[go: up one dir, main page]

MX2013002649A - Agente terapeutico contra el dolor. - Google Patents

Agente terapeutico contra el dolor.

Info

Publication number
MX2013002649A
MX2013002649A MX2013002649A MX2013002649A MX2013002649A MX 2013002649 A MX2013002649 A MX 2013002649A MX 2013002649 A MX2013002649 A MX 2013002649A MX 2013002649 A MX2013002649 A MX 2013002649A MX 2013002649 A MX2013002649 A MX 2013002649A
Authority
MX
Mexico
Prior art keywords
pain
therapeutic agent
inventors
useful
treatment
Prior art date
Application number
MX2013002649A
Other languages
English (en)
Inventor
Tetsuo Kiso
Mina Tsukamoto
Original Assignee
Astellas Pharma 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 Astellas Pharma Inc filed Critical Astellas Pharma Inc
Publication of MX2013002649A publication Critical patent/MX2013002649A/es

Links

Classifications

    • 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
    • A61K31/41961,2,4-Triazoles
    • 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
    • A61K31/4245Oxadiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular 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
    • 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]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Se proporciona un producto farmacéutico, particularmente, una composición farmacéutica que es útil para el tratamiento del dolor. Los actuales inventores han realizado estudios exhaustivos al usar los animales modelo con dolor para el propósito de proporcionar un agente terapéutico contra el dolor. Consecuentemente, han encontrado que el inhibidor de 11ß-hidroxiesteroide deshidrogenasa tipo 1 (11ß-HSD1, por sus siglas en inglés), particularmente, un compuesto de triazol que tiene un grupo cíclico en la posición 3 (o en la posición 5) de un anillo de triazol, tiene un buen efecto de mejorar el dolor crónico. Es decir, de acuerdo con la presente invención, una composición farmacéutica que comprende un inhibidor de 11ß-HSD1, particularmente, el compuesto de triazol de la presente invención, como un ingrediente activo, es útil para el tratamiento del dolor (particularmente, del dolor neuropático o de la fibromialgia).
MX2013002649A 2010-09-07 2011-09-06 Agente terapeutico contra el dolor. MX2013002649A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2010200305 2010-09-07
PCT/JP2011/070205 WO2012033070A1 (ja) 2010-09-07 2011-09-06 疼痛治療剤

Publications (1)

Publication Number Publication Date
MX2013002649A true MX2013002649A (es) 2013-04-05

Family

ID=45810669

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2013002649A MX2013002649A (es) 2010-09-07 2011-09-06 Agente terapeutico contra el dolor.

Country Status (23)

Country Link
US (2) US9765040B2 (es)
EP (1) EP2614824B1 (es)
JP (1) JP5822079B2 (es)
KR (1) KR101747486B1 (es)
CN (2) CN107041885A (es)
AU (1) AU2011299905B2 (es)
BR (1) BR112013005532A2 (es)
CA (1) CA2809778C (es)
CY (1) CY1116274T1 (es)
DK (1) DK2614824T3 (es)
EA (1) EA022338B1 (es)
ES (1) ES2533310T3 (es)
HR (1) HRP20150544T1 (es)
IL (1) IL224920A (es)
MX (1) MX2013002649A (es)
PH (1) PH12013500371A1 (es)
PL (1) PL2614824T3 (es)
PT (1) PT2614824E (es)
SI (1) SI2614824T1 (es)
TW (1) TWI486336B (es)
UA (1) UA112418C2 (es)
WO (1) WO2012033070A1 (es)
ZA (1) ZA201301458B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112014009524A2 (pt) 2011-10-18 2017-05-09 Astellas Pharma Inc composto heterocíclico bicíclico
US9994658B2 (en) 2015-10-02 2018-06-12 Exxonmobil Chemical Patents Inc. Polymerization process using bis phenolate compounds supported on organoaluminum treated layered silicate supports
WO2017096148A1 (en) * 2015-12-03 2017-06-08 Katz Robert S Methods and systems for diagnosing and treating fibromyalgia
RU2643583C1 (ru) * 2016-10-24 2018-02-02 Федеральное государственное бюджетное образовательное учреждение высшего образования "Уральский государственный медицинский университет" Министерства здравоохранения Российской Федерации (ФГБОУ ВО УГМУ Минздрава России) Способ лечения хронических болевых синдромов, сформировавшихся на основе посттравматического стрессового расстройства, сочетающегося с последствиями боевой черепно-мозговой травмы
WO2018117063A1 (ja) * 2016-12-20 2018-06-28 アステラス製薬株式会社 焦燥性興奮治療剤
AU2019384074B2 (en) * 2018-11-20 2025-04-10 Sparrow Pharmaceuticals, Inc. Methods for administering corticosteroids
AU2023273030A1 (en) 2022-05-16 2024-11-07 Sparrow Pharmaceuticals, Inc. Methods and compositions for treating glucocorticoid excess

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AUPR878201A0 (en) * 2001-11-09 2001-12-06 Fujisawa Pharmaceutical Co., Ltd. New compounds
AR040241A1 (es) 2002-06-10 2005-03-23 Merck & Co Inc Inhibidores de la 11-beta-hidroxiesteroide deshidrogrenasa 1 para el tratamiento de la diabetes obesidad y dislipidemia
JP4637578B2 (ja) 2002-08-09 2011-02-23 アストラゼネカ アクチボラグ 代謝調節型グルタミン酸受容体−5の調節因子としての1,2,4−オキサジアゾール類
JO2397B1 (en) 2002-12-20 2007-06-17 ميرك شارب اند دوم كوربوريشن Terazol derivatives as beta-hydroxy steroid dihydrogenase-1 inhibitors
EP1615698B1 (en) 2003-04-11 2010-09-29 High Point Pharmaceuticals, LLC New amide derivatives and pharmaceutical use thereof
EP1677819A1 (en) * 2003-10-10 2006-07-12 Novo Nordisk A/S Long-acting molecules in sustained release formulations
WO2005044192A2 (en) 2003-10-28 2005-05-19 Amgen Inc. Triazole compounds and uses related thereto
JP2005170939A (ja) * 2003-11-20 2005-06-30 Takeda Chem Ind Ltd 糖尿病の予防・治療剤
KR20060101772A (ko) 2003-12-19 2006-09-26 화이자 인코포레이티드 당뇨병 및 비만을 치료하기 위한,11-베타-하이드록시스테로이드 데하이드로게나제 유형1(11-베타-hsd-1)의 저해제로서의벤젠설폰일아미노-피리딘-2-일 유도체 및 관련 화합물
CN1909902A (zh) 2003-12-22 2007-02-07 伊莱利利公司 用于治疗糖尿病的作为ppar调节剂的三唑、噁二唑和噻二唑衍生物
WO2006030805A1 (ja) * 2004-09-16 2006-03-23 Astellas Pharma Inc. トリアゾール誘導体またはその塩
JP2008518903A (ja) 2004-11-02 2008-06-05 ファイザー・インク 置換および非置換アダマンチルアミドの新規化合物
WO2006134481A1 (en) 2005-06-16 2006-12-21 Pfizer Inc. Inhibitors of 11-beta hydroxysteroid dehydrogenase type 1
WO2006134467A1 (en) 2005-06-16 2006-12-21 Pfizer Inc. N-(pyridin-2-yl)-sulfonamide derivatives
CN101198605A (zh) 2005-06-16 2008-06-11 辉瑞大药厂 N-(吡啶-2-基)-磺酰胺衍生物
US7853951B2 (en) * 2005-07-25 2010-12-14 Intel Corporation Lock sequencing to reorder and grant lock requests from multiple program threads
EP1922068A4 (en) 2005-08-16 2010-08-11 Icagen Inc INHIBITORS OF VOLTAGE-CONTROLLED SODIUM CHANNELS
AR058807A1 (es) 2005-09-29 2008-02-27 Astrazeneca Ab 5-(fenilisoxazoletoxi)-triazol-3-il piridinas sustituidas, para el tratamiento de trastornos mediados por el receptor mglur5
TWI391378B (zh) 2006-03-16 2013-04-01 Astellas Pharma Inc 喹啉酮衍生物或其製藥學上可被容許之鹽
BRPI0708782A2 (pt) 2006-03-16 2011-06-14 Astellas Pharma Inc derivado de triazol ou um sal deste
SMT201700154T1 (it) * 2008-07-03 2017-05-08 Astellas Pharma Inc Derivato di triazolo o suo sale
FR2948211B1 (fr) * 2009-07-17 2011-08-05 Airbus Operations Sas Methode de routage des liaisons physiques d'une plateforme avionique
US8871208B2 (en) * 2009-12-04 2014-10-28 Abbvie Inc. 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors and uses thereof

Also Published As

Publication number Publication date
EA201390345A1 (ru) 2013-07-30
AU2011299905B2 (en) 2015-02-26
EP2614824B1 (en) 2015-03-11
CA2809778A1 (en) 2012-03-15
EP2614824A4 (en) 2014-02-12
CY1116274T1 (el) 2017-02-08
BR112013005532A2 (pt) 2016-05-03
JPWO2012033070A1 (ja) 2014-01-20
PL2614824T3 (pl) 2015-08-31
DK2614824T3 (en) 2015-03-23
CN103079564A (zh) 2013-05-01
US20130165491A1 (en) 2013-06-27
ES2533310T3 (es) 2015-04-09
KR101747486B1 (ko) 2017-06-14
PH12013500371A1 (en) 2013-04-01
US20170327474A1 (en) 2017-11-16
IL224920A (en) 2017-05-29
AU2011299905A1 (en) 2013-03-21
EP2614824A1 (en) 2013-07-17
CN107041885A (zh) 2017-08-15
EA022338B1 (ru) 2015-12-30
TWI486336B (zh) 2015-06-01
US9765040B2 (en) 2017-09-19
CN103079564B (zh) 2017-06-23
JP5822079B2 (ja) 2015-11-24
ZA201301458B (en) 2014-06-25
HRP20150544T1 (hr) 2015-06-19
KR20130114125A (ko) 2013-10-16
WO2012033070A1 (ja) 2012-03-15
SI2614824T1 (sl) 2015-05-29
CA2809778C (en) 2017-12-12
TW201302717A (zh) 2013-01-16
UA112418C2 (uk) 2016-09-12
PT2614824E (pt) 2015-05-28

Similar Documents

Publication Publication Date Title
PH12014500529A1 (en) Substituted n- [1-cyano-2- (phenyl) ethyl] -2-azabicyclo [2.2.1] heptane-3-carboxamide inhibitors of cathepsin c
NZ708593A (en) Novel pyrazole derivative
PH12013500145B1 (en) Agonists of gpr40
WO2013066839A3 (en) Compounds and methods
WO2013066835A3 (en) Compounds and methods
MX2013002649A (es) Agente terapeutico contra el dolor.
MX338554B (es) Compuestos de fenil carbamato para usarse en aliviar o tratar el dolor.
UA109661C2 (uk) Фармацевтична композиція співкристалів трамадолу і коксибів
MX2014007969A (es) Hidroxiamidas de ácido cinámico como inhibidores de la histona desacetilasa 8.
UA98839C2 (en) N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors
EA201291306A1 (ru) Состав сухого порошка, содержащий антимускариновое средство
WO2010087565A3 (ko) 피페린의 신규한 용도
MY167898A (en) Co-crystals and salts of ccr3-inhibitors
WO2013061004A8 (fr) Nouveaux composés di-substitués de la diamino-3,4-cyclobutène-3-dione-1,2 utiles dans le traitement de pathologies médiées par des chimiokines
MX2015001917A (es) Composiciones farmaceuticas de memantina.
WO2012128582A3 (en) A COMPOUND FOR INHIBITING HUMAN 11-β-HYDROXY STEROID DEHYDROGENASE TYPE 1, AND A PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
PH12019500618A1 (en) Pharmaceutical composition and method for treatment of non-alcoholic fatty liver disease
MX362830B (es) Agente terapeutico o profilactico para enfermedades del tracto biliar.
MY152040A (en) Triazolopyridazines as par1 inhibitors, production thereof, and use as medicaments
MY148732A (en) Triazolium salts as par1 inhibitors, production thereof, and use as medicaments
MY152685A (en) Imidazopyridazines as par1 inhibitors, production thereof, and use thereof as medicaments
GEP20257771B (en) Compounds and compositions as sppl2a inhibitors
EP2599487A4 (en) THERAPEUTIC OR PROPHYLACTIC AGENT FOR NEUROPATHIC PAIN
MX2010008586A (es) Amidas de acido 3-(4-fluorofenil)-3-hidroxi-2-amino-propionico y compuestos relacionados que tienen actividad analgesica.
HK1202117A1 (en) Substituted pyrazolyl-based carboxamide and urea derivatives bearing a phenyl moiety substituted with an so2-containing group as vanilloid receptor ligands

Legal Events

Date Code Title Description
FG Grant or registration