[go: up one dir, main page]

WO2008120655A1 - I型11βヒドロキシステロイド脱水素酵素阻害活性を有するオキサゾリジノン誘導体 - Google Patents

I型11βヒドロキシステロイド脱水素酵素阻害活性を有するオキサゾリジノン誘導体 Download PDF

Info

Publication number
WO2008120655A1
WO2008120655A1 PCT/JP2008/055827 JP2008055827W WO2008120655A1 WO 2008120655 A1 WO2008120655 A1 WO 2008120655A1 JP 2008055827 W JP2008055827 W JP 2008055827W WO 2008120655 A1 WO2008120655 A1 WO 2008120655A1
Authority
WO
WIPO (PCT)
Prior art keywords
optionally substituted
hydroxysteroid dehydrogenase
dehydrogenase type
inhibitory activity
oxazolidinone derivative
Prior art date
Application number
PCT/JP2008/055827
Other languages
English (en)
French (fr)
Inventor
Akiko Itai
Susumu Muto
Ryuko Tokuyama
Hiroshi Fukasawa
Takeshi Yanase
Original Assignee
Institute Of Medicinal Molecular Design, Inc.
Shionogi & 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 Institute Of Medicinal Molecular Design, Inc., Shionogi & Co., Ltd. filed Critical Institute Of Medicinal Molecular Design, Inc.
Priority to JP2009507492A priority Critical patent/JPWO2008120655A1/ja
Priority to EP08738977A priority patent/EP2141154A4/en
Priority to US12/594,093 priority patent/US7998992B2/en
Publication of WO2008120655A1 publication Critical patent/WO2008120655A1/ja
Priority to US13/173,819 priority patent/US20110294813A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/18Oxygen atoms
    • C07D263/20Oxygen atoms attached in position 2
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/4211,3-Oxazoles, e.g. pemoline, trimethadione
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic 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
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • 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
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • 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
    • 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
    • C07D413/12Heterocyclic 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 chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Child & Adolescent Psychology (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)

Abstract

I型11βヒドロキシステロイド脱水素酵素阻害剤として有用な化合物を提供する。 式: (式中、 R1は置換されていてもよいシクロアルキル、置換されていてもよいシクロアルキルアルキル、置換されていてもよいヘテロサイクルまたは置換されていてもよいヘテロサイクルアルキルであり、 Xは-O-、-NR3-、-NR3C(=O)-または-NR3S(=O)2-であり、 R2は置換されていてもよいアリール、置換されていてもよいアリールアルキル、置換されていてもよいヘテロアリールまたは置換されていてもよいヘテロアリールアルキルであり、 R3は水素または置換されていてもよいアルキルである。)で示される化合物、その製薬上許容される塩またはそれらの溶媒和物。
PCT/JP2008/055827 2007-03-30 2008-03-27 I型11βヒドロキシステロイド脱水素酵素阻害活性を有するオキサゾリジノン誘導体 WO2008120655A1 (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2009507492A JPWO2008120655A1 (ja) 2007-03-30 2008-03-27 I型11βヒドロキシステロイド脱水素酵素阻害活性を有するオキサゾリジノン誘導体
EP08738977A EP2141154A4 (en) 2007-03-30 2008-03-27 OXAZOLIDINONE DERIVATIVITY WITH HEMMETIC EFFECT ON TYPE I 11-HYDROXYSTEROIDDEHYDROGENASE
US12/594,093 US7998992B2 (en) 2007-03-30 2008-03-27 Oxazolidinone derivative having inhibitory activity on 11β-hydroxysteroid dehydrogenase type 1
US13/173,819 US20110294813A1 (en) 2007-03-30 2011-06-30 Oxazolidinone derivative having inhibitory activity on 11beta-hydroxysteroid dehydrogenase type 1

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007091023 2007-03-30
JP2007-091023 2007-03-30

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/173,819 Division US20110294813A1 (en) 2007-03-30 2011-06-30 Oxazolidinone derivative having inhibitory activity on 11beta-hydroxysteroid dehydrogenase type 1

Publications (1)

Publication Number Publication Date
WO2008120655A1 true WO2008120655A1 (ja) 2008-10-09

Family

ID=39808237

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/055827 WO2008120655A1 (ja) 2007-03-30 2008-03-27 I型11βヒドロキシステロイド脱水素酵素阻害活性を有するオキサゾリジノン誘導体

Country Status (4)

Country Link
US (2) US7998992B2 (ja)
EP (1) EP2141154A4 (ja)
JP (1) JPWO2008120655A1 (ja)
WO (1) WO2008120655A1 (ja)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
WO2011157827A1 (de) 2010-06-18 2011-12-22 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
WO2011161030A1 (de) 2010-06-21 2011-12-29 Sanofi Heterocyclisch substituierte methoxyphenylderivate mit oxogruppe, verfahren zu ihrer herstellung und ihre verwendung als gpr40 rezeptor modulatoren
WO2012004270A1 (de) 2010-07-05 2012-01-12 Sanofi Spirocyclisch substituierte 1,3-propandioxidderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012004269A1 (de) 2010-07-05 2012-01-12 Sanofi ( 2 -aryloxy -acetylamino) - phenyl - propionsäurederivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012010413A1 (de) 2010-07-05 2012-01-26 Sanofi Aryloxy-alkylen-substituierte hydroxy-phenyl-hexinsäuren, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
US8324265B2 (en) 2005-11-21 2012-12-04 Shionogi & Co., Ltd. Heterocyclic compounds having type I 11β hydroxysteroid dehydrogenase inhibitory activity
US8383622B2 (en) 2007-05-18 2013-02-26 Shionogi & Co., Ltd. Nitrogen-containing heterocyclic derivative having 11β-hydroxysteroid dehydrogenase type I inhibitory activity
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
US9527867B2 (en) 2013-04-16 2016-12-27 Actelion Pharmaceuticals Ltd. Antibacterial biaromatic derivatives

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200940551A (en) * 2008-02-20 2009-10-01 Actelion Pharmaceuticals Ltd Azatricyclic antibiotic compounds
PT2344495E (pt) 2008-10-07 2015-04-01 Actelion Pharmaceuticals Ltd Compostos antibióticos de oxazolidinona tricíclica

Citations (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3062828A (en) 1962-02-27 1962-11-06 Robins Co Inc A H 5-(alkoxyphenoxymethyl)-2-oxazolidones
GB938424A (en) 1958-12-09 1963-10-02 American Cyanamid Co Improvements in or relating to substituted oxazolidin-2-ones
DE2109651A1 (de) * 1970-02-27 1971-09-09 Imperial Chemical Industries Ltd , London Oxazolidinonderivate
JPS4920768A (ja) 1972-06-20 1974-02-23
DE2606140A1 (de) 1976-02-17 1977-08-25 Boehringer Sohn Ingelheim Neue derivate des 2-phenyl-2-hydroxyaethylamins
US4066628A (en) 1976-08-02 1978-01-03 Mitsubishi Chemical Industries Ltd. Oxazolidone catalyst
DD153682A1 (de) 1978-10-19 1982-01-27 Horst Bercher Verfahren zur herstellung neuer alkanolamine
EP0064294A1 (en) 1981-05-04 1982-11-10 G.D. Searle & Co. 1,5-Substituted isoquinoline derivatives
US4602093A (en) 1984-02-08 1986-07-22 Merck & Co., Inc. Novel substituted imidazoles, their preparation and use
JPS6322559A (ja) * 1986-07-03 1988-01-30 サノフイ インド−ル誘導体の立体特異的合成法
JPH05148247A (ja) 1991-11-28 1993-06-15 Otsuka Pharmaceut Co Ltd オキサゾリジン誘導体
WO1993022298A1 (fr) 1992-04-30 1993-11-11 Taiho Pharmaceutical Co., Ltd. Derive d'oxazolidine et son sel pharmaceutiquement acceptable
WO1994022857A1 (en) 1993-04-07 1994-10-13 Taiho Pharmaceutical Co., Ltd. Thiazolidine derivative and pharmaceutical composition containing the same
US5488064A (en) 1994-05-02 1996-01-30 Bristol-Myers Squibb Company Benzo 1,3 dioxole derivatives
US5606069A (en) 1993-12-13 1997-02-25 American Cyanamid Company β3 -adrenergic agents, benzodioxole dicarboxylates and their use in pharmaceutical compositions
JPH09194482A (ja) * 1996-01-16 1997-07-29 Bayer Ag ピリド−縮合したチエニル−およびフラニル−オキサゾリジノン類
WO1999003846A1 (de) * 1997-07-18 1999-01-28 Bayer Aktiengesellschaft Tricyclisch substituierte oxazolidinone
JPH1135534A (ja) 1997-07-17 1999-02-09 Sawai Seiyaku Kk フェノキシ酢酸誘導体
JPH11507330A (ja) * 1995-06-02 1999-06-29 シンセラボ オキサゾリジノン誘導体、その製造及び治療的使用
JP2000136186A (ja) * 1998-10-29 2000-05-16 Mitsui Chemicals Inc 2−オキサゾリドン誘導体の製造方法
JP2000290265A (ja) * 1999-04-05 2000-10-17 Daiso Co Ltd オキサゾリジン−2−オン類の製造方法
JP2001055383A (ja) 1999-08-19 2001-02-27 Kyowa Hakko Kogyo Co Ltd オキサゾリドン化合物の製造法
WO2001047919A1 (de) 1999-12-24 2001-07-05 Bayer Aktiengesellschaft Substituierte oxazolidinone und ihre verwendung im gebiet der blutgerinnung
JP2002517498A (ja) * 1998-06-05 2002-06-18 アストラゼネカ アクチボラグ 化学化合物
WO2002072542A2 (en) 2001-03-08 2002-09-19 Emory University Ph-dependent nmda receptor antagonists
JP2002326988A (ja) * 2001-03-27 2002-11-15 Warner Lambert Co サブタイプの選択的なn−メチル−d−アスパルテート拮抗薬としてのシクロヘキシルアミン誘導体
WO2003000256A1 (de) 2001-06-20 2003-01-03 Bayer Healthcare Ag Kombinationstherapie substituierter oxazolidinone
WO2005108360A1 (en) * 2004-05-07 2005-11-17 Janssen Pharmaceutica N.V. Pyrrolidin-2-one and piperidin-2-one derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors
WO2005108361A1 (en) * 2004-05-07 2005-11-17 Janssen Pharmaceutica N.V. Adamantyl pyrrolidin-2-one derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors
JP2006516991A (ja) * 2003-02-07 2006-07-13 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 抗菌剤
JP2006516989A (ja) * 2003-02-07 2006-07-13 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 抗菌剤として使用するための二環式環によりn−置換されたオキサゾリジノン誘導体
WO2006090792A1 (ja) 2005-02-24 2006-08-31 Nihon Nohyaku Co., Ltd. 新規なハロアルキルスルホンアニリド誘導体、除草剤及びその使用方法
WO2006104280A1 (ja) * 2005-03-31 2006-10-05 Takeda Pharmaceutical Company Limited 糖尿病の予防・治療剤
WO2006124490A2 (en) 2005-05-17 2006-11-23 Schering Corporation Heterocycles as nicotinic acid receptor agonists for the treatment of dyslipidemia
WO2007039134A1 (de) * 2005-10-04 2007-04-12 Bayer Healthcare Ag Kombinationstherapie mit substituierten oxazolidinonen zur prophylaxe und behandlung von cerebralen durchblutungsstörungen
WO2007118185A2 (en) 2006-04-07 2007-10-18 Abbott Laboratories Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4146638A (en) 1976-02-17 1979-03-27 Boehringer Ingelheim Gmbh N-(3-phenoxy-2-hydroxy-propyl)-n-(2-phenyl-2-hydroxy-ethyl)-amines
DE3406927A1 (de) 1984-02-25 1985-08-29 Hoechst Ag, 6230 Frankfurt Strahlungsempfindliches gemisch auf basis von saeurespaltbaren verbindungen
WO2006132197A1 (ja) 2005-06-07 2006-12-14 Shionogi & Co., Ltd. I型11βヒドロキシステロイド脱水素酵素阻害活性を有するヘテロ環化合物
CA2630665C (en) 2005-11-21 2011-03-15 Shionogi & Co., Ltd. Heterocyclic compound having inhibitory activity on 11-.beta.-hydroxysteroid dehydrogenase type i
US8017638B2 (en) 2006-03-30 2011-09-13 Shionogi & Co., Ltd. Isoxazole derivative and isothiazole derivative having inhibitory activity on 11β-hydroxysteroid dehydrogenase type 1

Patent Citations (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB938424A (en) 1958-12-09 1963-10-02 American Cyanamid Co Improvements in or relating to substituted oxazolidin-2-ones
US3062828A (en) 1962-02-27 1962-11-06 Robins Co Inc A H 5-(alkoxyphenoxymethyl)-2-oxazolidones
DE2109651A1 (de) * 1970-02-27 1971-09-09 Imperial Chemical Industries Ltd , London Oxazolidinonderivate
JPS4920768A (ja) 1972-06-20 1974-02-23
DE2606140A1 (de) 1976-02-17 1977-08-25 Boehringer Sohn Ingelheim Neue derivate des 2-phenyl-2-hydroxyaethylamins
US4066628A (en) 1976-08-02 1978-01-03 Mitsubishi Chemical Industries Ltd. Oxazolidone catalyst
DD153682A1 (de) 1978-10-19 1982-01-27 Horst Bercher Verfahren zur herstellung neuer alkanolamine
EP0064294A1 (en) 1981-05-04 1982-11-10 G.D. Searle & Co. 1,5-Substituted isoquinoline derivatives
US4602093A (en) 1984-02-08 1986-07-22 Merck & Co., Inc. Novel substituted imidazoles, their preparation and use
JPS6322559A (ja) * 1986-07-03 1988-01-30 サノフイ インド−ル誘導体の立体特異的合成法
JPH05148247A (ja) 1991-11-28 1993-06-15 Otsuka Pharmaceut Co Ltd オキサゾリジン誘導体
WO1993022298A1 (fr) 1992-04-30 1993-11-11 Taiho Pharmaceutical Co., Ltd. Derive d'oxazolidine et son sel pharmaceutiquement acceptable
WO1994022857A1 (en) 1993-04-07 1994-10-13 Taiho Pharmaceutical Co., Ltd. Thiazolidine derivative and pharmaceutical composition containing the same
US5606069A (en) 1993-12-13 1997-02-25 American Cyanamid Company β3 -adrenergic agents, benzodioxole dicarboxylates and their use in pharmaceutical compositions
US5488064A (en) 1994-05-02 1996-01-30 Bristol-Myers Squibb Company Benzo 1,3 dioxole derivatives
JPH11507330A (ja) * 1995-06-02 1999-06-29 シンセラボ オキサゾリジノン誘導体、その製造及び治療的使用
JPH09194482A (ja) * 1996-01-16 1997-07-29 Bayer Ag ピリド−縮合したチエニル−およびフラニル−オキサゾリジノン類
JPH1135534A (ja) 1997-07-17 1999-02-09 Sawai Seiyaku Kk フェノキシ酢酸誘導体
WO1999003846A1 (de) * 1997-07-18 1999-01-28 Bayer Aktiengesellschaft Tricyclisch substituierte oxazolidinone
JP2002517498A (ja) * 1998-06-05 2002-06-18 アストラゼネカ アクチボラグ 化学化合物
JP2000136186A (ja) * 1998-10-29 2000-05-16 Mitsui Chemicals Inc 2−オキサゾリドン誘導体の製造方法
JP2000290265A (ja) * 1999-04-05 2000-10-17 Daiso Co Ltd オキサゾリジン−2−オン類の製造方法
JP2001055383A (ja) 1999-08-19 2001-02-27 Kyowa Hakko Kogyo Co Ltd オキサゾリドン化合物の製造法
JP2003519141A (ja) * 1999-12-24 2003-06-17 バイエル アクチェンゲゼルシャフト 置換オキサゾリジノン及び血液凝固の分野におけるそれらの使用
WO2001047919A1 (de) 1999-12-24 2001-07-05 Bayer Aktiengesellschaft Substituierte oxazolidinone und ihre verwendung im gebiet der blutgerinnung
WO2002072542A2 (en) 2001-03-08 2002-09-19 Emory University Ph-dependent nmda receptor antagonists
JP2002326988A (ja) * 2001-03-27 2002-11-15 Warner Lambert Co サブタイプの選択的なn−メチル−d−アスパルテート拮抗薬としてのシクロヘキシルアミン誘導体
WO2003000256A1 (de) 2001-06-20 2003-01-03 Bayer Healthcare Ag Kombinationstherapie substituierter oxazolidinone
JP2006516991A (ja) * 2003-02-07 2006-07-13 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 抗菌剤
JP2006516989A (ja) * 2003-02-07 2006-07-13 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー 抗菌剤として使用するための二環式環によりn−置換されたオキサゾリジノン誘導体
WO2005108360A1 (en) * 2004-05-07 2005-11-17 Janssen Pharmaceutica N.V. Pyrrolidin-2-one and piperidin-2-one derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors
WO2005108361A1 (en) * 2004-05-07 2005-11-17 Janssen Pharmaceutica N.V. Adamantyl pyrrolidin-2-one derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors
WO2006090792A1 (ja) 2005-02-24 2006-08-31 Nihon Nohyaku Co., Ltd. 新規なハロアルキルスルホンアニリド誘導体、除草剤及びその使用方法
WO2006104280A1 (ja) * 2005-03-31 2006-10-05 Takeda Pharmaceutical Company Limited 糖尿病の予防・治療剤
WO2006124490A2 (en) 2005-05-17 2006-11-23 Schering Corporation Heterocycles as nicotinic acid receptor agonists for the treatment of dyslipidemia
WO2007039134A1 (de) * 2005-10-04 2007-04-12 Bayer Healthcare Ag Kombinationstherapie mit substituierten oxazolidinonen zur prophylaxe und behandlung von cerebralen durchblutungsstörungen
WO2007118185A2 (en) 2006-04-07 2007-10-18 Abbott Laboratories Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme

Non-Patent Citations (17)

* Cited by examiner, † Cited by third party
Title
ARCHIV DER PHARMAZIE, vol. 338, no. 4, 2005, pages 147
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 16, 2006, pages 5555
CHEMISCHE BERICHTE, vol. 93, 1960, pages 1975
CLIN. ENDOCRINOL, vol. 44, 1996, pages 493
J. CLIN. ENDOCRINOL. METAB., vol. 80, 1995, pages 3155
JOURNAL OF CHROMATOGRAPHY, A, vol. 740, no. 1, 1996, pages 11
JOURNAL OF COATINGS TECHNOLOGY, vol. 55, no. 700, 1983, pages 49
JOURNAL OF MEDICINAL CHEMISTRY, vol. 29, no. 6, 1986, pages 1065
JOURNAL OF POLYMER SCIENCE, PART A, vol. 27, no. 6, 1989, pages 1843
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 82, 1960, pages 1166
LANCET, vol. 349, 1997, pages 1210
MACROMOLECULES, vol. 14, no. 5, 1981, pages 1434
MAI A. ET AL.: "Synthesis and biochemical evaluation of (R)-5-acyloxymethy- and (S)-5-acylaminomethyl-3-(1H-pyrrol-1-yl)-2-oxazolidiones as new anti-monoamine oxidase (anti-MAO) agents", ARKIVOC, no. 5, 2004, pages 32 - 43 *
PAZDRO H. ET AL.: "N-mannich bases of some 5-aryloxymethy-2-oxazolidones", DISSERTATIONES PHARMACEUTICAE ET PHARMACOLOGICAE, vol. 22, no. 5, 1970, pages 297 - 303, XP008120815 *
PROC. NAT. ACAD. SCI. USA, vol. 94, 1997, pages 14924
TETRAHEDRON LETTERS, vol. 43, no. 46, 2002, pages 8327
TETRAHEDRON, vol. 43, no. 11, 1987, pages 2505

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8324265B2 (en) 2005-11-21 2012-12-04 Shionogi & Co., Ltd. Heterocyclic compounds having type I 11β hydroxysteroid dehydrogenase inhibitory activity
US8383622B2 (en) 2007-05-18 2013-02-26 Shionogi & Co., Ltd. Nitrogen-containing heterocyclic derivative having 11β-hydroxysteroid dehydrogenase type I inhibitory activity
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
WO2011157827A1 (de) 2010-06-18 2011-12-22 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
WO2011161030A1 (de) 2010-06-21 2011-12-29 Sanofi Heterocyclisch substituierte methoxyphenylderivate mit oxogruppe, verfahren zu ihrer herstellung und ihre verwendung als gpr40 rezeptor modulatoren
WO2012004270A1 (de) 2010-07-05 2012-01-12 Sanofi Spirocyclisch substituierte 1,3-propandioxidderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012004269A1 (de) 2010-07-05 2012-01-12 Sanofi ( 2 -aryloxy -acetylamino) - phenyl - propionsäurederivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012010413A1 (de) 2010-07-05 2012-01-26 Sanofi Aryloxy-alkylen-substituierte hydroxy-phenyl-hexinsäuren, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
US9527867B2 (en) 2013-04-16 2016-12-27 Actelion Pharmaceuticals Ltd. Antibacterial biaromatic derivatives

Also Published As

Publication number Publication date
US20100113448A1 (en) 2010-05-06
EP2141154A4 (en) 2011-06-01
EP2141154A1 (en) 2010-01-06
US7998992B2 (en) 2011-08-16
US20110294813A1 (en) 2011-12-01
JPWO2008120655A1 (ja) 2010-07-15

Similar Documents

Publication Publication Date Title
WO2008120655A1 (ja) I型11βヒドロキシステロイド脱水素酵素阻害活性を有するオキサゾリジノン誘導体
WO2008142986A1 (ja) I型11βヒドロキシステロイド脱水素酵素阻害活性を有する含窒素複素環誘導体
WO2009038064A1 (ja) I型11βヒドロキシステロイド脱水素酵素阻害活性を有する複素環誘導体
WO2009020140A1 (ja) アダマンチルウレア誘導体
TW200605883A (en) Condensed heterocycle derivative having HCV inhibitory activity
WO2005110410A3 (en) Kinase inhibitors as therapeutic agents
TW200640862A (en) Pyridyl acetic acid compounds
WO2007002313A3 (en) Phenylglycinamide and pyridylglycinamide derivatives useful as anticoagulants
TNSN08407A1 (en) Organic compounds
WO2005074603A3 (en) Aminobenzoxazoles as therapeutic agents
WO2010014930A3 (en) Piperidine derivatives as jak3 inhibitors
NO20072632L (no) Oksadiazolderivater som DGAT-inhibitorer
TW200730501A (en) Heterocyclic derivatives as inhibitors of 11-β-hydroxysteroid dehydrogenase I
WO2005097129A3 (en) 6-azaindole compound
EP1867331A4 (en) TRIAZOLE DERIVATIVE AND USE THEREOF
WO2008126901A1 (ja) 含窒素複素環化合物およびそれを含有する医薬組成物
WO2008114812A1 (ja) Jak阻害剤
MY146923A (en) Novel piperazine compound, and use thereof as hcv polymerase inhibitor
WO2008010048A3 (en) Novel 2-substituted methyl penam derivatives
WO2009020137A1 (ja) アミノピラゾールアミド誘導体
NO20072753L (no) 3-Etylidenhydrazinosubstituerte heterocykliske forbindelser som trombopoietinreseptoraktivatorer
MX2012002528A (es) Agente terapeutico para trastornos del estado de animo.
WO2008153042A1 (ja) 抗腫瘍剤
WO2009051223A1 (ja) 白内障処置のための医薬組成物
ATE489388T1 (de) Immunmodulierende heterocyclische verbindungen

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08738977

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2009507492

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 12594093

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 2008738977

Country of ref document: EP