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

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic 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
    • A61K31/403—Heterocyclic 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
    • A61K31/404—Indoles, e.g. pindolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/4245—Oxadiazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

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
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
US7868037B2 (en) 2004-07-14 2011-01-11 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7781478B2 (en) 2004-07-14 2010-08-24 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US8013006B2 (en) 2004-07-14 2011-09-06 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7772271B2 (en) 2004-07-14 2010-08-10 Ptc Therapeutics, Inc. Methods for treating hepatitis C
MX2007000762A (es) 2004-07-22 2007-04-02 Ptc Therapeutics Inc Tienopiridinas para tratamientode 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
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
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201242962A (en) * 2010-12-01 2012-11-01 Sumitomo Chemical Co Pyrimidine compound and use for pest control thereof
US8871758B2 (en) 2011-03-08 2014-10-28 Sanofi Tetrasubstituted oxathiazine derivatives, method for producing them, their use as medicine and drug containing said derivatives and the use thereof
EP2683699B1 (de) 2011-03-08 2015-06-24 Sanofi Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung
US8828994B2 (en) 2011-03-08 2014-09-09 Sanofi Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof
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
WO2012120052A1 (de) 2011-03-08 2012-09-13 Sanofi Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende 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
EP2760862B1 (en) 2011-09-27 2015-10-21 Sanofi 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
RU2631320C2 (ru) * 2011-12-06 2017-09-21 Санофи Кристаллические формы [(s)-1-карбамоил-2-(фенилпиримидин-2-иламино)этил]амида 2-(2-метиламинопиримидин-4-ил)-1н-индол-5-карбоновой кислоты
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
ES2697806T3 (es) * 2014-07-03 2019-01-28 Sanofi Sa [(S)-1-carbamoil-2-(fenil-pirimidin-2-il-amino)-etil]-amida del ácido 2-(2-metilamino-pirimidin-4-il)-1H-indol-5-carboxílico para uso en el tratamiento de dolor asociado a artrosis
JP2021530505A (ja) 2018-07-16 2021-11-11 ノバルティス アーゲー フェニルピペリジニルインドール誘導体を調製する化学的プロセス

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Also Published As

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

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