NO20075904L - Benzimidazolforbindelser - Google Patents

Benzimidazolforbindelser

Info

Publication number
NO20075904L
NO20075904L NO20075904A NO20075904A NO20075904L NO 20075904 L NO20075904 L NO 20075904L NO 20075904 A NO20075904 A NO 20075904A NO 20075904 A NO20075904 A NO 20075904A NO 20075904 L NO20075904 L NO 20075904L
Authority
NO
Norway
Prior art keywords
group
dioxan
dimethyl
secretion
hydrogen atom
Prior art date
Application number
NO20075904A
Other languages
English (en)
Other versions
NO339502B1 (no
Inventor
Tetsuya Kawahara
Shuhei Miyazawa
Hitoshi Harada
Hideaki Fujisaki
Atsuhiko Kubota
Junichi Nagakawa
Nobuhisa Watanabe
Masanobu Shinoda
Daisuke Iida
Hiroki Terauchi
Masato Ueda
Original Assignee
Eisai R&D Man 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 R&D Man Co Ltd filed Critical Eisai R&D Man Co Ltd
Publication of NO20075904L publication Critical patent/NO20075904L/no
Publication of NO339502B1 publication Critical patent/NO339502B1/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • 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
    • C07D405/14Heterocyclic 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 three or more hetero rings
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P1/06Anti-spasmodics, e.g. drugs for colics, esophagic dyskinesia
    • 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
    • A61P1/10Laxatives
    • 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
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • 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
    • A61P27/00Drugs for disorders of the senses
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/16Otologicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/10Spiro-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)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Immunology (AREA)
  • Nutrition Science (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

Det beskrives en ny kjemisk forbindelse som benyttes som terapeutisk eller profylaktisk middel for syrerelaterte sykdommer, med en utmerket inhibitorisk effekt mot sekresjon av gastrisk syre, en utmerket effekt mot å opprettholde den inhibitoriske effekt på sekresjon av gastrisk syre for derved å opprettholde en høy intragastrisk pH-verdi over lengre tid. Forbindelsen oppviser høy sikkerhet og en god fysikokjemisk stabilitet. Det beskrives således en forbindelse representert ved formel 1: der R1 og R3 kan være lik eller forskjellig og hver bety et hydrogenatom eller en C1- C6 alkylgruppe; R2 betyr en (5,5-dimetyl-1,3-dioksan-2-yl)metoksygruppe, 5,7-dioksaspiro[2.5]oct-6-ylmetoksygruppe, 1,5,9-trioksaspiro[5.5]undec-3-ylmetoksygruppe, eller (2,2-dimetyl-1,3-dioksan-5-yl)metoksygruppe; R4 , R5 , R6 og R7 er et hydrogenatom, halogenatom, C1-C6 alkylgruppe, C1-C6 haloalkylgruppe, C1-C6 alkoksygruppe eller C1-C6 haloalkoksygruppe; og W1 er en enkeltbinding, metylen- eller etylengruppe; eller et salt derav eller et solvat av disse.
NO20075904A 2005-04-15 2007-11-15 Benzimidazolforbindelser NO339502B1 (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2005117643 2005-04-15
US67584805P 2005-04-29 2005-04-29
PCT/JP2006/308069 WO2006112442A1 (ja) 2005-04-15 2006-04-17 ベンズイミダゾール化合物

Publications (2)

Publication Number Publication Date
NO20075904L true NO20075904L (no) 2007-11-15
NO339502B1 NO339502B1 (no) 2016-12-19

Family

ID=37115157

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20075904A NO339502B1 (no) 2005-04-15 2007-11-15 Benzimidazolforbindelser

Country Status (23)

Country Link
US (3) US20070015782A1 (no)
EP (1) EP1870409B1 (no)
JP (1) JP4949246B2 (no)
KR (1) KR101285696B1 (no)
AU (1) AU2006237974B2 (no)
BR (1) BRPI0608400B8 (no)
CA (1) CA2602610C (no)
CY (1) CY1110074T1 (no)
DE (1) DE602006014261D1 (no)
DK (1) DK1870409T3 (no)
ES (1) ES2344467T3 (no)
HK (1) HK1117826A1 (no)
HR (1) HRP20100389T1 (no)
IL (1) IL186282A (no)
ME (1) ME01855B (no)
NO (1) NO339502B1 (no)
NZ (1) NZ561920A (no)
PL (1) PL1870409T3 (no)
PT (1) PT1870409E (no)
RS (1) RS51389B (no)
RU (1) RU2409573C2 (no)
SI (1) SI1870409T1 (no)
WO (1) WO2006112442A1 (no)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070015782A1 (en) * 2005-04-15 2007-01-18 Eisai Co., Ltd. Benzimidazole compound
WO2007122686A1 (ja) * 2006-04-14 2007-11-01 Eisai R & D Management Co., Ltd. ベンズイミダゾール化合物
US20110009624A9 (en) * 2006-10-13 2011-01-13 Masato Ueda Benzimidazole compounds having gastric acid secretion inhibitory action
JP2009196894A (ja) * 2006-10-13 2009-09-03 Eisai R & D Management Co Ltd スルフィニルベンズイミダゾール化合物またはその塩の製造方法
TWI546306B (zh) * 2007-04-11 2016-08-21 第一三共股份有限公司 神經胺酸衍生物之製造方法
ES2381210T3 (es) 2007-12-18 2012-05-24 Nestec S.A. Sistema para la preparación de una bebida a partir de ingredientes facilitados por un elemento postizo codificado
AU2011272853A1 (en) 2010-07-01 2013-01-10 Amgen Inc. Heterocyclic compounds and their use as inhibitors of PI3K activity
JP6262733B2 (ja) 2012-09-04 2018-01-17 シャンハイ ヘンルイ ファーマスーティカル カンパニー リミテッドShanghai Hengrui Pharmaceutical Co., Ltd. イミダゾリン誘導体、その製造法、およびそれらの医薬への適用
EP2803666B1 (de) * 2013-05-17 2016-04-27 Symrise AG Cyclische Acetale und Ketale sowie deren Verwendung als Riechstoff
JP6377334B2 (ja) * 2013-10-25 2018-08-22 東洋鋼鈑株式会社 非線形光学色素、フォトリフラクティブ材料組成物、フォトリフラクティブ基材およびホログラム記録媒体
WO2016104668A1 (ja) * 2014-12-26 2016-06-30 国立大学法人 東京大学 光学活性のプロトンポンプ阻害化合物の製造方法
US10544113B2 (en) 2016-03-07 2020-01-28 National Health Research Institute Thiazolidinone compounds and use thereof
CN112457175B (zh) * 2020-11-03 2022-09-02 山东师范大学 一种制备1,3-二苄氧基-2-丙酮的方法

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE8300736D0 (sv) 1983-02-11 1983-02-11 Haessle Ab Novel pharmacologically active compounds
EP0187977B1 (en) 1984-12-18 1990-08-29 Otsuka Pharmaceutical Co., Ltd. Tetrahydroquinoline derivatives, process for preparing the same and anti-peptic ulcer compositions containg the same
JPS62277322A (ja) 1986-02-13 1987-12-02 Takeda Chem Ind Ltd 安定化された腸溶性抗潰瘍固形組成物
JPS62207271A (ja) 1986-03-06 1987-09-11 Yamanouchi Pharmaceut Co Ltd 2−ピリジルメチルチオ基または2−ピリジルメチルスルフイニル基で置換された縮合環化合物
GB2189699A (en) 1986-04-30 1987-11-04 Haessle Ab Coated acid-labile medicaments
JPH0643426B2 (ja) 1986-07-25 1994-06-08 東京田辺製薬株式会社 イミダゾ〔4,5−b〕ピリジン誘導体、その製造法及びそれを含有する抗潰瘍剤
US5026560A (en) 1987-01-29 1991-06-25 Takeda Chemical Industries, Ltd. Spherical granules having core and their production
JPH0222273A (ja) * 1987-07-21 1990-01-25 Yoshitomi Pharmaceut Ind Ltd ピリジン化合物およびその医薬用途
JPH0633261B2 (ja) 1988-01-22 1994-05-02 東京田辺製薬株式会社 新規なイミダゾ[4,5−bピリジン誘導体、その製造法及びそれを含有する抗潰瘍剤
PL166209B1 (pl) 1990-06-20 1995-04-28 Astra Ab Sposób wytwarzania nowych pochodnych benzimidazolu PL
SE9002206D0 (sv) * 1990-06-20 1990-06-20 Haessle Ab New compounds
JP2820829B2 (ja) 1991-03-07 1998-11-05 武田薬品工業株式会社 有核散剤およびその製造方法
JPH05117268A (ja) * 1991-10-22 1993-05-14 Yoshitomi Pharmaceut Ind Ltd ピリジン化合物
JPH05177268A (ja) 1992-01-09 1993-07-20 Amada Co Ltd 縦型パンチプレス
CN1148171C (zh) 1998-04-17 2004-05-05 大正制药株式会社 多单元缓释片剂
BR9912937A (pt) 1998-08-10 2001-05-08 Partnership Of Michael E Garst Pró-drogas de inibidores de bomba de prótons
TW404832B (en) 1999-01-27 2000-09-11 Nang Kuang Pharmaceutical Co L The oral medicine with good stability cotaining the omeprazole or the analogues
US6852739B1 (en) 1999-02-26 2005-02-08 Nitromed Inc. Methods using proton pump inhibitors and nitric oxide donors
EP1154771A4 (en) 1999-02-26 2005-04-20 Nitromed Inc INHIBITORS OF THE PROTON NITROSIS AND NITROSYL PUMP, COMPOSITIONS AND METHODS OF USE
ES2168043B1 (es) 1999-09-13 2003-04-01 Esteve Labor Dr Forma farmaceutica solida oral de liberacion modificada que contiene un compuesto de bencimidazol labil en medio acido.
AU2001296908A1 (en) 2000-09-29 2002-04-08 Geneva Pharmaceuticals, Inc. Proton pump inhibitor formulation
CN100562317C (zh) 2001-10-17 2009-11-25 武田药品工业株式会社 含大量酸不稳定药物的颗粒
JP4331930B2 (ja) 2001-10-17 2009-09-16 武田薬品工業株式会社 酸に不安定な薬物の高含量顆粒
JP2003137771A (ja) 2001-10-30 2003-05-14 Nichiko Pharmaceutical Co Ltd 難溶性薬物用医薬製剤
SE0203065D0 (sv) 2002-10-16 2002-10-16 Diabact Ab Gastric acid secretion inhibiting composition
MY148805A (en) 2002-10-16 2013-05-31 Takeda Pharmaceutical Controlled release preparation
US20040166162A1 (en) 2003-01-24 2004-08-26 Robert Niecestro Novel pharmaceutical formulation containing a proton pump inhibitor and an antacid
EP1602362B1 (en) 2003-03-12 2016-09-28 Takeda Pharmaceutical Company Limited Drug composition having active ingredient adhered at high concentration to spherical core
WO2005011637A1 (ja) 2003-08-04 2005-02-10 Eisai Co., Ltd. 用時分散型製剤
US20070015782A1 (en) * 2005-04-15 2007-01-18 Eisai Co., Ltd. Benzimidazole compound

Also Published As

Publication number Publication date
JPWO2006112442A1 (ja) 2008-12-11
US8124780B2 (en) 2012-02-28
JP4949246B2 (ja) 2012-06-06
EP1870409B1 (en) 2010-05-12
PT1870409E (pt) 2010-06-22
US20090203911A1 (en) 2009-08-13
DE602006014261D1 (en) 2010-06-24
DK1870409T3 (da) 2010-08-09
ES2344467T3 (es) 2010-08-27
IL186282A (en) 2014-05-28
AU2006237974B2 (en) 2011-07-07
PL1870409T3 (pl) 2010-10-29
US20070010542A1 (en) 2007-01-11
EP1870409A4 (en) 2009-09-23
US20070015782A1 (en) 2007-01-18
BRPI0608400A2 (pt) 2010-11-16
NZ561920A (en) 2010-01-29
KR101285696B1 (ko) 2013-07-12
RS51389B (en) 2011-02-28
IL186282A0 (en) 2008-01-20
RU2007138053A (ru) 2009-05-20
CA2602610A1 (en) 2006-10-26
NO339502B1 (no) 2016-12-19
BRPI0608400B8 (pt) 2021-05-25
ME01855B (me) 2011-02-28
RU2409573C2 (ru) 2011-01-20
KR20070120531A (ko) 2007-12-24
AU2006237974A1 (en) 2006-10-26
CY1110074T1 (el) 2015-01-14
HRP20100389T1 (hr) 2010-08-31
SI1870409T1 (sl) 2010-08-31
CA2602610C (en) 2013-01-22
EP1870409A1 (en) 2007-12-26
WO2006112442A1 (ja) 2006-10-26
US7425634B2 (en) 2008-09-16
BRPI0608400B1 (pt) 2020-05-05
HK1117826A1 (en) 2009-01-23

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