MA32301B1 - 1-aryl-3-amino-alcoxypyrazoles comme ligands de sigma augmentant l'effet analgesique d'opioides et attenuant la dependance a ceux-ci - Google Patents

1-aryl-3-amino-alcoxypyrazoles comme ligands de sigma augmentant l'effet analgesique d'opioides et attenuant la dependance a ceux-ci

Info

Publication number
MA32301B1
MA32301B1 MA33343A MA33343A MA32301B1 MA 32301 B1 MA32301 B1 MA 32301B1 MA 33343 A MA33343 A MA 33343A MA 33343 A MA33343 A MA 33343A MA 32301 B1 MA32301 B1 MA 32301B1
Authority
MA
Morocco
Prior art keywords
coccyberazole
opioids
aryl
amine
analgesic effect
Prior art date
Application number
MA33343A
Other languages
Arabic (ar)
English (en)
Inventor
Helmut Heinrich Buschmann
José Miguel Vela-Hernández
Daniel Zamanillo-Castanedo
Original Assignee
Esteve Labor Dr
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=39768934&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA32301(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Esteve Labor Dr filed Critical Esteve Labor Dr
Publication of MA32301B1 publication Critical patent/MA32301B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D231/18One oxygen or sulfur atom
    • C07D231/20One oxygen atom attached in position 3 or 5
    • C07D231/22One oxygen atom attached in position 3 or 5 with aryl radicals attached to ring nitrogen atoms
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41521,2-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. antipyrine, phenylbutazone, sulfinpyrazone
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41551,2-Diazoles non condensed and containing further heterocyclic rings
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/485Morphinan derivatives, e.g. morphine, codeine
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • 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
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Emergency Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Addiction (AREA)
  • Psychiatry (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Peptides Or Proteins (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)

Abstract

L'invention porte sur l'utilisation d'un groupe de ligands des récepteurs sigma de formule (i), pour la potentialisation de l'effet analgésique d'opioïdes et d'opiacés et en même temps pour diminuer la dépendance induite par ceux-ci.
MA33343A 2008-04-25 2010-11-11 1-aryl-3-amino-alcoxypyrazoles comme ligands de sigma augmentant l'effet analgesique d'opioides et attenuant la dependance a ceux-ci MA32301B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08380122A EP2116539A1 (fr) 2008-04-25 2008-04-25 1-aryl-3-aminoalkoxy-pyrazoles en tant que ligands améliorant les effets analgésiques des opioïdes et réduisant leur dépendance
PCT/EP2009/054974 WO2009130310A1 (fr) 2008-04-25 2009-04-24 1-aryl-3-amino-alcoxypyrazoles comme ligands de sigma augmentant l'effet analgésique d'opioïdes et atténuant la dépendance à ceux-ci

Publications (1)

Publication Number Publication Date
MA32301B1 true MA32301B1 (fr) 2011-05-02

Family

ID=39768934

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33343A MA32301B1 (fr) 2008-04-25 2010-11-11 1-aryl-3-amino-alcoxypyrazoles comme ligands de sigma augmentant l'effet analgesique d'opioides et attenuant la dependance a ceux-ci

Country Status (27)

Country Link
US (3) US8877753B2 (fr)
EP (3) EP2116539A1 (fr)
JP (1) JP5753076B2 (fr)
KR (1) KR101764817B1 (fr)
CN (1) CN102066334B (fr)
AU (1) AU2009239968B2 (fr)
BR (1) BRPI0910677A2 (fr)
CA (1) CA2722345C (fr)
CO (1) CO6410301A2 (fr)
CY (1) CY1115848T1 (fr)
DK (1) DK2276744T3 (fr)
EC (1) ECSP10010634A (fr)
ES (1) ES2526360T3 (fr)
HR (1) HRP20141263T1 (fr)
IL (1) IL208865B (fr)
MA (1) MA32301B1 (fr)
MX (1) MX2010011673A (fr)
MY (1) MY160800A (fr)
NZ (1) NZ588829A (fr)
PL (1) PL2276744T3 (fr)
PT (1) PT2276744E (fr)
RS (1) RS53717B1 (fr)
RU (1) RU2519060C2 (fr)
SG (1) SG190578A1 (fr)
SI (1) SI2276744T1 (fr)
UA (1) UA105900C2 (fr)
WO (1) WO2009130310A1 (fr)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2007002341A (es) * 2004-08-27 2007-09-25 Esteve Labor Dr Inhibidores del receptor sigma.
EP2116539A1 (fr) 2008-04-25 2009-11-11 Laboratorios Del. Dr. Esteve, S.A. 1-aryl-3-aminoalkoxy-pyrazoles en tant que ligands améliorant les effets analgésiques des opioïdes et réduisant leur dépendance
EP2335688A1 (fr) * 2009-11-25 2011-06-22 Laboratorios Del. Dr. Esteve, S.A. Compositions pharmaceutiques comprenant des ligands du récepteur sigma
EP2353591A1 (fr) * 2010-02-04 2011-08-10 Laboratorios Del. Dr. Esteve, S.A. Ligands sigma pour la potentialisation de l'effet analgésique d'opioïdes et d'opiacés dans la douleur post-opératoire et en atténuant la dépendance
EP2353598A1 (fr) 2010-02-04 2011-08-10 Laboratorios Del. Dr. Esteve, S.A. Ligands sigma pour utilisation dans la prévention et/ou le traitement de la douleur post-opératoire
EP2426112A1 (fr) * 2010-08-09 2012-03-07 Laboratorios Del. Dr. Esteve, S.A. Polymorphes et solvates de chlorhydrate de 4-[-2-[[5-méthyl-1-(2-naphtalényl)-1h-pyrazol-3-yl]oxy]éthyl]morpholine
EP2388005A1 (fr) 2010-05-21 2011-11-23 Laboratorios Del. Dr. Esteve, S.A. Ligands sigma pour la prévention et/ou le traitement du vomissement induit par la chimiothérapie ou la radiothérapie
EP2415471A1 (fr) * 2010-08-03 2012-02-08 Laboratorios Del. Dr. Esteve, S.A. Utilisation de ligands sigma dans l'hyperalgie induite par opioïdes
EP2426111A1 (fr) * 2010-08-09 2012-03-07 Laboratorios Del. Dr. Esteve, S.A. Formes cristallines de chlorhydrate de 4-[-2-[[5-méthyl-1-(2-naphtalényl)-1h-pyrazol-3-yl]oxy]éthyl]morpholine
EP2460519A1 (fr) 2010-12-03 2012-06-06 Laboratorios Del. Dr. Esteve, S.A. Utilisation de ligands sigma pour la douleur du cancer des os
EP2524694A1 (fr) 2011-05-19 2012-11-21 Laboratorios Del. Dr. Esteve, S.A. Utilisation de ligands sigma dans la douleur liée au diabète de type 2
EP2792352A1 (fr) * 2013-04-16 2014-10-22 Laboratorios Del. Dr. Esteve, S.A. Combinaisons comprenants un ligand de receptor Sigma et un ligand de réceptor adrénergic-alpha-2
EP2818166A1 (fr) * 2013-06-26 2014-12-31 Laboratorios del Dr. Esteve S.A. Utilisation de ligands des récepteurs sigma pour la prévention et le traitement de la douleur associée à la cystite interstitielle/au syndrome de la vessie douloureuse (IC/BPS)
EP3043795A1 (fr) * 2013-09-12 2016-07-20 Laboratorios Del. Dr. Esteve, S.A. Combinaisons d'anti-inflammatoire non stéroïdien (ains) et de ligand des récepteurs sigma
CN105873578A (zh) 2013-12-17 2016-08-17 埃斯蒂维实验室股份有限公司 血清素-去甲肾上腺素再摄取抑制剂(SNRIs)和σ受体配体组合物
WO2015091505A1 (fr) * 2013-12-17 2015-06-25 Laboratorios Del Dr. Esteve, S.A. Combinaisons de gabapentanoïdes et de ligands des récepteurs sigma
US11034669B2 (en) 2018-11-30 2021-06-15 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof
CN112341397B (zh) * 2019-08-09 2023-05-23 成都苑东生物制药股份有限公司 吡嗪类衍生物或盐、异构体、其制备方法及用途

Family Cites Families (133)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU11248A1 (ru) 1927-03-29 1929-09-30 В.С. Григорьев Способ очистки антрацена
US2908677A (en) 1955-03-30 1959-10-13 Eastman Kodak Co Nickel and cobalt complexes of pyrazolone monoazo compounds
US3428634A (en) 1965-03-13 1969-02-18 Acraf 3-tertiary amino alkoxy-1-hydrocarbon indazoles
CH471199A (de) 1965-07-06 1969-04-15 Sandoz Ag Verfahren zur Herstellung metallhaltiger Azofarbstoffe
DE2313722C3 (de) 1973-03-20 1987-04-16 Bayer Ag, 5090 Leverkusen Chromischkomplex-Farbstoff und dessen Verwendung zum Färben und Bedrucken von stickstoffhaltigen Fasermaterialien
IT1005472B (it) 1974-02-15 1976-08-20 Montedison Spa Procedimento per la preparazione del 2,5, dimetil 3,2h, furanone
DE2460891C2 (de) 1974-12-21 1982-09-23 Gödecke AG, 1000 Berlin 1-Aminomethyl-1-cycloalkanessigsäuren und deren Ester, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel
FR2301250A1 (fr) 1975-02-21 1976-09-17 Bellon Labor Sa Roger Nouveaux diaryl-1, 4o-aminoalcoxy-3 pyrazoles et leurs sels
CA1121651A (fr) 1978-07-27 1982-04-13 Chi-Kuen Shu Applications organoleptiques de 2,5-dialkyldihydrofuranones et 2,4,5-trialkyldihydrofuranones et de melanges des deux
US4207392A (en) 1978-10-30 1980-06-10 Eastman Kodak Company Heat developable and stabilizable photographic materials and process
FR2460299A1 (fr) 1979-07-05 1981-01-23 Bellon Labor Sa Roger Nouveaux derives du pyrazole et leur application therapeutique
US4234616A (en) 1979-08-03 1980-11-18 International Flavors & Fragrances Inc. Flavoring with mixtures of 2,5-dialkyl dihydrofuranones and 2,4,5-trialkyl dihydrofuranones
FR2472564A1 (fr) 1979-12-31 1981-07-03 Bellon Labor Sa Roger Nouveaux aryl-1 arylsulfonyl-4 1h-pyrazolols-3, et procede pour les preparer
US4826868A (en) 1986-05-29 1989-05-02 Ortho Pharmaceutical Corporation 1,5-Diaryl-3-substituted pyrazoles pharmaceutical compositions and use
GB8917069D0 (en) 1989-07-26 1989-09-13 Merck Sharp & Dohme Therapeutic agents
IL96507A0 (en) 1989-12-08 1991-08-16 Merck & Co Inc Nitrogen-containing spirocycles and pharmaceutical compositions containing them
EP0507863A4 (en) 1989-12-28 1993-07-07 Virginia Commonwealth University Sigma receptor ligands and the use thereof
JPH03232817A (ja) 1990-02-07 1991-10-16 Showa Yakuhin Kako Kk 貼付剤
EP0445974A3 (en) 1990-03-05 1992-04-29 Merck Sharp & Dohme Ltd. Spirocyclic antipsychotic agents
JPH04364129A (ja) 1990-10-26 1992-12-16 Asahi Chem Ind Co Ltd 6−置換アルコキシキノキサリン誘導体含有医薬組成物およびその製造法
AU9137091A (en) 1990-11-27 1992-06-25 Northwestern University Gaba and l-glutamic acid analogs for antiseizure treatment
NZ243065A (en) 1991-06-13 1995-07-26 Lundbeck & Co As H Piperidine derivatives and pharmaceutical compositions
US5240925A (en) 1991-08-26 1993-08-31 Rohm And Haas Company Fungicidal 2-aryl-2-cyano-2-(heterocyclylalkyl)ethyl-1,2,4-triazoles
FI945426A0 (fi) 1992-05-20 1994-11-18 Univ Northwestern GABA- ja L-glutamiinihappoanalogit kohtauksenvastaiseen käsittelyyn
GB9423542D0 (en) 1994-11-22 1995-01-11 Marples Brian A Pharmaceutical compounds
SG65637A1 (en) 1996-02-27 1999-06-22 Thomson Consumer Electronics Oscillation network in a digital timing recovery system
JPH1036259A (ja) 1996-04-11 1998-02-10 Kikkoman Corp 白内障の予防または治療薬剤
JPH1055048A (ja) 1996-08-08 1998-02-24 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料
WO1998031227A1 (fr) 1997-01-21 1998-07-23 Smithkline Beecham Corporation Nouveaux modulateurs de recepteurs de cannabinoides
WO1998041519A1 (fr) 1997-03-18 1998-09-24 Smithkline Beecham Corporation Nouveaux agonistes de recepteurs de cannabinoides
JP2001518912A (ja) 1997-04-14 2001-10-16 ソルフォード、ウルトラファイン、ケミカルズ、アンド、リサーチ、リミテッド モルヒネ誘導体
PL191496B1 (pl) 1997-07-02 2006-05-31 Merck & Co Inc Odmiana polimorficzna 2-(R)-{1-(R) -[3,5-bis(trifluorometylo)-fenylo]etoksy} -3-(S)-(4-fluoro) fenylo-4-[3-(5-okso-1H,4H-1,2,4-triazolo)metylo] morfoliny, sposób jej wytwarzania, zawierająca ją kompozycja farmaceutyczna i jej zastosowanie
CA2303244C (fr) 1997-10-27 2005-12-06 Warner-Lambert Company Acides amines cycliques et leurs derives utilises en tant qu'agents pharmaceutiques
JP2002508362A (ja) 1997-12-16 2002-03-19 ワーナー−ランバート・カンパニー 1−置換−1−アミノメチル−シクロアルカン誘導体(=ガバペンチン類縁体)、その製造および神経学的疾患の治療におけるその使用
TR200001794T2 (tr) 1997-12-16 2000-10-23 Warner-Lambert Company Farmasötik maddeler olarak yeni aminler
KR20010033153A (ko) 1997-12-16 2001-04-25 로즈 암스트롱, 크리스틴 에이. 트러트웨인 4(3)-치환-4(3)-아미노메틸-(티오)피란 또는 -피페리딘유도체(=가바펜틴 동족체), 그의 제법 및 신경 질환 치료용도
HUP0100310A3 (en) * 1997-12-22 2002-11-28 Euro Celtique Sa A method of preventing abuse of opioid dosage forms
EP2266564B1 (fr) * 1997-12-22 2013-03-13 Euro-Celtique S.A. Formulation pharmaceutique pour administration orale comprenant en combinaison un agoniste et un antagoniste des récepteurs opiacés
AU4198299A (en) * 1998-05-21 1999-12-06 Rae R. Matsumoto Compounds and uses thereof
WO1999061424A1 (fr) 1998-05-26 1999-12-02 Warner-Lambert Company Composes d'acide amines soumis a une contrainte de conformation et presentant une affinite pour la sous-unite alpha 2 delta d'un canal calcique
US6166072A (en) 1998-08-03 2000-12-26 Allelix Neuroscience, Inc. Amino acid derivatives
WO2000020005A1 (fr) 1998-10-01 2000-04-13 EGIS Gyógyszergyár Rt. Compositions pharmaceutiques renfermant un analgesique opiace et une substance synergique
GB9824310D0 (en) 1998-11-05 1998-12-30 Univ London Activators of soluble guanylate cyclase
CN1131221C (zh) * 1998-11-09 2003-12-17 参天制药株式会社 药物依赖症的治疗剂
JP3752580B2 (ja) * 1998-11-09 2006-03-08 参天製薬株式会社 薬物依存症治療剤
AU1602100A (en) 1998-11-25 2000-06-13 Warner-Lambert Company Improved gamma amino butyric acid analogs
NO310544B1 (no) 1999-01-04 2001-07-23 Algeta As Opparbeidelse og anvendelse av radium-223 til fremstilling av preparat samt kit til behandling av kalsifisert vev for palliasjon, benkreft-terapi og/eller overflatebehandling av ben
JP2002538221A (ja) 1999-03-10 2002-11-12 ワーナー−ランバート・カンパニー 抗てんかん作用を有する化合物を包含する鎮痛組成物およびその使用方法
DE60012508T2 (de) 1999-05-26 2005-06-23 Warner-Lambert Company Llc Aminosäuren mit polycyclischer struktur als pharmaka
BR0011039A (pt) 1999-05-28 2002-02-26 Warner Lambert Co Análogos de gaba substituìdos com 3-heteroarilalquila
WO2000073300A1 (fr) 1999-06-02 2000-12-07 Warner-Lambert Company Amino heterocycles convenant comme agents pharmaceutiques
US7091257B2 (en) 1999-07-27 2006-08-15 Alcatel Radiation-curable composition with simultaneous color formation during cure
US6469030B2 (en) 1999-11-29 2002-10-22 Adolor Corporation Methods for the treatment and prevention of ileus
US6492529B1 (en) 2000-01-18 2002-12-10 Boehringer Ingelheim Pharmaceuticals, Inc. Bis pyrazole-1H-pyrazole intermediates and their synthesis
CA2403328A1 (fr) 2000-04-03 2001-10-11 Sun Chemical Corporation Pigments de mono et de bishydrazone
DE60235619D1 (de) 2001-04-19 2010-04-22 Warner Lambert Co Kondensierte bizyklische oder trizyklische aminosäuren
AU2002308748A1 (en) 2001-05-16 2002-11-25 Vertex Pharmaceuticals Incorporated Heterocyclic substituted pyrazoles as inhibitors of src and other protein kinases
WO2002102387A1 (fr) 2001-06-18 2002-12-27 H. Lundbeck A/S Traitement de la douleur neuropathique
US6509367B1 (en) 2001-09-22 2003-01-21 Virginia Commonwealth University Pyrazole cannabinoid agonist and antagonists
RU2218187C2 (ru) 2002-02-11 2003-12-10 Ростовский научно-исследовательский онкологический институт Способ лечения болевого синдрома у онкологических больных
GB0206505D0 (en) 2002-03-19 2002-05-01 Euro Celtique Sa Pharmaceutical combination
EP1534680B1 (fr) 2002-08-14 2012-02-22 Pharmaco Investments, Inc. Inhibiteurs de prenylation et leurs methodes de synthese et d'utilisation
TW200413351A (en) 2002-08-21 2004-08-01 Astrazeneca Ab Chemical compounds
CN100486975C (zh) 2002-11-15 2009-05-13 杜邦公司 新的邻氨基苯甲酰胺杀虫剂
JP2004196678A (ja) 2002-12-17 2004-07-15 Dainippon Pharmaceut Co Ltd ピラゾール系誘導体
US7135575B2 (en) 2003-03-03 2006-11-14 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
EP1644026A4 (fr) 2003-06-12 2007-10-24 Ms Science Corp Ligands des recepteurs sigma pour regeneration neuronale et retablissement fonctionnel
WO2005061462A2 (fr) 2003-12-19 2005-07-07 Neurogen Corporation Modulateurs de recepteurs neurokinine 3 : derives pyrazoles de diaryle
EP1781272B1 (fr) 2004-07-24 2017-09-06 Laboratorios Del Dr. Esteve, S.A. Utilisation de composes actifs sur le recepteur sigma pour le traitement de l'allodynie mecanique
PT1781619E (pt) 2004-08-27 2011-11-04 Esteve Labor Dr Inibidores do recetor sigma
MX2007002341A (es) 2004-08-27 2007-09-25 Esteve Labor Dr Inhibidores del receptor sigma.
EP1634872A1 (fr) 2004-08-27 2006-03-15 Laboratorios Del Dr. Esteve, S.A. Dérivés de pyrazole en tant qu'inhibiteurs des récepteurs sigma
EP1634873A1 (fr) 2004-08-27 2006-03-15 Laboratorios Del Dr. Esteve, S.A. Inhibiteurs des récepteurs sigma
EP2325174A1 (fr) 2004-08-27 2011-05-25 Laboratorios Del. Dr. Esteve, S.A. Inhibiteurs de recepteur sigma
ES2251316B1 (es) 2004-10-14 2007-03-16 Laboratorios Del Dr. Esteve, S.A. Inhibidores del receptor sigma.
EP1632227A1 (fr) 2004-09-07 2006-03-08 Laboratorios del Dr. Esteve S.A. Dérivés des aryl (ou des heteroaryl) azolylcarbinols (en particulier cizolirtin citrate) pour le traitement de la dépendance des opioides
US20080161604A1 (en) 2005-04-26 2008-07-03 Sigma-Tau Industrie Farmaceutiche Riunite S.P.A. Acetyl L-Carnitine For Preventing Painful Peripheral Diabetic Neuropathy
JP2008179541A (ja) 2005-05-02 2008-08-07 Mochida Pharmaceut Co Ltd 神経因性疼痛治療薬
ITRM20050332A1 (it) * 2005-06-24 2006-12-25 Lay Line Genomics Spa Uso di molecole in grado di bloccare l'attivita' di trka per potenziare gli effetti di analgesici oppiacei sul dolore.
KR20080028964A (ko) 2005-06-27 2008-04-02 엑셀리시스, 인코포레이티드 피라졸계 lxr 변조제
WO2007025613A2 (fr) 2005-07-15 2007-03-08 Laboratorios Del Dr. Esteve, S.A. Utilisation de composes se liant au recepteur sigma pour traiter la douleur associee au diabete
EP1787679A1 (fr) 2005-07-29 2007-05-23 Laboratorios Del Dr. Esteve, S.A. Utilisation des composés attachés au sigma recepteur pour le traitement de la douleur associée avec diabète
WO2007041593A2 (fr) 2005-10-03 2007-04-12 Combinatorx, Incorporated Associations de medicaments empechant la formation de cicatrices et leur utilisation
US7872006B2 (en) 2005-10-21 2011-01-18 Mitsubishi Tanabe Pharma Corporation Pyrazole compounds having cannabinoid receptor (CB1) antagonizing activity
WO2007079086A1 (fr) 2005-12-28 2007-07-12 Coley Pharmaceutical Group, Inc. Composés imidazo cycliques substitués par des groupements pyrazoloalkyle et méthodes
EP1820502A1 (fr) 2006-02-10 2007-08-22 Laboratorios Del Dr. Esteve, S.A. Combinaisons de principes actifs comprenant de dérivés d' azolylcarbinol
US20090181976A1 (en) 2006-02-28 2009-07-16 Buschmann Helmut H Use of Compounds Binding to the Sigma Receptor for the Treatment of Metabolic Syndrome
JP2009528315A (ja) 2006-03-01 2009-08-06 ラボラトリオス・デル・ドクトル・エステベ・ソシエダッド・アノニマ シグマ受容体阻害剤としてのピラゾール誘導体
EP1829875A1 (fr) * 2006-03-01 2007-09-05 Laboratorios Del Dr. Esteve, S.A. Dérivés de pyrazole comme inhibiteurs de récepteur Sigma
EP1829873A1 (fr) 2006-03-02 2007-09-05 Laboratorios Del Dr. Esteve, S.A. Dérivés du pyrazole antagonistes des récepteurs sigma
EP1829866A1 (fr) 2006-03-02 2007-09-05 Laboratorios Del Dr. Esteve, S.A. Inhibiteurs des récepteurs sigma
CN101404933B (zh) 2006-03-22 2010-12-15 松下电器产业株式会社 血液检查装置
EP1847542A1 (fr) 2006-04-21 2007-10-24 Laboratorios del Dr. Esteve S.A. Dérivés de spiro[benzopyran] ou de spiro[benzofuran] comme antagonistes du récepteur sigma
ATE530175T1 (de) 2006-06-08 2011-11-15 Ucb Pharma Gmbh Therapeutische kombination für schmerzhafte medizinische zustände
RU2322977C1 (ru) 2006-08-01 2008-04-27 Закрытое акционерное общество "Физиофарм" Синтетическое анальгетическое средство и способ лечения на основе этого средства
WO2008015266A1 (fr) 2006-08-04 2008-02-07 Laboratorios Del Dr. Esteve, S.A. Composés diméthylcyclobutyle substitués, leur préparation et utilisation dans des médicaments
US7645767B2 (en) 2006-08-31 2010-01-12 Trinity Laboratories, Inc. Pharmaceutical compositions for treating chronic pain and pain associated with neuropathy
EP1921071A1 (fr) 2006-11-10 2008-05-14 Laboratorios del Dr. Esteve S.A. 1,2,3-Triazoles en tant qu'inhibiteurs du récepteur sigma
EP1921073A1 (fr) 2006-11-10 2008-05-14 Laboratorios del Dr. Esteve S.A. 1,2,4-Triazoles en tant qu'inhibiteurs du récepteur sigma
US20090018151A1 (en) 2007-02-23 2009-01-15 Ezekiel Fink Topical Treatment of Peripheral diabetic complications
KR100868353B1 (ko) 2007-03-08 2008-11-12 한국화학연구원 도파민 d4 수용체 길항제인 신규 피페라지닐프로필피라졸유도체, 이의 제조방법 및 이를 포함하는 약학적 조성물
GB0710981D0 (en) 2007-06-07 2007-07-18 Acacia Pharma Ltd New Therapeutic use
EP2191830A4 (fr) 2007-09-21 2011-11-23 Shionogi & Co Préparation solide comprenant un antagoniste du récepteur npyy5
EP2070933A1 (fr) 2007-12-07 2009-06-17 Laboratorios del Dr. Esteve S.A. Composants triazoliques tricycliques
EP2090311A1 (fr) 2008-02-18 2009-08-19 Laboratorios Del. Dr. Esteve, S.A. Utilisation de composés liés aux ligands de récepteur sigma pour le traitement de douleur neuropathique se développant suite à une chimiothérapie
DK2254579T3 (en) 2008-02-18 2018-04-09 Esteve Labor Dr Use of Compounds Binding to the Sigmar Receptor Ligands for the Treatment of Neuropathic Pain Developed by Chemotherapy
EP2112139A1 (fr) 2008-04-25 2009-10-28 Laboratorios Del. Dr. Esteve, S.A. Procédé pour la préparation d'intermédiaires naphthalen-2-yl-pyrazol-3-one utiles dans la synthèse d'inhibiteurs de récepteur sigma
EP2113501A1 (fr) 2008-04-25 2009-11-04 Laboratorios Del. Dr. Esteve, S.A. Pyrazoles de 5-Methyl-1-(naphthalen-2-YL)-1H- utiles en tant qu'inhibiteurs de récepteur sigma
EP2116539A1 (fr) 2008-04-25 2009-11-11 Laboratorios Del. Dr. Esteve, S.A. 1-aryl-3-aminoalkoxy-pyrazoles en tant que ligands améliorant les effets analgésiques des opioïdes et réduisant leur dépendance
RU2382646C1 (ru) 2008-11-20 2010-02-27 Федеральное государственное учреждение "Московский научно-исследовательский онкологический институт им. П.А. Герцена Федерального агентства по высокотехнологичной медицинской помощи" Способ профилактики и лечения послеоперационного болевого синдрома при обширных торакоабдоминальных операциях
US8192885B2 (en) 2009-01-26 2012-06-05 GM Global Technology Operations LLC Shutdown strategy for enhanced water management
EP2292236A1 (fr) 2009-08-14 2011-03-09 Laboratorios Del. Dr. Esteve, S.A. Ligands sigma pour la prévention ou le traitement de douleurs induites par la chimiothérapie
EP2335688A1 (fr) 2009-11-25 2011-06-22 Laboratorios Del. Dr. Esteve, S.A. Compositions pharmaceutiques comprenant des ligands du récepteur sigma
EP2361904A1 (fr) 2010-02-04 2011-08-31 Laboratorios Del. Dr. Esteve, S.A. Chlorhydrate de 4-[-2-[[5-méthyl-1-(2-naphtalényl)-1h-pyrazol-3-yl]oxy]éthyl]morpholine et formes cristallines correspondantes
DK2503993T3 (en) 2009-11-25 2016-08-22 Esteve Labor Dr Hydrochloridsalt af 4-[2-[[5-methyl-1-(2-naphthalenyl)-1H-pyrazol-3-yl]oxy]ethyl]-morpholin
EP2353591A1 (fr) 2010-02-04 2011-08-10 Laboratorios Del. Dr. Esteve, S.A. Ligands sigma pour la potentialisation de l'effet analgésique d'opioïdes et d'opiacés dans la douleur post-opératoire et en atténuant la dépendance
EP2426112A1 (fr) 2010-08-09 2012-03-07 Laboratorios Del. Dr. Esteve, S.A. Polymorphes et solvates de chlorhydrate de 4-[-2-[[5-méthyl-1-(2-naphtalényl)-1h-pyrazol-3-yl]oxy]éthyl]morpholine
CN102753155B (zh) 2010-02-04 2015-11-25 埃斯特韦实验室有限公司 4-[-2-[[5-甲基-1-(2-萘基)-1h-吡唑-3-基]氧基]乙基]吗啉盐酸盐多晶型体和溶剂化物
EP2353598A1 (fr) 2010-02-04 2011-08-10 Laboratorios Del. Dr. Esteve, S.A. Ligands sigma pour utilisation dans la prévention et/ou le traitement de la douleur post-opératoire
US20110269727A1 (en) 2010-04-29 2011-11-03 Toledano Annette C Composition to reduce allodynic back pain and related method of use
EP2388005A1 (fr) 2010-05-21 2011-11-23 Laboratorios Del. Dr. Esteve, S.A. Ligands sigma pour la prévention et/ou le traitement du vomissement induit par la chimiothérapie ou la radiothérapie
EP2395003A1 (fr) 2010-05-27 2011-12-14 Laboratorios Del. Dr. Esteve, S.A. Composés pyrazoliques en tant qu'inhibiteurs du récepteur sigma
EP2415471A1 (fr) 2010-08-03 2012-02-08 Laboratorios Del. Dr. Esteve, S.A. Utilisation de ligands sigma dans l'hyperalgie induite par opioïdes
EP2426111A1 (fr) 2010-08-09 2012-03-07 Laboratorios Del. Dr. Esteve, S.A. Formes cristallines de chlorhydrate de 4-[-2-[[5-méthyl-1-(2-naphtalényl)-1h-pyrazol-3-yl]oxy]éthyl]morpholine
EP2460804A1 (fr) 2010-12-03 2012-06-06 Laboratorios Del Dr. Esteve, S.A. Dérivés de 5-méthyl-1-(naphthalen-2-yl)-1h-pyrazole et leur utilisation dans la potentialisation de l'effet des analgésiques opioïdes
EP2460519A1 (fr) 2010-12-03 2012-06-06 Laboratorios Del. Dr. Esteve, S.A. Utilisation de ligands sigma pour la douleur du cancer des os
BR112013029201B1 (pt) 2011-05-13 2022-08-09 Array Biopharma Inc Compostos de pirrolidinil ureia e pirrolidinil tioureia, seu processo de preparação, seu uso e composições farmacêuticas
EP2524694A1 (fr) 2011-05-19 2012-11-21 Laboratorios Del. Dr. Esteve, S.A. Utilisation de ligands sigma dans la douleur liée au diabète de type 2
EP2792352A1 (fr) 2013-04-16 2014-10-22 Laboratorios Del. Dr. Esteve, S.A. Combinaisons comprenants un ligand de receptor Sigma et un ligand de réceptor adrénergic-alpha-2
EP2818166A1 (fr) 2013-06-26 2014-12-31 Laboratorios del Dr. Esteve S.A. Utilisation de ligands des récepteurs sigma pour la prévention et le traitement de la douleur associée à la cystite interstitielle/au syndrome de la vessie douloureuse (IC/BPS)
EP3043795A1 (fr) 2013-09-12 2016-07-20 Laboratorios Del. Dr. Esteve, S.A. Combinaisons d'anti-inflammatoire non stéroïdien (ains) et de ligand des récepteurs sigma
WO2015091505A1 (fr) 2013-12-17 2015-06-25 Laboratorios Del Dr. Esteve, S.A. Combinaisons de gabapentanoïdes et de ligands des récepteurs sigma
CN105873578A (zh) 2013-12-17 2016-08-17 埃斯蒂维实验室股份有限公司 血清素-去甲肾上腺素再摄取抑制剂(SNRIs)和σ受体配体组合物

Also Published As

Publication number Publication date
US9914705B2 (en) 2018-03-13
PT2276744E (pt) 2015-01-14
CA2722345C (fr) 2016-08-02
JP5753076B2 (ja) 2015-07-22
AU2009239968B2 (en) 2014-10-30
US20150018354A1 (en) 2015-01-15
US20110112095A1 (en) 2011-05-12
KR20110011640A (ko) 2011-02-08
CY1115848T1 (el) 2017-01-25
HRP20141263T1 (hr) 2015-03-13
KR101764817B1 (ko) 2017-08-14
UA105900C2 (uk) 2014-07-10
EP2276744B1 (fr) 2014-10-01
WO2009130310A1 (fr) 2009-10-29
EP2671875A1 (fr) 2013-12-11
SG190578A1 (en) 2013-06-28
CA2722345A1 (fr) 2009-10-29
SI2276744T1 (sl) 2015-02-27
RU2010147925A (ru) 2012-05-27
MX2010011673A (es) 2010-11-25
CN102066334A (zh) 2011-05-18
NZ588829A (en) 2013-10-25
US20190010128A1 (en) 2019-01-10
US8877753B2 (en) 2014-11-04
RS53717B1 (sr) 2015-04-30
EP2116539A1 (fr) 2009-11-11
HK1155724A1 (en) 2012-05-25
IL208865B (en) 2018-04-30
MY160800A (en) 2017-03-31
IL208865A0 (en) 2011-01-31
RU2519060C2 (ru) 2014-06-10
ECSP10010634A (es) 2010-12-30
JP2011518807A (ja) 2011-06-30
PL2276744T3 (pl) 2015-03-31
CO6410301A2 (es) 2012-03-30
BRPI0910677A2 (pt) 2020-08-25
ES2526360T3 (es) 2015-01-09
EP2276744A1 (fr) 2011-01-26
DK2276744T3 (en) 2015-01-12
CN102066334B (zh) 2015-07-22
AU2009239968A1 (en) 2009-10-29

Similar Documents

Publication Publication Date Title
MA32301B1 (fr) 1-aryl-3-amino-alcoxypyrazoles comme ligands de sigma augmentant l'effet analgesique d'opioides et attenuant la dependance a ceux-ci
EA201170884A1 (ru) Производные пиперидина, пригодные в качестве антагонистов орексина
DE602007012072D1 (de) Orantagonisten
DK2112153T3 (da) Fremgangsmåde til reduktion af alpha, beta-umættede ketoner i opioidsammensætninger
ATE446856T1 (de) Kautschukmischungen
GEP20146124B (en) Novel ccr2 receptor antagonists and usage thereof
PL2069332T3 (pl) Związki azetydynowe jako antagoniści receptorów oreksynowych
CL2011003347A1 (es) Composicion farmaceutica que comprende un conjugado, correspondiente a benzoato de hidrocodona ; y uso en el tratamiento de una enfermedad, trastorno o afeccion mediada por la union de un opioide a receptores opioides.
MA32774B1 (fr) Antagonistes de récepteur de mélanocortine
MX2009009690A (es) Derivados de tiazolidina como antagonistas del receptor de orexina.
MX2011011127A (es) 3-azabiciclo[4.1.0] heptanos usados como antagonistas de orexina.
CY1110648T1 (el) Ενωσεις τροπανιου
UA102858C2 (ru) Производные пиридино-пиридинонов, способ их получения и применения в терапии
UA107784C2 (en) Inhibitor of melanin production
TW200942524A (en) Novel aminomethyl benzene derivatives
MY157533A (en) Effervescent compositions
ECSP10010491A (es) Composiciones fungicidas con 3'-bromo-2,3,4,6'-tetrametoxi-2',6-dimetilbenzofenona
TR201109686T2 (tr) Olmesartan'ın Farmasötik Bileşimleri.
DE502006005053D1 (de) Spritzbare akustikmassen
ATE491764T1 (de) Auto-adhäsiver klebstoff
MX2009007292A (es) Composicion anestesica en aerosol.
UA96476C2 (ru) Фармацевтические композиции, которые содержат ирбесартан
WO2010054003A3 (fr) Modulateurs méthylindazole de récepteurs 5-ht3
IT1397508B1 (it) Procedimento per regolare un'oscillazione eccitata
DK2081944T3 (da) Nye morfin-derivater