CN101903377B - 6H-二苯并[b，e]氧杂环庚烷衍生的非类固醇矿皮质激素受体拮抗剂 - Google Patents

6H-二苯并[b，e]氧杂环庚烷衍生的非类固醇矿皮质激素受体拮抗剂 Download PDF

Info

Publication number
CN101903377B
CN101903377B CN200880121527.2A CN200880121527A CN101903377B CN 101903377 B CN101903377 B CN 101903377B CN 200880121527 A CN200880121527 A CN 200880121527A CN 101903377 B CN101903377 B CN 101903377B
Authority
CN
China
Prior art keywords
compound
methyl
oxepane
pharmaceutically acceptable
formula
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.)
Expired - Fee Related
Application number
CN200880121527.2A
Other languages
English (en)
Chinese (zh)
Other versions
CN101903377A (zh
Inventor
K·加瓦迪纳斯
P·K·贾达夫
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.)
Eli Lilly and Co
Original Assignee
Eli Lilly and 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40430143&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CN101903377(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Eli Lilly and Co filed Critical Eli Lilly and Co
Publication of CN101903377A publication Critical patent/CN101903377A/zh
Application granted granted Critical
Publication of CN101903377B publication Critical patent/CN101903377B/zh
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/02—Heterocyclic 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
    • C07D405/06—Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
    • A61P5/40—Mineralocorticosteroids, e.g. aldosterone; Drugs increasing or potentiating the activity of mineralocorticosteroids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
    • A61P5/42—Drugs for disorders of the endocrine system of the suprarenal hormones for decreasing, blocking or antagonising the activity of mineralocorticosteroids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Hospice & Palliative Care (AREA)
  • Emergency Medicine (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Steroid Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
CN200880121527.2A 2007-12-19 2008-12-09 6H-二苯并[b，e]氧杂环庚烷衍生的非类固醇矿皮质激素受体拮抗剂 Expired - Fee Related CN101903377B (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US1477607P 2007-12-19 2007-12-19
US61/014776 2007-12-19
PCT/US2008/085997 WO2009085584A1 (en) 2007-12-19 2008-12-09 6h-dibenz0 [b, e] oxepine derived nonsteroidal mineralocorticoid receptor antagonists

Publications (2)

Publication Number Publication Date
CN101903377A CN101903377A (zh) 2010-12-01
CN101903377B true CN101903377B (zh) 2014-07-09

Family

ID=40430143

Family Applications (1)

Application Number Title Priority Date Filing Date
CN200880121527.2A Expired - Fee Related CN101903377B (zh) 2007-12-19 2008-12-09 6H-二苯并[b，e]氧杂环庚烷衍生的非类固醇矿皮质激素受体拮抗剂

Country Status (33)

Country Link
US (1) US7994164B2 (enExample)
EP (2) EP2537845B1 (enExample)
JP (1) JP5562866B2 (enExample)
KR (1) KR101254382B1 (enExample)
CN (1) CN101903377B (enExample)
AR (1) AR069554A1 (enExample)
AU (1) AU2008343524B2 (enExample)
BR (1) BRPI0820805A2 (enExample)
CA (1) CA2710409C (enExample)
CL (1) CL2008003600A1 (enExample)
CO (1) CO6300953A2 (enExample)
DK (1) DK2235007T3 (enExample)
DO (1) DOP2010000185A (enExample)
EA (1) EA017668B1 (enExample)
EC (2) ECSP10010266A (enExample)
ES (2) ES2396605T3 (enExample)
GT (1) GT201000179A (enExample)
HR (1) HRP20120916T1 (enExample)
IL (1) IL206353A (enExample)
MA (1) MA31910B1 (enExample)
MX (1) MX2010006911A (enExample)
MY (1) MY150474A (enExample)
NZ (1) NZ586300A (enExample)
PE (1) PE20091057A1 (enExample)
PL (1) PL2235007T3 (enExample)
PT (1) PT2235007E (enExample)
RS (1) RS52594B (enExample)
SI (1) SI2235007T1 (enExample)
TN (1) TN2010000292A1 (enExample)
TW (1) TWI431010B (enExample)
UA (1) UA100131C2 (enExample)
WO (1) WO2009085584A1 (enExample)
ZA (1) ZA201004257B (enExample)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009018657A1 (en) 2007-08-03 2009-02-12 Boehringer Ingelheim International Gmbh Viral polymerase inhibitors
EP2234977A4 (en) 2007-12-19 2011-04-13 Boehringer Ingelheim Int VIRAL POLYMERASE INHIBITORS
WO2010104721A1 (en) * 2009-03-12 2010-09-16 Eli Lilly And Company Mineralocorticoid receptor antagonist and methods of use
EP2568986B1 (en) 2010-05-10 2016-01-13 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and compositions for the treatment of fluid accumulation in and/ or under the retina
EP2582365B1 (en) 2010-06-16 2019-03-20 INSERM (Institut National de la Santé et de la Recherche Médicale) Compositions for stimulating reepithelialisation during wound healing
CN102060670A (zh) * 2011-01-04 2011-05-18 常州大学 一种2-溴-6-氟苯甲醇的制备方法
MD20150103A2 (ro) 2013-05-02 2016-02-29 Pfizer Inc. Derivaţi ai imidazo-triazinei ca inhibitori ai PDE10
AR099416A1 (es) 2014-02-28 2016-07-20 Lilly Co Eli Terapia combinada para la hipertensión resistente
ME03316B (me) 2014-06-30 2019-10-20 Astrazeneca Ab Benzoksazinon amidi као modulatori mineralokorтikoidnog receptora
JP2017531684A (ja) * 2014-11-21 2017-10-26 イーライ リリー アンド カンパニー 腎障害の治療のための１，２−ベンゾチアゾール化合物
US20180280414A1 (en) 2015-10-13 2018-10-04 Inserm (Institut National De La Sante Et De La Recherche Medicale) Methods and pharmaceutical compositions for the treatment of choroidal neovascularisation
EP3490606B8 (en) 2016-07-26 2024-04-10 INSERM (Institut National de la Santé et de la Recherche Médicale) Antagonist of mineralocorticoid receptor for the treatment of osteoarthritis
WO2018054357A1 (zh) * 2016-09-24 2018-03-29 山东亨利医药科技有限责任公司 含盐皮质激素受体拮抗剂的药物组合物及其用途
EP4118235B1 (en) 2020-03-11 2026-08-05 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods of determining whether a subject has or is at risk of having a central serous chorioretinopathy
WO2023031277A1 (en) 2021-08-31 2023-03-09 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for the treatment of ocular rosacea
CN117510398A (zh) * 2023-11-02 2024-02-06 上海诺丁太生物科技有限公司 一种高光学纯度(3r,4r)/(3s,4s)-n-boc-4-氨基-3-羟基哌啶的制备方法

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4072756A (en) * 1973-05-17 1978-02-07 Sandoz Ltd. Tricyclo piperidino ketones and soporific compositions thereof
SE426341C (sv) * 1980-02-14 1985-09-23 Fagersta Ab Sett att forhindra korrosion i en forbrenningsanleggnings kylare och skorsten vid kylning av rokgaser
FR2603713B1 (fr) * 1986-09-10 1992-07-24 Canon Kk Derive nouveau de 5h-dibenzo(a,d)cycloheptane-(ene)ylidene, son procede de production et support electrophotographique photosensible le contenant
US4999363A (en) * 1988-06-09 1991-03-12 Kyowa Hakko Kogyo Co., Ltd. Tricyclic compounds
GB8914061D0 (en) * 1989-06-19 1989-08-09 Wellcome Found Agents for potentiating the effects of antitumour agents and combating multiple drug resistance
US5378701A (en) * 1991-12-27 1995-01-03 Kyowa Hakko Kogyo Tricyclic compounds
US6372779B1 (en) 1997-12-29 2002-04-16 Ortho Pharmaceutical Corporation Anti-inflammatory compounds
EP1154997A4 (en) 1999-01-26 2002-11-04 Dana Farber Cancer Inst Inc PHARMACEUTICALLY ACTIVE COMPOUNDS AND METHODS OF USE
ES2260497T7 (es) * 2001-11-21 2009-11-05 Millennium Pharmaceuticals, Inc. Antagonistas de receptores de quimioquininas y metodos de uso de los mismos.
TW200400816A (en) * 2002-06-26 2004-01-16 Lilly Co Eli Tricyclic steroid hormone nuclear receptor modulators
WO2005066153A1 (en) 2003-12-19 2005-07-21 Eli Lilly And Company Tricyclic steroid hormone nuclear receptor modulators
DE602004014640D1 (de) * 2003-12-19 2008-08-07 Lilly Co Eli Tricyclische modulatoren von nuklearen steroidhormonrezeptoren
TWI350168B (en) 2004-05-07 2011-10-11 Incyte Corp Amido compounds and their use as pharmaceuticals
RU2007107177A (ru) * 2004-07-28 2008-09-10 Айрм Ллк (Bm) Соединения и композиции, как модуляторы ядерных рецепторов стероидных гормонов
SG161261A1 (en) 2004-11-10 2010-05-27 Incyte Corp Lactam compounds and their use as pharmaceuticals
ES2375877T3 (es) 2006-10-31 2012-03-07 Pfizer Products Inc. Compuestos de pirazolina como antagonistas de receptores de mineralocorticoides.
JP2010522732A (ja) 2007-03-29 2010-07-08 ナームローゼ・フエンノートチヤツプ・オルガノン 鉱質コルチコイド受容体アンタゴニスト
PE20091339A1 (es) 2007-12-21 2009-09-26 Glaxo Group Ltd Derivados de oxadiazol con actividad sobre receptores s1p1
GB0725102D0 (en) 2007-12-21 2008-01-30 Glaxo Group Ltd Compounds
WO2009094157A1 (en) 2008-01-25 2009-07-30 Arena Pharmaceuticals, Inc. Dihydro- 1h- pyrrolo [1,2-a] indol-1-yl carboxylic derivatives which act as s1p1 agonists
WO2010104721A1 (en) 2009-03-12 2010-09-16 Eli Lilly And Company Mineralocorticoid receptor antagonist and methods of use

Also Published As

Publication number Publication date
MA31910B1 (fr) 2010-12-01
PT2235007E (pt) 2013-01-22
HRP20120916T1 (hr) 2012-12-31
AR069554A1 (es) 2010-02-03
EP2537845A1 (en) 2012-12-26
EA201070762A1 (ru) 2010-12-30
ES2459318T3 (es) 2014-05-09
UA100131C2 (uk) 2012-11-26
MY150474A (en) 2014-01-30
AU2008343524B2 (en) 2012-03-08
DOP2010000185A (es) 2010-09-15
PE20091057A1 (es) 2009-07-20
ZA201004257B (en) 2011-11-30
PL2235007T3 (pl) 2013-03-29
TN2010000292A1 (en) 2011-11-11
CN101903377A (zh) 2010-12-01
NZ586300A (en) 2012-06-29
JP2011507868A (ja) 2011-03-10
EP2235007B1 (en) 2012-10-31
HK1144284A1 (en) 2011-02-11
CA2710409C (en) 2012-11-06
KR101254382B1 (ko) 2013-04-15
CO6300953A2 (es) 2011-07-21
TWI431010B (zh) 2014-03-21
BRPI0820805A2 (pt) 2015-06-16
ECSP12012048A (es) 2012-08-31
RS52594B (sr) 2013-04-30
EA017668B1 (ru) 2013-02-28
ECSP10010266A (es) 2010-07-30
GT201000179A (es) 2012-04-16
CL2008003600A1 (es) 2010-02-19
KR20100082866A (ko) 2010-07-20
ES2396605T3 (es) 2013-02-22
SI2235007T1 (sl) 2013-01-31
EP2537845B1 (en) 2014-03-19
US7994164B2 (en) 2011-08-09
TW200930721A (en) 2009-07-16
WO2009085584A1 (en) 2009-07-09
IL206353A0 (en) 2010-12-30
CA2710409A1 (en) 2009-07-09
US20090163472A1 (en) 2009-06-25
EP2235007A1 (en) 2010-10-06
IL206353A (en) 2014-06-30
DK2235007T3 (da) 2012-12-17
MX2010006911A (es) 2010-10-05
AU2008343524A1 (en) 2009-07-09
JP5562866B2 (ja) 2014-07-30

Similar Documents

Publication Publication Date Title
TWI431010B (zh) 礦皮質素受體拮抗劑及使用方法
TWI609018B (zh) 新穎雙環衍生物
CN107849017A (zh) 作为magl抑制剂的1,1,1‑三氟‑3‑羟基丙‑2‑基氨基甲酸酯衍生物及1,1,1‑三氟‑4‑羟基丁‑2‑基氨基甲酸酯衍生物
TW201249845A (en) Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors
CN108697710B (zh) 作为nik抑制剂的新颖的经取代的氰基吲哚啉衍生物
WO2012011591A1 (ja) 縮合複素環化合物およびその用途
KR20100031578A (ko) 5-ｈｔ6 수용체 친화성을 갖는 4'-치환된 화합물
JP7295019B2 (ja) ７－置換１－アリール－ナフチリジン－３－カルボン酸アミドおよびその使用
CN105308045A (zh) 新的3，4-二氢-2h-异喹啉-1-酮和2，3-二氢-异吲哚-1-酮化合物
CN113677673A (zh) Trpc6的抑制剂
US8658638B2 (en) Mineralocorticoid receptor antagonist and methods of use
CN105143205A (zh) 新的3,4-二氢-2h-异喹啉-1-酮和2,3-二氢-异吲哚-1-酮化合物
EP1497292A1 (en) Azaindolylpiperidine derivatives as antihistaminic and antiallergic agents
HK1144284B (en) 6h-dibenz0 [b, e] oxepine derived nonsteroidal mineralocorticoid receptor antagonists
TW202607004A (zh) ６，７－二氫－５Ｈ－吡咯並〔１，２ａ〕咪唑類衍生物及其製備方法和用途
Bhalay Preparation of tyrosine amide derivatives as Rho-​ kinase inhibitors
HK40065851B (en) Iso-citrate dehydrogenase (idh) inhibitor
HK40065851A (en) Iso-citrate dehydrogenase (idh) inhibitor

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
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20140709

Termination date: 20161209

CF01 Termination of patent right due to non-payment of annual fee