AR052902A1 - Derivados de piridazina, composicion farmaceutica que los contiene y su uso como agentes terapeuticos para enfermedades mediadas por la estearoil-coa desaturasa - Google Patents

Derivados de piridazina, composicion farmaceutica que los contiene y su uso como agentes terapeuticos para enfermedades mediadas por la estearoil-coa desaturasa

Info

Publication number
AR052902A1
AR052902A1 ARP060100466A ARP060100466A AR052902A1 AR 052902 A1 AR052902 A1 AR 052902A1 AR P060100466 A ARP060100466 A AR P060100466A AR P060100466 A ARP060100466 A AR P060100466A AR 052902 A1 AR052902 A1 AR 052902A1
Authority
AR
Argentina
Prior art keywords
alkyl
group
hydrogen
cycloalkyl
heterocyclyl
Prior art date
Application number
ARP060100466A
Other languages
English (en)
Original Assignee
Xenon Pharmaceuticals 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 Xenon Pharmaceuticals Inc filed Critical Xenon Pharmaceuticals Inc
Publication of AR052902A1 publication Critical patent/AR052902A1/es

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-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
    • C07D237/20—Nitrogen atoms
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • 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
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-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
    • C07D237/22—Nitrogen and oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-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
    • C07D237/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen

Landscapes

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

Abstract

Composiciones farmacéuticas que comprenden los compuestos de formula (1) y su uso en el tratamiento de trastornos del metabolismo de los lípidos. Reivindicacion 10: Un compuesto caracterizado porque responde a la formula (1), donde x y y son cada uno en forma independiente 1, 2 o 3; W es un enlace directo, -C(O)N(R1)-; -C(O)N[C(O)R1a]-, -N(R1)C(O)N(R1)- -N(R1)C(O)-, -OC(O)N(R1)-, -N(R1)S(O)p- (donde p es 1 o 2), -S(O)pN(R1)- (donde p es 1 o 2), -C(O)-, -OS(O)2N(R1)-, -OC(O)-, -C(O)O-, - N(R1)C(O)O-, -N(R1)C(=NR1a)N(R1)-, -N(R1)C(= S)N(R1)-, -N(R1)C(=NR1a)-, o -C(=NR1a)N(R1)-; V es -C(O)-, -C(O)O-, -C(S)-, -C(O)N(R1)-, -S(O)t- (donde t es 0, 1 o 2), -S(O)pN(R1)- (donde p es 1 o 2), -C(R10)H-, o -C(=NR1a)-; cada R1 se selecciona en forma independiente del grupo formado por hidrogeno; alquilo C1-6 opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo formado por halo, metilo o trifluorometilo; alquilo C2-C6 opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo formado por metoxi e hidroxilos; R1a se selecciona del grupo formado por hidrogeno, -OR1, ciano, alquilo C1-6 cicloalquil alquilo; R2 se selecciona del grupo formado por alquilo C1-12, alquenilo C2-12, hidroxialquilo C2-12, hidroxialquenilo C2-12, alcoxi C1-12, alcoxialquilo C2-C12, cicloalquilo C3-C12, cicloalquilC4-C12- alquilo, arilo, aralquilo C7-C12, heterociclilo C3-12, heterociclilC3-C12-alquilo, heteroarilo C1-12, y heteroarilC3-12-alquilo; o R2 es una estructura de anillos multiples que tiene entre 2 y 4 anillos en donde los anillos se seleccionan en forma independiente del grupo formado por cicloalquilo, heterociclilo, arilo y heteroarilo y donde algunos o todos los anillos puede estar fusionados entre sí; R3 se selecciona del grupo formado por alquilo C1-12, alquenilo C2-12, hidroxialquilo C2-12, hidroxialquenilo C2-12, alcoxi C1-12, alcoxialquilo C2-C12, cicloalquilo C3-C12, cicloalquilC4-C12-alquilo, arilo, aralquilo C7- C12, heterociclilo C3-12, heterociclilC3-C12-alquilo, heteroarilo C1-12, y heteroarilC3-12-alquilo; o R3 es una estructura de anillos multiples que tiene entre 2 y 4 anillos en donde los anillos se seleccionan en forma independiente del grupo formado por cicloalquilo, heterociclilo, arilo y heteroarilo y donde algunos o todos los anillos puede estar fusionados entre sí; R4 y R5 se seleccionan cada uno en forma independiente entre hidrogeno, fluoro, cloro, metilo, metoxi, trifluorometilo, ciano, nitro, o -N(R12)2; R6, R6a, R7, R7a, R8, R8a, R9, y R9a se seleccionan cada uno en forma independiente entre hidrogeno o alquilo C1-3; o R6 y R6a juntos, o R7 y R7a juntos, o R8 y R8a juntos, o R9 y R9a juntos son un grupo oxo, con la salvedad de que cuando V es -C(O)-, R7 y R7a juntos o R8 y R8a juntos no forman un grupo oxo, mientras que los restantes R6, R6a, R7, R7a, R8, R8a, R9, y R9a se seleccionan cada uno en forma independiente entre hidrogeno o alquilo C1-3; o uno de R6, R6a, R7, y R7a junto con uno de R8, R8a, R9 y R9a forman un puente alquileno, mientras que los restantes R6, R6a, R7, R7a, R8, R8a, R9, y R9a se seleccionan cada uno en forma independiente entre hidrogeno o alquilo C1-3; R10 es hidrogeno o alquilo C1-3; y cada R12 se selecciona en forma independiente entre hidrogeno, o alquilo C1-6; un estereoisomero, enantiomero, o tautomero del mismo, una sal aceptable para uso farmacéutico del mismo, una composicion farmacéutica del mismo o una prodroga del mismo.
ARP060100466A 2005-02-09 2006-02-09 Derivados de piridazina, composicion farmaceutica que los contiene y su uso como agentes terapeuticos para enfermedades mediadas por la estearoil-coa desaturasa AR052902A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US11/055,034 US7754711B2 (en) 2003-07-30 2005-02-09 Pyridazine derivatives and their use as therapeutic agents

Publications (1)

Publication Number Publication Date
AR052902A1 true AR052902A1 (es) 2007-04-11

Family

ID=36646207

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060100466A AR052902A1 (es) 2005-02-09 2006-02-09 Derivados de piridazina, composicion farmaceutica que los contiene y su uso como agentes terapeuticos para enfermedades mediadas por la estearoil-coa desaturasa

Country Status (16)

Country Link
US (1) US7754711B2 (es)
EP (1) EP1851205B1 (es)
JP (1) JP5114212B2 (es)
CN (2) CN102600162A (es)
AR (1) AR052902A1 (es)
AT (1) ATE553096T1 (es)
AU (2) AU2006212763A1 (es)
BR (1) BRPI0606817A2 (es)
CA (1) CA2597069C (es)
ES (1) ES2385577T3 (es)
GT (1) GT200600045A (es)
MX (1) MX2007009593A (es)
MY (1) MY141939A (es)
PE (2) PE20061065A1 (es)
TW (1) TWI320316B (es)
WO (1) WO2006086447A2 (es)

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ATE553096T1 (de) 2012-04-15
CN102600162A (zh) 2012-07-25
JP5114212B2 (ja) 2013-01-09
CA2597069A1 (en) 2006-08-17
AU2010227003B2 (en) 2012-06-14
CN101160289A (zh) 2008-04-09
ES2385577T3 (es) 2012-07-26
TW200638935A (en) 2006-11-16
AU2006212763A1 (en) 2006-08-17
MX2007009593A (es) 2007-10-16
JP2008530098A (ja) 2008-08-07
TWI320316B (en) 2010-02-11
EP1851205A2 (en) 2007-11-07
EP1851205B1 (en) 2012-04-11
WO2006086447A3 (en) 2007-04-05
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WO2006086447A2 (en) 2006-08-17
PE20100561A1 (es) 2010-08-25
CA2597069C (en) 2011-09-20
MY141939A (en) 2010-07-30
US20060009459A1 (en) 2006-01-12
US7754711B2 (en) 2010-07-13
AU2010227003A1 (en) 2010-10-28
BRPI0606817A2 (pt) 2009-07-14

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