MXPA04003354A - Derivados de acido [[2-(amino-3,4-dioxo-1-ciclobuten-1-il)amino]alquilico] para tratamiento de dolor. - Google Patents

Derivados de acido [[2-(amino-3,4-dioxo-1-ciclobuten-1-il)amino]alquilico] para tratamiento de dolor.

Info

Publication number
MXPA04003354A
MXPA04003354A MXPA04003354A MXPA04003354A MXPA04003354A MX PA04003354 A MXPA04003354 A MX PA04003354A MX PA04003354 A MXPA04003354 A MX PA04003354A MX PA04003354 A MXPA04003354 A MX PA04003354A MX PA04003354 A MXPA04003354 A MX PA04003354A
Authority
MX
Mexico
Prior art keywords
alkyl
amino
pain
dioxo
treatment
Prior art date
Application number
MXPA04003354A
Other languages
English (en)
Inventor
Maria Zaleska Margaret
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Publication of MXPA04003354A publication Critical patent/MXPA04003354A/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D243/00Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
    • C07D243/06Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
    • C07D243/10Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/12Ketones
    • A61K31/122Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid or pantothenic acid
    • A61K31/198Alpha-amino acids, e.g. alanine or edetic acid [EDTA]
    • 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
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/662Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Esta invencion proporciona un metodo para tratar el dolor en un mamifero que incluye administrar a un mamifero en necesidad de tal tratamiento una cantidad efectiva para tratar el dolor de un compuesto de la formula (I): donde R1 es H, alquilo o fenilalquilo; R2 es H, alquilo, alquenilo o fenilalquilo; o R1 y R2, tomados conjuntamente como Z, son -CH2CH2-, -CH2C(R6)(R7)CH2- o -CH2C(R8)(R9)-C(R10)(R11)CH2-, donde R6, R8 y R10 son, independientemente, H, alquilo o hidroxilo y R7, R9 R11 son, independientemente, H, o alquilo; A es alquileno o alquenileno; X es CO2R3, P(O)(OR4)(OR5), 3,5 dioxo-1,2,4-oxadiazolidin-2-ilo o 5-tetrazolilo, en los cuales R3, R4 y R5 son, independientemente, H o alquilo; o composiciones farmaceuticas para tratar el dolor que contienen una cantidad efectiva para tratar el dolor del compuesto de la formula (I).
MXPA04003354A 2001-10-10 2002-10-09 Derivados de acido [[2-(amino-3,4-dioxo-1-ciclobuten-1-il)amino]alquilico] para tratamiento de dolor. MXPA04003354A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32824501P 2001-10-10 2001-10-10
PCT/US2002/032252 WO2003031416A2 (en) 2001-10-10 2002-10-09 [[2-(amino-3,4-dioxo-1cyclobuten-1-yl)amino]alkyl]-acid derivatives for the treatment of pain

Publications (1)

Publication Number Publication Date
MXPA04003354A true MXPA04003354A (es) 2004-09-28

Family

ID=23280159

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA04003354A MXPA04003354A (es) 2001-10-10 2002-10-09 Derivados de acido [[2-(amino-3,4-dioxo-1-ciclobuten-1-il)amino]alquilico] para tratamiento de dolor.

Country Status (27)

Country Link
US (2) US7098200B2 (es)
EP (1) EP1434588B1 (es)
JP (1) JP4350512B2 (es)
KR (1) KR100922703B1 (es)
CN (1) CN100448449C (es)
AR (1) AR036764A1 (es)
AT (1) ATE515266T1 (es)
AU (1) AU2009201746A1 (es)
BR (1) BR0213237A (es)
CA (1) CA2461348C (es)
CY (1) CY1111909T1 (es)
DK (1) DK1434588T3 (es)
EA (1) EA009993B1 (es)
ES (1) ES2367356T3 (es)
HK (1) HK1064609A1 (es)
HU (1) HUP0401773A3 (es)
IL (2) IL161275A0 (es)
MX (1) MXPA04003354A (es)
NO (1) NO20041378L (es)
NZ (1) NZ532159A (es)
PL (1) PL368863A1 (es)
PT (1) PT1434588E (es)
SI (1) SI1434588T1 (es)
TW (1) TWI321472B (es)
UA (1) UA78529C2 (es)
WO (1) WO2003031416A2 (es)
ZA (1) ZA200403406B (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI1839654T1 (sl) 2002-11-22 2010-08-31 Gruenenthal Gmbh Uporaba (1R, 2R)-3-(3-dimetilamino-1-etil-2-metil- propil)-fenola za zdravljenje vnetne bolečine
BRPI0409255A (pt) 2003-04-09 2006-03-28 Wyeth Corp derivados de ácido 2-(8,9-dioxo-2,6-diazabi-ciclo(5.2.0)non-1(7)-en-2-il)alquil fosfÈnico e seu uso como antagonistas de receptores de d-asparto de -n-metila (nmda)
WO2004091633A1 (en) * 2003-04-09 2004-10-28 Wyeth Pharmaceutical compositions for intranasal administration of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.o]non-1 (7)-en-2-yl)alkyl] phosphonic acid and derivatives and methods of use thereof
US20050142192A1 (en) * 2003-10-15 2005-06-30 Wyeth Oral administration of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)alkyl] phosphonic acid and derivatives
GT200400213A (es) * 2003-10-22 2007-09-05 Metodos para la preparacion del acido {2-[(8,9)-dioxo-2,6-diaza-biciclo[5.2.0]-non-1(7)-en-2-il]etil} fosfonico y esteres del mismo
KR20070100233A (ko) * 2004-10-08 2007-10-10 와이어쓰 [2-(8,9-디옥소-2,6-디아자바이사이클로[5.2.0]논-1(7)-엔-2-일)알킬]포스폰산의 유도체 및 이의 제조 방법
BRPI0815821A2 (pt) * 2007-08-27 2015-02-18 Wyeth Llc Composições e métodos que empregam antagonistas nmda para alcançar um efeito poupador de anestésico.
AU2010213580A1 (en) 2009-02-13 2011-09-08 Allergan, Inc. Pharmaceutical compositions comprising (3-(1-(1H-imidazol-4-yl)ethyl)-2-methylphenyl)methanol
WO2010108063A1 (en) 2009-03-19 2010-09-23 Wyeth Llc Methods for the preparation of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)ethyl]phosphonic acid and precursors thereof
WO2013078151A1 (en) 2011-11-21 2013-05-30 Allergan, Inc. Pharmaceutical compositions comprising 4-[1-(2,3-dimethylphenyl)ethyl]-3h-imidazole derivatives for treating retinal diseases
US10292989B2 (en) 2014-03-28 2019-05-21 University Of Virginia Patent Foundation General anesthetics that are not neurotoxic

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5168103A (en) 1991-01-22 1992-12-01 American Home Products Corporation [[2-(amino-3,4-dioxo-1-cyclobuten-1-yl) amino]alkyl]-acid derivatives
US5124319A (en) * 1991-10-11 1992-06-23 American Home Products Corporation Benzimidazole phosphono-amino acids
DK124393D0 (da) 1993-11-03 1993-11-03 Lundbeck & Co As H Compounds
AT400440B (de) * 1993-12-06 1995-12-27 Vianova Kunstharz Ag Verfahren zur herstellung von wasserverdünnbaren lackbindemitteln und deren verwendung
TW427904B (en) 1995-12-07 2001-04-01 American Home Prod Neuroprotective agents
UA52698C2 (uk) 1996-10-04 2003-01-15 Х. Луннбек А/С Похідні (3-алкоксіізоксазол-4-іл)заміщеної 2-амінокарбонової кислоти та їх сірковмісні аналоги, фармацевтична композиція на їх основі
EP1000072B1 (en) 1997-08-01 2003-02-19 Wyeth Process for the preparation of [2-((8,9)- dioxo-2,6-diazabicyclo [5.2.0]-non-1(7)-en-2-yl)-ethyl] phosphonic acid
US5990307A (en) * 1997-08-01 1999-11-23 American Home Products Corporation Process for the preparation of [2-((8.9)-Dioxo-2,6-Diazabicyclo [5.2.0]-Non-1(7)-en-2yl) Ethyl]Phosphonic acid
US6362371B1 (en) 1998-06-08 2002-03-26 Advanced Medicine, Inc. β2- adrenergic receptor agonists
US6225343B1 (en) * 1999-06-16 2001-05-01 Nastech Pharmaceutical Company, Inc. Compositions and methods comprising morphine gluconate
US20030158254A1 (en) 2002-01-24 2003-08-21 Xenoport, Inc. Engineering absorption of therapeutic compounds via colonic transporters
US20040082543A1 (en) 2002-10-29 2004-04-29 Pharmacia Corporation Compositions of cyclooxygenase-2 selective inhibitors and NMDA receptor antagonists for the treatment or prevention of neuropathic pain

Also Published As

Publication number Publication date
CA2461348C (en) 2011-02-15
NO20041378L (no) 2004-05-28
CY1111909T1 (el) 2015-11-04
ES2367356T3 (es) 2011-11-02
KR20050034604A (ko) 2005-04-14
EA009993B1 (ru) 2008-06-30
HK1064609A1 (en) 2005-02-04
KR100922703B1 (ko) 2009-10-22
JP2005508950A (ja) 2005-04-07
EA200400523A1 (ru) 2004-08-26
EP1434588A2 (en) 2004-07-07
CN1568189A (zh) 2005-01-19
WO2003031416A3 (en) 2003-08-14
HUP0401773A2 (hu) 2005-01-28
AU2009201746A1 (en) 2009-05-28
IL161275A0 (en) 2004-09-27
ATE515266T1 (de) 2011-07-15
PT1434588E (pt) 2011-09-05
UA78529C2 (en) 2007-04-10
US7098200B2 (en) 2006-08-29
PL368863A1 (en) 2005-04-04
JP4350512B2 (ja) 2009-10-21
DK1434588T3 (da) 2011-08-15
US20030114444A1 (en) 2003-06-19
HUP0401773A3 (en) 2005-06-28
ZA200403406B (en) 2007-04-25
CN100448449C (zh) 2009-01-07
WO2003031416A2 (en) 2003-04-17
IL161275A (en) 2009-09-01
SI1434588T1 (sl) 2011-10-28
EP1434588B1 (en) 2011-07-06
CA2461348A1 (en) 2003-04-17
NZ532159A (en) 2006-02-24
TWI321472B (en) 2010-03-11
US20060205696A1 (en) 2006-09-14
US7759346B2 (en) 2010-07-20
BR0213237A (pt) 2004-09-28
AR036764A1 (es) 2004-09-29

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