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

WO2008142986A1 - 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 - 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含窒素複素環誘導体 Download PDF

Info

Publication number
WO2008142986A1
WO2008142986A1 PCT/JP2008/058461 JP2008058461W WO2008142986A1 WO 2008142986 A1 WO2008142986 A1 WO 2008142986A1 JP 2008058461 W JP2008058461 W JP 2008058461W WO 2008142986 A1 WO2008142986 A1 WO 2008142986A1
Authority
WO
WIPO (PCT)
Prior art keywords
optionally substituted
hydrogen
substituted alkyl
hydroxysteroid dehydrogenase
dehydrogenase type
Prior art date
Application number
PCT/JP2008/058461
Other languages
English (en)
French (fr)
Inventor
Koji Masuda
Tomoyuki Ogawa
Takuji Nakatani
Original Assignee
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
Priority to JP2009515137A priority Critical patent/JP4671369B2/ja
Priority to CA2689659A priority patent/CA2689659C/en
Priority to DK08764258T priority patent/DK2163543T3/en
Priority to CN200880025349.3A priority patent/CN101754954B/zh
Priority to MX2009012283A priority patent/MX2009012283A/es
Priority to BRPI0811191-0A2A priority patent/BRPI0811191A2/pt
Priority to PL08764258T priority patent/PL2163543T3/pl
Priority to EP08764258.3A priority patent/EP2163543B1/en
Application filed by Shionogi & Co., Ltd. filed Critical Shionogi & Co., Ltd.
Priority to KR1020127009630A priority patent/KR101376432B1/ko
Priority to US12/599,133 priority patent/US8383622B2/en
Priority to ES08764258.3T priority patent/ES2535317T3/es
Priority to AU2008252185A priority patent/AU2008252185B2/en
Publication of WO2008142986A1 publication Critical patent/WO2008142986A1/ja
Priority to HK10107274.0A priority patent/HK1140766A1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • 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
    • A61K31/4151,2-Diazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • 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
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D231/16Halogen atoms or nitro radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D231/18One oxygen or sulfur atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D231/18One oxygen or sulfur atom
    • C07D231/20One oxygen atom attached in position 3 or 5
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D231/38Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (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(Ⅰ): (式中、 環Aは、(ⅠⅠ) であり、 環Bは、置換されていてもよいヘテロアリール(ただし、置換されていてもよいイソキサゾールは除く。)または置換されていてもよいヘテロサイクルであり、 R1は水素または置換されていてもよいアルキルであり、 R2は-OR5、-SR5、ハロゲンまたはハロゲン化アルキル等であり、 R3は置換されていてもよいアルキル等であり、 R4は置換されていてもよいアルキル等あり、 R5は置換されていてもよいアルキル等であり、 R6は水素等であり、 R7およびR8は各々独立して水素等であり、 R10およびR11は各々独立して水素等であり、 R12は置換されていてもよいアルキル等であり、 mおよびpは各々独立して1~3の整数である。)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/JP2008/058461 2007-05-18 2008-05-07 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 WO2008142986A1 (ja)

Priority Applications (13)

Application Number Priority Date Filing Date Title
PL08764258T PL2163543T3 (pl) 2007-05-18 2008-05-07 Heterocykliczna pochodna zawierająca azot o aktywności hamującej dehydrogenazę 11-beta-hydroksysteroidową typu I
DK08764258T DK2163543T3 (en) 2007-05-18 2008-05-07 Nitrogenholdigt heterocyklisk derivat med 11beta-hydroxysteroiddehydrogenase-type 1-inhibitorisk aktivitet
CN200880025349.3A CN101754954B (zh) 2007-05-18 2008-05-07 具有11β-羟基类固醇脱氢酶Ⅰ型抑制活性的含氮杂环衍生物
MX2009012283A MX2009012283A (es) 2007-05-18 2008-05-07 Derivado heterociclico que contiene nitrogeno que tiene actividad inhibitoria de 11beta-hidroxiesteroide-deshidrogenasa tipo 1.
BRPI0811191-0A2A BRPI0811191A2 (pt) 2007-05-18 2008-05-07 Derivado heterocíclico contendo nitrogênio tendo atividade inibitória para 11beta-hidroxiesteroide deidrogenase tipo 1
JP2009515137A JP4671369B2 (ja) 2007-05-18 2008-05-07 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
EP08764258.3A EP2163543B1 (en) 2007-05-18 2008-05-07 Nitrogen-containing heterocyclic derivative having 11 beta-hydroxysteroid dehydrogenase type i inhibitory activity
CA2689659A CA2689659C (en) 2007-05-18 2008-05-07 Nitrogen-containing heterocyclic derivative having 11.beta.-hydroxysteroid dehydrogenase type 1 inhibitory activity
KR1020127009630A KR101376432B1 (ko) 2007-05-18 2008-05-07 11β-하이드록시스테로이드 탈수소효소 유형 1 저해 활성을 갖는 질소-함유 헤테로환형 유도체
US12/599,133 US8383622B2 (en) 2007-05-18 2008-05-07 Nitrogen-containing heterocyclic derivative having 11β-hydroxysteroid dehydrogenase type I inhibitory activity
ES08764258.3T ES2535317T3 (es) 2007-05-18 2008-05-07 Derivado heterocíclico que contiene nitrógeno que tiene actividad inhibidora de la 11 beta-hidroxiesteroide deshidrogenasa de tipo 1
AU2008252185A AU2008252185B2 (en) 2007-05-18 2008-05-07 Nitrogen-containing heterocyclic derivative having 11 beta-hydroxysteroid dehydrogenase type I inhibitory activity
HK10107274.0A HK1140766A1 (en) 2007-05-18 2010-07-29 Nitrogen-containing heterocyclic derivative having 11 beta-hydroxysteroid dehydrogenase type i inhibitory activity 11- i

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2007132259 2007-05-18
JP2007-132259 2007-05-18
JP2007327114 2007-12-19
JP2007-327114 2007-12-19

Publications (1)

Publication Number Publication Date
WO2008142986A1 true WO2008142986A1 (ja) 2008-11-27

Family

ID=40031701

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/058461 WO2008142986A1 (ja) 2007-05-18 2008-05-07 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

Country Status (16)

Country Link
US (1) US8383622B2 (ja)
EP (1) EP2163543B1 (ja)
JP (2) JP4671369B2 (ja)
KR (2) KR101376432B1 (ja)
CN (2) CN103288738B (ja)
AU (1) AU2008252185B2 (ja)
BR (1) BRPI0811191A2 (ja)
CA (1) CA2689659C (ja)
DK (1) DK2163543T3 (ja)
ES (1) ES2535317T3 (ja)
HK (1) HK1140766A1 (ja)
MX (1) MX2009012283A (ja)
PL (1) PL2163543T3 (ja)
RU (1) RU2455285C2 (ja)
TW (1) TWI426902B (ja)
WO (1) WO2008142986A1 (ja)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7816391B2 (en) 2007-02-12 2010-10-19 Astrazeneca Ab Chemical compounds
EP2243479A2 (en) 2009-04-20 2010-10-27 Abbott Laboratories Novel amide and amidine derivates and uses thereof
US7951833B2 (en) 2008-02-04 2011-05-31 Astrazeneca Ab Crystalline forms of 4-[4-(2-adamantylcarbamoyl)-5-tert-butyl-pyrazol-1-yl]Benzoic acid 471
US7964618B2 (en) 2006-11-03 2011-06-21 Astrazeneca Ab Chemical compounds
WO2011078101A1 (ja) 2009-12-22 2011-06-30 塩野義製薬株式会社 アダマンタンアミン誘導体
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
WO2011142359A1 (ja) * 2010-05-10 2011-11-17 日産化学工業株式会社 スピロ化合物及びアディポネクチン受容体活性化薬
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
WO2012004269A1 (de) 2010-07-05 2012-01-12 Sanofi ( 2 -aryloxy -acetylamino) - phenyl - propionsäurederivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012004270A1 (de) 2010-07-05 2012-01-12 Sanofi Spirocyclisch substituierte 1,3-propandioxidderivate, 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
WO2012020724A1 (ja) 2010-08-09 2012-02-16 塩野義製薬株式会社 アミノアダマンタンカルバメート誘導体の製造方法
WO2012124781A1 (ja) 2011-03-17 2012-09-20 塩野義製薬株式会社 ピラゾールカルボン酸誘導体の製造方法
US8324265B2 (en) 2005-11-21 2012-12-04 Shionogi & Co., Ltd. Heterocyclic compounds having type I 11β hydroxysteroid dehydrogenase inhibitory activity
US8383381B2 (en) 2007-09-27 2013-02-26 Shjonogi & Co., Ltd. Method for producing hydroxylated adaivjantane using cytochrome P450
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
JP2014517013A (ja) * 2011-06-10 2014-07-17 エスケー バイオファーマシューティカルズ カンパニー リミテッド 5−カルバモイルアダマンタン−2−イルアミド誘導体、その薬学的に許容可能な塩およびその製造方法
WO2017094743A1 (ja) * 2015-11-30 2017-06-08 塩野義製薬株式会社 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医薬組成物

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8871208B2 (en) * 2009-12-04 2014-10-28 Abbvie Inc. 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors and uses thereof
CA2809112A1 (en) * 2010-09-03 2012-03-08 Dainippon Sumitomo Pharma Co., Ltd. Cyclic amide derivative
RU2533558C1 (ru) * 2013-08-06 2014-11-20 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) Способ получения 1-(1-адамантил)-3,4-динитро-5-(o-r)-1h-пиразолов
RU2532268C1 (ru) * 2013-08-06 2014-11-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Волгоградский государственный технический университет" (ВолгГТУ) Способ получения 1-(1-адамантил)-3,4-динитро-5(n-нитропиразолил)-1h-пиразолов
CN111423396B (zh) * 2020-04-30 2023-01-06 沈阳药科大学 一种sEH抑制剂及其制备方法和应用

Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998041519A1 (en) 1997-03-18 1998-09-24 Smithkline Beecham Corporation Novel cannabinoid receptor agonists
WO2001023358A1 (fr) 1999-09-27 2001-04-05 Sagami Chemical Research Center Derives pyrazole, intermediaires pour la preparation de ces derives, procedes de preparation des derives et intermediaires, et herbicides dont ces derives sont le principe actif
WO2005016877A2 (en) 2003-08-07 2005-02-24 Merck & Co., Inc. Pyrazole carboxamides as inhibitors of 11-beta-hydroxysteroid dehydrogenase-1
WO2005061462A2 (en) 2003-12-19 2005-07-07 Neurogen Corporation Diaryl pyrazole derivatives and their use as neurokinin-3 receptor modulators
WO2005108368A1 (en) 2004-04-29 2005-11-17 Abbott Laboratories Adamantyl-acetamide derivatives as inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme
US20050277647A1 (en) 2004-04-29 2005-12-15 Link James T Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme
WO2006024627A2 (en) 2004-08-30 2006-03-09 Janssen Pharmaceutica N.V. N-2 adamantanyl-2-phenoxy-acetamide derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors
WO2006074330A2 (en) 2005-01-05 2006-07-13 Abbott Laboratories Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme
WO2006074244A2 (en) 2005-01-05 2006-07-13 Abbott Laboratories Adamantyl derivatives as inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme
WO2006106052A1 (en) 2005-04-05 2006-10-12 F. Hoffmann-La Roche Ag Pyrazoles
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
WO2007058346A1 (ja) 2005-11-21 2007-05-24 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
WO2007107470A2 (en) 2006-03-22 2007-09-27 F. Hoffmann-La Roche Ag Pyrazoles as 11-beta-hsd-1
WO2007114124A1 (ja) * 2006-03-30 2007-10-11 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イソキサゾール誘導体およびイソチアゾール誘導体
WO2007114125A1 (ja) * 2006-03-31 2007-10-11 Shionogi & Co., Ltd. 微生物によるアダマンタン水酸化体の製造方法
WO2007144394A2 (en) * 2006-06-16 2007-12-21 High Point Pharmaceuticals, Llc. Pharmaceutical use of substituted piperidine carboxamides
WO2008012532A2 (en) * 2006-07-27 2008-01-31 Astrazeneca Ab : pyridine-3-carboxamide compounds and their use for inhibiting 11-beta-hydroxysteroid dehydrogenase
WO2008053652A1 (fr) * 2006-11-02 2008-05-08 Shionogi & Co., Ltd. Procédé de fabrication d'hydroxyadamantane-amine

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4226877A (en) * 1979-05-14 1980-10-07 Abbott Laboratories Pyrazoles active in the central nervous system
JPS60214785A (ja) 1984-03-27 1985-10-28 Nissan Chem Ind Ltd ピラゾ−ルスルホニルウレア誘導体、および植物生長調節剤または除草剤
JPH01207289A (ja) 1987-10-19 1989-08-21 Mitsui Toatsu Chem Inc アシルアミノアセトニトリル誘導体の製造法
AU626402B2 (en) 1989-04-19 1992-07-30 Sumitomo Chemical Company, Limited An amide compound and its production and use
DE69322118T2 (de) 1992-04-17 1999-05-20 Hodogaya Chemical Co., Ltd., Tokio/Tokyo Amino-Thiazolderivate und ihre Anwendung als Fungizide
IL105939A0 (en) 1992-06-11 1993-10-20 Rhone Poulenc Agriculture Herbicidal compounds and compositions
GB9517622D0 (en) 1995-08-29 1995-11-01 Univ Edinburgh Regulation of intracellular glucocorticoid concentrations
AU2001276378A1 (en) 2000-07-05 2002-01-14 Bayer Aktiengesellschaft Regulation of human 11 beta-hydroxysteroid dehydrogenase 1-like enzyme
GB0107383D0 (en) 2001-03-23 2001-05-16 Univ Edinburgh Lipid profile modulation
TWI296619B (ja) 2001-05-31 2008-05-11 Nihon Nohyaku Co Ltd
AR040241A1 (es) 2002-06-10 2005-03-23 Merck & Co Inc Inhibidores de la 11-beta-hidroxiesteroide deshidrogrenasa 1 para el tratamiento de la diabetes obesidad y dislipidemia
JP2004065194A (ja) 2002-08-09 2004-03-04 Sumitomo Chem Co Ltd 脂肪細胞関連因子の分析方法
WO2004056744A1 (en) 2002-12-23 2004-07-08 Janssen Pharmaceutica N.V. Adamantyl acetamides as hydroxysteroid dehydrogenase inhibitors
WO2004076418A1 (en) 2003-02-28 2004-09-10 Galderma Research & Development, S.N.C. Ligands that modulate lxr-type receptors
US7449464B2 (en) * 2003-03-12 2008-11-11 Kudos Pharmaceuticals Limited Phthalazinone derivatives
DE602004027171D1 (de) 2003-04-11 2010-06-24 High Point Pharmaceuticals Llc Verbindungen mit Aktivität an der 11Beta-Hydroxasteroiddehydrogenase
WO2005070889A1 (en) 2004-01-23 2005-08-04 E.I. Dupont De Nemours And Company Herbicidal amides
US7354938B2 (en) 2004-03-23 2008-04-08 Amgen Inc. Pyrazole compounds and uses related thereto
JP2007261945A (ja) 2004-04-07 2007-10-11 Taisho Pharmaceut Co Ltd チアゾール誘導体
US20050245533A1 (en) * 2004-04-29 2005-11-03 Hoff Ethan D Inhibitors of the 11-beta-hydroxysteroid dehydrogenaseType 1 enzyme and their therapeutic application
US20050245532A1 (en) * 2004-04-29 2005-11-03 Hoff Ethan D Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme and their therapeutic application
US20050261302A1 (en) * 2004-04-29 2005-11-24 Hoff Ethan D Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme and their therapeutic application
MXPA06012831A (es) 2004-05-06 2007-01-26 Pfizer Nuevos compuestos de derivados de morfolina y prolina.
MXPA06012929A (es) 2004-05-07 2007-01-26 Janssen Pharmaceutica Nv Derivados de adamantil pirrolidin-2-ona como inhibidores de 11-beta hidroxiesteroide deshidrogenasa.
JP2007538102A (ja) 2004-05-20 2007-12-27 バイエル・フアーマシユーチカルズ・コーポレーシヨン 糖尿病の処置に有用な5−アニリノ−4−ヘテロアリールピラゾール誘導体
MY141198A (en) 2004-08-30 2010-03-31 Janssen Pharmaceutica Nv Tricyclic adamantylamide derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors
US20090093463A1 (en) 2004-11-02 2009-04-09 Agouron Pharmaceuticals Inc. Novel compounds of substituted and unsubtituted adamantyl amides
US20060148871A1 (en) * 2005-01-05 2006-07-06 Rohde Jeffrey J Metabolic stabilization of substituted adamantane
GB0506133D0 (en) 2005-03-24 2005-05-04 Sterix Ltd Compound
CA2610172A1 (en) 2005-06-08 2006-12-14 Japan Tobacco Inc. Heterocyclic compound
JP2007262022A (ja) 2006-03-29 2007-10-11 Mochida Pharmaceut Co Ltd 新規2−チオフェンカルボキサミド誘導体
WO2008044656A1 (fr) 2006-10-06 2008-04-17 Taisho Pharmaceutical Co., Ltd. Dérivé d'imidazolidinone
US20080200444A1 (en) 2006-10-20 2008-08-21 Arete Therapeutics, Inc. Soluble epoxide hydrolase inhibitors
TW200827346A (en) 2006-11-03 2008-07-01 Astrazeneca Ab Chemical compounds
TW200836719A (en) 2007-02-12 2008-09-16 Astrazeneca Ab Chemical compounds
JPWO2008120655A1 (ja) 2007-03-30 2010-07-15 株式会社医薬分子設計研究所 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
BRPI0811191A2 (pt) 2007-05-18 2014-10-29 Shionogi & Co Derivado heterocíclico contendo nitrogênio tendo atividade inibitória para 11beta-hidroxiesteroide deidrogenase tipo 1
US8222417B2 (en) 2007-06-27 2012-07-17 Taisho Pharmaceutical Co., Ltd Compound having 11β-HSD1 inhibitory activity
WO2009010416A2 (en) 2007-07-17 2009-01-22 F. Hoffmann-La Roche Ag Inhibitors of 11b-hydroxysteroid dehydrogenase
US7977358B2 (en) 2007-07-26 2011-07-12 Hoffmann-La Roche Inc. Pyrazol derivatives
WO2009056881A1 (en) 2007-10-29 2009-05-07 Astrazeneca Ab Chemical compounds 313
CA2703781A1 (en) 2007-11-06 2009-05-14 Astrazeneca Ab 4-[4-(2-adamantylcarbamoyl)-5-tert-butyl-pyrazol-1-yl]benzoic acid - 465
WO2009098501A1 (en) 2008-02-04 2009-08-13 Astrazeneca Ab Novel crystalline forms of 4- [4- (2-adamantylcarbam0yl) -5-tert-butyl-pyrazol-1-yl] benzoic acid
BRPI0910734A2 (pt) 2008-04-22 2015-09-29 Astrazeneca Ab composto, composição farmacêutica, e, processo para preparar um composto ou um sal farmaceuticamente aceitável do mesmo.

Patent Citations (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998041519A1 (en) 1997-03-18 1998-09-24 Smithkline Beecham Corporation Novel cannabinoid receptor agonists
WO2001023358A1 (fr) 1999-09-27 2001-04-05 Sagami Chemical Research Center Derives pyrazole, intermediaires pour la preparation de ces derives, procedes de preparation des derives et intermediaires, et herbicides dont ces derives sont le principe actif
JP2007501789A (ja) * 2003-08-07 2007-02-01 メルク エンド カムパニー インコーポレーテッド 11−β−ヒドロキシステロイドデヒドロゲナーゼ−1の阻害剤としてのピラゾールカルボキサミド
WO2005016877A2 (en) 2003-08-07 2005-02-24 Merck & Co., Inc. Pyrazole carboxamides as inhibitors of 11-beta-hydroxysteroid dehydrogenase-1
WO2005061462A2 (en) 2003-12-19 2005-07-07 Neurogen Corporation Diaryl pyrazole derivatives and their use as neurokinin-3 receptor modulators
WO2005108368A1 (en) 2004-04-29 2005-11-17 Abbott Laboratories Adamantyl-acetamide derivatives as inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme
US20050277647A1 (en) 2004-04-29 2005-12-15 Link James T Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme
WO2006024627A2 (en) 2004-08-30 2006-03-09 Janssen Pharmaceutica N.V. N-2 adamantanyl-2-phenoxy-acetamide derivatives as 11-beta hydroxysteroid dehydrogenase inhibitors
WO2006074330A2 (en) 2005-01-05 2006-07-13 Abbott Laboratories Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme
WO2006074244A2 (en) 2005-01-05 2006-07-13 Abbott Laboratories Adamantyl derivatives as inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme
WO2006106052A1 (en) 2005-04-05 2006-10-12 F. Hoffmann-La Roche Ag Pyrazoles
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
WO2007058346A1 (ja) 2005-11-21 2007-05-24 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
EP1953145A1 (en) 2005-11-21 2008-08-06 Shionogi & Co., Ltd. Heterocyclic compound having inhibitory activity on 11- -hydroxysteroid dehydrogenase type i
WO2007107470A2 (en) 2006-03-22 2007-09-27 F. Hoffmann-La Roche Ag Pyrazoles as 11-beta-hsd-1
WO2007114124A1 (ja) * 2006-03-30 2007-10-11 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イソキサゾール誘導体およびイソチアゾール誘導体
WO2007114125A1 (ja) * 2006-03-31 2007-10-11 Shionogi & Co., Ltd. 微生物によるアダマンタン水酸化体の製造方法
WO2007144394A2 (en) * 2006-06-16 2007-12-21 High Point Pharmaceuticals, Llc. Pharmaceutical use of substituted piperidine carboxamides
WO2008012532A2 (en) * 2006-07-27 2008-01-31 Astrazeneca Ab : pyridine-3-carboxamide compounds and their use for inhibiting 11-beta-hydroxysteroid dehydrogenase
WO2008053652A1 (fr) * 2006-11-02 2008-05-08 Shionogi & Co., Ltd. Procédé de fabrication d'hydroxyadamantane-amine

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
CLIN. ENDOCRINOL, vol. 44, 1996, pages 493
J. CLIN. ENDOCRINOL. METAB., vol. 80, 1995, pages 3155
LANCET, vol. 349, 1997, pages 1210
PROC. NAT. ACAD. SCI. USA, vol. 94, 1997, pages 14924
See also references of EP2163543A4 *

Cited By (32)

* 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
US8673938B2 (en) 2006-11-03 2014-03-18 Astrazeneca Ab Chemical compounds
US7964618B2 (en) 2006-11-03 2011-06-21 Astrazeneca Ab Chemical compounds
US8344016B2 (en) 2007-02-12 2013-01-01 Astrazeneca Ab Pyrazole derivatives as 11-beta-HSD1 inhibitors
US7816391B2 (en) 2007-02-12 2010-10-19 Astrazeneca Ab Chemical compounds
US8383622B2 (en) 2007-05-18 2013-02-26 Shionogi & Co., Ltd. Nitrogen-containing heterocyclic derivative having 11β-hydroxysteroid dehydrogenase type I inhibitory activity
US8383381B2 (en) 2007-09-27 2013-02-26 Shjonogi & Co., Ltd. Method for producing hydroxylated adaivjantane using cytochrome P450
US8614080B2 (en) 2007-09-27 2013-12-24 Shionogi & Co., Ltd. Method for producing hydroxylated adamantane using cytochrome P450
US7951833B2 (en) 2008-02-04 2011-05-31 Astrazeneca Ab Crystalline forms of 4-[4-(2-adamantylcarbamoyl)-5-tert-butyl-pyrazol-1-yl]Benzoic acid 471
US8507493B2 (en) 2009-04-20 2013-08-13 Abbvie Inc. Amide and amidine derivatives and uses thereof
EP2243479A2 (en) 2009-04-20 2010-10-27 Abbott Laboratories Novel amide and amidine derivates and uses thereof
CN102762531B (zh) * 2009-12-22 2015-12-02 盐野义制药株式会社 金刚烷胺衍生物
CN102762531A (zh) * 2009-12-22 2012-10-31 盐野义制药株式会社 金刚烷胺衍生物
WO2011078101A1 (ja) 2009-12-22 2011-06-30 塩野義製薬株式会社 アダマンタンアミン誘導体
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
WO2011142359A1 (ja) * 2010-05-10 2011-11-17 日産化学工業株式会社 スピロ化合物及びアディポネクチン受容体活性化薬
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
WO2012004269A1 (de) 2010-07-05 2012-01-12 Sanofi ( 2 -aryloxy -acetylamino) - phenyl - propionsäurederivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
WO2012004270A1 (de) 2010-07-05 2012-01-12 Sanofi Spirocyclisch substituierte 1,3-propandioxidderivate, 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
KR101519280B1 (ko) 2010-08-09 2015-05-11 시오노기세이야쿠가부시키가이샤 아미노아다만탄카르바메이트 유도체의 제조 방법
TWI511958B (zh) * 2010-08-09 2015-12-11 Shionogi & Co 胺基金剛烷胺基甲酸酯衍生物之製造方法
CN103209957A (zh) * 2010-08-09 2013-07-17 盐野义制药株式会社 氨基金刚烷氨基甲酸酯衍生物的制备方法
WO2012020724A1 (ja) 2010-08-09 2012-02-16 塩野義製薬株式会社 アミノアダマンタンカルバメート誘導体の製造方法
JP5812295B2 (ja) * 2010-08-09 2015-11-11 塩野義製薬株式会社 アミノアダマンタンカルバメート誘導体の製造方法
WO2012124781A1 (ja) 2011-03-17 2012-09-20 塩野義製薬株式会社 ピラゾールカルボン酸誘導体の製造方法
JPWO2012124781A1 (ja) * 2011-03-17 2014-07-24 塩野義製薬株式会社 ピラゾールカルボン酸誘導体の製造方法
JP6080165B2 (ja) * 2011-03-17 2017-02-15 塩野義製薬株式会社 ピラゾールカルボン酸誘導体の製造方法
JP2014517013A (ja) * 2011-06-10 2014-07-17 エスケー バイオファーマシューティカルズ カンパニー リミテッド 5−カルバモイルアダマンタン−2−イルアミド誘導体、その薬学的に許容可能な塩およびその製造方法
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
WO2017094743A1 (ja) * 2015-11-30 2017-06-08 塩野義製薬株式会社 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医薬組成物

Also Published As

Publication number Publication date
ES2535317T3 (es) 2015-05-08
JP2011098974A (ja) 2011-05-19
EP2163543A1 (en) 2010-03-17
PL2163543T3 (pl) 2015-06-30
CA2689659C (en) 2012-10-23
EP2163543B1 (en) 2015-03-04
JPWO2008142986A1 (ja) 2010-08-05
KR101376432B1 (ko) 2014-05-16
RU2455285C2 (ru) 2012-07-10
AU2008252185A1 (en) 2008-11-27
CN103288738B (zh) 2016-03-16
BRPI0811191A2 (pt) 2014-10-29
KR20140057689A (ko) 2014-05-13
CN101754954A (zh) 2010-06-23
RU2009147015A (ru) 2011-06-27
US20100240659A1 (en) 2010-09-23
CA2689659A1 (en) 2008-11-27
US8383622B2 (en) 2013-02-26
TWI426902B (zh) 2014-02-21
HK1140766A1 (en) 2010-10-22
CN103288738A (zh) 2013-09-11
AU2008252185B2 (en) 2012-02-16
KR20100008382A (ko) 2010-01-25
CN101754954B (zh) 2015-11-25
TW200901973A (en) 2009-01-16
DK2163543T3 (en) 2015-04-27
JP5252515B2 (ja) 2013-07-31
JP4671369B2 (ja) 2011-04-13
MX2009012283A (es) 2009-11-25
EP2163543A4 (en) 2010-08-11

Similar Documents

Publication Publication Date Title
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
DK1533292T3 (da) Dibenzylaminforbindelse og medicinsk anvendelse deraf
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
TW200732333A (en) An oxime derivative and preparations thereof
MX2009004920A (es) Nuevos derivados de aminopirimidina como inhibidores de plk1.
TW200605883A (en) Condensed heterocycle derivative having HCV inhibitory activity
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
TN2011000362A1 (en) Pyridazinone compounds
EP2017278A4 (en) DIHYDROPYRAZOLOPYRIMIDINONDERIVAT
NO20065012L (no) Tetrahydronaftyridin-derivater og fremgangsmate for fremstilling av disse
RS53451B (en) INHIBITORI P70 S6 KINAZE
WO2008136444A1 (ja) 縮合複素環誘導体
WO2009069736A1 (ja) 含窒素化合物
MX2009009525A (es) Activador de glucocinasa.
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
WO2008111604A1 (ja) 新規なベンジル(ヘテロサイクリックメチル)アミン構造を有するピリミジン化合物及びこれを含有する医薬
WO2008140066A3 (en) Pyridone derivatives as p38a mapk inhibitors
MY169179A (en) Novel piperidine compound or salt thereof
IN2012DN00770A (ja)
NO20075617L (no) 4-fenyl-5-okso-1,4,5,6,7,8-heksahydrokinolinderivater for behandling av infertilitet
MX2010001566A (es) Derivado de aminopirazolamida.
WO2005003087A3 (en) Oxazole derivatives as antibacterial agents
WO2009009531A3 (en) Pyrimidinecarboxamide derivatives for the treatment of hiv infections
TNSN08161A1 (en) 6-heteroarylpyridoindolone derivatives, their preparation and therapeutic use thereof
TW200517387A (en) Compounds exhibiting thrombopoietin receptor agonism

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200880025349.3

Country of ref document: CN

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

Ref document number: 08764258

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2009515137

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 12599133

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 2008252185

Country of ref document: AU

Ref document number: MX/A/2009/012283

Country of ref document: MX

ENP Entry into the national phase

Ref document number: 20097023969

Country of ref document: KR

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2689659

Country of ref document: CA

Ref document number: 6775/CHENP/2009

Country of ref document: IN

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2008252185

Country of ref document: AU

Date of ref document: 20080507

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2008764258

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2009147015

Country of ref document: RU

ENP Entry into the national phase

Ref document number: PI0811191

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20091118