CO5031285A1 - Triarilimidazoles - Google Patents
TriarilimidazolesInfo
- Publication number
- CO5031285A1 CO5031285A1 CO00026001A CO00026001A CO5031285A1 CO 5031285 A1 CO5031285 A1 CO 5031285A1 CO 00026001 A CO00026001 A CO 00026001A CO 00026001 A CO00026001 A CO 00026001A CO 5031285 A1 CO5031285 A1 CO 5031285A1
- Authority
- CO
- Colombia
- Prior art keywords
- triarilimidazoles
- andone
- 6alkyl
- chr
- pharmaceuticals
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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 two hetero rings
- C07D401/04—Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic 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
- C07D413/04—Heterocyclic 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
Abstract
Un compuesto de la fórmula (I) o una sal farmacéuticamenteaceptable del mismo:en la que R1 es naftilo, antracenilo, o fenilo opcionalmente sustituido con uno o más sustituyentes seleccionados del grupo constituido por halo, alcoxi C1-6 , alquil C1-6 -tio, alquilo C1-6 , -O-(CH2 )n -Ph, -S-(CH2 )n -Ph, ciano, fenilo y CO2 R, en donde R es hidrógeno o alquilo C1-6 y n es 0, 1, 2 ó 3; o R1 es fenilo condensado con un anillo cíclico aromático o no aromático de 5-7 miembros, en donde dicho anillo cíclico contiene opcionalmente hasta dos heteroátomos, seleccionados independientemente entre N, O y S;R2 es H, NH(CH2 )n -Ph o NH-alquilo C1-6 , en donde n es 0, 1, 2 ó 3;R3 es CO2 H, CONH2 , CN, NO2 , alquil C1-6 -tio, SO2 -alquilo C1-6 , alcoxi C1-6 , SONH2 , CONHOH, NH2 , CHO, CH2 OH, CH2 NH2 ó CO2 R, en donde R es hidrógeno o alquilo C1-6 ; y uno de X1 y X2 es N o CR´; y el otro es NR´ o CHR´ en donde R´ es hidrógeno, OH, alquilo C1-6 o cicloalquilo C3-7 ; o cuando uno de X1 y X2 es N o CR´ , entonces el otro puede ser S u O.Un método para inhibir la ruta que produce señales por medio de TGF-ß en mamíferos, que comprende administrar a un mamífero que necesita de dicho tratamiento, una cantidad terapéuticamente eficaz de un compuesto según una cualquiera de las reivindicaciones 1 a 8, o una de sus sales farmacéuticamente aceptables.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12868799P | 1999-04-09 | 1999-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO5031285A1 true CO5031285A1 (es) | 2001-04-27 |
Family
ID=22436501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO00026001A CO5031285A1 (es) | 1999-04-09 | 2000-04-10 | Triarilimidazoles |
Country Status (9)
Country | Link |
---|---|
US (1) | US6465493B1 (es) |
EP (1) | EP1169317B1 (es) |
JP (1) | JP2002541253A (es) |
AT (1) | ATE231143T1 (es) |
AU (1) | AU4798000A (es) |
CO (1) | CO5031285A1 (es) |
DE (1) | DE60001229T2 (es) |
ES (1) | ES2187473T3 (es) |
WO (1) | WO2000061576A1 (es) |
Families Citing this family (62)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0007405D0 (en) * | 2000-03-27 | 2000-05-17 | Smithkline Beecham Corp | Compounds |
AU2000250285B2 (en) * | 2000-05-19 | 2006-05-04 | The Government Of The United States Of America, Represented By The Secretary Of The Department Of Health And Human Services | Inhibition of SMAD3 to prevent fibrosis and improve wound healing |
JP2004517068A (ja) * | 2000-11-16 | 2004-06-10 | スミスクライン・ビーチャム・コーポレイション | 化合物 |
GB0100762D0 (en) * | 2001-01-11 | 2001-02-21 | Smithkline Beecham Plc | Novel use |
GB0102672D0 (en) * | 2001-02-02 | 2001-03-21 | Glaxo Group Ltd | Compounds |
GB0102665D0 (en) * | 2001-02-02 | 2001-03-21 | Glaxo Group Ltd | Compounds |
UA76461C2 (en) | 2001-05-24 | 2006-08-15 | Lilly Co Eli | Pyrrazole derivatives as pharmaceutical agents, use thereof, a pharmaceutical composition on their basis |
GB0127430D0 (en) * | 2001-11-15 | 2002-01-09 | Smithkline Beecham Corp | Compounds |
AR039241A1 (es) * | 2002-04-04 | 2005-02-16 | Biogen Inc | Heteroarilos trisustituidos y metodos para su produccion y uso de los mismos |
EP1554272B1 (en) | 2002-08-09 | 2006-10-25 | Eli Lilly And Company | Benzimidazoles and benzothiazoles as inhibitors of map kinase |
UA80295C2 (en) | 2002-09-06 | 2007-09-10 | Biogen Inc | Pyrazolopyridines and using the same |
CN1681501A (zh) | 2002-09-18 | 2005-10-12 | 辉瑞产品公司 | 作为转化生长因子(tgf)抑制剂的吡唑衍生物 |
BR0314286A (pt) | 2002-09-18 | 2005-08-02 | Pfizer Prod Inc | Compostos de isotiazol e isoxazol como inibidores do fator de crescimento transformante (tgf) |
EA200500378A1 (ru) * | 2002-09-18 | 2005-08-25 | Пфайзер Продактс Инк. | Новые соединения имидазола в качестве ингибиторов трансформирующего фактора роста (tgf) |
PL375974A1 (en) | 2002-09-18 | 2005-12-12 | Pfizer Products Inc. | Triazole derivatives as transforming growth factor (tgf) inhibitors |
MXPA05002332A (es) * | 2002-09-18 | 2005-06-08 | Pfizer Prod Inc | Nuevos compuestos de oxazol y tiazol como inhibidores del factor de crecimiento transformador (tgf). |
US20040192583A1 (en) * | 2002-12-19 | 2004-09-30 | Satyanarayana Medicherla | Treatment of obesity and associated conditions with TGF-beta inhibitors |
AU2003300099A1 (en) * | 2003-01-02 | 2004-07-29 | Millennium Pharmaceuticals, Inc. | COMPOSITIONS AND METHODS FOR INHIBITING TGF-Beta |
PA8595001A1 (es) | 2003-03-04 | 2004-09-28 | Pfizer Prod Inc | Nuevos compuestos heteroaromaticos condensados que son inhibidores del factor de crecimiento transforante (tgf) |
JPWO2004108160A1 (ja) * | 2003-06-05 | 2006-07-27 | 日本新薬株式会社 | 骨形成促進増強剤及びそのスクリーニング方法 |
CA2539162A1 (en) * | 2003-09-17 | 2005-03-31 | Sumitomo Chemical Company, Limited | Cinnamoyl derivatives and use thereof |
JP4815773B2 (ja) * | 2003-09-17 | 2011-11-16 | 住友化学株式会社 | シンナモイル化合物及びその用途 |
JP2006104061A (ja) * | 2003-09-17 | 2006-04-20 | Sumitomo Chemical Co Ltd | シンナモイル化合物含有i型コラーゲン遺伝子転写抑制組成物。 |
RU2367661C2 (ru) | 2004-03-05 | 2009-09-20 | Тайсо Фармасьютикал Ко., Лтд. | Производные тиазола |
US20080319012A1 (en) | 2004-04-21 | 2008-12-25 | In2Gen Co., Ltd. | 2-Pyridyl substituted imidazoles as ALK5 and/or ALK4 inhibitors |
KR100749566B1 (ko) * | 2004-04-21 | 2007-08-16 | 이화여자대학교 산학협력단 | Alk5 및/또는 alk4 억제제로 유효한 2-피리딜이치환된 이미다졸 유도체 |
US7429604B2 (en) * | 2004-06-15 | 2008-09-30 | Bristol Myers Squibb Company | Six-membered heterocycles useful as serine protease inhibitors |
JP2008506787A (ja) * | 2004-07-29 | 2008-03-06 | シェーリング−プラウ・リミテッド | 動物においてミオスタチン活性を調節または阻害して赤身組織の成長増加を導くalk5インヒビターの使用 |
WO2007011626A2 (en) | 2005-07-14 | 2007-01-25 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
KR100694181B1 (ko) * | 2005-11-25 | 2007-03-12 | 연세대학교 산학협력단 | 근원세포 또는 근섬유로부터 신경세포 분화를 유도하는화합물, 이를 포함하는 약학적 조성물, 신경세포 분화를유도하는 방법 및 신경세포 분화를 유도하는 화합물을검색하는 스크리닝 방법 |
WO2008066626A2 (en) | 2006-10-25 | 2008-06-05 | The Rockefeller University | METHODS FOR THE TREATMENT OF Aβ RELATED DISORDERS AND COMPOSITIONS THEREFOR |
WO2008071605A2 (en) * | 2006-12-15 | 2008-06-19 | F. Hoffmann-La Roche Ag | Methods of treating inflammatory diseases |
EP2108017A2 (en) * | 2007-01-30 | 2009-10-14 | Biogen Idec MA, Inc. | Imidazolone compounds as tgf-beta family type i receptors, alk5 and/or alk4 antagonists |
WO2008136739A1 (en) * | 2007-05-04 | 2008-11-13 | Jana Pickova | Compound feed for aquaculture |
GB0715087D0 (en) | 2007-08-03 | 2007-09-12 | Summit Corp Plc | Drug combinations for the treatment of duchenne muscular dystrophy |
RS55735B1 (sr) | 2007-08-03 | 2017-07-31 | Summit (Oxford) Ltd | Kombinacije lekova za lečenje dišenove mišićne distrofije |
WO2009047163A1 (en) * | 2007-10-10 | 2009-04-16 | F. Hoffmann-La Roche Ag | Methods of treating inflammatory diseases |
AU2012203026B2 (en) * | 2008-03-21 | 2014-06-12 | Novartis Ag | Novel heterocyclic compounds and uses thereof |
US8865732B2 (en) | 2008-03-21 | 2014-10-21 | Novartis Ag | Heterocyclic compounds and uses thereof |
US8080568B1 (en) | 2010-06-29 | 2011-12-20 | Ewha University - Industry Collaboration Foundation | 2-pyridyl substituted imidazoles as therapeutic ALK5 and/or ALK4 inhibitors |
US8513222B2 (en) | 2010-06-29 | 2013-08-20 | EWHA University—Industry Collaboration Foundation | Methods of treating fibrosis, cancer and vascular injuries |
USRE47141E1 (en) | 2010-06-29 | 2018-11-27 | EWHA University—Industry Collaboration Foundation | Methods of treating fibrosis, cancer and vascular injuries |
US9446175B2 (en) * | 2011-06-03 | 2016-09-20 | Yale University | Compositions and methods for treating and preventing neointimal stenosis |
TR201808033T4 (tr) | 2011-07-13 | 2018-06-21 | Tiumbio Co Ltd | Alk5 ve veya alk4 inhibitörleri olarak 2 pridil ikameli imidazollar. |
DK2855665T3 (da) | 2012-05-30 | 2019-11-04 | Univ Cornell | Tilvejebringelse af funktionelle og bestandige endotele celler fra humane amnionvæske-afledte celler |
ES2791778T3 (es) | 2012-08-01 | 2020-11-05 | Ikaika Therapeutics Llc | Mitigación del daño tisular y la fibrosis a través de anticuerpos anti-LTBP4 |
CN105229144A (zh) | 2013-02-22 | 2016-01-06 | 细胞动力学国际有限公司 | 通过组合的遗传工程和化学工程经由正向编程产生肝细胞 |
US9242969B2 (en) | 2013-03-14 | 2016-01-26 | Novartis Ag | Biaryl amide compounds as kinase inhibitors |
US10961531B2 (en) | 2013-06-05 | 2021-03-30 | Agex Therapeutics, Inc. | Compositions and methods for induced tissue regeneration in mammalian species |
WO2015106158A1 (en) | 2014-01-09 | 2015-07-16 | Intra-Cellular Therapies, Inc. | Organic compounds |
US11078462B2 (en) | 2014-02-18 | 2021-08-03 | ReCyte Therapeutics, Inc. | Perivascular stromal cells from primate pluripotent stem cells |
KR102346489B1 (ko) | 2014-04-18 | 2021-12-31 | 교토후고리츠다이가쿠호진 | 골아 세포의 조제 방법 및 골아 세포 유도제 |
WO2015164228A1 (en) | 2014-04-21 | 2015-10-29 | Cellular Dynamics International, Inc. | Hepatocyte production via forward programming by combined genetic and chemical engineering |
US10240127B2 (en) | 2014-07-03 | 2019-03-26 | ReCyte Therapeutics, Inc. | Exosomes from clonal progenitor cells |
UY36294A (es) | 2014-09-12 | 2016-04-29 | Novartis Ag | Compuestos y composiciones como inhibidores de quinasa |
US11541149B2 (en) | 2015-12-11 | 2023-01-03 | Research Institute At Nationwide Children's Hospital | Systems and methods for optimized patient specific tissue engineering vascular grafts |
CN113347990A (zh) | 2018-12-21 | 2021-09-03 | 西北大学 | 膜联蛋白在预防和治疗肌膜损伤中的用途 |
WO2020139977A1 (en) | 2018-12-26 | 2020-07-02 | Northwestern University | Use of glucocorticoid steroids in preventing and treating conditions of muscle wasting, aging and metabolic disorder |
US20230090552A1 (en) | 2020-01-08 | 2023-03-23 | Synthis Therapeutics, Inc. | Alk5 inhibitor conjugates and uses thereof |
JP2023533850A (ja) | 2020-07-15 | 2023-08-04 | キエシ・フアルマチエウテイチ・ソチエタ・ペル・アチオニ | Alk5阻害剤としてのピリドオキサジンアミノ誘導体 |
BR112023000588A8 (pt) | 2020-07-15 | 2023-05-09 | Chiesi Farm Spa | Derivados de piridazinil amino como inibidores de alk5 |
WO2023208986A1 (en) | 2022-04-27 | 2023-11-02 | Chiesi Farmaceutici S.P.A. | Imidazole derivatives as alk5 inhibitors |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB138101A (es) | ||||
CH561716A5 (es) * | 1971-05-10 | 1975-05-15 | Ciba Geigy Ag | |
US5656644A (en) | 1994-07-20 | 1997-08-12 | Smithkline Beecham Corporation | Pyridyl imidazoles |
DE69433501T2 (de) * | 1993-11-08 | 2004-11-04 | Smithkline Beecham Corp. | Oxazole zur behandlung von zytokinvermittelten erkrankungen |
US5776954A (en) | 1996-10-30 | 1998-07-07 | Merck & Co., Inc. | Substituted pyridyl pyrroles, compositions containing such compounds and methods of use |
WO1998022109A1 (en) | 1996-11-20 | 1998-05-28 | Merck & Co., Inc. | Triaryl substituted imidazoles as glucagon antagonists |
JPH11180958A (ja) * | 1997-12-24 | 1999-07-06 | Yamanouchi Pharmaceut Co Ltd | 新規アミン誘導体 |
-
2000
- 2000-04-06 DE DE60001229T patent/DE60001229T2/de not_active Expired - Fee Related
- 2000-04-06 EP EP00930101A patent/EP1169317B1/en not_active Expired - Lifetime
- 2000-04-06 ES ES00930101T patent/ES2187473T3/es not_active Expired - Lifetime
- 2000-04-06 US US09/958,639 patent/US6465493B1/en not_active Expired - Fee Related
- 2000-04-06 WO PCT/US2000/009147 patent/WO2000061576A1/en active IP Right Grant
- 2000-04-06 AU AU47980/00A patent/AU4798000A/en not_active Abandoned
- 2000-04-06 JP JP2000610849A patent/JP2002541253A/ja not_active Withdrawn
- 2000-04-06 AT AT00930101T patent/ATE231143T1/de not_active IP Right Cessation
- 2000-04-10 CO CO00026001A patent/CO5031285A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
US6465493B1 (en) | 2002-10-15 |
ES2187473T3 (es) | 2003-06-16 |
ATE231143T1 (de) | 2003-02-15 |
DE60001229T2 (de) | 2003-10-30 |
WO2000061576A1 (en) | 2000-10-19 |
DE60001229D1 (de) | 2003-02-20 |
EP1169317B1 (en) | 2003-01-15 |
EP1169317A1 (en) | 2002-01-09 |
JP2002541253A (ja) | 2002-12-03 |
AU4798000A (en) | 2000-11-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CO5031285A1 (es) | Triarilimidazoles | |
CO5280078A1 (es) | Compuestos | |
AP1614A (en) | New heterocyclic compounds, their preparation and their use as medicaments, in particular as anti-bacterial agents. | |
BG106586A (en) | Pyrazolopyramidines as therapeutic agents | |
MXPA03002911A (es) | Compuestos quimicos. | |
ATE416157T1 (de) | Inhibitoren von integrin alpha-v-beta-6 | |
MXPA02012076A (es) | Compuestos quimicos. | |
AU2001266575A1 (en) | Chemical compounds | |
TR200002605T2 (tr) | Nitrik oksit sentaz inhibitörleri olarak faydalı halojene amidino amino asit türevleri | |
GEP20053626B (en) | Substituted 8-Arylquinoline Phosphodiesterase-4 Inhibitors, Pharmaceutical Composition Containing Them and Use Thereof | |
WO2002062767A1 (fr) | Nouveaux derives de quinazoline | |
MY117092A (en) | Chemotherapeutic pyrrolocarbazole derivatives | |
TR200201128T2 (tr) | PDE4 inhibitörleri olarak tetrahidrotiyopiranfitalazinon türevleri. | |
CA2412596A1 (en) | Cyclic gmp-specific phosphodiesterase inhibitors | |
AU3626895A (en) | Quinazolinone pharmaceuticals and use thereof | |
TR200001909T2 (tr) | Matris metaloprotez inhibitörleri. | |
NO20022123L (no) | Osoksazolderivater for anvendelse som inhibitorer for fosfodiesterase VII | |
ATE213241T1 (de) | Amidin- und isothioharnstoffderivate als inhibitoren der stickstoffoxid-synthase | |
ATE330958T1 (de) | Pyrazino 1'2':1,6öpyrido 3,4-böindolderivate | |
HRP20010885B1 (en) | Ethanesulfonyl-piperidine derivatives | |
ATE286887T1 (de) | Antibakterielle mittel | |
TR200001122T2 (tr) | Farmasötikler olarak bifenil türevleri. | |
SE9901901D0 (sv) | Compounds | |
IL159493A0 (en) | Pharmaceutical formulation containing an ltb4 antagonist | |
SE9603284D0 (sv) | New compounds |