxicsoport és hasonlók; R11 és R12 vagy R12 és R13 együtt 5-8 tagúheterociklusos gyűrűt alkothat. A találmány a vegyületek sóit, avegyületeket tartalmazó gyógyszerészeti készítményeket és a vegyületekalkalmazását is magában foglalja. Ó
HU0400467A 2001-04-19 2002-04-19 2-iminopyrrolidine derivatives, pharmaceutical compositions containing them and their use HUP0400467A3 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2001121829 2001-04-19
JP2001269422 2001-09-05
PCT/JP2002/003961 WO2002085855A1 (fr) 2001-04-19 2002-04-19 Derives de 2-iminopyrrolidine

Publications (2)

Publication Number Publication Date
HUP0400467A2 true HUP0400467A2 (hu) 2005-02-28
HUP0400467A3 HUP0400467A3 (en) 2012-08-28

Family

ID=26613890

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0400467A HUP0400467A3 (en) 2001-04-19 2002-04-19 2-iminopyrrolidine derivatives, pharmaceutical compositions containing them and their use

Country Status (22)

Country Link
US (6) US7476688B2 (hu)
EP (6) EP1391451B1 (hu)
JP (6) JP3795458B2 (hu)
KR (2) KR100749794B1 (hu)
CN (3) CN100402499C (hu)
AT (3) ATE534627T1 (hu)
AU (1) AU2005202135B2 (hu)
BR (1) BR0208985A (hu)
CA (1) CA2446924C (hu)
CZ (1) CZ303865B6 (hu)
DE (2) DE60233043D1 (hu)
ES (1) ES2462995T3 (hu)
HK (1) HK1086269A1 (hu)
HU (1) HUP0400467A3 (hu)
IL (2) IL158491A0 (hu)
MX (1) MXPA03009497A (hu)
NO (1) NO327849B1 (hu)
NZ (1) NZ528820A (hu)
PL (1) PL368109A1 (hu)
RU (1) RU2270192C2 (hu)
WO (4) WO2002085855A1 (hu)
ZA (1) ZA200308064B (hu)

Families Citing this family (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6346510B1 (en) * 1995-10-23 2002-02-12 The Children's Medical Center Corporation Therapeutic antiangiogenic endostatin compositions
US7235567B2 (en) 2000-06-15 2007-06-26 Schering Corporation Crystalline polymorph of a bisulfate salt of a thrombin receptor antagonist
DK1598338T5 (da) 2001-04-18 2010-01-18 Euro Celtique Sa 1-(4-piperidinyl)-1,3-dihydro-2H-indol-2-on-derivater og relaterede forbindelser som nociceptinanaloger og ORL1-ligander til behandlingen af smerte
EP1391451B1 (en) 2001-04-19 2011-11-23 Eisai R&D Management Co., Ltd. 2-iminopyrrolidine derivates
US8048917B2 (en) 2005-04-06 2011-11-01 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
US7186855B2 (en) 2001-06-11 2007-03-06 Xenoport, Inc. Prodrugs of GABA analogs, compositions and uses thereof
US7049333B2 (en) * 2002-06-04 2006-05-23 Sanofi-Aventis Deutschland Gmbh Substituted thiophenes: compositions, processes of making, and uses in disease treatment and diagnosis
AU2003252259A1 (en) * 2002-07-26 2004-02-16 Nihon Nohyaku Co., Ltd. Novel haloalkylsulfonanilide derivatives, herbicides and usage thereof
CA2515715C (en) * 2003-02-19 2012-05-08 Eisai Co., Ltd. Methods for producing cyclic benzamidine derivatives
JP4786147B2 (ja) * 2003-06-26 2011-10-05 武田薬品工業株式会社 カンナビノイド受容体調節剤
US20070243632A1 (en) * 2003-07-08 2007-10-18 Coller Barry S Methods for measuring platelet reactivity of patients that have received drug eluting stents
ES2378544T3 (es) * 2003-07-08 2012-04-13 Accumetrics, Inc. Activación selectiva de plaquetas para el seguimiento de terapia con antagonistas de ADP
WO2005032464A2 (en) * 2003-09-30 2005-04-14 Merck & Co., Inc. Phenyl pyrrolidine ether tachykinin receptor antagonists
EP1677783A2 (en) 2003-10-08 2006-07-12 Nicholas Piramal India Limited Fibrinogen receptor antagonists and their use
KR20060108691A (ko) * 2003-11-28 2006-10-18 상꾜 가부시키가이샤 헤테로아릴고리를 갖는 고리상 아민 유도체
JP4749702B2 (ja) * 2003-11-28 2011-08-17 第一三共株式会社 ヘテロアリール環を有する環状アミン誘導体
US7301036B2 (en) * 2003-12-19 2007-11-27 Merck & Co., Inc. Cyclic guanidines, compositions containing such compounds and methods of use
EP1721610B1 (en) * 2004-03-04 2009-05-13 Eisai R&D Management Co., Ltd. Composition containing benzamidine derivative and method for stabilizing benzamidine derivative
EP1751150A2 (en) * 2004-05-19 2007-02-14 Neurosearch A/S Novel azabicyclic aryl derivatives
JP4820295B2 (ja) * 2004-08-16 2011-11-24 エーザイ・アール・アンド・ディー・マネジメント株式会社 イソインドール誘導体の製造方法
US7956222B2 (en) 2004-08-17 2011-06-07 Eisai R&D Management Co., Ltd Methods for producing dibromofluorobenzene derivatives
AU2005277203A1 (en) * 2004-08-20 2006-03-02 Entremed, Inc. Compositions and methods comprising proteinase activated receptor antagonists
WO2006041119A1 (ja) * 2004-10-13 2006-04-20 Eisai R & D Management Co., Ltd. ヒドラジド誘導体
JP2007084440A (ja) * 2004-11-09 2007-04-05 Eisai R & D Management Co Ltd トロンビン受容体アンタゴニストを有効成分とするくも膜下出血に伴う血管攣縮の治療剤
JPWO2006051623A1 (ja) * 2004-11-09 2008-05-29 エーザイ株式会社 トロンビン受容体アンタゴニストを有効成分とするくも膜下出血に伴う血管攣縮の治療剤
WO2006051648A1 (ja) * 2004-11-09 2006-05-18 Eisai R & D Management Co., Ltd. トロンビン受容体アンタゴニストを有効成分とするくも膜下出血に伴う血管攣縮の治療剤
DE102004061748A1 (de) * 2004-12-22 2006-07-06 Bayer Healthcare Ag Azetidin-substituierte Pyrazoline
DE102004061750A1 (de) * 2004-12-22 2006-07-06 Bayer Healthcare Ag Heteroaryl-substituierte Pyrazoline
CN100366595C (zh) * 2005-02-28 2008-02-06 北京金源化学集团有限公司 一种经由中间体2-氟-6-卤代苯酚制备1,2-二烷氧基-3-氟苯的方法
US7786330B2 (en) 2005-02-28 2010-08-31 Asahi Glass Company, Limited Process for producing 1,2-dialkoxy-3-fluorobenzene
EP1867331A4 (en) * 2005-04-06 2009-04-08 Takeda Pharmaceutical TRIAZOL DERIVATIVE AND ITS USE
US7595169B2 (en) * 2005-04-27 2009-09-29 Accumetrics, Inc. Method for determining percent platelet aggregation
US20090306059A1 (en) * 2005-05-13 2009-12-10 Tomio Kimura Cyclic amine derivative having substituted alkyl group
JP2007001974A (ja) * 2005-05-27 2007-01-11 Sankyo Co Ltd ヘテロアリール環を有する環状アミン誘導体を含有する医薬組成物
EP2308852A1 (de) 2005-08-21 2011-04-13 Abbott GmbH & Co. KG 5-Ring-Heteroaromaten-Verbindungen und ihre Verwendung als Bindungspartner für 5-HT5-Rezeptoren
ES2530398T3 (es) * 2005-09-15 2015-03-02 Ucb Pharma Sa Pirrolidin-2-onas 4-sustituidas y su uso
CN101371545A (zh) * 2006-01-12 2009-02-18 诺基亚公司 通信系统中的导频加扰
WO2007084728A2 (en) * 2006-01-19 2007-07-26 Abbott Laboratories 2-imino-benzimidazoles
WO2007102563A1 (ja) * 2006-03-02 2007-09-13 Eisai R & D Management Co., Ltd. 炎症性マーカー測定によるトロンビン受容体アンタゴニストの効果の判定方法
DE602007011231D1 (de) * 2006-03-24 2011-01-27 Eisai R&D Man Co Ltd Triazolonderivat
TWI367112B (en) 2006-06-30 2012-07-01 Schering Corp Immediate-release tablet formulations of a thrombin receptor antagonist
DE102006036023A1 (de) * 2006-08-02 2008-02-07 Sanofi-Aventis Imino-imidazo-pyridinderivate mit antithrombotischer Aktivität
JPWO2008023438A1 (ja) 2006-08-25 2010-01-07 旭硝子株式会社 1,2−ジアルコキシ−3−フルオロベンゼンの製造方法
JPWO2008026527A1 (ja) * 2006-08-28 2010-01-21 株式会社カネカ 3−シアノピロリジン誘導体およびその塩の製造方法
GB2446652A (en) * 2007-02-16 2008-08-20 Inion Ltd Osteogenic compounds
US20090022729A1 (en) * 2007-04-13 2009-01-22 Nigel Mackman Methods and compositions for treating cardiac dysfunctions
CN101675342A (zh) * 2007-05-03 2010-03-17 阿库米特里克斯股份有限公司 测量凝血酶受体拮抗剂对血小板聚集的抑制的方法
TWI417100B (zh) * 2007-06-07 2013-12-01 Astrazeneca Ab 二唑衍生物及其作為代謝型麩胺酸受體增效劑-842之用途
US7807690B2 (en) * 2007-09-21 2010-10-05 Eisai R&D Management Co., Ltd. 2,3-dihydro-iminoisoindole derivatives
DE502008003324D1 (de) * 2007-11-30 2011-06-01 Bayer Schering Pharma Ag Heteroaryl-substituierte piperidine
EP2241315B1 (en) * 2008-01-11 2013-12-11 Eisai R&D Management Co., Ltd. Pharmaceutical composition, use of 2-iminopyrrolidine derivative for production of pharmaceutical composition, and kit for treatment or amelioration of heart diseases
MY148732A (en) * 2008-02-05 2013-05-31 Sanofi Aventis Triazolium salts as par1 inhibitors, production thereof, and use as medicaments
BRPI0907486A2 (pt) * 2008-02-05 2015-07-14 Sanofi Aventis Triazolpiridazinas como inibidores de par1, sua produção e uso como medicamentos
PL2240179T3 (pl) * 2008-02-05 2017-08-31 Sanofi Imidazopirydazyny jako inhibitory PAR1, ich wytwarzanie i zastosowanie jako leku
ES2400322T3 (es) 2008-02-05 2013-04-09 Sanofi Derivados de SF5 como inhibidores de PAR-1, su preparación y utilización como medicamento
JP2011515493A (ja) * 2008-03-27 2011-05-19 バーンハム インスティトゥート フォー メディカル リサーチ 抗原受容体により誘導されるNF−κBの活性化の阻害剤
US20100056519A1 (en) * 2008-07-15 2010-03-04 Serebruany Victor L Composition and method for reducing platelet activation and for the treatment of thrombotic events
EP2166009A1 (en) * 2008-09-23 2010-03-24 Genkyo Tex Sa Pyrazolo pyridine derivatives as nadph oxidase inhibitors
EP2166008A1 (en) * 2008-09-23 2010-03-24 Genkyo Tex Sa Pyrazolo pyridine derivatives as NADPH oxidase inhibitors
EA201100874A1 (ru) 2008-12-08 2012-01-30 Бёрингер Ингельхайм Интернациональ Гмбх Соединения для лечения рака
WO2011015381A1 (en) * 2009-08-05 2011-02-10 Celltrend Gmbh Method for prognosis of pulmonary arterial hypertension by detecting anti-par1-antibodies
WO2011035332A1 (en) 2009-09-21 2011-03-24 Chemocentryx, Inc. Pyrrolidinone carboxamide derivatives as chemerin-r ( chemr23 ) modulators
US8673890B2 (en) * 2009-10-29 2014-03-18 Janssen Pharmaceutica Nv 2,3-dihydro-1H-isoindol-1-imine derivatives useful as thrombin PAR-1 receptor antagonist
ES2532902T3 (es) 2010-04-16 2015-04-01 Sanofi Piridil-vinil-pirroles tricíclicos como inhibidores de PAR1
WO2011128420A1 (de) 2010-04-16 2011-10-20 Sanofi Pyridyl-vinyl-pyrazolo-chinoline als par1-inhibitoren
CN102241621A (zh) * 2010-05-11 2011-11-16 江苏恒瑞医药股份有限公司 5,5-双取代-2-亚氨基吡咯烷类衍生物、其制备方法及其在医药上的应用
JPWO2012014889A1 (ja) * 2010-07-29 2013-09-12 エーザイ・アール・アンド・ディー・マネジメント株式会社 フタロニトリル誘導体の製造方法
CN102442965B (zh) * 2010-09-30 2013-12-11 天津药物研究院 用于治疗血栓性疾病的par-1拮抗剂及其制备方法和用途
CN102757396B (zh) * 2011-04-28 2014-10-15 天津药物研究院 含苯并五元杂环的环外亚胺化合物、其制备方法和用途
MX359634B (es) 2011-12-21 2018-10-03 Novira Therapeutics Inc Agentes antivirales contra la hepatitis b.
WO2014046125A1 (ja) * 2012-09-20 2014-03-27 エーザイ・アール・アンド・ディー・マネジメント株式会社 トロンビン受容体アンタゴニストを有効成分とする肺高血圧症の予防治療剤
PL2961732T3 (pl) 2013-02-28 2017-09-29 Janssen Sciences Ireland Uc Sulfamoilo-aryloamidy i ich stosowanie jako leków do leczenia wirusowego zapalenia wątroby typu B
MX366787B (es) 2013-05-17 2019-07-23 Janssen Sciences Ireland Uc Derivados de sulfamoiltiofenamida y su uso como medicamentos para tratar la hepatitis b.
JO3603B1 (ar) 2013-05-17 2020-07-05 Janssen Sciences Ireland Uc مشتقات سلفامويل بيرولاميد واستخدامها كادوية لمعالجة التهاب الكبد نوع بي
UY35750A (es) 2013-09-26 2015-04-30 Mnemosyne Pharmaceuticals Inc Moduladores octahidro-ciclopenta[c] pirrol negativos de nr2b
EA031804B1 (ru) 2014-02-03 2019-02-28 Вайтаи Фармасьютиклз, Инк. Дигидропирролопиридиновые ингибиторы ror-гамма
CN104086501B (zh) * 2014-07-23 2016-02-17 张远强 一种par-1拮抗剂、其制备方法和用途
SG11201702362SA (en) 2014-10-14 2017-04-27 Vitae Pharmaceuticals Inc Dihydropyrrolopyridine inhibitors of ror-gamma
US9663515B2 (en) 2014-11-05 2017-05-30 Vitae Pharmaceuticals, Inc. Dihydropyrrolopyridine inhibitors of ROR-gamma
US9845308B2 (en) 2014-11-05 2017-12-19 Vitae Pharmaceuticals, Inc. Isoindoline inhibitors of ROR-gamma
WO2016085224A2 (en) * 2014-11-25 2016-06-02 Institute For Basic Science N-heterocyclic carbene nitric oxide radical and application thereof
KR101657054B1 (ko) 2014-11-25 2016-09-19 기초과학연구원 N-헤테로고리 카벤 일산화질소 라디칼 화합물 및 그 응용
WO2016114386A1 (ja) * 2015-01-15 2016-07-21 国立研究開発法人国立精神・神経医療研究センター 進行型免疫性脱髄疾患治療剤
US10301261B2 (en) 2015-08-05 2019-05-28 Vitae Pharmaceuticals, Llc Substituted indoles as modulators of ROR-gamma
CN108463458B (zh) 2015-11-20 2022-02-01 生命医药有限责任公司 ROR-γ的调节剂
TWI757266B (zh) 2016-01-29 2022-03-11 美商維它藥物有限責任公司 ROR-γ調節劑
WO2017181141A2 (en) 2016-04-15 2017-10-19 Novira Therapeutics, Inc. Combinations and methods comprising a capsid assembly inhibitor
US9481674B1 (en) 2016-06-10 2016-11-01 Vitae Pharmaceuticals, Inc. Dihydropyrrolopyridine inhibitors of ROR-gamma
JP2020528904A (ja) 2017-07-24 2020-10-01 ヴァイティー ファーマシューティカルズ,エルエルシー RORγの阻害剤
WO2019018975A1 (en) 2017-07-24 2019-01-31 Vitae Pharmaceuticals, Inc. INHIBITORS OF ROR GAMMA
US10844044B2 (en) 2018-06-14 2020-11-24 Vanderbilt University WDR5 inhibitors and modulators
CN109053546B (zh) * 2018-07-05 2021-04-27 中国科学院兰州化学物理研究所 一种苯酞类衍生物及其制备方法和应用
US10807959B2 (en) 2018-08-16 2020-10-20 Vanderbilt University WDR5-MLL1 inhibitors and modulators
WO2022051384A1 (en) * 2020-09-01 2022-03-10 Albert Einstein College Of Medicine Compounds and methods for inhibition of bax-mediated cell death
KR102517368B1 (ko) * 2020-09-03 2023-03-31 경희대학교 산학협력단 항진균 활성을 갖는 신규한 이미다졸 유도체의 염 및 이의 용도
CN114181088B (zh) * 2021-12-21 2024-05-17 大连大学 一种离子液体[TEA][TfOH]2催化制备α-卤代苯乙酮类化合物的方法
KR20230163654A (ko) * 2022-05-24 2023-12-01 주식회사 이노보테라퓨틱스 벤조퓨라닐 히드록시페닐 메타논 옥심 유도체 및 이의 용도
CN115521266A (zh) * 2022-10-25 2022-12-27 广东医科大学 一种乙烯基异噁唑烷衍生物的制备方法
CN116675677B (zh) * 2023-08-02 2023-09-26 中国林业科学研究院林产化学工业研究所 一种c8漆酚衍生物及其制备方法和应用

Family Cites Families (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR8129E (fr) 1906-03-09 1908-01-20 Zeiss Carl Soc Garniture de canon munie d'une lunette de visée
US6087380A (en) * 1949-11-24 2000-07-11 Boehringer Ingelheim Pharma Kg Disubstituted bicyclic heterocycles, the preparations and the use thereof as pharmaceutical compositions
JPS4842875B1 (hu) 1969-01-29 1973-12-14
US3717648A (en) * 1970-10-21 1973-02-20 Sterling Drug Inc 1-phenyl-azacarbocyclic-2-imines
DE2154525A1 (de) 1970-11-05 1972-06-15 Carlo Erba S.P.A., Mailand (Italien) Isoindolinderivate und Verfahren zu ihrer Herstellung
US4118504A (en) 1970-11-05 1978-10-03 Carlo Erba Isoindoline derivatives for treating pain
GB1344663A (en) 1970-11-10 1974-01-23 Erba Carlo Spa Isoindoline compounds
ZA722407B (en) 1971-05-13 1973-01-31 Richardson Merrell Inc Substituted cycloalkyl lactamimides
JPS512868B2 (hu) 1971-09-30 1976-01-29
US3773788A (en) 1971-11-26 1973-11-20 Standard Oil Co Method for the preparation of n-(substituted phenyl)-2-iminopyrrolidines
US3920688A (en) * 1973-02-05 1975-11-18 Monsanto Co 2-imino derivatives of substituted imidazoles
US3859302A (en) 1973-02-05 1975-01-07 Monsanto Co Preparation of 2-imino-imidazole derivatives
US3904395A (en) 1973-02-05 1975-09-09 Monsanto Co 2-Imino derivatives of substituted imidazoles
US3887577A (en) 1973-07-05 1975-06-03 Monsanto Co Process for the preparation of 2-imino derivatives of substituted imidazoles
US4126611A (en) * 1973-08-09 1978-11-21 Richardson-Merrell Inc. Substituted cycloalkyl lactamimides
DE2430354A1 (de) 1974-06-25 1976-01-15 Basf Ag Neue substituierte 1-amino-isoindole, verfahren zu deren herstellung sowie diese enthaltende pharmazeutische zubereitungen
JPS5122720A (ja) 1974-08-19 1976-02-23 Sumitomo Chemical Co Jukyobaifuanteigatadofutaroshianinganryono seizoho
GB1476949A (en) 1974-11-20 1977-06-16 Wyeth John & Brother Ltd Imidazo-1,2-a-benzimidazole and pyrimido-1,2-a-benzimidazole derivatives their preparation and their pharmaceutical compositions
GB1484615A (en) * 1974-11-23 1977-09-01 Lepetit Spa Tricyclic n-containing derivatives
US4004016A (en) 1975-08-11 1977-01-18 E. R. Squibb & Sons, Inc. Amino-benzimidazole derivatives
JPS5371063A (en) 1976-12-03 1978-06-24 Grelan Pharmaceut Co Ltd Preparation of 4-(1-9x9-2-isoindolinyl)acetophenone
US4521793A (en) 1982-02-27 1985-06-04 Asahi Kasei Kogyo Kabushiki Kaisha Coloring method and color-forming material
JPS6222760A (ja) 1985-07-24 1987-01-30 Sankyo Co Ltd イソインドリン誘導体及びそれを有効成分とする農園芸用殺菌剤
US5002941A (en) 1985-12-12 1991-03-26 Smithkline Beecham Corporation Pyrrolo(1,2-a)imidazole and imidazo(1,2-a)pyridine derivatives and their use as 5-lipoxygenase pathway inhibitors
FR2595521B1 (fr) * 1986-03-07 1988-10-21 Electricite De France Dispositif de telecomptage
ES2005450A6 (es) 1987-11-16 1989-03-01 Gema Sa Procedimiento para la preparacion de derivados n(4-etil-2,3-dioxo)-piperacin-1-iln-carbonilo.
JP2805867B2 (ja) 1989-07-19 1998-09-30 日本電気株式会社 電子写真感光体
US5145818A (en) * 1989-12-29 1992-09-08 Mitsui Petrochemical Industries, Ltd. Olefin polymerization catalyst and process for the polymerization of olefins
US5258387A (en) 1990-08-21 1993-11-02 Hoffmann-La Roche Inc. Tricyclic pyridone derivatives
CA2048003A1 (en) 1990-08-21 1992-02-22 Serge Burner Tricyclic pyridone derivatives
GB2266642B (en) * 1991-01-03 1995-08-16 Sasktel Data collection network apparatus and method
EP0509582B1 (en) * 1991-04-16 1996-09-04 Koninklijke Philips Electronics N.V. SMD-resistor
CA2134347C (en) * 1993-02-26 2003-04-29 Koichi Yasumura Thiazole or imidazole derivatives as maillard reaction inhibitors
JPH0732103A (ja) 1993-07-19 1995-02-03 Sumitomo Metal Ind Ltd 溶融金属の鋳造用ノズル
AU688811B2 (en) 1993-10-21 1998-03-19 G.D. Searle & Co. Amidino derivatives useful as nitric oxide synthase inhibitors
CN1070191C (zh) 1994-08-12 2001-08-29 富山化学工业株式会社 新的喹诺酮-或萘酮-羧酸衍生物或其盐
US5629322A (en) 1994-11-15 1997-05-13 Merck & Co., Inc. Cyclic amidine analogs as inhibitors of nitric oxide synthase
JP3666922B2 (ja) 1995-02-21 2005-06-29 山本化成株式会社 カルボン酸塩、その製造方法および該塩化合物を用いる感熱記録材料
TW401408B (en) 1995-07-21 2000-08-11 Fujisawa Pharmaceutical Co Heterocyclic compounds having prostaglandin I2 agonism
WO1998000408A1 (en) 1996-07-02 1998-01-08 Novartis Ag N-phenylimino heterocyclic derivatives and their use as herbicides
JP2707239B2 (ja) * 1996-07-26 1998-01-28 日本バイエルアグロケム株式会社 シアノアルキルーヘテロ環式化合物及び殺虫剤
IL129298A0 (en) * 1996-10-02 2000-02-17 Janssen Pharmaceutica Nv PDE iv inhibiting 2-cyanoiminoimidazole derivatives
US5977134A (en) 1996-12-05 1999-11-02 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
FR2757053B1 (fr) 1996-12-12 1999-01-22 Oreal Utilisation de derives de la di-imino-isoindoline ou de la 3-amino-isoindolone pour la teinture des fibres keratiniques et compositions de teinture les renfermant
PE121699A1 (es) * 1997-02-18 1999-12-08 Boehringer Ingelheim Pharma Heterociclos biciclicos disustituidos como inhibidores de la trombina
US6187799B1 (en) 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
JP2002510313A (ja) * 1997-06-26 2002-04-02 イーライ・リリー・アンド・カンパニー 抗血栓物質
US6465484B1 (en) * 1997-09-26 2002-10-15 Merck & Co., Inc. Angiogenesis inhibitors
PT1036072E (pt) 1997-11-25 2004-08-31 Schering Corp Antagonistas de receptores de trombina
US6114532A (en) * 1998-02-03 2000-09-05 Boehringer Ingelheim Pharma Kg Bicyclic heterocycles, the preparation thereof, and their use as pharmaceuticals
AU2720199A (en) * 1998-02-03 1999-08-23 Boehringer Ingelheim Pharma Kg Five-membered, benzo-condensed heterocycles used as antithrombotic agents
US6194447B1 (en) 1998-07-02 2001-02-27 Neurosearch A/S Bis (benzimidazole) derivatives serving as potassium blocking agents
DE69924493T2 (de) 1998-07-02 2005-09-15 Neurosearch A/S Kaliumkanal-blockierende mittel
WO2000053582A1 (en) 1999-03-05 2000-09-14 Suntory Limited HETEROCYCLIC COMPOUNDS HAVING EFFECT OF ACTIVATING NICOTINIC ACETYLCHOLINE α4β2 RECEPTOR
US6376530B1 (en) 1999-05-10 2002-04-23 Merck & Co., Inc. Cyclic amidines useful as NMDA NR2B antagonists
JP3647338B2 (ja) * 1999-11-11 2005-05-11 富士通株式会社 画像信号解像度変換方法及び装置
ES2265447T3 (es) * 2000-11-10 2007-02-16 Eli Lilly And Company Agonistas de receptor beta-3 de oxindol-3-sustituido.
JP2002155060A (ja) 2000-11-15 2002-05-28 Japan Tobacco Inc イミダゾール化合物及びその用途
EP1391451B1 (en) 2001-04-19 2011-11-23 Eisai R&D Management Co., Ltd. 2-iminopyrrolidine derivates
JP4151310B2 (ja) 2001-05-22 2008-09-17 Dic株式会社 硬化性不飽和樹脂組成物
US6726177B2 (en) 2002-07-02 2004-04-27 Value Valves Co., Ltd. Valve with improved junk ring structure
JP3725843B2 (ja) * 2002-07-05 2005-12-14 ローム株式会社 反射型センサ
CA2515715C (en) 2003-02-19 2012-05-08 Eisai Co., Ltd. Methods for producing cyclic benzamidine derivatives

Also Published As

Publication number Publication date
KR20030090764A (ko) 2003-11-28
JP4516922B2 (ja) 2010-08-04
EP1386912A1 (en) 2004-02-04
US7476688B2 (en) 2009-01-13
US20050004197A1 (en) 2005-01-06
NO20034632L (no) 2003-12-19
EP1394152A1 (en) 2004-03-03
JPWO2002085855A1 (ja) 2004-08-12
US20090215795A1 (en) 2009-08-27
CN1503784A (zh) 2004-06-09
EP1386912A4 (en) 2006-02-01
US7304083B2 (en) 2007-12-04
WO2002088092A1 (fr) 2002-11-07
EP1394152A4 (en) 2005-02-02
EP1391456B1 (en) 2009-07-22
JP4464928B2 (ja) 2010-05-19
US20050245592A1 (en) 2005-11-03
KR100749795B1 (ko) 2007-08-17
AU2005202135B2 (en) 2007-11-15
EP2385039B1 (en) 2014-03-12
DE60231608D1 (de) 2009-04-30
ES2462995T3 (es) 2014-05-27
CN1754880A (zh) 2006-04-05
JPWO2002088094A1 (ja) 2004-08-12
JPWO2002085850A1 (ja) 2004-08-12
US7244730B2 (en) 2007-07-17
ATE538090T1 (de) 2012-01-15
CN1321996C (zh) 2007-06-20
MXPA03009497A (es) 2004-05-24
WO2002088094A1 (fr) 2002-11-07
EP2385039A1 (en) 2011-11-09
JP3795458B2 (ja) 2006-07-12
JPWO2002088092A1 (ja) 2004-08-12
PL368109A1 (en) 2005-03-21
JP4251872B2 (ja) 2009-04-08
CA2446924A1 (en) 2002-10-31
EP1614680A3 (en) 2006-02-01
AU2002255269B2 (en) 2007-03-15
EP1391451B1 (en) 2011-11-23
DE60233043D1 (de) 2009-09-03
ATE425964T1 (de) 2009-04-15
CZ303865B6 (cs) 2013-05-29
BR0208985A (pt) 2004-03-09
ATE534627T1 (de) 2011-12-15
US20050004204A1 (en) 2005-01-06
CN1733725A (zh) 2006-02-15
EP1614680B1 (en) 2011-12-21
HUP0400467A3 (en) 2012-08-28
AU2005202135A1 (en) 2005-06-09
NO20034632D0 (no) 2003-10-16
EP1391451A1 (en) 2004-02-25
US20040254376A1 (en) 2004-12-16
JP4445201B2 (ja) 2010-04-07
EP1614680A2 (en) 2006-01-11
CZ20032824A3 (en) 2004-04-14
JP4220249B2 (ja) 2009-02-04
CN1243735C (zh) 2006-03-01
EP1391456A4 (en) 2006-02-01
CA2446924C (en) 2011-02-08
WO2002085855A1 (fr) 2002-10-31
RU2270192C2 (ru) 2006-02-20
KR100749794B1 (ko) 2007-08-17
EP1386912B1 (en) 2009-03-18
HK1086269A1 (en) 2006-09-15
IL158491A0 (en) 2004-05-12
CN100402499C (zh) 2008-07-16
US20040242627A1 (en) 2004-12-02
WO2002085850A1 (fr) 2002-10-31
RU2003133664A (ru) 2005-05-10
IL158491A (en) 2010-12-30
NO327849B1 (no) 2009-10-05
JP2006225393A (ja) 2006-08-31
NZ528820A (en) 2007-01-26
EP1391456A1 (en) 2004-02-25
JP2006206595A (ja) 2006-08-10
ZA200308064B (en) 2005-04-26
EP1391451A4 (en) 2006-02-01
KR20050059343A (ko) 2005-06-17

Similar Documents

Publication Publication Date Title
HUP0400467A2 (hu) 2-Iminopirrolidin-származékok, ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk
HUP0300350A2 (hu) Új 3-amino-azetidin-származékok, előállításuk és ezeket tartalmazó gyógyszerkészítmények
HUP0303841A2 (hu) 2,4-Diszubsztituált-5-pirimidinkarboxamid-származékok mint KCNQ káliumcsatorna modulátorok és ezeket tartalmazó gyógyszerkészítmények és előállításuk
HUP0401503A2 (hu) Indol, aza-indol és hasonló heterociklikus amido-piperazin-származékok és ezeket tartalmazó gyógyszerkészítmények
HUP0302480A2 (hu) Piridinonszármazékok ateroszklerózis kezelésére, eljárás ezek előállítására és ezeket tartalmazó gyógyszerkészítmények
HUP0302435A2 (hu) 11-Béta-hidroxiszteroid dehidrogenáz 1 típusú enzimet gátló anyagok és ezeket tartalmazó gyógyszerkészítmények
HUP0302367A2 (hu) HIV Integráz inhibitorokként hasznos aza- és poliazanaftalenil-karboxamidok, ezeket tartalmazó gyógyszerkészítmények
PL396946A1 (pl) Pochodne pirazolu i kompozycje farmaceutyczne zawierające je oraz ich zastosowanie do leczenia HIV
HUP0300565A2 (hu) PDE 5 inhibitor hatású 8-kinolin-xantin- és 8-izo-kinolin-xantin-származékok, alkalmazásuk, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények
HUP0302167A2 (hu) Metabotropikus glutamát receptor antagonista hatású kinolinszármazékok, a vegyületeket tartalmazó gyógyszerkészítmények és eljárás előállításukra
HUP0302487A2 (hu) Új mandulasavszármazékok és felhasználásuk trombin inhibitorokként, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények
HUP0302603A2 (hu) Nitrogéntartalmú aromás származékok és ezeket tartalmazó gyógyászati készítmények
HUP0400202A2 (hu) Metalloproteináz inhibitor, hatású imidazolidin-dion-származékok alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények
HUP0400828A2 (hu) Kondenzált heterociklikus aminopirimidinek, alkalmazásuk és az ezeket tartalmazó gyógyszerkészítmények
HUP0400636A2 (hu) Azetidinszármazékokat tartalmazó gyógyszerkészítmények, új azetidinszármazékok és előállításuk
HUP0303283A2 (hu) Új piridinilcsoporttal szubsztituált pirazolopiridin-származékok, előállításuk és alkalmazásuk szív- és keringési betegségek kezelésére alkalmas gyógyszerkészítmény előállítására
NO20004778L (no) Amidderivater og nociceptin antagonister
CY1111822T1 (el) Παραγωγα σπειροϊνδολινοπιπεριδινης ονες
HUP0203453A2 (en) Quinazoline derivatives as vegf inhibitors, process for their preparation, pharmaceutical compositions containing them and their use
HUP0400451A2 (hu) Pirrolszármazékok és ezeket tartalmazó gyógyászati készítmények
HUP0401982A2 (hu) Indolizinszármazékok, eljárás előállításukra és a vegyületeket tartalmazó gyógyászati készítmények
ATE297910T1 (de) Retinoid x rezeptormodulatoren
CO5550439A2 (es) Compuestos derivados de arilsulfonil-piperazina que tienen afinidad al receptor 5-ht6 y composiciones farmaceuticas que los contienen
HUP0402675A2 (hu) HIV integráz inhibitor hatású hidroxilaminszármazékok, az ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk
HRP20050213A2 (en) 2,4-substituted indoles and their use as 5-ht6 modulators

Legal Events

Date Code Title Description
GB9A Succession in title

Owner name: EISAI R&D MANAGEMENT CO., LTD., JP

Free format text: FORMER OWNER(S): EISAI CO., LTD., JP

FD9A Lapse of provisional protection due to non-payment of fees