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NI200800169A - Uso de derivados de sulfamidas heterocíclicas benzo-fusionadas para el tratamiento del dolor - Google Patents

Uso de derivados de sulfamidas heterocíclicas benzo-fusionadas para el tratamiento del dolor

Info

Publication number
NI200800169A
NI200800169A NI200800169A NI200800169A NI200800169A NI 200800169 A NI200800169 A NI 200800169A NI 200800169 A NI200800169 A NI 200800169A NI 200800169 A NI200800169 A NI 200800169A NI 200800169 A NI200800169 A NI 200800169A
Authority
NI
Nicaragua
Prior art keywords
pain
treatment
benzo
fused heterocyclic
derivatives
Prior art date
Application number
NI200800169A
Other languages
English (en)
Inventor
B Reitz Allen
L Smith-Swintosky Virginia
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of NI200800169A publication Critical patent/NI200800169A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D321/00Heterocyclic compounds containing rings having two oxygen atoms as the only ring hetero atoms, not provided for by groups C07D317/00 - C07D319/00
    • C07D321/02Seven-membered rings
    • C07D321/10Seven-membered rings condensed with carbocyclic rings or ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/357Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • 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
    • 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
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Pyrane Compounds (AREA)

Abstract

La presente invención es un método para el tratamiento del dolor que comprende la administración a un sujeto en necesidad del mismo una cantidad terapéuticamente eficaz de uno o más derivados novedosos de sulfamidas heterocíclicas benzo-fusionadas de la fórmula (I) y fórmula (II) como se describen en el presente documento. La presente invención también está dirigida a métodos para el tratamiento del dolor que comprenden la co-terapia con agente(s) anagésico(s) y un compuesto de la fórmula (I) o fórmula (II) como se describen aquí.
NI200800169A 2005-12-19 2008-06-18 Uso de derivados de sulfamidas heterocíclicas benzo-fusionadas para el tratamiento del dolor NI200800169A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US75168605P 2005-12-19 2005-12-19
US77381206P 2006-02-15 2006-02-15
US11/612,071 US8716231B2 (en) 2005-12-19 2006-12-18 Use of benzo-fused heterocycle sulfamide derivatives for the treatment of pain

Publications (1)

Publication Number Publication Date
NI200800169A true NI200800169A (es) 2012-05-28

Family

ID=38007332

Family Applications (1)

Application Number Title Priority Date Filing Date
NI200800169A NI200800169A (es) 2005-12-19 2008-06-18 Uso de derivados de sulfamidas heterocíclicas benzo-fusionadas para el tratamiento del dolor

Country Status (26)

Country Link
US (1) US8716231B2 (es)
EP (1) EP1973540B1 (es)
JP (1) JP5190377B2 (es)
KR (1) KR20080077025A (es)
CN (1) CN101378746B (es)
AT (1) ATE447948T1 (es)
AU (1) AU2006331734B2 (es)
BR (1) BRPI0620018A2 (es)
CA (1) CA2634115C (es)
CR (1) CR10167A (es)
CY (1) CY1109732T1 (es)
DE (1) DE602006010442D1 (es)
DK (1) DK1973540T3 (es)
EA (1) EA016302B1 (es)
ES (1) ES2335699T3 (es)
HR (1) HRP20100007T1 (es)
IL (1) IL192100A0 (es)
MY (1) MY150903A (es)
NI (1) NI200800169A (es)
NO (1) NO20083005L (es)
NZ (1) NZ569040A (es)
PL (1) PL1973540T3 (es)
PT (1) PT1973540E (es)
RS (1) RS51249B (es)
SI (1) SI1973540T1 (es)
WO (1) WO2007075752A1 (es)

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MY147767A (en) 2004-06-16 2013-01-31 Janssen Pharmaceutica Nv Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders
EA200702558A1 (ru) * 2005-05-20 2008-06-30 Янссен Фармацевтика Н. В. Способ получения производных сульфамида
US8937096B2 (en) 2005-12-19 2015-01-20 Janssen Pharmaceutica Nv Use of benzo-fused heterocyle sulfamide derivatives for the treatment of mania and bipolar disorder
US8497298B2 (en) 2005-12-19 2013-07-30 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for lowering lipids and lowering blood glucose levels
US20070155827A1 (en) * 2005-12-19 2007-07-05 Smith-Swintosky Virginia L Use of benzo-fused heterocycle sulfamide derivatives for the treatment of depression
US8691867B2 (en) 2005-12-19 2014-04-08 Janssen Pharmaceutica Nv Use of benzo-fused heterocycle sulfamide derivatives for the treatment of substance abuse and addiction
AU2007253814A1 (en) 2006-05-19 2007-11-29 Janssen Pharmaceutica N.V. Co-therapy for the treatment of epilepsy
US20090247616A1 (en) * 2008-03-26 2009-10-01 Smith-Swintosky Virginia L Use of benzo-fused heterocyle sulfamide derivatives for the treatment of anxiety
US20090247617A1 (en) * 2008-03-26 2009-10-01 Abdel-Magid Ahmed F Process for the preparation of benzo-fused heteroaryl sulfamates
CN102015674B (zh) * 2008-04-29 2014-10-29 Nsab神经研究瑞典公司分公司 多巴胺神经传递调节剂
US20110105462A1 (en) * 2008-04-29 2011-05-05 Nsab, Filial Af Neurosearch Sweden Ab, Sverige Modulators of dopamine neurotransmission
RU2010141964A (ru) * 2008-04-29 2012-06-10 НСАБ, Филиаль аф НьюроСерч Свиден АБ, Сверийе (DK) Модуляторы дофаминовой нейротрансмиссии
CA2729056A1 (en) 2008-06-23 2010-01-21 Janssen Pharmaceutica Nv Crystalline form of (2s)-(-)-n-(6-chloro-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-sulfamide
US8815939B2 (en) * 2008-07-22 2014-08-26 Janssen Pharmaceutica Nv Substituted sulfamide derivatives
AU2012314317A1 (en) 2011-09-29 2014-04-03 Janssen Pharmaceutica Nv Improved process for the preparation of sulfamide derivatives
JP2014528953A (ja) 2011-09-29 2014-10-30 ヤンセン ファーマシューティカ エヌ.ベー. スルファミド誘導体の調製プロセス
BR112016012833B1 (pt) 2013-12-19 2022-11-16 Eisai R&D Management Co. Ltd Agente terapêutico e/ou preventivo compreendendo derivado de 1-indansulfamida para dor
JP7439096B2 (ja) 2018-09-04 2024-02-27 田辺三菱製薬株式会社 疼痛を処置するためにフェノキシプロピルアミン化合物を使用する方法
RU2712918C1 (ru) * 2019-08-01 2020-02-03 Федеральное государственное бюджетное учреждение "Ростовский научно-исследовательский онкологический институт" Министерства здравоохранения Российской Федерации Способ предотвращения острой боли при выполнении химического плевродеза после радикальных торакопластических операций онкологического характера

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JP2009520035A (ja) 2009-05-21
JP5190377B2 (ja) 2013-04-24
NO20083005L (no) 2008-09-16
PL1973540T3 (pl) 2010-04-30
IL192100A0 (en) 2009-08-03
MY150903A (en) 2014-03-14
WO2007075752A1 (en) 2007-07-05
ATE447948T1 (de) 2009-11-15
EP1973540B1 (en) 2009-11-11
AU2006331734A1 (en) 2007-07-05
HRP20100007T1 (hr) 2010-02-28
DE602006010442D1 (de) 2009-12-24
CY1109732T1 (el) 2014-09-10
DK1973540T3 (da) 2010-02-01
CN101378746B (zh) 2013-07-17
RS51249B (sr) 2010-12-31
CA2634115C (en) 2014-11-18
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ES2335699T3 (es) 2010-03-31
EA016302B1 (ru) 2012-04-30
BRPI0620018A2 (pt) 2011-10-25
KR20080077025A (ko) 2008-08-20
CN101378746A (zh) 2009-03-04
US8716231B2 (en) 2014-05-06
AU2006331734B2 (en) 2012-12-20
CR10167A (es) 2009-01-16
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CA2634115A1 (en) 2007-07-05

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