AR036905A1 - Derivados del 3-azabiciclo[3.1.0]hexano, composiciones farmaceuticas que los contienen, su uso en un metodo para tratar un trastorno o afeccion en un mamifero, e intermediarios utiles para su sintesis - Google Patents

Derivados del 3-azabiciclo[3.1.0]hexano, composiciones farmaceuticas que los contienen, su uso en un metodo para tratar un trastorno o afeccion en un mamifero, e intermediarios utiles para su sintesis

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Publication number
AR036905A1
AR036905A1 ARP020103960A ARP020103960A AR036905A1 AR 036905 A1 AR036905 A1 AR 036905A1 AR P020103960 A ARP020103960 A AR P020103960A AR P020103960 A ARP020103960 A AR P020103960A AR 036905 A1 AR036905 A1 AR 036905A1
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AR
Argentina
Prior art keywords
alkyl
optionally
cycloalkyl
heterocycloalkyl
halogen
Prior art date
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ARP020103960A
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English (en)
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Pfizer Prod Inc
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Publication of AR036905A1 publication Critical patent/AR036905A1/es

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/10Laxatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10Drugs for genital or sexual disorders; Contraceptives for impotence
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
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    • 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
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/32Alcohol-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/34Tobacco-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P3/04Anorexiants; Antiobesity agents
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    • A61P37/08Antiallergic agents
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/52Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/04Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
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  • Psychiatry (AREA)
  • Reproductive Health (AREA)
  • Endocrinology (AREA)
  • Hospice & Palliative Care (AREA)
  • Obesity (AREA)
  • Otolaryngology (AREA)
  • Pulmonology (AREA)
  • Hematology (AREA)
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  • Diabetes (AREA)
  • Child & Adolescent Psychology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Un compuesto derivado del 3-azabiciclo [3.1.0] hexano de fórmula (1), donde X es H, halógeno, -OH, -CN, -alquilo C1-4 sustituido con 1 a 3 átomos de halógeno ó -O(alquil C1-4), estando el alquilo C1-4 de -O(alquil C1-4) opcionalmente sustituido con 1 a 3 átomos de halógeno; Q es halógeno, -OH, -O-(alquil C1-4) -NH2, -NH(alquil C1-4), -N(alquil C1-4) (alquil C1-4), -C(=O)NH2, -C(=O)NH(alquil C1-4), -C(=O)N(alquil C1-4) (alquil C1-4), -NHS(=O)2H, ó -NHS(=O)2R11; ó Q puede formar un anillo cicloalquilo ó heterocicloalquilo de 5 ó 6 miembros con cualquier átomo de carbono adyacente al átomo de carbono al que está unido, formando así un sistema de anillo bicíclico condensado con el fenilo al que está unido, comprendiendo dicho heterocicloalquilo de 1 a 3 heterorestos seleccionados entre O, S, -C(=O) y N, y conteniendo opcionalmente dicho cicloalquilo o heterocicloalquilo 1 o 2 dobles enlaces; R1 y R2 están conectados, con el carbono al que están unidos, para formar un cicloalquilo C3-7 ó un heterocicloalquilo de 4-7 miembros que comprende de 1 a 3 heterorestos seleccionados entre O, S, -C(=O) y N; y en el que dicho cicloalquilo ó heterocicloalquilo contiene opcionalmente 1 ó 2 dobles enlaces; y estando dicho cicloalquilo ó heterocicloalquilo opcionalmente condensado con un grupo arilo C6-14 ó un heteroarilo de 5-14 miembros; en el que dicho cicloalquilo C3-7 ó el heterocicloalquilo de 4-7 miembros formado por R1 y R2 pueden cada uno opcionalmente estar sustituido con 1 a 3 grupos R12, y cada uno de dichos arilo o heteroarilo opcionalmente condensado pueden estar sustituidos opcional e independientemente con 1 a 6 grupos R12, seleccionándose los grupos R12 entre R13, R16, -alquilo C1-4 que contiene 1 ó 2 enlaces insaturados, halógeno, -OR13, -NO2-CN, -cicloalquilo C3-6, -NR13R14, -NR13C(=O)R14, -C(=O)NR13R14, -OC(=O)R13, -C(=O)OR13, -C(=O)R13, -NR13, -NR13C(=O)R14, -NR13C(=O)ONR14R15, -NR13S(=O)2R14 y -S(=O)2R13; R3 es alquilo C1-4, conteniendo opcionalmente dicho alquilo C1-4 uno o dos enlaces insaturados; R4 es -alquilo C1-4 que puede opcionalmente contener 1 ó 2 enlaces insaturados, -OH, -CN, NO2, -OR16, -NH2, NHR16, NHR16R17 ó -NHC(=O)R16; R5 y R6 son cada uno independientemente H ó metilo; R6, R7, R9 y R10 son H; R11 se selecciona entre alquilo C1-4, -(alquilen C1-4)-O-(alquil C1-4), 4-(1-metilimidazol), -(alquilen C1-4)-NH2, -(alquilen C1-4)-NH(alquil C1-4), -(alquilen C1-4)-N(alquil C1-4) (alquil C1-4); cada R13, R14 y R15 se selecciona independientemente entre H, R16, alquilo C1-4, halógeno, -OH, -SH, -NH2, -NH(alquil C1-4),-N(alquil C1-4) (alquil C1-4), -O(alquil C1-4), -S(alquil C1-4), -CN, -NO2, -C(=O) (alquil C1-4), -C(=O)OH, -C(=O)O(alquil C1-4), -NHC(=O) (alquil C1-4), -C(=O)NH2, y -C(=O)N(alquil C1-4) (alquil C1-4), ó R13 y R14 cuando en -NR13R14, pueden estar opcionalmente conectados para formar un grupo heterocicloalquilo o heteroarilo de 4 a 6 miembros, cuyo grupo heteroarilo opcionalmente comprende de 1 a 3 heterorestos adicionales seleccionados entre N, S, O y C(=O); cada R16 y R17 se selecciona independientemente entre arilo C6-14 y heteroarilo de 5-14 miembros, en el que dicho heteroarilo comprende de 1 a 3 heterorestos seleccionados entre O, S, -C(=O) y N, y estando dicho arilo y heteroarilo opcionalmente sustituidos con 1 a 3 sustituyentes seleccionados entre alquilo C1-4 que opcionalmente contiene 1 ó 2 enlaces insaturados, halógeno, -OH -SH, -NH2, -NH(alquil C1-4), -N(alquil C1-4) (alquil C1-4), -O(alquil C1-4), -S(alquil C1-4), -CN, -NO2, -C(=O) (alquil C1-4), -NHC(=O) (alquil C1-4), -C(=O)NH2, y -C(=O)N(alquil C1-4) (alquil C1-4); y n es un número entero seleccionado entre 1, 2, 3, 4 y 5; ó una sal farmacéuticamente aceptable de éste. Los compuestos de fórmula (1) tienen actividad como antagonistas del receptor de opioides. Además se describen composiciones farmacéuticas, procedimientos terapéuticos que comprenden los compuestos de fórmula (1) y compuestos intermediarios útiles para su síntesis. Estos compuestos son de aplicación para tratar trastornos y estados como colon irritable, dependencia ó adicción a drogas y depuración y también ciertos trastornos de la alimentación.
ARP020103960A 2001-10-22 2002-10-21 Derivados del 3-azabiciclo[3.1.0]hexano, composiciones farmaceuticas que los contienen, su uso en un metodo para tratar un trastorno o afeccion en un mamifero, e intermediarios utiles para su sintesis AR036905A1 (es)

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US33851101P 2001-10-22 2001-10-22

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EP (1) EP1440059B1 (es)
JP (2) JP4155522B2 (es)
KR (1) KR100621292B1 (es)
CN (1) CN100368398C (es)
AP (1) AP1816A (es)
AR (1) AR036905A1 (es)
AT (1) ATE392415T1 (es)
AU (1) AU2002329557B2 (es)
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Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1379246E (pt) 2001-04-18 2009-01-14 Euro Celtique Sa Análogos de nociceptina
PT1440059E (pt) * 2001-10-22 2008-05-16 Pfizer Prod Inc Derivados do 3-azabiciclo(3.1.0)hexano como antagonistas de receptores opióides
EP1615894A2 (en) * 2003-04-14 2006-01-18 Pfizer Products Inc. 3-azabicyclo 3.2.1 octane derivatives
US20050043327A1 (en) * 2003-08-21 2005-02-24 Pfizer Inc Pharmaceutical composition for the prevention and treatment of addiction in a mammal
US7153976B2 (en) * 2003-10-06 2006-12-26 Pfizer Inc. Purification process for an azabicyclo[3.1.0]hexane compound
WO2005037216A2 (en) * 2003-10-14 2005-04-28 Pfizer Products Inc. Bicyclic [3.1.0] derivatives as glycine transporter inhibitors
CN1867548A (zh) * 2003-10-16 2006-11-22 辉瑞产品公司 3-氮杂双环[3.1.0]己烷衍生物的制备
PT2060570E (pt) * 2004-02-23 2012-05-07 Glaxo Group Ltd Derivados de azabiciclo(3.1.0)-hexano úteis como moduladores dos receptores d3 da dopamina
EP1726590A4 (en) * 2004-03-05 2009-07-15 Banyu Pharma Co Ltd D RIV CYCLOALKANOPYRIDINE
WO2006064779A1 (ja) * 2004-12-14 2006-06-22 Shionogi & Co., Ltd. 6’位にカルボキシを有するインドロモルヒナン誘導体
GB0512099D0 (en) * 2005-06-14 2005-07-20 Glaxo Group Ltd Compounds
GB0517191D0 (en) 2005-08-22 2005-09-28 Glaxo Group Ltd Compounds
US7592461B2 (en) 2005-12-21 2009-09-22 Bristol-Myers Squibb Company Indane modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
MY145633A (en) * 2006-03-01 2012-03-15 Theravance Inc 8-azabicyclo[3.2.1]octane compounds as mu opioid receptor antagonists
WO2008075162A2 (en) * 2006-12-15 2008-06-26 Pfizer Limited Selective mu opioid receptor antagonists for the treatment of female sexual dysfunction
TWI409067B (zh) * 2007-02-28 2013-09-21 Theravance Inc 8-氮雜雙環〔3.2.1〕辛烷化合物之結晶型
EP2185553B1 (en) * 2007-08-27 2012-06-27 Theravance, Inc. Amidoalkyl-8-azabicyclo[3.2.1]octane compounds as mu opioid receptor antagonists
ATE502939T1 (de) * 2007-08-27 2011-04-15 Theravance Inc Disubstituierte alkyl-8-azabicycloä3.2.1üoktan- verbindungen als mu-opioid-rezeptorantagonisten
TWI423801B (zh) * 2007-08-27 2014-01-21 Theravance Inc 作為μ類鴉片受體拮抗劑之8-氮雜雙環〔3.2.1〕辛基-2-羥基苯甲醯胺化合物
EP2195313B1 (en) * 2007-08-27 2014-04-02 Theravance, Inc. Heteroarylalkyl-8-azabicyclo[3.2.1]octane compounds as mu opioid receptor antagonists
JP2013542929A (ja) 2010-09-28 2013-11-28 パナセア バイオテック リミテッド 新規ビシクロ環化合物
MX2016006482A (es) * 2013-11-20 2016-12-09 Sanwa Kagaku Kenkyusho Co Derivado novedoso de 3-azabiciclo[3.1.0]hexano y uso del mismo para proposito medico.
KR20180004734A (ko) * 2015-05-20 2018-01-12 가부시키가이샤산와카가쿠켄큐쇼 신규 3-아자비시클로[3.1.0]헥산 유도체의 염의 결정 및 그의 의약 용도
AU2018229062A1 (en) 2017-03-02 2019-09-26 Ube Industries, Ltd. Therapeutic agent for alcohol use disorders

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2099214A (en) * 1937-11-16 Process fob forming the sulphuric
US2099216A (en) * 1934-05-04 1937-11-16 Frederick H Nass Metal testing machine
US3004340A (en) * 1959-09-24 1961-10-17 Bernice L Collins Kitchen utensil
US3078282A (en) * 1960-01-02 1963-02-19 Bayer Ag Anthraquinone dyestuffs
DE3851081T2 (de) 1987-04-16 1995-02-16 Lilly Co Eli Piperidine als Opioid-Antagoniste.
JPH04155522A (ja) * 1990-10-19 1992-05-28 Nec Corp ファースト・イン・ランダム・アウト回路
CZ284993B6 (cs) 1991-03-29 1999-04-14 Eli Lilly And Company Derivát piperidinu
US5159081A (en) 1991-03-29 1992-10-27 Eli Lilly And Company Intermediates of peripherally selective n-carbonyl-3,4,4-trisubstituted piperidine opioid antagonists
GB9725114D0 (en) * 1997-11-28 1998-01-28 Pfizer Ltd Treatment of pruritus
GB9810671D0 (en) * 1998-05-18 1998-07-15 Pfizer Ltd Anti-pruritic agents
TWI244481B (en) * 1998-12-23 2005-12-01 Pfizer 3-azabicyclo[3.1.0]hexane derivatives useful in therapy
GB9912413D0 (en) * 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912415D0 (en) * 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912410D0 (en) * 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
GB9912411D0 (en) * 1999-05-28 1999-07-28 Pfizer Ltd Compounds useful in therapy
US20020064825A1 (en) * 2000-05-19 2002-05-30 Lewis Marilyn Evelyn Novel polypeptide
GB0015562D0 (en) * 2000-06-23 2000-08-16 Pfizer Ltd Heterocycles
US20020025948A1 (en) * 2000-06-23 2002-02-28 Banks Bernard Joseph 3-azabicyclo[3.1.0]hexane derivatives useful in therapy
US20030207876A1 (en) * 2000-06-23 2003-11-06 Banks Bernard Joseph 3-Azabicyclo[3.1.0]hexane derivatives useful in therapy
DE10042885A1 (de) * 2000-08-31 2002-03-14 Heidelberger Druckmasch Ag Bogentransportzylinder
PT1440059E (pt) 2001-10-22 2008-05-16 Pfizer Prod Inc Derivados do 3-azabiciclo(3.1.0)hexano como antagonistas de receptores opióides
EP1513813B1 (en) 2002-05-30 2005-11-02 Eli Lilly And Company Opioid receptor antagonists
US7056930B2 (en) * 2003-04-14 2006-06-06 Pfizer Inc. 2-Azabicyclo[3.3.1]nonane derivatives
US20040204453A1 (en) * 2003-04-14 2004-10-14 Pfizer Inc 4-Phenyl-piperidine compounds and their use as modulators of opioid receptors
US20050043327A1 (en) * 2003-08-21 2005-02-24 Pfizer Inc Pharmaceutical composition for the prevention and treatment of addiction in a mammal
US7153976B2 (en) * 2003-10-06 2006-12-26 Pfizer Inc. Purification process for an azabicyclo[3.1.0]hexane compound

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