PE130999A1 - 4-oxo-naftiridin-3-carboxamidas sustituidas; ligandos de receptor cerebral gaba - Google Patents

4-oxo-naftiridin-3-carboxamidas sustituidas; ligandos de receptor cerebral gaba

Info

Publication number
PE130999A1
PE130999A1 PE1998001100A PE00110098A PE130999A1 PE 130999 A1 PE130999 A1 PE 130999A1 PE 1998001100 A PE1998001100 A PE 1998001100A PE 00110098 A PE00110098 A PE 00110098A PE 130999 A1 PE130999 A1 PE 130999A1
Authority
PE
Peru
Prior art keywords
alkyl
naftiridin
oxo
cycloalkyl
leaguards
Prior art date
Application number
PE1998001100A
Other languages
English (en)
Inventor
Pamela Albaugh
Robert W Desimone
Gang Liu
Original Assignee
Neurogen 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 Neurogen Corp filed Critical Neurogen Corp
Publication of PE130999A1 publication Critical patent/PE130999A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02Muscle relaxants, e.g. for tetanus or cramps
    • 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
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Neurology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

SE REFIERE A UN COMPUESTO DE FORMULA I; X ES H, HALOGENO, -OR1, ALQUILO C1-C6, FENIL, NAFTIL, 1-(5,6,7,8-TETRAHIDRO)NAFTIL, CARBOCICLO DE 3-7 MIEMBROS, ENTRE OTROS; Y ES ALQUILO C1-C8 OPCIONALMENTE SUSTITUIDO, CARBOCICLO DE 3-7 MIEMBROS; R1 ES H, ALQUILO C1-C6, CICLOALQUILO C3-C7 OPCIONALMENTE SUSTITUIDO; R2 Y R3 SON H, ALQUILO, ARIL, CICLOALQUILO C3-C7 OPCIONALMENTE SUSTITUIDO; R4 ES R1; R5 Y R6 SON R2 Y R3; R7 ES H, ALQUILO C1-C6, CICLOALQUILO C3-C7; R8 ES ALQUILO C1-C6, CICLOALQUILO C3-C7 O FENIL. SON COMPUESTOS PREFERIDOS N-n-BUTIL-6-BENCILAMINO-4-OXO-1,4-DIHIDRO-1,5-NAFTIRIDIN-3-CARBOXAMIDA, N-[2-ETILTIO)ETIL]-6-BENCILAMINO-4-OXO-1,4-DIHIDRO-1,5-NAFTIRIDIN-3-CARBOXAMIDA, ENTRE OTROS. EL COMPUESTO I ES UN ANTAGONISTA, AGONISTA O ANTAGONISTA INVERSO ALTAMENTE SELECTIVO PARA LOS RECEPTORES GABAa Y PUEDEN SER UTILES EN EL DIAGNOSTICO Y TRATAMIENTO DE LA ANSIEDAD, SINDROME DE DOWN, TRASTORNOS DEL SUENO, SOBREDOSIS DE BENZODIAZEPINAS Y PARA MEJORAR EL ESTADO DE ALERTA
PE1998001100A 1997-08-25 1998-11-13 4-oxo-naftiridin-3-carboxamidas sustituidas; ligandos de receptor cerebral gaba PE130999A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US91818097A 1997-08-25 1997-08-25

Publications (1)

Publication Number Publication Date
PE130999A1 true PE130999A1 (es) 1999-12-16

Family

ID=25439933

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1998001100A PE130999A1 (es) 1997-08-25 1998-11-13 4-oxo-naftiridin-3-carboxamidas sustituidas; ligandos de receptor cerebral gaba

Country Status (24)

Country Link
EP (1) EP1007526A1 (es)
JP (1) JP2001514181A (es)
KR (1) KR20010023313A (es)
CN (1) CN1268136A (es)
AP (1) AP2000001742A0 (es)
AU (1) AU753800B2 (es)
BG (1) BG104192A (es)
BR (1) BR9811362A (es)
CA (1) CA2301599C (es)
EG (1) EG21717A (es)
HU (1) HUP0003258A3 (es)
IL (1) IL134291A0 (es)
IS (1) IS5382A (es)
LV (1) LV12539B (es)
NO (1) NO20000822L (es)
NZ (1) NZ502548A (es)
OA (1) OA11293A (es)
PE (1) PE130999A1 (es)
PL (1) PL338783A1 (es)
SI (1) SI20270A (es)
SK (1) SK2162000A3 (es)
TW (1) TW574221B (es)
WO (1) WO1999010347A1 (es)
YU (1) YU10500A (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1177177B1 (en) * 1999-05-06 2005-02-23 Neurogen Corporation Substituted 4-oxo-quinoline-3-carboxamides: gaba brain receptor ligands
US6448246B1 (en) 1999-05-25 2002-09-10 Neurogen Corporation Substituted 4H-1,4-benzothiazine-2-carboxamide: GABA brain receptor ligands
US6562822B2 (en) 2000-07-12 2003-05-13 Pharmacia & Upjohn Company Heterocyle carboxamides as antiviral agents
US6730682B2 (en) 2000-07-12 2004-05-04 Pharmacia & Upjohn Company Heterocycle carboxamides as antiviral agents
US6559145B2 (en) 2000-07-12 2003-05-06 Pharmacia & Upjohn Company Heterocycle carboxamides as antiviral agents
ATE430745T1 (de) 2000-10-12 2009-05-15 Merck & Co Inc Aza- und polyaza naphthalenyl karboxamide als inhibitoren der hiv-integrase
AU1532802A (en) 2000-10-12 2002-04-22 Merck & Co Inc Aza- and polyaza-naphthalenyl-carboxamides useful as hiv integrase inhibitors
US6841558B2 (en) 2000-10-12 2005-01-11 Merck & Co., Inc. Aza-and polyaza-naphthalenyl carboxamides useful as HIV intergrase inhibitors
US20020151591A1 (en) * 2000-10-17 2002-10-17 Anabella Villalobos Combination use of acetylcholinesterase inhibitors and GABAa inverse agonists for the treatment of cognitive disorders
OA12554A (en) * 2001-03-01 2006-06-07 Pfizer Prod Inc Use of GABA a inverse agonists in combination withnicotine receptor partial agonists, estrogen, sel ective estrogen modulators, or bitamin E for the treatment of cognitive disorders.
AR036256A1 (es) 2001-08-17 2004-08-25 Merck & Co Inc Sal sodica de un inhibidor de integrasa del vih, procesos para su preparacion, composiciones farmaceuticas que lo contienen y su uso para la manufactura de un medicamento
AU2003216049B2 (en) 2002-01-17 2008-07-17 Merck Sharp & Dohme Corp. Hydroxynaphthyridinone carboxamides useful as HIV integrase inhibitors
WO2003077857A2 (en) 2002-03-15 2003-09-25 Merck & Co., Inc. N-(substituted benzyl)-8-hydroxy-1,6-naphthyridine-7- carboxamides useful as hiv integrase inhibitors
WO2004106336A1 (en) * 2003-05-27 2004-12-09 Pfizer Products Inc. Process for the preparation and purification of 1,5-naphthyridine-3-carboxyamides
WO2004106334A2 (en) * 2003-05-28 2004-12-09 Pfizer Products Inc. Process for the preparation of 1,5-naphthyridine-3-carboxy amides by direct ester amidation
PL2074123T3 (pl) * 2006-10-16 2013-04-30 Bionomics Ltd Nowe związki o działaniu przeciwlękowym
JP2010510314A (ja) * 2006-11-22 2010-04-02 シーサイド セラピューティクス,エルエルシー 精神遅滞、ダウン症候群、脆弱x症候群および自閉症の治療方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR204813A1 (es) * 1972-05-08 1976-03-05 Yamanouchi Pharma Co Ltd Proceso para la preparacion de derivados de ampilicina
GB1433774A (en) * 1973-02-26 1976-04-28 Allen & Hanburys Ltd Heterocyclic compounds apparatus for conveying articles
US4374138A (en) * 1981-11-13 1983-02-15 Warner-Lambert Company Antibacterial amide compounds, compositions, and methods of use
DD295360A5 (de) * 1987-07-03 1991-10-31 Akad Wissenschaften Verfahren zur Herstellung von aktivierten Carbonsäureestern
DD279887A1 (de) * 1987-07-03 1990-06-20 Inst Pharmakologische Forschun Verfahren zur herstellung von d-alpha-(4(1h)-1,5-naphthyridon-3-carboxamido)-benzylpenicillin und anderen beta-lactamantibiotika
DD279875A1 (de) * 1987-07-03 1990-06-20 Inst Pharmakologische Forschun Verfahren zur herstellung von aktivierten carbonsaeureestern
JPS6461461A (en) * 1987-09-01 1989-03-08 Otsuka Pharma Co Ltd Benzohetero ring derivative

Also Published As

Publication number Publication date
BG104192A (en) 2001-05-31
AU9117398A (en) 1999-03-16
IL134291A0 (en) 2001-04-30
BR9811362A (pt) 2000-08-22
SK2162000A3 (en) 2001-03-12
KR20010023313A (ko) 2001-03-26
NO20000822D0 (no) 2000-02-18
LV12539A (en) 2000-10-20
YU10500A (sh) 2002-10-18
CA2301599C (en) 2003-03-25
OA11293A (en) 2002-11-19
AP2000001742A0 (en) 2000-02-24
HUP0003258A3 (en) 2001-05-28
EG21717A (en) 2002-02-27
NO20000822L (no) 2000-04-13
HUP0003258A2 (en) 2001-03-28
EP1007526A1 (en) 2000-06-14
SI20270A (sl) 2000-12-31
CA2301599A1 (en) 1999-03-04
WO1999010347A1 (en) 1999-03-04
CN1268136A (zh) 2000-09-27
IS5382A (is) 2000-02-22
JP2001514181A (ja) 2001-09-11
NZ502548A (en) 2002-06-28
LV12539B (en) 2001-01-20
TW574221B (en) 2004-02-01
PL338783A1 (en) 2000-11-20
AU753800B2 (en) 2002-10-31

Similar Documents

Publication Publication Date Title
PE130999A1 (es) 4-oxo-naftiridin-3-carboxamidas sustituidas; ligandos de receptor cerebral gaba
DK0613458T3 (da) Acykliske ethylendiaminderivater som substans P receptorantagonister
PE91798A1 (es) Pirrolicarboxanilidas condensadas: utiles como ligandos receptores
PE20021094A1 (es) Derivados de ciclohexano-1,4-diamina sustituidos
AR062299A1 (es) Derivados de bencimidazol
DK0641328T3 (da) Broforbundne, azabicykliske derivater som substans P-antagonister
MX9702601A (es) AGONISTAS beta-ADRENERGICOS HETEROCICLICOS.
PE46899A1 (es) Derivados de n-fenil-sulfonamida
PE109598A1 (es) Pirrolcarboxamidas condensadas, utiles como ligandos de receptores cerebrales gaba
PE20020917A1 (es) Derivados de imidazol como bloqueadores del receptor n-metil-d-aspartato
ES2059327T3 (es) Derivados de tetrahidronaftaleno y de indano, obtencion de los mismos y utilizacion en preparados farmaceuticos.
NO940927L (no) Kondenserte tricykliske nitrogenholdige heterocykler som substans-P-reseptor-antagonister
PE20030417A1 (es) Derivados de urea como antagonistas del receptor vainilloide
RU2004126613A (ru) Замещенные индолы в качестве агонистов альфа-1
HUP0000079A2 (hu) Indán- és dihidroindolszármazékok
PE20010205A1 (es) Derivados 3-sustituido de 2-carboxiciclopropil glicina como agonistas de glutamato
OA09579A (en) Certain imidazoquinoxalines a new class of gaba brain receptor ligands
ATE428694T1 (de) N-ä1h-indol-5-ylünaphthalin-1-sulphonamid- derivate und verwandte verbindungen als serotonin 5-ht6 rezeptor antagonisten zur behandlung von erkrankungen des zentralen nervensystems
ATE247639T1 (de) Arylsubstituierte cyclische amine als selektive dopamin-d3-liganden
RU2004139099A (ru) 1-(аминоалкил)-3-сульфонилиндольные и -индазольные производные в качестве лигандов 5-гидрокситриптамина-6
PE20030718A1 (es) Lactamas como antagonistas de taquiquininas
ES2130135T3 (es) Nuevos compuestos heterociclicos de 6,7,8,9-tetrahidro-3h-benz(e)indol con actividad terapeutica sobre el sistema nervioso central.
DE60003899D1 (de) Aryl-annellierte disubstituierte pyridine : nk3 rezeptor-liganden
HUP0001165A2 (hu) NK1 és NK2 antagonista hatású acil-amino-alkil-amid-származékok, a vegyületeket tartalmazó gyógyszerkészítmények, eljárás előállításukra
PE20021018A1 (es) DERIVADOS DE ß - CARBOLINA

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed