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ES2180338T3 - Antagonistas del receptor de crf y metodos relacionados. - Google Patents

Antagonistas del receptor de crf y metodos relacionados.

Info

Publication number
ES2180338T3
ES2180338T3 ES99960363T ES99960363T ES2180338T3 ES 2180338 T3 ES2180338 T3 ES 2180338T3 ES 99960363 T ES99960363 T ES 99960363T ES 99960363 T ES99960363 T ES 99960363T ES 2180338 T3 ES2180338 T3 ES 2180338T3
Authority
ES
Spain
Prior art keywords
crf
related methods
crf receptor
pharmaceutically acceptable
treatment
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 - Lifetime
Application number
ES99960363T
Other languages
English (en)
Inventor
Mustapha Haddach
Jodie Nelson
Brian P Dyck
Zhiqiang Guo
Charles Q Huang
James R Mccarthy
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.)
Neurocrine Biosciences Inc
Original Assignee
Neurocrine Biosciences Inc
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 Neurocrine Biosciences Inc filed Critical Neurocrine Biosciences Inc
Application granted granted Critical
Publication of ES2180338T3 publication Critical patent/ES2180338T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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
    • C07D471/12Heterocyclic 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 three hetero rings
    • C07D471/16Peri-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/02Drugs for disorders of the endocrine system of the hypothalamic hormones, e.g. TRH, GnRH, CRH, GRH, somatostatin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/16Peri-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (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)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Endocrinology (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Input Circuits Of Receivers And Coupling Of Receivers And Audio Equipment (AREA)
  • Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)

Abstract

Un compuesto que tiene la estructura siguiente: con inclusión de sus estereoisómeros, profármacos y sales farmacéuticamente aceptables, en la cual: n es 1 ó 2; A y C son cada uno independientemente nitrógeno, carbono o CH; B es nitrógeno o CR3; con las condiciones de que al menos uno de A, B y C es nitrógeno; A, B y C no son todos ellos nitrógeno; y A - B o B - C es un enlace doble; X es nitrógeno o CH; Ar es arilo, arilo sustituido, heteroarilo, o heteroarilo sustituido; R es un sustituyente opcional que, en cada caso, es independientemente alquilo, alquilidenilo, arilalquilo o heteroarilalquilo, en el cual m es 0, 1, 2 ¿ o 3 y representa el número de sustituyentes R; R1 es - C(H)0, 1(R4)(R5) o - SO2R5; R2 es hidrógeno o alquilo; R3 es hidrógeno, alquilo o haloalquilo; R4 es hidrógeno, ceto, alquilo, alquilidenilo, o halo; y R5 es un radical de la fórmula - Y - Z - R6, en la cual Y es un alcanodiílo, alcanodiílo sustituido, o un enlace directo, Z es NH, - N(R7), O, S, SO2, C(=O), C(=O)O, OC(=O), NHC(=O), C(=O)NH, NH(SO2), (SO2)NH, NR8C(=O)O, o un enlace directo; R6 es hidrógeno, alquilo, alquilo sustituido, arilo, arilo sustituido, arilalquilo, arilalquilo sustituido, heterociclo, heterociclo sustituido, heterocicloalquilo, o heterocicloalquilo sustituido; o R7 y R8 son iguales o diferentes y son independientemente alquilo, alquilo sustituido, arilo, arilo sustituido, arilalquilo, arilalquilo sustituido, heterociclo, heterociclo sustituido, heterocicloalquilo, o heterocicloalquilo sustituido; o R6 y R7, considerados junto con el átomo de nitrógeno al cual están unidos, forman un anillo heterocíclico o anillo heterocíclico sustituido; o R4 y R5, considerados juntos, forman ciclo - alquilo, cicloalquilo sustituido, cicloalquilcicloalquilo, cicloalquilcicloalquilo sustituido, cicloalquil arilo, cicloalquilarilo sustituido, cicloalquilheterociclo, o ciclo - alquilheterociclo sustituido.
ES99960363T 1998-11-12 1999-11-12 Antagonistas del receptor de crf y metodos relacionados. Expired - Lifetime ES2180338T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US19107398A 1998-11-12 1998-11-12
US37083799A 1999-08-09 1999-08-09
US40136499A 1999-09-21 1999-09-21

Publications (1)

Publication Number Publication Date
ES2180338T3 true ES2180338T3 (es) 2003-02-01

Family

ID=27392849

Family Applications (1)

Application Number Title Priority Date Filing Date
ES99960363T Expired - Lifetime ES2180338T3 (es) 1998-11-12 1999-11-12 Antagonistas del receptor de crf y metodos relacionados.

Country Status (17)

Country Link
US (1) US6514982B1 (es)
EP (1) EP1129091B1 (es)
JP (1) JP2002529465A (es)
KR (1) KR20010080990A (es)
CN (1) CN1217945C (es)
AT (1) ATE225349T1 (es)
AU (1) AU755552B2 (es)
CA (1) CA2350642A1 (es)
DE (1) DE69903333T2 (es)
DK (1) DK1129091T3 (es)
ES (1) ES2180338T3 (es)
HK (1) HK1038926B (es)
IL (1) IL142893A0 (es)
NO (1) NO20012194D0 (es)
NZ (1) NZ510955A (es)
PT (1) PT1129091E (es)
WO (1) WO2000027846A2 (es)

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EP1129091B1 (en) * 1998-11-12 2002-10-02 Neurocrine Biosciences, Inc. Crf receptor antagonists and methods relating thereto
US6531475B1 (en) 1998-11-12 2003-03-11 Neurocrine Biosciences, Inc. CRF receptor antagonists and methods relating thereto
WO2001058489A1 (en) * 2000-02-14 2001-08-16 Japan Tobacco Inc. Preventives/remedies for postoperative stress
JP2003533530A (ja) 2000-05-18 2003-11-11 ニューロクライン バイオサイエンシーズ, インコーポレイテッド Crfレセプターアンタゴニスト
KR20030060927A (ko) * 2000-11-03 2003-07-16 뉴로크린 바이오사이언시즈 인코퍼레이티드 Crf 수용체 길항제 및 이와 관련된 방법
KR100843281B1 (ko) 2000-12-28 2008-07-09 오노 야꾸힝 고교 가부시키가이샤 삼환식 복소환 유도체 화합물 및 그 화합물을 유효성분으로 하는 의약
WO2002064592A1 (en) * 2000-12-28 2002-08-22 Neurocrine Biosciences, Inc. Tricyclic crf receptor antagonists
AU2002249474B2 (en) * 2001-04-30 2006-01-12 Glaxo Group Limited Crf receptor antagonists
EP1392689B1 (en) 2001-05-21 2006-10-25 Neurocrine Biosciences, Inc. Tri- and tetraaza-acenaphthylen derivatives as crf receptor antagonists
US7273871B2 (en) 2001-07-17 2007-09-25 Sb Pharmco Puerto Rico Inc. Phenyl-5,6,6A,7,8,9-hexahydro-4H-1,4,9-triaza-phenalene derivatives as CRF antagonists
GB0117395D0 (en) * 2001-07-17 2001-09-05 Glaxo Group Ltd Chemical compounds
EP2335700A1 (en) 2001-07-25 2011-06-22 Boehringer Ingelheim (Canada) Ltd. Hepatitis C virus polymerase inhibitors with a heterobicylic structure
AU2004249629B2 (en) 2003-06-25 2009-07-30 Ono Pharmaceutical Co., Ltd. Methanesulfonic acid salt of pyrazolopyrimidine compound, crystal thereof, and process for producing the same
US20060024661A1 (en) * 2003-07-30 2006-02-02 The Regents Of The University Of California Modulation of CRF potentiation of NMDA receptor currents via CRF receptor 2
JP2007501822A (ja) * 2003-08-12 2007-02-01 エフ.ホフマン−ラ ロシュ アーゲー コルチコトロピン放出性因子(crf)アンタゴニストとしてのスピロ置換テトラヒドロキナゾリン
EP1697362B1 (en) * 2003-12-22 2008-03-05 SB Pharmco Puerto Rico Inc. Crf receptor antagonists and methods relating thereto
IN2012DN04853A (es) 2004-02-20 2015-09-25 Boehringer Ingelheim Int
WO2005087775A1 (ja) * 2004-03-15 2005-09-22 Ono Pharmaceutical Co., Ltd. 三環式複素環化合物およびその化合物を有効成分として含有する医薬組成物
US7869958B2 (en) * 2004-08-09 2011-01-11 Research Development Foundation Structure-based modulators of B1 G-protein coupled receptors
AU2008211729A1 (en) 2007-02-01 2008-08-07 Astrazeneca Ab 5,6,7,8-tetrahydropteridine derivatives as HSP90 inhibitors
US8343983B2 (en) * 2009-03-31 2013-01-01 Arqule, Inc. Substituted pyrazolo-pyrimidine compounds
CA2764885C (en) * 2009-06-08 2018-05-15 Takeda Pharmaceutical Company Limited Dihydropyrrolonaphtyridinone compounds as inhibitors of jak
WO2011082273A2 (en) * 2009-12-30 2011-07-07 Arqule, Inc. Substituted pyrrolo-aminopyrimidine compounds
CN113416191A (zh) * 2021-04-27 2021-09-21 西安交通大学 一种合成三环骨架2-吡啶酮/2-吡啶亚胺类化合物的方法

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EP1129091B1 (en) * 1998-11-12 2002-10-02 Neurocrine Biosciences, Inc. Crf receptor antagonists and methods relating thereto

Also Published As

Publication number Publication date
CA2350642A1 (en) 2000-05-18
IL142893A0 (en) 2002-04-21
HK1038926B (en) 2003-07-18
AU1725800A (en) 2000-05-29
DK1129091T3 (da) 2002-11-04
CN1217945C (zh) 2005-09-07
EP1129091B1 (en) 2002-10-02
NO20012194L (no) 2001-05-03
DE69903333D1 (de) 2002-11-07
EP1129091A2 (en) 2001-09-05
NZ510955A (en) 2003-01-31
KR20010080990A (ko) 2001-08-25
WO2000027846A3 (en) 2000-11-16
ATE225349T1 (de) 2002-10-15
CN1328559A (zh) 2001-12-26
WO2000027846A2 (en) 2000-05-18
NO20012194D0 (no) 2001-05-03
DE69903333T2 (de) 2003-08-07
HK1038926A1 (en) 2002-05-10
PT1129091E (pt) 2003-02-28
AU755552B2 (en) 2002-12-12
JP2002529465A (ja) 2002-09-10
US6514982B1 (en) 2003-02-04

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