CO5690585A2 - Uso de inhibidores de la ikb-quinasa para el tratamiento del dolor - Google Patents

Uso de inhibidores de la ikb-quinasa para el tratamiento del dolor

Info

Publication number
CO5690585A2
CO5690585A2 CO05013333A CO05013333A CO5690585A2 CO 5690585 A2 CO5690585 A2 CO 5690585A2 CO 05013333 A CO05013333 A CO 05013333A CO 05013333 A CO05013333 A CO 05013333A CO 5690585 A2 CO5690585 A2 CO 5690585A2
Authority
CO
Colombia
Prior art keywords
unsubstituted
substituted
heterocycle
heteroaryl
aryl
Prior art date
Application number
CO05013333A
Other languages
English (en)
Inventor
Martin Michaelis
Original Assignee
Sanofi Aventis Deutschland
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 Sanofi Aventis Deutschland filed Critical Sanofi Aventis Deutschland
Publication of CO5690585A2 publication Critical patent/CO5690585A2/es

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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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
    • 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
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • 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
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Paper (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

1.- Uso de inhibidores de la I?B-quinasa para producir fármacos para tratar dolores.2.- Uso del compuesto de la fórmula I y/o una forma estereoisomérica del compuesto de la fórmula I y/o una sal fisiológicamente tolerada del compuesto de la fórmula I, para producir fármacos para tratar dolores, donde E es un átomo de N o el radical -C(R19)-, donde R19 es un átomo de hidrógeno o el radical R9, uno de los sustituyentes R1, R2, R3 y R4 es un radical de la fórmula II,en la que D es -C(O)-, S(O)- o -S(O)2R8 es un átomo de hidrógeno o alquilo-(C1-C4)-, R9 es 1. un radical característico de aminoácido, 2. arilo, en el cual el arilo está sustituido o insustituido, 3. heteroarilo con de 5 a 14 anillos, en el cual el heteroarilo es sustituido o insustituido, 4. un heterociclo con de 5 a 12 anillos, en el cual el heterociclo es sustituido o insustituido, 5. alquilo-(C1-C6)-, en el que el alquilo es lineal o ramificado y está sustituido o insustituido, una dos o tres veces, independientemente uno de otro, por 5.1 arilo, en el que el arilo está insustituido o sustituido, 5.2 heteroarilo, con 5-14 anillos, en el que el heteroarilo está insustituido o sustituido, 5.3 un heterociclo con 5-12 anillos, en el que el heterociclo está insustituido o sustituido, 5.4 - O-R11, 5.5 = O, 5.6 halógeno, 5.7 -CN, 5.8 -CF3, ...
CO05013333A 2002-08-17 2005-02-15 Uso de inhibidores de la ikb-quinasa para el tratamiento del dolor CO5690585A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE10237723A DE10237723A1 (de) 2002-08-17 2002-08-17 Verwendung von IKappaB-Kinase Inhibitoren in der Schmerztherapie

Publications (1)

Publication Number Publication Date
CO5690585A2 true CO5690585A2 (es) 2006-10-31

Family

ID=31968975

Family Applications (1)

Application Number Title Priority Date Filing Date
CO05013333A CO5690585A2 (es) 2002-08-17 2005-02-15 Uso de inhibidores de la ikb-quinasa para el tratamiento del dolor

Country Status (34)

Country Link
EP (1) EP1531819B1 (es)
JP (1) JP4504811B2 (es)
KR (2) KR20110135428A (es)
CN (1) CN100398107C (es)
AR (1) AR043045A1 (es)
AT (1) ATE418336T1 (es)
AU (1) AU2003271555B2 (es)
BR (1) BR0313555A (es)
CA (1) CA2495455C (es)
CO (1) CO5690585A2 (es)
CR (1) CR7716A (es)
CY (1) CY1108874T1 (es)
DE (2) DE10237723A1 (es)
DK (1) DK1531819T3 (es)
EC (1) ECSP055609A (es)
ES (1) ES2320118T3 (es)
HK (1) HK1079426A1 (es)
HR (1) HRP20050041B1 (es)
IL (1) IL166780A (es)
MA (1) MA27334A1 (es)
MX (1) MXPA05001218A (es)
MY (1) MY138059A (es)
NO (1) NO334309B1 (es)
OA (1) OA12907A (es)
PL (1) PL212356B1 (es)
PT (1) PT1531819E (es)
RS (1) RS51878B (es)
RU (1) RU2320338C2 (es)
SI (1) SI1531819T1 (es)
TN (1) TNSN05044A1 (es)
TW (1) TWI325782B (es)
UA (1) UA80837C2 (es)
WO (1) WO2004022057A1 (es)
ZA (1) ZA200500323B (es)

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US7718644B2 (en) 2004-01-22 2010-05-18 The Trustees Of Columbia University In The City Of New York Anti-arrhythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) and uses thereof
US7879840B2 (en) 2005-08-25 2011-02-01 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the RyR receptors
US8022058B2 (en) 2000-05-10 2011-09-20 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the RyR receptors
DE10237722A1 (de) * 2002-08-17 2004-08-19 Aventis Pharma Deutschland Gmbh Indol- oder Benzimidazolderivate zur Modulation der IKappaB-Kinase
US8710045B2 (en) 2004-01-22 2014-04-29 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the ryanodine receptors
BRPI0511834A (pt) 2004-07-14 2008-01-08 Ptc Therapeutics Inc métodos por tratar hepatite c
US7781478B2 (en) 2004-07-14 2010-08-24 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7772271B2 (en) 2004-07-14 2010-08-10 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7868037B2 (en) 2004-07-14 2011-01-11 Ptc Therapeutics, Inc. Methods for treating hepatitis C
WO2006019832A1 (en) 2004-07-22 2006-02-23 Ptc Therapeutics, Inc. Thienopyridines for treating hepatitis c
DE102005025225A1 (de) * 2005-06-01 2006-12-07 Sanofi-Aventis Deutschland Gmbh Verfahren zur Herstellung von 2-(2-Amino-pyrimidin-4-yl)-1H-indol-5-carbonsäure-derivaten
US7704990B2 (en) 2005-08-25 2010-04-27 The Trustees Of Columbia University In The City Of New York Agents for preventing and treating disorders involving modulation of the RyR receptors
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
AR072297A1 (es) 2008-06-27 2010-08-18 Novartis Ag Derivados de indol-2-il-piridin-3-ilo, composicion farmaceutica que los comprende y su uso en medicamentos para el tratamiento de enfermedades mediadas por la sintasa aldosterona.
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
EP2582709B1 (de) 2010-06-18 2018-01-24 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
JP5790440B2 (ja) * 2010-12-01 2015-10-07 住友化学株式会社 ピリミジン化合物およびその有害生物防除用途
EP2766349B1 (de) 2011-03-08 2016-06-01 Sanofi Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung
EP2683700B1 (de) 2011-03-08 2015-02-18 Sanofi Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2012120053A1 (de) 2011-03-08 2012-09-13 Sanofi Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2012120054A1 (de) 2011-03-08 2012-09-13 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
WO2012120055A1 (de) 2011-03-08 2012-09-13 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
EP2532755A1 (en) * 2011-06-10 2012-12-12 Sanofi-Aventis Methods and uses based on Slfn2 expression and relating to the identification and profiling of compounds for use in the treatment or prevention of pain
WO2013045413A1 (en) 2011-09-27 2013-04-04 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
CN104105483B (zh) * 2011-12-06 2017-03-22 赛诺菲 2‑(2‑甲基氨基‑嘧啶‑4‑基)‑1h‑吲哚‑5‑羧酸[(s)‑1‑氨甲酰基‑2‑(苯基‑嘧啶‑2‑基‑氨基)‑乙基]‑酰胺的晶体形式
EP3184095A1 (en) 2013-05-23 2017-06-28 IP Gesellschaft für Management mbH Administration units comprising polymorph 1 of 2-(2-methylamino-pyrimidin-4-yl]-1h-indole-5-carboxylic acid [(s)-1-carbamoyl-2-(phenyl-pyrimidin-2-yl-amino)-ethyl]-amide
JO3425B1 (ar) 2013-07-15 2019-10-20 Novartis Ag مشتقات البابيريدينيل-اندول واستخدامها كعامل متمم لمثبطات b
US9968605B2 (en) * 2014-07-03 2018-05-15 Sanofi 2-(2-methylamino-pyrimidin-4-yl)-1h-indole-5-carboxylic acid [(S)-1-carbamoyl-2-(phenyl-pyrimidin-2-yl-amino)-ethyl]-amide for use in the treatment of pain associated to osteoarthritis
KR20210032950A (ko) 2018-07-16 2021-03-25 노파르티스 아게 페닐피페리디닐 인돌 유도체를 제조하기 위한 화학적 방법

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AU769350B2 (en) * 1999-06-23 2004-01-22 Sanofi-Aventis Deutschland Gmbh Substituted benzimidazole
DE19951360A1 (de) * 1999-10-26 2001-05-03 Aventis Pharma Gmbh Substituierte Indole
DE10237722A1 (de) * 2002-08-17 2004-08-19 Aventis Pharma Deutschland Gmbh Indol- oder Benzimidazolderivate zur Modulation der IKappaB-Kinase

Also Published As

Publication number Publication date
TW200417370A (en) 2004-09-16
NO334309B1 (no) 2014-02-03
OA12907A (en) 2006-10-13
CY1108874T1 (el) 2014-07-02
AU2003271555B2 (en) 2009-03-26
EP1531819B1 (de) 2008-12-24
RU2320338C2 (ru) 2008-03-27
TWI325782B (en) 2010-06-11
CA2495455A1 (en) 2004-03-18
PL373568A1 (en) 2005-09-05
RS51878B (sr) 2012-02-29
HRP20050041A2 (hr) 2006-04-30
JP4504811B2 (ja) 2010-07-14
TNSN05044A1 (en) 2007-05-14
WO2004022057A1 (de) 2004-03-18
RS20050070A (en) 2007-06-04
HRP20050041B1 (hr) 2013-07-31
ATE418336T1 (de) 2009-01-15
JP2005539053A (ja) 2005-12-22
IL166780A0 (en) 2006-01-15
AR043045A1 (es) 2005-07-13
PL212356B1 (pl) 2012-09-28
DE50310980D1 (de) 2009-02-05
MXPA05001218A (es) 2005-05-16
MY138059A (en) 2009-04-30
CN100398107C (zh) 2008-07-02
ECSP055609A (es) 2005-04-18
EP1531819A1 (de) 2005-05-25
CA2495455C (en) 2011-01-11
DE10237723A1 (de) 2004-07-08
KR20050058339A (ko) 2005-06-16
KR101119845B1 (ko) 2012-02-28
MA27334A1 (fr) 2005-05-02
DK1531819T3 (da) 2009-04-20
SI1531819T1 (sl) 2009-06-30
HK1079426A1 (en) 2006-04-07
KR20110135428A (ko) 2011-12-16
ES2320118T3 (es) 2009-05-19
BR0313555A (pt) 2005-07-12
CN1674899A (zh) 2005-09-28
PT1531819E (pt) 2009-02-18
CR7716A (es) 2008-11-25
RU2005107419A (ru) 2005-08-10
IL166780A (en) 2011-11-30
NO20051339L (no) 2005-05-03
UA80837C2 (uk) 2007-11-12
AU2003271555A1 (en) 2004-03-29
ZA200500323B (en) 2006-02-22

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