[go: up one dir, main page]

ES2191484T3 - Compuestos heterociclicos como inhibidores de enzimas de rotamasa. - Google Patents

Compuestos heterociclicos como inhibidores de enzimas de rotamasa.

Info

Publication number
ES2191484T3
ES2191484T3 ES99963123T ES99963123T ES2191484T3 ES 2191484 T3 ES2191484 T3 ES 2191484T3 ES 99963123 T ES99963123 T ES 99963123T ES 99963123 T ES99963123 T ES 99963123T ES 2191484 T3 ES2191484 T3 ES 2191484T3
Authority
ES
Spain
Prior art keywords
alkyl
aryl
independently selected
halogen
cycloalkyl
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES99963123T
Other languages
English (en)
Inventor
Mark Ian Kemp
Michael John Palmer
Mark Allen Sanner
Martin James Wythes
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Corp Belgium
Pfizer Corp SRL
Original Assignee
Pfizer Corp Belgium
Pfizer Corp SRL
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 Pfizer Corp Belgium, Pfizer Corp SRL filed Critical Pfizer Corp Belgium
Application granted granted Critical
Publication of ES2191484T3 publication Critical patent/ES2191484T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • 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
    • 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
    • A61P21/04Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
    • 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
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/16Otologicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Psychology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Ophthalmology & Optometry (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Un compuesto de fórmula (I): **(Fórmula)** o una sal farmacéuticamente aceptable del mismo, en el que A es un alquileno C3 - C5 no ramificado opcionalmente sustituido con un alquilo C1 - C6; X es O, S, NH o N(alquilo C1 - C6); Y es O, S, NH o N(alquilo C1 - C6); R es un grupo heterocíclico de anillo no aromático de 4 a 6 eslabones unido por un átomo de carbono, que contiene un heteroátomo de nitrógeno, estando dicho grupo opcionalmente sustituído con 1, 2, ó 3 sustituyente(s) cada uno de ellos independientemente seleccionado de alquilo C1 - C6, alquenilo C2 - C6, cicloalquilo C3 - C7, arilo, het, - CO2 (alquilo C1 - C6), - CO (het), - CONR5R6 y - CO (arilo), estando dicho alquilo y alquenilo opcionalmente sustituidos por 1 ó 2 sustituyente(s) cada uno de ellos seleccionados independientemente de cicloalquilo C3 - C7, arilo, het, - O (arilo), - O (alquileno C1 - C2)arilo, - CO (het), - CONR5R6 y - CO (arilo); R1, R2, R3 y R4 se seleccionan independientemente de H, halógeno, alquilo C1 - C6,cicloalquilo C3 - C7, haloalquilo C1 - C6), alcoxi C1 - C6, - CONR5R6, cicloalcoxi C3 - C7, cicloalquilo C3 - C7 - alquileno (C2 - C4), cicloalquilo (C3 - C7)alcoxi (C2 - C4) y - CO2(alquilo C1 - C6); R5 y R6 son, bien cada uno de ellos independientemente seleccionados entre H y alquilo C1 - C6, o bien, cuando se consideran juntos, representan un alquileno C3 - C5 no ramificado; ¿arilo¿ significa fenilo, opcionalmente sustituido con 1, 2 ó 3 sustituyente(s) cada uno de ellos independientemente seleccionado entre alquilo C1 - C6, alcoxi C1 - C6, halógeno, CONR5R6, halógeno(alquilo C1 - C6) y - NR5R6; y ¿het¿ significa un grupo heterocíclico de anillo monocíclico de 5 ó 6 eslabones, o de anillo bicíclico de 8, 9 ó 10 eslabones, que contiente de 1 a 3 heteroátomos cada uno de ellos independientemente seleccionado entre N, O y S, dicho grupo puede estar opcionalmente sustituido con 1, 2 ó 3 sustituyente(s) cada uno de ellos seleccionado independientemente entre alquilo C1 - C6, alcoxi C1 - C6,halógeno, halógeno(alquilo C1 - C6), fenilo y - NR5R6.
ES99963123T 1998-07-21 1999-06-28 Compuestos heterociclicos como inhibidores de enzimas de rotamasa. Expired - Lifetime ES2191484T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9815880.1A GB9815880D0 (en) 1998-07-21 1998-07-21 Heterocycles

Publications (1)

Publication Number Publication Date
ES2191484T3 true ES2191484T3 (es) 2003-09-01

Family

ID=10835920

Family Applications (1)

Application Number Title Priority Date Filing Date
ES99963123T Expired - Lifetime ES2191484T3 (es) 1998-07-21 1999-06-28 Compuestos heterociclicos como inhibidores de enzimas de rotamasa.

Country Status (45)

Country Link
US (2) US6372736B1 (es)
EP (1) EP1100797B1 (es)
JP (2) JP3795329B2 (es)
KR (2) KR100468185B1 (es)
CN (3) CN1511837A (es)
AP (1) AP2001002046A0 (es)
AR (1) AR019427A1 (es)
AT (1) ATE233261T1 (es)
AU (1) AU765925B2 (es)
BG (1) BG105254A (es)
BR (1) BR9912330A (es)
CA (1) CA2338214C (es)
CO (1) CO5080782A1 (es)
CR (1) CR6073A (es)
DE (1) DE69905582T2 (es)
DK (1) DK1100797T3 (es)
DZ (1) DZ2851A1 (es)
EA (1) EA003513B1 (es)
EE (1) EE200100044A (es)
ES (1) ES2191484T3 (es)
GB (1) GB9815880D0 (es)
GE (1) GEP20033028B (es)
GT (1) GT199900115A (es)
HK (1) HK1039779A1 (es)
HN (1) HN1999000106A (es)
HR (1) HRP20010052A2 (es)
HU (1) HUP0103413A3 (es)
ID (1) ID26991A (es)
IL (1) IL140244A0 (es)
IS (1) IS5790A (es)
MA (1) MA24936A1 (es)
MY (1) MY118222A (es)
NO (1) NO20010322L (es)
NZ (2) NZ522270A (es)
OA (1) OA11585A (es)
PA (1) PA8478501A1 (es)
PE (1) PE20001037A1 (es)
PL (1) PL345734A1 (es)
SI (1) SI1100797T1 (es)
SK (1) SK772001A3 (es)
SV (1) SV1999000102A (es)
TN (1) TNSN99147A1 (es)
TR (1) TR200100135T2 (es)
TW (1) TWI229672B (es)
WO (1) WO2000005232A1 (es)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9815696D0 (en) * 1998-07-20 1998-09-16 Pfizer Ltd Heterocyclics
GB9815880D0 (en) * 1998-07-21 1998-09-16 Pfizer Ltd Heterocycles
ID28787A (id) 1998-11-03 2001-07-05 Basf Ag 2-fenilbenzimidazol tersubstitusi, pembuatannya dan penggunaannya
CO5261615A1 (es) 1999-12-01 2003-03-31 Agouron Pharma Compuestos, composiciones y metodos para estimular el crecimiento y elongacion de neuronas
FR2805818B1 (fr) * 2000-03-03 2002-04-26 Aventis Pharma Sa Derives d'azetidine, leur preparation et les compositions pharmaceutiques les contenant
DE10124953A1 (de) * 2001-05-21 2002-12-12 Marlies Knipper Substanz für die therapeutische Behandlung von Tinnitus
ES2383123T3 (es) * 2004-06-29 2012-06-18 Aventis Pharmaceuticals Inc. Composición de unión a FKBP y su uso farmacéutico
US7728026B2 (en) * 2005-04-11 2010-06-01 Abbott Laboratories, Inc. 2-substituted-1 h-benzimidazile-4-carboxamides are PARP inhibitors
TWI375673B (en) * 2005-04-11 2012-11-01 Abbott Lab 1h-benzimidazole-4-carboxamides substituted with a quaternary carbon at the 2-position are potent parp inhibitors
CN101316834A (zh) * 2005-09-29 2008-12-03 艾博特公司 在2位取代有苯基的1h-苯并咪唑-4-甲酰胺是强效parp抑制剂
CN101309908A (zh) * 2005-11-15 2008-11-19 艾博特公司 作为有效parp抑制剂的取代的1h-苯并咪唑-4-甲酰胺化合物
DK1976828T3 (en) 2005-12-29 2017-03-06 Celtaxsys Inc DIAMINE DERIVATIVES AS INhibitors of Leukotriene A4 HYDROLASE
RU2462458C2 (ru) * 2006-02-10 2012-09-27 Байомарин Ига Лимитед Лечение миодистрофии дюшена
KR101472248B1 (ko) 2006-02-10 2014-12-16 서미트 코포레이션 피엘씨 뒤시엔느 근이영양증의 치료
GB0602768D0 (en) * 2006-02-10 2006-03-22 Vastox Plc Treatment of muscular dystrophy
EP2012780B1 (en) * 2006-05-02 2012-04-11 Abbott Laboratories Substituted 1h-benzimidazole-4-carboxamides are potent parp inhibitors
ES2387471T3 (es) 2006-12-20 2012-09-24 Amgen Inc. Compuestos heterocíclicos y su uso en el tratamiento de la inflamación, la angiogénesis y el cáncer
CL2008000666A1 (es) * 2007-03-07 2008-06-13 Xenon Pharmaceuticals Inc Compuestos derivados de triciclos sustituidos, inhibidores del transportador de metales divalentes-1; y uso para tratar una enfermedad asociada con un trastorno del hierro.
US8067613B2 (en) * 2007-07-16 2011-11-29 Abbott Laboratories Benzimidazole poly(ADP ribose)polymerase inhibitors
AR068332A1 (es) * 2007-08-03 2009-11-11 Summit Corp Plc Combinaciones de drogas para el tratamiento de la distrofia muscular de duchenne
GB0715939D0 (en) * 2007-08-15 2007-09-26 Vastox Plc Method of treatment of duchenne muscular dystrophy
GB0715937D0 (en) * 2007-08-15 2007-09-26 Vastox Plc Method of treatment og duchenne muscular dystrophy
DE102008060549A1 (de) 2008-12-04 2010-06-10 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Wirkstoff-Peptid-Konstrukt zur extrazellulären Anreicherung
WO2010083199A1 (en) * 2009-01-19 2010-07-22 Abbott Laboratories Benzthiazole inhibitors of poly(adp-ribose)polymerase
GB0905664D0 (en) * 2009-04-02 2009-05-13 Summit Corp Plc Compounds for treatment of duchenne muscular dystrophy
ES2864862T3 (es) 2013-03-12 2021-10-14 Celltaxis Llc Métodos de inhibición de la leucotrieno A4 hidrolasa
CA2906035A1 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
RU2690489C2 (ru) 2013-03-14 2019-06-04 Селтакссис, Инк. Ингибиторы лейкотриен а4-гидролазы
WO2014152518A2 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
AR100530A1 (es) * 2014-05-19 2016-10-12 Merial Inc Compuestos antihelmínticos
WO2019232306A1 (en) 2018-05-31 2019-12-05 Celtaxsys, Inc. Method of reducing pulmonary exacerbations in respiratory disease patients
CN109111376B (zh) * 2018-09-18 2021-09-14 四川医立特生物医药有限公司 一种2,5-双脱氧链霉胺衍生物及其应用

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5612332A (en) * 1984-03-19 1997-03-18 Alteon Inc. Di- and triaminoguanidines, and methods of use
JPS6428245A (en) 1987-07-22 1989-01-30 Sumitomo Electric Industries Production of fluoride glass
MX9202466A (es) 1991-05-24 1994-06-30 Vertex Pharma Compuestos inmunosupresores novedosos.
CO4520280A1 (es) * 1993-10-26 1997-10-15 Boehringer Ingelheim Pharma Derivados de pirrolidina, inhibidores de la bioscientesis de leucotrienos
DE19514313A1 (de) 1994-08-03 1996-02-08 Bayer Ag Benzoxazolyl- und Benzothiazolyloxazolidinone
US5859031A (en) 1995-06-07 1999-01-12 Gpi Nil Holdings, Inc. Small molecule inhibitors of rotamase enzyme activity
US5696135A (en) * 1995-06-07 1997-12-09 Gpi Nil Holdings, Inc. Inhibitors of rotamase enzyme activity effective at stimulating neuronal growth
US5801197A (en) * 1995-10-31 1998-09-01 Gpi Nil Holdings, Inc. Rotamase enzyme activity inhibitors
US5786378A (en) * 1996-09-25 1998-07-28 Gpi Nil Holdings, Inc. Heterocyclic thioesters
US5801187A (en) * 1996-09-25 1998-09-01 Gpi-Nil Holdings, Inc. Heterocyclic esters and amides
US5840736A (en) 1996-11-13 1998-11-24 Vertex Pharmaceuticals Incorporated Methods and compositions for stimulating neurite growth
US5780484A (en) 1996-11-13 1998-07-14 Vertex Pharmaceuticals Incorporated Methods for stimulating neurite growth with piperidine compounds
US5811434A (en) 1996-11-13 1998-09-22 Vertex Pharmacueticals Incorporated Methods and compositions for stimulating neurite growth
US5721256A (en) 1997-02-12 1998-02-24 Gpi Nil Holdings, Inc. Method of using neurotrophic sulfonamide compounds
GB9815696D0 (en) * 1998-07-20 1998-09-16 Pfizer Ltd Heterocyclics
GB9815880D0 (en) * 1998-07-21 1998-09-16 Pfizer Ltd Heterocycles

Also Published As

Publication number Publication date
PE20001037A1 (es) 2000-10-11
HUP0103413A3 (en) 2002-10-28
JP3795329B2 (ja) 2006-07-12
TWI229672B (en) 2005-03-21
TNSN99147A1 (fr) 2005-11-10
EE200100044A (et) 2002-06-17
GT199900115A (es) 2001-01-10
PL345734A1 (en) 2002-01-02
IL140244A0 (en) 2002-02-10
NZ522270A (en) 2004-03-26
HN1999000106A (es) 1999-11-11
AP2001002046A0 (en) 2001-03-31
GB9815880D0 (en) 1998-09-16
CA2338214C (en) 2006-08-01
HUP0103413A2 (hu) 2002-05-29
JP2004002374A (ja) 2004-01-08
US6372736B1 (en) 2002-04-16
DE69905582D1 (de) 2003-04-03
NZ508838A (en) 2002-12-20
AU4285899A (en) 2000-02-14
CO5080782A1 (es) 2001-09-25
WO2000005232A1 (en) 2000-02-03
CN1174978C (zh) 2004-11-10
KR100468185B1 (ko) 2005-01-26
EA200100052A1 (ru) 2001-06-25
DZ2851A1 (fr) 2004-02-04
BG105254A (en) 2001-10-31
HRP20010052A2 (en) 2001-12-31
CR6073A (es) 2004-04-29
IS5790A (is) 2000-12-22
KR100450008B1 (ko) 2004-09-24
JP2002521382A (ja) 2002-07-16
NO20010322D0 (no) 2001-01-19
CN1310718A (zh) 2001-08-29
CN1511837A (zh) 2004-07-14
CN1611499A (zh) 2005-05-04
DE69905582T2 (de) 2003-09-04
DK1100797T3 (da) 2003-04-22
US6562964B1 (en) 2003-05-13
EP1100797A1 (en) 2001-05-23
SK772001A3 (en) 2001-12-03
SV1999000102A (es) 2000-07-06
AR019427A1 (es) 2002-02-20
AU765925B2 (en) 2003-10-02
KR20040062640A (ko) 2004-07-07
ID26991A (id) 2001-02-22
GEP20033028B (en) 2003-07-25
HK1039779A1 (zh) 2002-05-10
TR200100135T2 (tr) 2001-06-21
MA24936A1 (fr) 2000-04-01
CA2338214A1 (en) 2000-02-03
OA11585A (en) 2004-07-26
SI1100797T1 (en) 2003-06-30
BR9912330A (pt) 2001-04-17
PA8478501A1 (es) 2000-05-24
EA003513B1 (ru) 2003-06-26
MY118222A (en) 2004-09-30
EP1100797B1 (en) 2003-02-26
ATE233261T1 (de) 2003-03-15
NO20010322L (no) 2001-03-15
KR20010071013A (ko) 2001-07-28

Similar Documents

Publication Publication Date Title
ES2191484T3 (es) Compuestos heterociclicos como inhibidores de enzimas de rotamasa.
AR055592A1 (es) Derivados de 2-amino-5-cicloalquil-hidantoina como moduladores y/o inhibidores de la beta-secretasa(bace)
AR117916A1 (es) Compuesto heterocíclico y su uso
DK0606024T3 (da) Erythromycinderivater, en fremgangsmåde til deres fremstilling samt deres anvendelse som lægemidler
RS52397B (en) PYRIDO / 2,1-A / ISOCHINOLINE DERIVATIVES AS DPP-IV INHIBITORS
AR035548A1 (es) Compuestos organicos
PE20010152A1 (es) Derivados heterociclicos utiles como agentes anticancerosos
AR056536A1 (es) Compuestos de 2-amino-5- [4-(difluormetoxi)fenil]-5-fenilimidazolona como inhibidores de la beta secretasa (bace)
CO5721002A2 (es) Derivados de acido 3-(4-benciloxifenil) propanoico
ES2179490T3 (es) Derivados de 1,2,4-triazolo(3,4-a)ftalazina sustituidos como ligandos de gaba alfa 5.
AR055878A1 (es) Derivados de ciclopropanocarboxamida
ES2196772T3 (es) Compuestos amino ciclicos.
CO5640140A2 (es) Inhibidores de actividad de akt
AR055144A1 (es) Inhibidor de secrecion acida
CO5160347A1 (es) Derivados de acido carbamico
AR040031A1 (es) Compuestos de pirazol-pirimidina anilina utiles como inhibidores de cinasa y composiciones farmaceuticas que los contienen
AR006720A1 (es) Un compuesto derivado de azahexano heterociclico, su uso para la preparacion de una composicion farmaceutica, procedimiento para prepararlo y una composicion farmaceutica que lo comprende
DK1020439T3 (da) Inhibitorer af CETP-aktivitet
WO2007149448A3 (en) Pyrazinones as cellular proliferation inhibitors
AR031597A1 (es) Compuestos piperidinos,un proceso para su preparacion, composiciones farmaceuticas,y el uso de dichos compuestos para la fabricacion de un medicamento para uso como inhibidores ccr-3
CO6331462A2 (es) Compuesto de fenil pirrol o una sal farmaceuticamente aceptable del mismo con actividad activadora de la glucoquinasa
ECSP066415A (es) 2-carbonilamino-6-piperidinaminopiridinas sustituidas y 1-carbonilamino-3-piperidinaminobenzenos sustituidos como 5-ht1f agonistas
CO4990932A1 (es) Derivados de 2,1,3-benzotiadiazol y proceso para su preparacion
DK1031569T3 (da) Salt af et 7-isoindolinquinoloncarboxylsyre-derivat, monohydrat deraf og sammensætning, der indeholder dette som aktiv bestanddel
CO4900047A1 (es) Amidas del acido 4-(n -benzoilamino)-penten-2-enoico que tienen actividad como antagonistas de neuroquinina