[go: up one dir, main page]

AR009484A1 - Un compuesto de acido n-sustituido-2-amino-4-fenil-4-oxo-butanoico, su utilizacion como inhibidor de la quinurenina-3-hidroxilasa y una composicionfarmaceutica que lo comprende. - Google Patents

Un compuesto de acido n-sustituido-2-amino-4-fenil-4-oxo-butanoico, su utilizacion como inhibidor de la quinurenina-3-hidroxilasa y una composicionfarmaceutica que lo comprende.

Info

Publication number
AR009484A1
AR009484A1 ARP970103945A ARP970103945A AR009484A1 AR 009484 A1 AR009484 A1 AR 009484A1 AR P970103945 A ARP970103945 A AR P970103945A AR P970103945 A ARP970103945 A AR P970103945A AR 009484 A1 AR009484 A1 AR 009484A1
Authority
AR
Argentina
Prior art keywords
phenyl
alkyl
alkenyl
benzyl
substituted
Prior art date
Application number
ARP970103945A
Other languages
English (en)
Original Assignee
Pharmacia & Upjohn Spa
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 Pharmacia & Upjohn Spa filed Critical Pharmacia & Upjohn Spa
Publication of AR009484A1 publication Critical patent/AR009484A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/46Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/47Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • A61P27/06Antiglaucoma agents or miotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/03Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C311/06Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by carboxyl groups

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)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Ophthalmology & Optometry (AREA)
  • Psychology (AREA)
  • Communicable Diseases (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Oncology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Compuestos de ácido N-sustituido-2-amino-4-oxo butanoico de la formula (I) donde cada uno de los grupos X e Y son, de manera independiente, hidrogeno,halogeno, nitro, alquilo C1-C6; alquenilo C2-C4; alquinilo C2-C4; alcoxi C1-C6; alquiltio C1-C6; SOR2 o SO2R2, donde R2 es alquilo C2-C6, fenilo o bencilo; oSO2N(R3)2, donde cada uno de los grupos R3 son, de manera independiente, hidrogeno, alquilo C1-C6, alquenilo C2-C4, alquinilo C2-C4, fenilo o bencilo; Res hidroxi, -OR5, donde R5 es alquilo C1-C6, alquenilo C2-C4, alquinilo C2-C4 o bencilo; -N(R3)OR3, donde cada R3 es tal como se la definiera antes; W es-COOR4, -COR4 o -SO2R4, donde R4 es alquilo C1-C6, un alquenilo C2-C4 opcionalemente sustituido, un fenilo o bencilo opcionalmente sustituido;-CONHR5 o -CSNHR5, donde R5 es tal como se definiría antes; tricloroacetilo; o trifluoroacetilo; o las sales farmacéuticamente aceptables de ls mismos, parasu utilizacion como un medicamento, en particular como un inhibidor dela quinurenina 3-hidroxilasa, la utilizacion de tales compuestos; composicionesfarmacéuticas que los comprenden; un grupo de compuestos seleccionados de tales compuestos de formula (I), ya sea, en la forma de enantiomeros simples o comouna mezcla de enantiomeros o una sal farmacéuticamente aceptable de los mismos.
ARP970103945A 1996-09-03 1997-08-29 Un compuesto de acido n-sustituido-2-amino-4-fenil-4-oxo-butanoico, su utilizacion como inhibidor de la quinurenina-3-hidroxilasa y una composicionfarmaceutica que lo comprende. AR009484A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9618349.6A GB9618349D0 (en) 1996-09-03 1996-09-03 N-substituted 2-amino-4-phenyl-4-oxo-butanoic acid derivatives with kynurenine-3-hydroxylase inhibitory activity

Publications (1)

Publication Number Publication Date
AR009484A1 true AR009484A1 (es) 2000-04-26

Family

ID=10799321

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP970103945A AR009484A1 (es) 1996-09-03 1997-08-29 Un compuesto de acido n-sustituido-2-amino-4-fenil-4-oxo-butanoico, su utilizacion como inhibidor de la quinurenina-3-hidroxilasa y una composicionfarmaceutica que lo comprende.

Country Status (9)

Country Link
US (1) US6207709B1 (es)
EP (1) EP0931056A1 (es)
JP (1) JP2001501179A (es)
AR (1) AR009484A1 (es)
AU (1) AU4117297A (es)
CA (1) CA2263250A1 (es)
GB (1) GB9618349D0 (es)
WO (1) WO1998009938A1 (es)
ZA (1) ZA977833B (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9725055D0 (en) * 1997-11-26 1998-01-28 Pharmacia & Upjohn Spa 1,3,4-thiadiazoles compounds
US6541521B1 (en) 1999-07-12 2003-04-01 Warner-Lambert Company Benzene butyric acids and their derivatives as inhibitors of matrix metalloproteinases
IT1317049B1 (it) * 2000-06-23 2003-05-26 Sigma Tau Ind Farmaceuti Composti utili per la preparazione di medicamenti ad attivita'inibitrice della fosfodiesterasi iv.
JP2005060311A (ja) * 2003-08-13 2005-03-10 Mochida Pharmaceut Co Ltd N−(ベンゾイル)アミノ酸誘導体を有効成分とするニューロパシー性疼痛治療剤
KR100560845B1 (ko) 2003-10-09 2006-03-13 에스케이 텔레콤주식회사 Mm-mb 단말기의 모뎀 간 절체 방법
EP2054397B1 (en) * 2006-08-16 2015-10-07 The J. David Gladstone Institutes, A Testamentary Trust Established under The Will of J. David Gladstone Small molecule inhibitors of kynurenine-3-monooxygenase
DK2420494T3 (en) 2006-08-16 2015-01-12 J David Gladstone Inst A Testamentary Trust Established Under The Will Of J David Gladstone Use of thiadiazole compounds as inhibitors of kynurenine 3-monooxygenase
US11229810B2 (en) * 2017-05-17 2022-01-25 University Of Virginia Patent Foundation Methods and systems for producing neuronal lesions using magnetic resonance and acoustic energy
MX2020003811A (es) 2017-10-05 2021-01-15 Biogen Inc Proceso para preparar derivados de alfa-carboxamida pirrolidina.
CN112236412B (zh) 2018-02-09 2024-01-30 维斯塔津治疗公司 4-氯代犬尿氨酸及中间体的合成
KR20210150528A (ko) * 2019-04-10 2021-12-10 바이오젠 인크. 알파-카르복스아미드 피롤리딘 유도체 제조 방법

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4758661A (en) * 1986-06-24 1988-07-19 Merck & Co., Inc. Chiral synthesis of (+)-trans-1a,2,3,4a,5,6-hexahydro-9-hydroxy-4-propyl-4H-naphth[1,2-b]-1,4-oxazine
US5495044A (en) * 1991-04-18 1996-02-27 University Of Georgia Research Foundation, Inc. Inhibitors of kynureninase
IT1265101B1 (it) * 1993-07-23 1996-10-30 Erba Carlo Spa Derivati dell'acido 2-ammino-4-fenil-4-osso butirrico
US5519055A (en) * 1993-08-06 1996-05-21 University Of Maryland At Baltimore Substituted kynurenines and process for their preparation
GB9521486D0 (en) * 1995-10-20 1995-12-20 Pharmacia Spa Fluoro-substituted benzoylpropionic acid derivatives

Also Published As

Publication number Publication date
GB9618349D0 (en) 1996-10-16
AU4117297A (en) 1998-03-26
US6207709B1 (en) 2001-03-27
WO1998009938A1 (en) 1998-03-12
JP2001501179A (ja) 2001-01-30
EP0931056A1 (en) 1999-07-28
ZA977833B (en) 1998-03-02
CA2263250A1 (en) 1998-03-12

Similar Documents

Publication Publication Date Title
AR009484A1 (es) Un compuesto de acido n-sustituido-2-amino-4-fenil-4-oxo-butanoico, su utilizacion como inhibidor de la quinurenina-3-hidroxilasa y una composicionfarmaceutica que lo comprende.
ES2094721T3 (es) Analogos de la camptotecina solubles en agua.
AR029766A1 (es) Compuesto inhibidor de quinasa y uso del mismo para preparar una composicion farmaceutica
AR037329A1 (es) Compuestos pirazolo pirimidinona, procedimientos para la preparacion de los mismos, composiciones farmaceuticas de los mismos y usos de los mismos en la preparacion de medicamentos
AR040474A1 (es) Derivados de tiofenolglicosido, procedimientos para la preparacion de los mismos, medicamentos que contienen estos compuestos, y el uso de los mismos
ES2076253T3 (es) N-(ariloxialquil)-heteroarilpiperidinas y -heteroarilpiperazinas, un procedimiento para su preparacion y su uso como medicamentos.
MX9204622A (es) Nuevos derivados de 3,5-di-tert-butil-4-hidroxifenilo, procedimiento para su preparacion y composicion farmaceutica que los contiene.
RU2002129575A (ru) Бензоилпиразолы и их применение в качестве гербицидов
DK0880508T3 (da) Quinazolinderivater som VEGF-inhibitorer
AR021482A1 (es) Compuestos de 4-carboxiamino-1,2,3,4-tetrahidroquinolinas, composiciones farmaceuticas, kit, y uso de los mismos.
BG102764A (en) Derivatives of pyrimidin-4-on as pesticides
AR041271A1 (es) Quinazolinonas espirocondensadas y su uso como inhibidores de la fosfodiesterasa
ES2142486T3 (es) Formulaciones liquidas y procedimiento destinadas a prolongar la vida en jarron de flores cortadas.
KR940009185A (ko) 피라졸로[4,3-c]피리딘 및 세로토닌 재흡수 억제제로서의 이의 용도
PA8444901A1 (es) Derivados de 5-aroilnaftaleno como agentes anti-inflamatorios
AR029001A1 (es) Derivados de bencil-3,4-metilendioxicinamico y el uso de los mismos para la manufactura de un medicamento
FI945582A0 (fi) Substituoidut (aryylialkyyliaminobentsyyli) aminopropioniamidijohdannaiset, niiden valmistus ja käyttö anti-epileptisinä, neuroprotektiivisina ja antidepressiivisina aineina
ATE182330T1 (de) 1,4-dihydropyridin-derivate, verfahren zu ihrer herstellung und diese enthaltende therapeutische zusammensetzung
AR001768A1 (es) Derivados de ciclolignano utiles como antineoplasicos composiciones farmaceuticas que los contienen y proceso para preparar dichos derivados
AR006553A1 (es) COMPUESTOS ESPIRO[CICLOPENT[b] INDOLPIPERIDINAS] PARTICULARMENTE UTILES PARA ALIVIAR LA DISFUNCION DE LA MEMORIA, INTERMEDIARIOS, COMPOSICIONESFARMACEUTICAS, USOS Y PROCEDIMIENTOS DE PREPARACION DE DICHOS COMPUESTOS.
FR2858320B1 (fr) Utilisation d'un derive d'acide (dihydro)jasmonique comme agent desquamant.
ES2076201T3 (es) Derivados de 3-piperidinil-indazol antihipertensivos.
ATE216392T1 (de) 7-oxo-2,3,7,14-tetrahydro-1h-benzo(b)pyrano(3,2 h)acridincarboxylatderivate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische zubereitungen
ES2190941T3 (es) Derivados de bencilaminodiacetamidas, composiciones, composiciones que los incluyen, procedimiento de preparacion y utilizaciones.
RU99120174A (ru) Гидрометильные производные 2-амино-1,2,3,4-тетрагидронафталина в качестве сердечно-сосудистого агента