[go: up one dir, main page]

AR071111A1 - Derivados de amidas del acido 3-trifluorometil-pirazin-2-carboxilico como agentes para aumentar el hdl-colesterol, composiciones farmaceuticas y un metodo para su preparacion. - Google Patents

Derivados de amidas del acido 3-trifluorometil-pirazin-2-carboxilico como agentes para aumentar el hdl-colesterol, composiciones farmaceuticas y un metodo para su preparacion.

Info

Publication number
AR071111A1
AR071111A1 ARP090101125A ARP090101125A AR071111A1 AR 071111 A1 AR071111 A1 AR 071111A1 AR P090101125 A ARP090101125 A AR P090101125A AR P090101125 A ARP090101125 A AR P090101125A AR 071111 A1 AR071111 A1 AR 071111A1
Authority
AR
Argentina
Prior art keywords
hydrogen
cholesterol
agents
preparation
pirazin
Prior art date
Application number
ARP090101125A
Other languages
English (en)
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR071111A1 publication Critical patent/AR071111A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
    • C07D241/20Nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
    • C07D241/24Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Estos compuestos se utilizan para la preparacion de medicamentos para el tratamiento y/o la profilaxis de enfermedades que pueden tratarse con agentes para aumentar el HDL-colesterol, tal como, de una forma preferible, la dislipemia. Reivindicacion 1: Compuestos de la formula general (1) en donde, R1 es cicloalquilo, el cual se encuentra insustituido o sustituido por hidroxi o hidroxialquilo inferior, o CH2-CR9R10-cicloalquilo, R9 es hidrogeno o alquilo inferior; R10 es hidrogeno o hidroxi; R2, es hidrogeno; R3, se selecciona de entre el grupo consistente en cicloalquilalquilo inferior, alcoxialquilo inferior, halogenoalquilo inferior, heteroarilalquilo inferior, en donde, el grupo heteroarilo, se encuentra insustituido o mono- o disustituido por alquilo inferior; y fenilo, es cual se encuentra insustituido o mono- o di-sustituido por halogeno; R4 y R8, de una forma independiente la una con respecto a la otra, son hidrogeno o halogeno; R5, R6 y R7, de una forma independiente la una con respecto a la otra se seleccionan de entre el grupo consistente en hidrogeno, alquilo inferior, alcoxi inferior, halogeno, halogenoalquilo inferior, halogenoalcoxi inferior, alquilsulfonilamino inferior y ciano; y sus sales farmacéuticamente aceptables.
ARP090101125A 2008-03-31 2009-03-30 Derivados de amidas del acido 3-trifluorometil-pirazin-2-carboxilico como agentes para aumentar el hdl-colesterol, composiciones farmaceuticas y un metodo para su preparacion. AR071111A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP08153802 2008-03-31

Publications (1)

Publication Number Publication Date
AR071111A1 true AR071111A1 (es) 2010-05-26

Family

ID=40585575

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP090101125A AR071111A1 (es) 2008-03-31 2009-03-30 Derivados de amidas del acido 3-trifluorometil-pirazin-2-carboxilico como agentes para aumentar el hdl-colesterol, composiciones farmaceuticas y un metodo para su preparacion.

Country Status (14)

Country Link
US (1) US8088920B2 (es)
EP (1) EP2271632B1 (es)
JP (1) JP5243596B2 (es)
KR (1) KR101307066B1 (es)
CN (1) CN101981015B (es)
AR (1) AR071111A1 (es)
AU (1) AU2009231376A1 (es)
CA (1) CA2718645A1 (es)
ES (1) ES2408961T3 (es)
IL (1) IL208022A0 (es)
MX (1) MX2010009999A (es)
PE (1) PE20091711A1 (es)
TW (1) TW200944514A (es)
WO (1) WO2009121741A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2009003222A (es) * 2006-10-04 2009-04-06 Hoffmann La Roche Derivados de 3-piridinocarboxamida y 2-pirazinocarboxamida como agentes elevadores de colesterol de lipoproteina de alta densidad.
WO2012031817A1 (en) * 2010-09-09 2012-03-15 F. Hoffmann-La Roche Ag Determination of abca1 protein levels in cells
US8410107B2 (en) 2010-10-15 2013-04-02 Hoffmann-La Roche Inc. N-pyridin-3-yl or N-pyrazin-2-yl carboxamides
US8669254B2 (en) 2010-12-15 2014-03-11 Hoffman-La Roche Inc. Pyridine, pyridazine, pyrimidine or pyrazine carboxamides as HDL-cholesterol raising agents
EP2567959B1 (en) 2011-09-12 2014-04-16 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
US9403808B2 (en) * 2011-10-28 2016-08-02 Hoffmann-La Roche Inc. Pyrazine derivatives

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4293552A (en) * 1978-02-27 1981-10-06 Eli Lilly And Company Novel 1-(mono-o-substituted benzoyl)-3-(substituted pyrazinyl) ureas
US6930111B2 (en) * 2001-07-19 2005-08-16 Cv Therapeutics, Inc. Substituted heterocyclic compounds
JP4712865B2 (ja) * 2005-04-06 2011-06-29 エフ.ホフマン−ラ ロシュ アーゲー Cb1逆アゴニストとしてのピリジン−3−カルボキサミド誘導体
US7629346B2 (en) 2006-06-19 2009-12-08 Hoffmann-La Roche Inc. Pyrazinecarboxamide derivatives as CB1 antagonists
US7781593B2 (en) * 2006-09-14 2010-08-24 Hoffmann-La Roche Inc. 5-phenyl-nicotinamide derivatives
MX2009003316A (es) 2006-10-04 2009-04-09 Hoffmann La Roche Derivados de pirazina-2-carboxamida como moduladores receptores de cb2.
MX2009003222A (es) 2006-10-04 2009-04-06 Hoffmann La Roche Derivados de 3-piridinocarboxamida y 2-pirazinocarboxamida como agentes elevadores de colesterol de lipoproteina de alta densidad.

Also Published As

Publication number Publication date
CN101981015B (zh) 2013-08-21
US20090247550A1 (en) 2009-10-01
EP2271632A1 (en) 2011-01-12
JP5243596B2 (ja) 2013-07-24
TW200944514A (en) 2009-11-01
ES2408961T3 (es) 2013-06-24
KR101307066B1 (ko) 2013-09-11
CN101981015A (zh) 2011-02-23
WO2009121741A1 (en) 2009-10-08
MX2010009999A (es) 2010-09-30
PE20091711A1 (es) 2009-11-13
AU2009231376A1 (en) 2009-10-08
IL208022A0 (en) 2010-12-30
CA2718645A1 (en) 2009-10-08
EP2271632B1 (en) 2013-04-17
KR20100119819A (ko) 2010-11-10
US8088920B2 (en) 2012-01-03
JP2011516445A (ja) 2011-05-26

Similar Documents

Publication Publication Date Title
AR082914A1 (es) Heteroarilmetilamidas utiles para tratar enfermedades cardiovasculares y dislipemias, composiciones farmaceuticas que las contienen y proceso de preparacion de los mismos
UY35243A (es) Inhibidores de fosfatidilinositol 3-cinasa
UY35242A (es) Inhibidores de fosfatidilinositol 3-quinasa
ECSP16082790A (es) Composición de control de enfermedades de plantas y método para controlar enfermedades de plantas mediante su aplicación
UY35146A (es) Compuestos y composiciones para el tratamiento de enfermedades parasitarias
AR079226A1 (es) Espiroindolinona- pirrolidinas, procesos de preparacion y uso de los mismos para el tratamiento y profilaxis del cancer
UY37007A (es) Compuestos derivados de purinas, estimuladores de genes de interferón
CL2017002207A1 (es) Inhibidores del factor beta de crecimiento de transformación (tgf-beta)
AR086357A1 (es) Derivados de indazol sustituidos activos como inhibidores de quinasas
UY35617A (es) Inhibidores de la fosfatidilinositol 3-quinasa
ES2564010T3 (es) Composición farmacéutica para tratar o prevenir el glaucoma
UY32582A (es) Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero
AR062769A1 (es) Derivados de 5- fenil- nicotilamida
AR103222A1 (es) Procedimiento para la preparación de análogos de 4-fenil-5-alcoxicarbonil-2-tiazol-2-il-1,4-dihidropirimidina
UY35641A (es) PROCEDIMIENTO DE SÍNTESIS PARA PREPARAR ANÁLOGOS MACROCÍCLICOS C1-CETO DE HALICONDRINA B, E INTERMEDIARIOS ÚTILES INCLUYENDO INTERMEDIARIOS CONTENIENDO GRUPOS ?SO2-(p-TOLILO)
AR108101A1 (es) Compuestos agonistas de gpr119 y método para tratar enfermedades y afecciones mediado a través de gpr119
CU20140072A7 (es) Derivados de dihidro-oxazina y dihidro-pirido-oxazina
PE20140192A1 (es) Derivados de bencimidazol como inhibidores de cinasa pi3
CR11757A (es) Compuestos de triazina como inhibidores mtor y quinasa pi3
CL2012000001A1 (es) Compuestos derivados de heteroarilo-pirazolopirimidina-carboxamida, inhibidores de jak; composicion farmaceutica que los comprende; utiles para el tratamiento de la artritis reumatoide, enfermedad de chron, dermatitis, psoriasis, entre otros.
AR076360A1 (es) Derivados de 3,3'-espiroindolinona y su uso en el tratamiento del cancer
TN2014000254A1 (en) Substituted triazolopyridines and their use as ttk inhibitors
AR071111A1 (es) Derivados de amidas del acido 3-trifluorometil-pirazin-2-carboxilico como agentes para aumentar el hdl-colesterol, composiciones farmaceuticas y un metodo para su preparacion.
EA201490272A1 (ru) Новые 4-пиперидинильные соединения для применения в качестве ингибиторов танкиразы
PE20141380A1 (es) Imidazopiridazinas como inhibidores de quinasa akt

Legal Events

Date Code Title Description
FB Suspension of granting procedure