BR112014001018A2 - derivado de azabenzimidazol tendo atividade de ativação de ampk - Google Patents

derivado de azabenzimidazol tendo atividade de ativação de ampk

Info

Publication number
BR112014001018A2
BR112014001018A2 BR112014001018A BR112014001018A BR112014001018A2 BR 112014001018 A2 BR112014001018 A2 BR 112014001018A2 BR 112014001018 A BR112014001018 A BR 112014001018A BR 112014001018 A BR112014001018 A BR 112014001018A BR 112014001018 A2 BR112014001018 A2 BR 112014001018A2
Authority
BR
Brazil
Prior art keywords
substituted
group
hydrogen atom
unsubstituted
unsubstituted alkyl
Prior art date
Application number
BR112014001018A
Other languages
English (en)
Inventor
Akira Ino
Eiichi Kojima
Keisuke Tonogaki
Manabu Katou
Masafumi Iwatsu
Masahiko Fujioka
Naoki Ohyabu
Nobuyuki Tanaka
Yu Hinata
Original Assignee
Shionogi & Co
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 Shionogi & Co filed Critical Shionogi & Co
Publication of BR112014001018A2 publication Critical patent/BR112014001018A2/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • C07D451/06Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

resumo patente de invenção: "derivado de azabenzimidazol tendo atividade de ativação de ampk". a presente invenção refere-se a um composto que é útil como um ativador de ampk. um composto representado pela fórmula (em que r4 representa um átomo de hidrogênio, ou um grupo alquila substituído ou não substituídoa, r1, r2 e r3 independentemente representam um átomo de hidrogênio, um átomo de halogênio, um grupo hidróxi, um grupo ciano, um grupo nitro, um grupo carbóxi, um grupo alquila substituído ou não substituído ou similares, em que um caso onde r1, r2 e r3 representam um átomo de hidrogênio simultaneamente é excluído; x representa uma ligação simples, -s-, -o-, -nr5-, -c(=o)- ou similares; r5 representa um átomo de hidrogênio, ou um grupo alquila substituído ou não substituído, e y representa um grupo cicloalquila substituído ou não substituído, um grupo cicloalquenila substituído ou não substituído, um grupo heterociclila substituído ou não substituído ou similares) ou um sal farmaceuticamente aceitável do mesmo.
BR112014001018A 2011-07-15 2012-07-13 derivado de azabenzimidazol tendo atividade de ativação de ampk BR112014001018A2 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2011156297 2011-07-15
JP2012055785 2012-03-13
PCT/JP2012/067889 WO2013011932A1 (ja) 2011-07-15 2012-07-13 Ampk活性化作用を有するアザベンズイミダゾール誘導体

Publications (1)

Publication Number Publication Date
BR112014001018A2 true BR112014001018A2 (pt) 2017-01-10

Family

ID=47558110

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112014001018A BR112014001018A2 (pt) 2011-07-15 2012-07-13 derivado de azabenzimidazol tendo atividade de ativação de ampk

Country Status (11)

Country Link
US (2) US9567330B2 (pt)
EP (2) EP2733141B1 (pt)
JP (2) JP6108467B2 (pt)
KR (1) KR20140040801A (pt)
CN (1) CN103781786A (pt)
AU (1) AU2012284955A1 (pt)
BR (1) BR112014001018A2 (pt)
CA (1) CA2841906A1 (pt)
MX (1) MX2014000452A (pt)
RU (1) RU2014105650A (pt)
WO (1) WO2013011932A1 (pt)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2617722B1 (en) * 2010-09-10 2016-03-23 Shionogi & Co., Ltd. Hetero ring-fused imidazole derivative having ampk activating effect
EP2677869B1 (en) * 2011-02-25 2017-11-08 Merck Sharp & Dohme Corp. Novel cyclic azabenzimidazole derivatives useful as anti-diabetic agents
SG11201408178TA (en) * 2012-06-19 2015-01-29 Sunovion Pharmaceuticals Inc Heteroaryl compounds and methods of use thereof
EP2888006B1 (en) * 2012-08-22 2019-04-24 Merck Sharp & Dohme Corp. Novel azabenzimidazole tetrahydropyran derivatives useful as ampk activators
WO2014069426A1 (ja) * 2012-10-31 2014-05-08 塩野義製薬株式会社 Ampk活性化作用を有するベンズイミダゾールおよびアザベンズイミダゾール誘導体
EP2963013A4 (en) * 2013-02-27 2016-09-14 Shionogi & Co INDOLE AND AZAINDOLE DERIVATIVES HAVING AMPK ACTIVATION ACTIVITY EACH
WO2014139388A1 (en) 2013-03-14 2014-09-18 Merck Sharp & Dohme Corp. Novel indole derivatives useful as anti-diabetic agents
WO2014175330A1 (ja) * 2013-04-24 2014-10-30 塩野義製薬株式会社 Ampk活性化作用を有する5-オキシベンズイミダゾールおよび5-オキシアザベンズイミダゾール誘導体
JP6474804B2 (ja) * 2013-10-31 2019-02-27 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング アザベンゾイミダゾール誘導体
US9980948B2 (en) 2014-08-27 2018-05-29 Shionogi & Co., Ltd. Azaindole derivative having AMPK-activating activity
WO2016057931A1 (en) 2014-10-10 2016-04-14 The Research Foundation For The State University Of New York Trifluoromethoxylation of arenes via intramolecular trifluoromethoxy group migration
AU2015338042A1 (en) 2014-10-28 2017-04-27 Shionogi & Co., Ltd. Heterocyclic derivative having AMPK activating effect
CN109071536A (zh) 2016-02-26 2018-12-21 盐野义制药株式会社 具有ampk活化作用的5-苯基氮杂吲哚衍生物
EP3450435A4 (en) * 2016-04-26 2019-09-18 Shionogi & Co., Ltd SUBSTITUTED AZABENZIMIDAZOLE DERIVATIVE IN POSITION 5 HAVING AN AMPK ACTIVATION ACTION
CN109476661A (zh) * 2016-05-20 2019-03-15 盐野义制药株式会社 具有ampk活化作用的5-取代苯并咪唑及5-取代氮杂苯并咪唑衍生物
CN111423435B (zh) * 2020-03-30 2021-10-15 厦门大学 (1H-咪唑并[4,5-b]吡啶-6-基)吡啶衍生物及其应用
US11691963B2 (en) 2020-05-06 2023-07-04 Ajax Therapeutics, Inc. 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors
EP4153589A4 (en) 2020-05-19 2024-06-12 Kallyope, Inc. AMPK ACTIVATORS
WO2021263039A1 (en) 2020-06-26 2021-12-30 Kallyope, Inc. Ampk activators
TW202334139A (zh) 2021-11-09 2023-09-01 美商雅捷可斯治療公司 作為jak2抑制劑之6-雜芳氧基苯并咪唑及氮雜苯并咪唑
WO2023097190A1 (en) * 2021-11-23 2023-06-01 Kallyope, Inc. Ampk activators
TW202340185A (zh) * 2021-11-23 2023-10-16 美商克力歐普股份有限公司 Ampk活化劑

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1186504A (en) * 1966-10-15 1970-04-02 Fisons Pest Control Ltd Substituted Heterocyclic Compounds
BE788065A (fr) * 1971-08-26 1973-02-26 Degussa Nouvelles aza-benzimidazoles et procede pour leur preparation
JPS62145084A (ja) * 1985-12-20 1987-06-29 Tokyo Tanabe Co Ltd イミダゾ〔4,5−b〕ピリジン誘導体
JP2546841B2 (ja) * 1986-07-25 1996-10-23 東京田辺製薬株式会社 新規なイミダゾ〔4,5−b〕ピリジン誘導体、その製造法及びそれを含有する抗潰瘍剤
US5332744A (en) * 1989-05-30 1994-07-26 Merck & Co., Inc. Substituted imidazo-fused 6-membered heterocycles as angiotensin II antagonists
IL94390A (en) 1989-05-30 1996-03-31 Merck & Co Inc The 6-membered trans-nitrogen-containing heterocycles are compressed with imidazo and pharmaceutical preparations containing them
JPH04120079A (ja) * 1989-12-22 1992-04-21 Takeda Chem Ind Ltd 縮合イミダゾール誘導体
DE4309969A1 (de) * 1993-03-26 1994-09-29 Bayer Ag Substituierte heteroanellierte Imidazole
KR0151816B1 (ko) 1994-02-08 1998-10-15 강박광 신규의 치환된 피리딜 이미다졸 유도체 및 그의 제조방법
US6348474B1 (en) 1997-06-27 2002-02-19 Fujisawa Pharmaceutical Co., Ltd. Sulfonamide compounds and medicinal use thereof
PL200694B1 (pl) 1999-06-28 2009-01-30 Janssen Pharmaceutica Nv Pochodna benzoimidazolu lub imidazopirydyny, sposób jej otrzymywania i zastosowanie oraz kompozycja farmaceutyczna i sposób jej otrzymywania
US6969712B2 (en) * 2000-11-15 2005-11-29 Banyu Pharmaceutical Co., Ltd. Benzimidazole derivatives
WO2003045929A1 (fr) * 2001-11-26 2003-06-05 Takeda Chemical Industries, Ltd. Derive bicyclique, procede de production de ce derive et utilisation correspondante
DE60305446T4 (de) 2002-01-07 2009-07-09 Eisai R&D Management Co., Ltd. Desazapurine und deren verwendung
US7138399B2 (en) 2002-03-27 2006-11-21 Altana Pharma Ag Alkoxypyridine-derivatives
US7105526B2 (en) * 2002-06-28 2006-09-12 Banyu Pharmaceuticals Co., Ltd. Benzimidazole derivatives
EP1719765A4 (en) * 2004-02-19 2009-01-07 Banyu Pharma Co Ltd NEW SULFONAMIDE DERIVATIVE
WO2005082905A1 (ja) 2004-02-26 2005-09-09 Kyowa Hakko Kogyo Co., Ltd. 二環性複素環化合物
ES2241496B1 (es) 2004-04-15 2006-12-01 Almirall Prodesfarma, S.A. Nuevos derivados de piridina.
TW200606163A (en) * 2004-04-22 2006-02-16 Eisai Co Ltd Imidazopyridine compound
WO2008031788A1 (en) * 2006-09-12 2008-03-20 Nycomed Gmbh Aminoazepine derivatives as highly efficient inhibitors of the inducible nitric oxide synthase
EP1988091B1 (en) * 2007-02-07 2015-06-10 Kyowa Hakko Kirin Co., Ltd. Tricyclic compounds
CN101492446A (zh) * 2008-01-25 2009-07-29 山东轩竹医药科技有限公司 新的吡啶并咪唑衍生物
BRPI0905952A2 (pt) 2008-02-04 2015-06-30 Mercury Therapeutics Composto e sais do mesmo e compição farmacêutica
EP2265609B1 (en) * 2008-02-29 2012-09-05 Array Biopharma, Inc. Imdizo [4. 5-b] pyridine derivatives used as raf inhibitors
CA2727928A1 (en) * 2008-06-18 2009-12-23 Merck Sharp & Dohme Corp. Inhibitors of janus kinases
MY157330A (en) 2008-06-24 2016-05-31 Sanofi Aventis Substituted isoquinolinones as rho kinase inhibitors
MX2011003239A (es) 2008-09-26 2011-04-28 Merck Sharp & Dohme Nuevos derivados de bencimidazol ciclicos utiles como agentes anti-diabeticos.
US8232409B2 (en) * 2008-10-15 2012-07-31 Janssen Pharmaceutica N.V. Heterocyclic benzimidazoles as TRPM8 modulators
WO2010047982A1 (en) 2008-10-22 2010-04-29 Merck Sharp & Dohme Corp. Novel cyclic benzimidazole derivatives useful anti-diabetic agents
JP2012507530A (ja) 2008-10-29 2012-03-29 メルク・シャープ・エンド・ドーム・コーポレイション 有用な抗糖尿病剤である新規な環状ベンズイミダゾール誘導体
JP5557845B2 (ja) 2008-10-31 2014-07-23 メルク・シャープ・アンド・ドーム・コーポレーション 糖尿病用剤として有用な新規環状ベンゾイミダゾール誘導体
JP5762971B2 (ja) 2008-12-03 2015-08-12 プレシディオ ファーマシューティカルズ インコーポレイテッド Hcvns5aの阻害剤
EP2400846B1 (en) 2009-02-27 2016-10-05 Enanta Pharmaceuticals, Inc. Hepatitis c virus inhibitors
KR101117128B1 (ko) * 2009-06-02 2012-03-14 한국화학연구원 페닐테트라졸 유도체 또는 이의 약학적으로 허용가능한 염을 유효성분으로 포함하는 골다공증 또는 비만의 예방 또는 치료용 약학적 조성물
US8372862B2 (en) 2009-06-02 2013-02-12 Korea Research Institute Of Chemical Technology Pharmaceutical composition for preventing or treating osteoporosis or obesity comprising phenyltetrazole derivative
JP2011088833A (ja) * 2009-10-20 2011-05-06 Shionogi & Co Ltd Npyy5受容体拮抗作用を有するスルファミド誘導体
EP2512480A4 (en) * 2009-12-14 2013-05-15 Enanta Pharm Inc HEPATITIS C-VIRUS HEMMER
JP5475488B2 (ja) * 2010-02-03 2014-04-16 株式会社三共 遊技機
EP2538784B1 (en) 2010-02-25 2015-09-09 Merck Sharp & Dohme Corp. Benzimidazole derivatives useful anti-diabetic agents
US9060971B2 (en) 2010-03-04 2015-06-23 Enanta Pharmaceuticals, Inc. Combination pharmaceutical agents as inhibitors of HCV replication
JP5585873B2 (ja) * 2010-09-03 2014-09-10 独立行政法人産業技術総合研究所 イオン液体を用いた環境浄化方法およびその装置
EP2617722B1 (en) 2010-09-10 2016-03-23 Shionogi & Co., Ltd. Hetero ring-fused imidazole derivative having ampk activating effect
WO2012070114A1 (ja) 2010-11-24 2012-05-31 塩野義製薬株式会社 Npy y5受容体拮抗作用を有するスルファミド誘導体
EP2677869B1 (en) * 2011-02-25 2017-11-08 Merck Sharp & Dohme Corp. Novel cyclic azabenzimidazole derivatives useful as anti-diabetic agents
JP2014519378A (ja) * 2011-05-27 2014-08-14 ネステク ソシエテ アノニム 着脱可能なノズル回転モジュールを伴う飲料ディスペンサ
CN102863428B (zh) 2011-07-09 2014-12-24 广东东阳光药业有限公司 作为丙型肝炎病毒抑制剂的螺环化合物

Also Published As

Publication number Publication date
EP3495366A1 (en) 2019-06-12
US20140194420A1 (en) 2014-07-10
EP2733141A1 (en) 2014-05-21
US10093670B2 (en) 2018-10-09
US20170107219A1 (en) 2017-04-20
US9567330B2 (en) 2017-02-14
AU2012284955A1 (en) 2014-02-27
JP6108467B2 (ja) 2017-04-05
EP2733141B1 (en) 2019-01-09
JPWO2013011932A1 (ja) 2015-02-23
JP6292692B2 (ja) 2018-03-14
CA2841906A1 (en) 2013-01-24
RU2014105650A (ru) 2015-08-27
KR20140040801A (ko) 2014-04-03
CN103781786A (zh) 2014-05-07
WO2013011932A1 (ja) 2013-01-24
MX2014000452A (es) 2014-03-21
EP2733141A4 (en) 2015-03-04
JP2017101049A (ja) 2017-06-08

Similar Documents

Publication Publication Date Title
BR112014001018A2 (pt) derivado de azabenzimidazol tendo atividade de ativação de ampk
BR112012027373A2 (pt) composição pesticida e seu uso
BR112013025732A2 (pt) composto de imidazo-oxazina ou sal do mesmo
BR112012014858A2 (pt) agente antiplaqueta
NI201100223A (es) Derivados de imidazolidina 2 -0ne 1,3 - disustituidos como inhibidores de cyp 17
BRPI0821653B8 (pt) composto de piridina substituída com anel heterocíclico e grupo fosfonoximetila ou um sal do mesmo, composição farmacêutica compreendendo-os e uso dos mesmos para tratar uma doença fungíca
BRPI0720993B8 (pt) usos de compostos análogos de ciclopamina
BRPI0818193B8 (pt) composto, composição farmacêutica, e, uso de um composto
SV2009003376A (es) Derivados de aril isoxazolinas insecticidas
PH12017500048A1 (en) Pyridone derivative having tetrahydropyranylmethyl group
BR112015018738A8 (pt) compostos de tetra-hidropirrolotiazina, seus usos, e composição farmacêutica
ECSP099552A (es) Compuestos triciclicos, composiciones y procedimientos
CR20190465A (es) COMPOSICIONES PARA EL CONTROL DE PLAGAS QUE INCLUYE UN DERIVADO DE IMINOPIRIDINA NOVEDOSO (Divisional 2014-0450)
BR112012030711A2 (pt) derivado de purinona
CR20190244A (es) Agentes control de plaga
BR112016011755A2 (pt) derivado de ureia ou sal farmacologicamente aceitável do mesmo
BR112013011593A2 (pt) cristal de derivado de morfinan 7-carbamoíla-6,7-insaturada e método para produzir o mesmo
BRPI1013482B8 (pt) método para produzir um composto
BR112013028598A2 (pt) método para promover o crescimento de plantas
BR112015029348A2 (pt) inibidores da bace
BRPI1009212B8 (pt) Composto de piperazina capaz de inibir a prostaglandina d sintase, seus usos e composição farmacêutica
BR112013028486A2 (pt) método para promover crescimento de planta
BR112014026198A2 (pt) compostos pirazol como inibidores de sglt1
BR112014031616A2 (pt) compostos de fenoxietil piperidina
BR112012021198A2 (pt) composto de pirazolopirimidina e seu uso como inibidores de pde10

Legal Events

Date Code Title Description
B08F Application fees: application dismissed [chapter 8.6 patent gazette]
B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]