CN101787016B - 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物 - Google Patents

用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物 Download PDF

Info

Publication number
CN101787016B
CN101787016B CN2010101438299A CN201010143829A CN101787016B CN 101787016 B CN101787016 B CN 101787016B CN 2010101438299 A CN2010101438299 A CN 2010101438299A CN 201010143829 A CN201010143829 A CN 201010143829A CN 101787016 B CN101787016 B CN 101787016B
Authority
CN
China
Prior art keywords
pyridine
alkyl
group
base
methyl
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
CN2010101438299A
Other languages
English (en)
Chinese (zh)
Other versions
CN101787016A (zh
Inventor
W·麦克考尔
M·帕克
J·S·斯科特
P·R·O·怀塔摩尔
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AstraZeneca AB
Original Assignee
AstraZeneca AB
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 AstraZeneca AB filed Critical AstraZeneca AB
Publication of CN101787016A publication Critical patent/CN101787016A/zh
Application granted granted Critical
Publication of CN101787016B publication Critical patent/CN101787016B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • C07D213/82Amides; Imides in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/4402Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
    • 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
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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
    • C07D413/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
CN2010101438299A 2006-11-03 2007-10-31 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物 Active CN101787016B (zh)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US86430306P 2006-11-03 2006-11-03
US86424706P 2006-11-03 2006-11-03
US60/864303 2006-11-03
US60/864247 2006-11-03
US60/864,303 2006-11-03
US60/864,247 2006-11-03

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CN2007800491675A Division CN101573336B (zh) 2006-11-03 2007-10-31 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物

Publications (2)

Publication Number Publication Date
CN101787016A CN101787016A (zh) 2010-07-28
CN101787016B true CN101787016B (zh) 2013-08-28

Family

ID=39304797

Family Applications (3)

Application Number Title Priority Date Filing Date
CN2010101438299A Active CN101787016B (zh) 2006-11-03 2007-10-31 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物
CN2012100119350A Pending CN102603711A (zh) 2006-11-03 2007-10-31 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物
CN2007800491675A Expired - Fee Related CN101573336B (zh) 2006-11-03 2007-10-31 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物

Family Applications After (2)

Application Number Title Priority Date Filing Date
CN2012100119350A Pending CN102603711A (zh) 2006-11-03 2007-10-31 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物
CN2007800491675A Expired - Fee Related CN101573336B (zh) 2006-11-03 2007-10-31 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物

Country Status (30)

Country Link
US (3) US7964618B2 (enExample)
EP (2) EP2086939B8 (enExample)
JP (1) JP5165688B2 (enExample)
KR (1) KR101465275B1 (enExample)
CN (3) CN101787016B (enExample)
AR (1) AR063458A1 (enExample)
AT (1) ATE475649T1 (enExample)
AU (1) AU2007315955B2 (enExample)
BR (1) BRPI0717970C1 (enExample)
CA (1) CA2668006C (enExample)
CL (1) CL2007003176A1 (enExample)
CO (1) CO6321130A2 (enExample)
CY (1) CY1110813T1 (enExample)
DE (1) DE602007008137D1 (enExample)
DK (1) DK2086939T3 (enExample)
ES (2) ES2423206T3 (enExample)
HR (1) HRP20100522T1 (enExample)
IL (1) IL198231A0 (enExample)
MX (1) MX2009004707A (enExample)
NO (1) NO20091603L (enExample)
NZ (1) NZ576501A (enExample)
PE (1) PE20081487A1 (enExample)
PL (1) PL2086939T3 (enExample)
PT (1) PT2086939E (enExample)
RS (1) RS51451B (enExample)
RU (1) RU2451674C2 (enExample)
SI (1) SI2086939T1 (enExample)
TW (1) TW200827346A (enExample)
UY (1) UY30681A1 (enExample)
WO (1) WO2008053194A2 (enExample)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2443689C2 (ru) 2005-11-21 2012-02-27 Сионоги Энд Ко., Лтд. ГЕТЕРОЦИКЛИЧЕСКИЕ СОЕДИНЕНИЯ, ОБЛАДАЮЩИЕ ИНГИБИРУЮЩЕЙ АКТИВНОСТЬЮ ПО ОТНОШЕНИЮ К 11β-ГИДРОКСИСТЕРОИДДЕГИДРОГЕНАЗЕ 1 ТИПА
TW200827346A (en) * 2006-11-03 2008-07-01 Astrazeneca Ab Chemical compounds
US8314119B2 (en) 2006-11-06 2012-11-20 Abbvie Inc. Azaadamantane derivatives and methods of use
TW200836719A (en) * 2007-02-12 2008-09-16 Astrazeneca Ab Chemical compounds
ES2535317T3 (es) 2007-05-18 2015-05-08 Shionogi & Co., Ltd. Derivado heterocíclico que contiene nitrógeno que tiene actividad inhibidora de la 11 beta-hidroxiesteroide deshidrogenasa de tipo 1
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
JP5441705B2 (ja) * 2007-10-15 2014-03-12 武田薬品工業株式会社 アミド化合物およびその用途
WO2009056881A1 (en) * 2007-10-29 2009-05-07 Astrazeneca Ab Chemical compounds 313
SA109300090B1 (ar) * 2008-02-04 2011-10-03 استرازينيكا ايه بي صور متبلرة جديدة من 4- [4- (2- أدامنتيل كربامويل) -5- ثلاثي- بيوتيل – بيرازول -1- يل] حمض بنزويك 471
JP2011518216A (ja) * 2008-04-22 2011-06-23 アストラゼネカ アクチボラグ 置換ピリミジン−5−カルボキサミド
US8507493B2 (en) 2009-04-20 2013-08-13 Abbvie Inc. Amide and amidine derivatives and uses thereof
WO2010144647A1 (en) 2009-06-12 2010-12-16 Bristol-Myers Squibb Company Nicotinamide compounds useful as kinase modulators
WO2011049520A1 (en) * 2009-10-20 2011-04-28 Astrazeneca Ab Adamantyl iminocarbonyl-substituted pyrimidines as inhibitors of 1 1 betahsd1
CN102712607B (zh) * 2009-11-24 2016-06-22 阿勒根公司 作为具有治疗效用的受体调节剂的化合物
US8871208B2 (en) * 2009-12-04 2014-10-28 Abbvie Inc. 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors and uses thereof
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
KR20110123657A (ko) * 2010-05-07 2011-11-15 에스케이케미칼주식회사 피콜린아마이드 및 피리미딘-4-카복사미드 화합물, 이의 제조방법 및 이를 함유하는 약제학적 조성물
US8933024B2 (en) 2010-06-18 2015-01-13 Sanofi Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
CN106074548A (zh) 2010-09-23 2016-11-09 艾伯维巴哈马有限公司 氮杂金刚烷衍生物的一水合物
US8471027B2 (en) * 2011-04-06 2013-06-25 Hoffmann-La Roche Inc. Adamantyl compounds
US8980904B2 (en) * 2011-07-21 2015-03-17 Xuanzhu Pharma Co., Ltd. Heterocyclic substituted pyrimidine compound
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
CN102659657B (zh) * 2012-04-24 2014-08-06 徐州医学院 一种蛋白酶抑制剂pf429242的合成方法
MA37764A1 (fr) 2012-06-20 2016-01-29 Hoffmann La Roche Composés n-alkyltriazole utilisés comme antagonistes de lpar
MA37765A1 (fr) 2012-06-20 2017-04-28 Hoffmann La Roche Composés de pyrazole substitués utilisés comme antagonistes de lpar
EP3821892A1 (en) 2019-11-12 2021-05-19 University of Leeds (s)-2-(1-(5-(cyclohexylcarbamoyl)-6-(propylthio)pyridin-2-yl)piperidin-3-yl) acetic acid for use in treating wounds
GB202216324D0 (en) * 2022-11-02 2022-12-14 Cerevance Ltd Novel compounds
GB202408335D0 (en) 2024-06-11 2024-07-24 Astrazeneca Ab Therapies for wound treatment

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1741986A (zh) * 2003-01-24 2006-03-01 诺瓦提斯公司 酰胺衍生物及其作为11-β羟类固醇脱氢酶抑制剂的用途

Family Cites Families (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GR66581B (enExample) 1978-02-21 1981-03-27 Delalande Sa
CA1307786C (en) 1984-12-14 1992-09-22 Keiichi Yokoyama Quinazoline derivatives and antihypertensive preparations containing same as effective components
CA2383466C (en) 1999-09-16 2009-08-25 Tanabe Seiyaku Co., Ltd. Aromatic nitrogen-containing 6-membered cyclic compounds
FR2803592A1 (fr) * 2000-01-06 2001-07-13 Aventis Cropscience Sa Nouveaux derives de l'acide 3-hydroxypicolinique, leur procede de preparation et compositions fongicides les contenant.
US7273868B2 (en) 2000-04-28 2007-09-25 Tanabe Seiyaku Co., Ltd. Pyrazine derivatives
WO2002020463A2 (en) 2000-09-05 2002-03-14 Tularik Inc. Fxr modulators
IL155202A0 (en) 2000-10-20 2003-11-23 Biocryst Pharm Inc Biaryl compounds as serine protease inhibitors
SE0102764D0 (sv) 2001-08-17 2001-08-17 Astrazeneca Ab Compounds
JP2005528395A (ja) 2002-04-05 2005-09-22 ザ ユニバーシティ オブ エディンバラ 組成物
WO2004039795A2 (en) * 2002-10-29 2004-05-13 Fujisawa Pharmaceutical Co., Ltd. Amide compounds for the treatment of hyperlipidemia
SE0300457D0 (sv) * 2003-02-19 2003-02-19 Astrazeneca Ab Novel compounds
SE0300458D0 (sv) * 2003-02-19 2003-02-19 Astrazeneca Ab Novel compounds
JP4432901B2 (ja) 2003-02-26 2010-03-17 萬有製薬株式会社 ヘテロアリールカルバモイルベンゼン誘導体
EP1615698B1 (en) 2003-04-11 2010-09-29 High Point Pharmaceuticals, LLC New amide derivatives and pharmaceutical use thereof
AU2004265299B2 (en) 2003-08-07 2008-05-01 Merck & Co., Inc. Pyrazole carboxamides as inhibitors of 11-beta-hydroxysteroid dehydrogenase-1
BRPI0414313A (pt) 2003-09-11 2006-11-07 Kemia Inc inibidores de citocinas
GB0327761D0 (en) 2003-11-29 2003-12-31 Astrazeneca Ab Compounds
KR20060101772A (ko) 2003-12-19 2006-09-26 화이자 인코포레이티드 당뇨병 및 비만을 치료하기 위한,11-베타-하이드록시스테로이드 데하이드로게나제 유형1(11-베타-hsd-1)의 저해제로서의벤젠설폰일아미노-피리딘-2-일 유도체 및 관련 화합물
DE602005009500D1 (de) 2004-02-24 2008-10-16 Glaxo Group Ltd Pyridinderivate und deren verwendung als modulatoren des cb2-rezeptors
JP2007531753A (ja) * 2004-03-31 2007-11-08 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 非イミダゾール系複素環式化合物
JP2007536369A (ja) 2004-05-06 2007-12-13 ファイザー・インク プロリン及びモルホリン誘導体の新規化合物
TW200600086A (en) 2004-06-05 2006-01-01 Astrazeneca Ab Chemical compound
PT1763517E (pt) 2004-06-28 2011-07-01 Hoffmann La Roche Derivados de pirimidina como inibidores 11beta-hsd1
JP2008518903A (ja) 2004-11-02 2008-06-05 ファイザー・インク 置換および非置換アダマンチルアミドの新規化合物
WO2006050476A2 (en) 2004-11-03 2006-05-11 Vertex Pharmaceuticals Incorporated Pyrimidine derivatives as ion channel modulators and methods of use
AU2006204017B2 (en) 2005-01-05 2011-10-06 Abbvie Inc. 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
ATE435207T1 (de) 2005-04-06 2009-07-15 Hoffmann La Roche Pyridin-3-carbonsäureamidderivate als cb1-inverse agonisten
WO2006106423A2 (en) 2005-04-07 2006-10-12 Pfizer Inc. Amino sulfonyl derivatives as inhibitors of human 11-.beta.-hydrosysteroid dehydrogenase
EP1879881A2 (en) 2005-04-14 2008-01-23 Bristol-Myers Squibb Company Inhibitors of 11-beta hydroxysteroid dehydrogenase type i
JP2008542247A (ja) 2005-05-24 2008-11-27 アストラゼネカ アクチボラグ グルコキナーゼモジュレーターとしての2−フェニル置換イミダゾール[4,5b]ピリジン/ピラジンおよびプリン誘導体
EP1894919B1 (en) 2005-06-07 2012-03-28 Shionogi & Co., Ltd. Heterocyclic compound having type i 11 beta hydroxysteroid dehydrogenase inhibitory activity
WO2006132436A1 (ja) 2005-06-08 2006-12-14 Japan Tobacco Inc. 複素環化合物
WO2006134467A1 (en) 2005-06-16 2006-12-21 Pfizer Inc. N-(pyridin-2-yl)-sulfonamide derivatives
JP4651714B2 (ja) 2005-07-09 2011-03-16 アストラゼネカ アクチボラグ 糖尿病の治療においてglk活性化剤として使用するためのヘテロアリールベンズアミド誘導体
EP1915367A1 (en) 2005-08-09 2008-04-30 AstraZeneca AB Heteroarylcarbamoylbenzene derivatives for the treatment of diabetes
JP2009513711A (ja) 2005-11-01 2009-04-02 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ グルコキナーゼのアロステリックモジュレーターとしての置換ピロロン
WO2007052843A1 (ja) 2005-11-04 2007-05-10 Takeda Pharmaceutical Company Limited 複素環アミド化合物およびその用途
RU2443689C2 (ru) 2005-11-21 2012-02-27 Сионоги Энд Ко., Лтд. ГЕТЕРОЦИКЛИЧЕСКИЕ СОЕДИНЕНИЯ, ОБЛАДАЮЩИЕ ИНГИБИРУЮЩЕЙ АКТИВНОСТЬЮ ПО ОТНОШЕНИЮ К 11β-ГИДРОКСИСТЕРОИДДЕГИДРОГЕНАЗЕ 1 ТИПА
US20070197530A1 (en) 2006-01-31 2007-08-23 Yun-Long Li Amido compounds and their use as pharmaceuticals
RS54216B1 (sr) 2006-03-22 2015-12-31 F. Hoffmann-La Roche Ag. Pirazoli kao 11-beta-hsd-1
BRPI0710669A2 (pt) 2006-04-07 2011-08-16 High Point Pharmaceuticals Llc compostos ativos de dehidrogenase de 11b-hidroxiesteróide tipo 1
EP2012775A1 (en) 2006-04-27 2009-01-14 Solvay Pharmaceuticals GmbH Use of cbx cannabinoid receptor modulators as potassium channel modulators
WO2008012532A2 (en) 2006-07-27 2008-01-31 Astrazeneca Ab : pyridine-3-carboxamide compounds and their use for inhibiting 11-beta-hydroxysteroid dehydrogenase
TW200827346A (en) 2006-11-03 2008-07-01 Astrazeneca Ab Chemical compounds
TW200836719A (en) 2007-02-12 2008-09-16 Astrazeneca Ab Chemical compounds
ES2535317T3 (es) 2007-05-18 2015-05-08 Shionogi & Co., Ltd. Derivado heterocíclico que contiene nitrógeno que tiene actividad inhibidora de la 11 beta-hidroxiesteroide deshidrogenasa de tipo 1
BRPI0814825A2 (pt) 2007-07-17 2015-02-03 Hoffmann La Roche Composto, processo para a preparação do composto, composição farmacêutica que o compreende, seu uso e métodos para o tratamento ou profilaxia de diabetes, obesidade, distúrbios de alimentação ou dislipimedia e diabetes do tipo ii
MX2010005048A (es) * 2007-11-06 2010-07-28 Astrazeneca Ab Acido 4-[4-(2-adamantilcarbamoil)-5-terc-butil-pirazol-1-il]benzoi c-465.
SA109300090B1 (ar) * 2008-02-04 2011-10-03 استرازينيكا ايه بي صور متبلرة جديدة من 4- [4- (2- أدامنتيل كربامويل) -5- ثلاثي- بيوتيل – بيرازول -1- يل] حمض بنزويك 471
JP2011518216A (ja) 2008-04-22 2011-06-23 アストラゼネカ アクチボラグ 置換ピリミジン−5−カルボキサミド
JP2012516327A (ja) 2009-01-30 2012-07-19 アストラゼネカ アクチボラグ カルボキシ含有ピラゾールアミド化合物を製造するための新規な方法
WO2011049520A1 (en) * 2009-10-20 2011-04-28 Astrazeneca Ab Adamantyl iminocarbonyl-substituted pyrimidines as inhibitors of 1 1 betahsd1

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1741986A (zh) * 2003-01-24 2006-03-01 诺瓦提斯公司 酰胺衍生物及其作为11-β羟类固醇脱氢酶抑制剂的用途

Also Published As

Publication number Publication date
SI2086939T1 (sl) 2010-10-29
BRPI0717970A2 (pt) 2013-11-05
CL2007003176A1 (es) 2008-07-25
UY30681A1 (es) 2008-07-03
IL198231A0 (en) 2009-12-24
RU2009115830A (ru) 2010-12-10
AU2007315955A1 (en) 2008-05-08
PL2086939T3 (pl) 2011-09-30
JP2010508338A (ja) 2010-03-18
WO2008053194A2 (en) 2008-05-08
KR101465275B1 (ko) 2014-11-27
US20080269288A1 (en) 2008-10-30
EP2086939B1 (en) 2010-07-28
EP2233480B1 (en) 2013-05-29
CN102603711A (zh) 2012-07-25
NO20091603L (no) 2009-05-28
TW200827346A (en) 2008-07-01
RS51451B (sr) 2011-04-30
ATE475649T1 (de) 2010-08-15
BRPI0717970B8 (pt) 2020-12-01
BRPI0717970C1 (pt) 2021-05-25
KR20090075865A (ko) 2009-07-09
DK2086939T3 (da) 2010-10-11
AR063458A1 (es) 2009-01-28
HRP20100522T1 (hr) 2010-11-30
PE20081487A1 (es) 2009-01-11
JP5165688B2 (ja) 2013-03-21
US8673938B2 (en) 2014-03-18
PT2086939E (pt) 2010-09-17
CN101573336B (zh) 2012-03-21
US20090306075A1 (en) 2009-12-10
MX2009004707A (es) 2009-05-15
EP2086939A2 (en) 2009-08-12
CA2668006A1 (en) 2008-05-08
NZ576501A (en) 2011-03-31
CN101787016A (zh) 2010-07-28
AU2007315955B2 (en) 2011-04-14
EP2233480A1 (en) 2010-09-29
CN101573336A (zh) 2009-11-04
ES2347491T3 (es) 2010-10-29
US7964618B2 (en) 2011-06-21
EP2086939B8 (en) 2011-06-22
CO6321130A2 (es) 2011-09-20
HK1135090A1 (en) 2010-05-28
DE602007008137D1 (en) 2010-09-09
BRPI0717970B1 (pt) 2019-10-22
US20090312372A1 (en) 2009-12-17
ES2423206T3 (es) 2013-09-18
RU2451674C2 (ru) 2012-05-27
CA2668006C (en) 2016-05-24
WO2008053194A3 (en) 2008-10-02
CY1110813T1 (el) 2015-06-10

Similar Documents

Publication Publication Date Title
CN101787016B (zh) 用作11-β-HSD1抑制剂的吡啶甲酰胺类化合物
CN105682661B (zh) 某些化学实体、组合物和方法
DE69718177T2 (de) Substituierte pyrimidinderivate und ihre pharmazeutische anwendung
KR101921486B1 (ko) PARP억제제인 4H-피라졸로[1,5-a]벤즈이미다졸 화합물의 아날로그
KR20110002475A (ko) 치환 피리미딘-5-카르복시아미드 281
EP1396488A1 (en) Fused heterocyclic compound and medicinal use thereof
EP2788349A1 (en) Kinase inhibitors
CN105722835A (zh) 3-芳基-5-取代的-异喹啉-1-酮化合物及它们的疗法应用
CA2955062A1 (en) Novel 2,5-substituted pyrimidines as pde inhibitors
MX2013000359A (es) Compuesto de piridina sustituida.
WO2024153143A1 (zh) 含氮并环类化合物及其应用
WO2025147320A1 (en) Stat6 inhibitors and uses thereof
HK1135090B (en) Pyridine carboxamides as 11-beta-hsd1 inhibitors
HK1230174B (zh) 嘧啶吡唑基衍生物及其作为irak抑制剂的用途
SA07280596B1 (ar) مركبات بيريدين الأميد وأستخدامها كمثبطات إنزيم β-11 هيدروكسى ستيرويد ديهيدروجينيز من النوع الأول
JPWO1999038867A1 (ja) ▲iv▼型ホスホジエステラーゼ阻害作用を有する1−シクロアルキル−1,8−ナフチリジン−4−オン誘導体

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant