[go: up one dir, main page]

GT200400268A - Pirido[2,3-d] pirimidina-2,4-diaminas como inhibidores de pde 2 - Google Patents

Pirido[2,3-d] pirimidina-2,4-diaminas como inhibidores de pde 2

Info

Publication number
GT200400268A
GT200400268A GT200400268A GT200400268A GT200400268A GT 200400268 A GT200400268 A GT 200400268A GT 200400268 A GT200400268 A GT 200400268A GT 200400268 A GT200400268 A GT 200400268A GT 200400268 A GT200400268 A GT 200400268A
Authority
GT
Guatemala
Prior art keywords
pde
inhibitors
diaminas
pirimidina
pirido
Prior art date
Application number
GT200400268A
Other languages
English (en)
Inventor
Thomas Arthur Beyer
Robert James Chambers
Kelvin Lam
Mei Li
Andrew Ian Morrell
David Duane Thompson
Original Assignee
Pfizer
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 filed Critical Pfizer
Publication of GT200400268A publication Critical patent/GT200400268A/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/08Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
    • 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
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • 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
    • A61P35/00Antineoplastic agents
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Cardiology (AREA)
  • Reproductive Health (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Endocrinology (AREA)
  • Pregnancy & Childbirth (AREA)
  • Diabetes (AREA)
  • Gynecology & Obstetrics (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

LA PRESENTE INVENCION SE REFIERE A COMPUESTOS DE LA FORMULA GENERAL I EN LA QUE R1,R2,X,Y,N, SON GRUPOS FUNCIONALES DESCRITOS EN EL EXPEDIENTE. ESTOS COMPUESTOS SON UTILES COMO INHIBIDORES DE LA PDE 2 POR LO QUE SON DE UTILIDAD EN UNA AMPLIA VARIEDAD DE PATOLOGIAS TALES COMO OSTEOPOROSIS, HIPERTENSION PULMONAR, ANGIOGENESIS VASCULAR, DEMENCIA, ENTRE OTRAS MENCIONADAS EN LA SOLICITUD. T2004
GT200400268A 2003-12-16 2004-12-15 Pirido[2,3-d] pirimidina-2,4-diaminas como inhibidores de pde 2 GT200400268A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US52999403P 2003-12-16 2003-12-16

Publications (1)

Publication Number Publication Date
GT200400268A true GT200400268A (es) 2005-09-20

Family

ID=34710150

Family Applications (1)

Application Number Title Priority Date Filing Date
GT200400268A GT200400268A (es) 2003-12-16 2004-12-15 Pirido[2,3-d] pirimidina-2,4-diaminas como inhibidores de pde 2

Country Status (39)

Country Link
US (1) US20070135457A1 (es)
EP (1) EP1697356B1 (es)
JP (1) JP4073944B2 (es)
KR (1) KR100816179B1 (es)
CN (1) CN100439366C (es)
AP (1) AP2006003632A0 (es)
AR (1) AR046766A1 (es)
AT (1) ATE387446T1 (es)
AU (1) AU2004303609A1 (es)
BR (1) BRPI0417663A (es)
CA (1) CA2549510A1 (es)
CL (1) CL2008001920A1 (es)
DE (1) DE602004012154T2 (es)
DK (1) DK1697356T3 (es)
EA (1) EA010424B1 (es)
EC (1) ECSP066643A (es)
ES (1) ES2299888T3 (es)
GE (1) GEP20094720B (es)
GT (1) GT200400268A (es)
HN (1) HN2004000538A (es)
HR (1) HRP20080142T3 (es)
IL (1) IL175813A0 (es)
IS (1) IS8474A (es)
MA (1) MA28270A1 (es)
MX (1) MXPA06006777A (es)
NL (1) NL1027787C2 (es)
NO (1) NO20063231L (es)
PE (1) PE20050681A1 (es)
PL (1) PL1697356T3 (es)
PT (1) PT1697356E (es)
RS (1) RS50575B (es)
SI (1) SI1697356T1 (es)
SV (1) SV2005001979A (es)
TN (1) TNSN06186A1 (es)
TW (1) TWI291961B (es)
UA (1) UA83091C2 (es)
UY (1) UY28671A1 (es)
WO (1) WO2005061497A1 (es)
ZA (1) ZA200604970B (es)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1960372B1 (en) * 2005-12-15 2015-12-09 Rigel Pharmaceuticals, Inc. Kinase inhibitors and their uses
KR20090098783A (ko) * 2006-09-21 2009-09-17 토시키 오구로 경조직 재생 촉진제
WO2009116577A1 (ja) * 2008-03-18 2009-09-24 日産化学工業株式会社 1-(置換フェニル)-1-置換シリルエーテル、アルコールまたはケトンの製造方法および中間体
WO2010062366A1 (en) * 2008-10-31 2010-06-03 Arginetix, Inc. Compositions and methods of treating endothelial disorders
US8680116B2 (en) 2009-07-22 2014-03-25 Merck Sharp & Dohme Corp. Quinolinone PDE2 inhibitors
US8440710B2 (en) 2009-10-15 2013-05-14 Hoffmann-La Roche Inc. HSL inhibitors useful in the treatment of diabetes
US9540379B2 (en) 2011-01-31 2017-01-10 Boehringer Ingelheim International Gmbh (1,2,4)triazolo[4,3-A]quinoxaline derivatives as inhibitors of phosphodiesterases
CN103596958A (zh) 2011-04-20 2014-02-19 葛兰素集团有限公司 用作抗结核病化合物的四氢吡唑并[1,5-a]嘧啶
US9469637B2 (en) 2012-04-25 2016-10-18 Takeda Pharmaceutical Company Limited Nitrogenated heterocyclic compound
JP6205356B2 (ja) 2012-07-13 2017-09-27 武田薬品工業株式会社 複素環化合物
US20140045856A1 (en) 2012-07-31 2014-02-13 Boehringer Ingelheim International Gmbh 4-Methyl-2,3,5,9,9b-pentaaza-cyclopenta[a]naphthalenes
WO2014142255A1 (ja) 2013-03-14 2014-09-18 武田薬品工業株式会社 複素環化合物
EP3018126A4 (en) 2013-07-03 2016-12-07 Takeda Pharmaceuticals Co HETEROCYCLIC CONNECTION
EP3018123B1 (en) 2013-07-03 2023-05-10 Takeda Pharmaceutical Company Limited Amide compound
US20160159808A1 (en) * 2013-07-24 2016-06-09 Takeda Pharmaceutical Company Limited Heterocyclic compound
US9815796B2 (en) 2013-12-23 2017-11-14 Merck Sharp & Dohme Corp. Pyrimidone carboxamide compounds as PDE2 inhibitors
JP6696904B2 (ja) 2014-01-08 2020-05-20 イントラ−セルラー・セラピーズ・インコーポレイテッドIntra−Cellular Therapies, Inc. 製剤および医薬組成物
MX380860B (es) * 2014-08-01 2025-03-12 Firmenich & Cie Dispersion solida de compuestos con sabor de amida.
WO2016090380A1 (en) 2014-12-06 2016-06-09 Intra-Cellular Therapies, Inc. Organic compounds
HK1244427A1 (zh) 2014-12-06 2018-08-10 Intra-Cellular Therapies, Inc. 有机化合物
WO2016145614A1 (en) 2015-03-17 2016-09-22 Merck Sharp & Dohme Corp. Triazolyl pyrimidinone compounds as pde2 inhibitors
US10287269B2 (en) 2015-03-26 2019-05-14 Merck Sharp & Dohme Corp. Pyrazolyl pyrimidinone compounds as PDE2 inhibitors
WO2016179059A1 (en) 2015-05-05 2016-11-10 Merck Sharp & Dohme Corp. Heteroaryl-pyrimidinone compounds as pde2 inhibitors
WO2016183741A1 (en) 2015-05-15 2016-11-24 Merck Sharp & Dohme Corp. Pyrimidinone amide compounds as pde2 inhibitors
WO2016191935A1 (en) 2015-05-29 2016-12-08 Merck Sharp & Dohme Corp. 6-alkyl dihydropyrazolopyrimidinone compounds as pde2 inhibitors
WO2016192083A1 (en) 2015-06-04 2016-12-08 Merck Sharp & Dohme Corp. Dihydropyrazolopyrimidinone compounds as pde2 inhibitors
WO2016209749A1 (en) 2015-06-25 2016-12-29 Merck Sharp & Dohme Corp. Substituted pyrazolo/imidazolo bicyclic compounds as pde2 inhibitors
WO2017000276A1 (en) 2015-07-01 2017-01-05 Merck Sharp & Dohme Corp. Bicyclic heterocyclic compounds as pde2 inhibitors
WO2017000277A1 (en) * 2015-07-01 2017-01-05 Merck Sharp & Dohme Corp. Substituted triazolo bicycliccompounds as pde2 inhibitors
EP3156405A1 (en) 2015-10-13 2017-04-19 Boehringer Ingelheim International GmbH Spirocyclic ether derivatives of pyrazolo[1,5-a]pyrimidine-3-carboxamide
GB201700814D0 (en) * 2017-01-17 2017-03-01 Liverpool School Tropical Medicine Compounds
EP3713572B1 (en) 2017-11-23 2025-07-30 Oslo University Hospital HF Treatment of tachycardia
CN109758458B (zh) * 2019-03-05 2021-02-23 中国人民解放军陆军军医大学第二附属医院 抑制Crif1与PKA相互作用的化合物的应用
WO2022187411A1 (en) * 2021-03-02 2022-09-09 Kumquat Biosciences Inc. Heterocycles and uses thereof
IL316144A (en) 2022-04-20 2024-12-01 Kumquat Biosciences Inc Macrocyclic heterocycles and their uses

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2749344A (en) * 1953-01-02 1956-06-05 Burroughs Wellcome Co Pyrimidine compounds
US3021332A (en) * 1954-01-04 1962-02-13 Burroughs Wellcome Co Pyrido (2, 3-d) pyrimidine compounds and method of making
US2926166A (en) * 1954-01-04 1960-02-23 Burroughs Wellcome Co Pyrido (2, 3-d) pyrimidine compounds and method of making
US2924599A (en) * 1956-07-16 1960-02-09 Anchor Chemical Company Ltd Derivatives of 1:3:5-triazanaphthalene
US2937284A (en) * 1958-05-01 1960-05-17 Burroughs Wellcome Co 2, 4-diamino-5, 6-dialkylpyrido (2, 3-d) pyrimidines and method
US3288792A (en) * 1962-07-05 1966-11-29 Burroughs Wellcome Co Method of preparing 2, 4-diamino-6-alkylpyrido (2, 3-d) pyrimidines
DE3422824A1 (de) * 1984-06-20 1986-01-02 Celamerck Gmbh & Co Kg, 6507 Ingelheim Neue herbizid wirksame sulfonylharnstoffe
US6194166B1 (en) * 1993-05-24 2001-02-27 Takara Shuzo Co., Ltd. Gene regulating aureobasidin sensitivity
US5547954A (en) 1994-05-26 1996-08-20 Fmc Corporation 2,4-Diamino-5,6-disubstituted-and 5,6,7-trisubstituted-5-deazapteridines as insecticides
US6262059B1 (en) * 1995-06-07 2001-07-17 Cell Pathways, Inc. Method of treating a patient having precancerous lesions with quinazoline derivatives
US6184226B1 (en) * 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
PE20030008A1 (es) * 2001-06-19 2003-01-22 Bristol Myers Squibb Co Inhibidores duales de pde 7 y pde 4

Also Published As

Publication number Publication date
JP2007513996A (ja) 2007-05-31
AP2006003632A0 (en) 2006-06-30
ZA200604970B (en) 2007-11-28
HN2004000538A (es) 2008-02-21
SV2005001979A (es) 2005-12-13
BRPI0417663A (pt) 2007-04-03
TNSN06186A1 (fr) 2007-11-15
UA83091C2 (en) 2008-06-10
KR100816179B1 (ko) 2008-03-28
WO2005061497A1 (en) 2005-07-07
CN1894245A (zh) 2007-01-10
ECSP066643A (es) 2006-10-25
NL1027787A1 (nl) 2005-06-21
CA2549510A1 (en) 2005-07-07
PE20050681A1 (es) 2005-10-04
AU2004303609A1 (en) 2005-07-07
IS8474A (is) 2006-05-18
JP4073944B2 (ja) 2008-04-09
ATE387446T1 (de) 2008-03-15
US20070135457A1 (en) 2007-06-14
CN100439366C (zh) 2008-12-03
SI1697356T1 (sl) 2008-06-30
ES2299888T3 (es) 2008-06-01
NL1027787C2 (nl) 2006-03-09
HRP20080142T3 (en) 2008-06-30
NO20063231L (no) 2006-07-11
IL175813A0 (en) 2006-10-05
EP1697356B1 (en) 2008-02-27
MXPA06006777A (es) 2006-08-23
DE602004012154D1 (de) 2008-04-10
EA010424B1 (ru) 2008-08-29
EP1697356A1 (en) 2006-09-06
DK1697356T3 (da) 2009-01-12
TWI291961B (en) 2008-01-01
DE602004012154T2 (de) 2009-03-12
TW200522952A (en) 2005-07-16
PT1697356E (pt) 2008-05-05
EA200600973A1 (ru) 2006-10-27
KR20060105776A (ko) 2006-10-11
UY28671A1 (es) 2005-07-29
AR046766A1 (es) 2005-12-21
RS50575B (sr) 2010-05-07
PL1697356T3 (pl) 2008-07-31
MA28270A1 (fr) 2006-11-01
GEP20094720B (en) 2009-06-25
CL2008001920A1 (es) 2008-10-17

Similar Documents

Publication Publication Date Title
GT200400268A (es) Pirido[2,3-d] pirimidina-2,4-diaminas como inhibidores de pde 2
GT200300028A (es) Derivados iii de dihidrobenzodiacepina-2-ona
GT200400020A (es) Compuestos de triazol utiles en terapia
GT200300098A (es) Inhibidores de metaloproteinasa de aril-heteroariloxi-ariloxi-pirimidina-2,4,6-triona
GT200300297A (es) Inhibidores benzamidicos del receptor p2x7
GT200300087A (es) 2-(2,6-diclorofenil)-diarilimidazoles
GT200300093A (es) Inhibidores de metaloproteinasa de heteroariloxi-aril-espiro-pirimidina-2,4,6-triona n-sustituida
GT200300171A (es) Derivados de heterobiarilo como inhibidores de metaloproteinasa de la matriz
GT200500101A (es) Compuestos de metil-aril o heteroaril-amida sustituida
GT200800258A (es) Compuestos de pirrolo-pirimidina y sus usos
GT200300097A (es) Inhibidores de metaloproteinasa de triaril-oxi-aril-espiro-pirimidina-2,4,6-triona
GT200500103A (es) 4-fenilamino-quinazolin-6-il-amidas
GT200600246A (es) Formulacion de 1-[(3-hidroxi-adamant-1-ilamino)-acetil]-pirrolidin-2(s)-carbonitrilo de liberacion modificada
GT200300226A (es) 4-piperazinilbencenosulfonilindoles y usos de los mismos
GT200200220A (es) Nuevos derivados de pirrolidina
GT200400133AA (es) Derivados de pirrolo[3,4-c] pirazol, activos como inhibidores de quinasa, proceso para su preparacion y composiciones farmaceuticas que los comprenden. (solicitud fraccionaria no. 1, derivada de la patente no. pi-2004-0133).
GT200500008A (es) Intermediarios de quinolina como inhibidores de receptores de tirosina quinasas y la sintesis de los mismos
GT200200027A (es) Pirimidinas biciclicas como inhibidores de metaloproteinasas de matriz
GT200100148A (es) Derivados de 4-fenil-piridina.
GT200300284A (es) Derivados de 3h-quinazolin-4-ona
GT200400117A (es) Derivados de imidazol
GT200400188A (es) 5-arilpirimidinas como agentes anticancerigenos
GT200200280A (es) Lactamas como antagonistas de taquiquininas
GT200500292A (es) Derivados de 2-amido-4-feniltiazol, su preparacion y su aplicacion en terapeutica
GT200300082A (es) Inhibidores triariloxiariloxipirimidina-2,4,6-triona de metaloproteinasa