BR0013113A - Piridazinas substituìdas e piridazinas fundidas com atividade inibidora da angiogênese - Google Patents
Piridazinas substituìdas e piridazinas fundidas com atividade inibidora da angiogêneseInfo
- Publication number
- BR0013113A BR0013113A BR0013113-0A BR0013113A BR0013113A BR 0013113 A BR0013113 A BR 0013113A BR 0013113 A BR0013113 A BR 0013113A BR 0013113 A BR0013113 A BR 0013113A
- Authority
- BR
- Brazil
- Prior art keywords
- pyridazines
- substituted
- fused
- angiogenesis
- inhibiting activity
- Prior art date
Links
- 150000004892 pyridazines Chemical class 0.000 title abstract 5
- 230000033115 angiogenesis Effects 0.000 title abstract 4
- 230000002401 inhibitory effect Effects 0.000 title abstract 3
- 239000000463 material Substances 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 241000124008 Mammalia Species 0.000 abstract 1
- 230000002159 abnormal effect Effects 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
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
- C07D401/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
-
- 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
- A61P17/06—Antipsoriatics
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic 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
- C07D417/14—Heterocyclic 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Ophthalmology & Optometry (AREA)
- Dermatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Patente de Invenção: "PIRIDAZINAS SUBSTITUìDAS E PIRIDAZINAS FUNDIDAS COM ATIVIDADE INIBIDORA DA ANGIOGêNESE". Piridazinas substituídas e fundidas tendo atividade de inibição da angiogênese e fórmula estrutural generalizada (I) em que o anel contendo A, B, D, E e L é um heterociclo contendo nitrogênio; grupos X e Y podem ser qualquer um de uma variedade de unidades de articulação definidas; R^ 1^ e R^ 2^ podem ser substituintes independentes definidos ouo juntos podem ser uma ponte de definição do anel; o anel J pode ser um grupo de arila, piridila ou cicloalquila; e os grupos G podem ser qualquer um de uma variedade de substituintes definidos. As composições farmacêuticas contendo estes materiais, e métodos de tratamento de um mamífero tendo uma condição caracterizada por angiogênese anormal ou processos de hipermeabilidade usando estes materiais são também apresentados.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37132299A | 1999-08-10 | 1999-08-10 | |
| PCT/US2000/021579 WO2001010859A1 (en) | 1999-08-10 | 2000-08-08 | Substituted pyridazines and fused pyridazines with angiogenesis inhibiting activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BR0013113A true BR0013113A (pt) | 2002-04-30 |
Family
ID=23463486
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR0013113-0A BR0013113A (pt) | 1999-08-10 | 2000-08-08 | Piridazinas substituìdas e piridazinas fundidas com atividade inibidora da angiogênese |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP1208096B1 (pt) |
| JP (1) | JP2003506447A (pt) |
| KR (1) | KR20020019969A (pt) |
| CN (1) | CN1378543A (pt) |
| AR (1) | AR025068A1 (pt) |
| AT (1) | ATE265448T1 (pt) |
| AU (1) | AU775237B2 (pt) |
| BR (1) | BR0013113A (pt) |
| CA (1) | CA2381621A1 (pt) |
| CO (1) | CO5180637A1 (pt) |
| DE (1) | DE60010280T2 (pt) |
| ES (1) | ES2219382T3 (pt) |
| IL (1) | IL147885A0 (pt) |
| MX (1) | MXPA02001324A (pt) |
| NO (1) | NO20020569L (pt) |
| NZ (1) | NZ517087A (pt) |
| PE (1) | PE20010494A1 (pt) |
| WO (1) | WO2001010859A1 (pt) |
| ZA (1) | ZA200200691B (pt) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6689883B1 (en) | 1999-09-28 | 2004-02-10 | Bayer Pharmaceuticals Corporation | Substituted pyridines and pyridazines with angiogenesis inhibiting activity |
| CO5200835A1 (es) * | 1999-09-28 | 2002-09-27 | Bayer Corp | Piridinas y piridacinas sustituidas con actividad de inhibicion de angiogenesis |
| US7977333B2 (en) | 2000-04-20 | 2011-07-12 | Bayer Healthcare Llc | Substituted pyridines and pyridazines with angiogenesis inhibiting activity |
| GB0111078D0 (en) | 2001-05-04 | 2001-06-27 | Novartis Ag | Organic compounds |
| SI1427420T1 (sl) * | 2001-09-12 | 2006-12-31 | Novartis Ag | Uporaba kombinacije, ki vsebuje 4-piridilmetilftalazine za zdravljenje raka |
| MXPA04005561A (es) * | 2001-12-21 | 2004-12-06 | Bayer Pharmaceuticals Corp | Terapias de combinacion anti-angiogenesis que comprenden derivados de piridazina o piridina. |
| US7015227B2 (en) | 2002-06-21 | 2006-03-21 | Cgi Pharmaceuticals, Inc. | Certain amino-substituted monocycles as kinase modulators |
| WO2004028542A1 (en) * | 2002-09-24 | 2004-04-08 | Novartis Ag | Use of 4-pyridylmethyl-phthalazine derivatives for the manufacture of a medicament for the treatment of myelodysplastic syndromes |
| US20060058313A1 (en) * | 2002-11-12 | 2006-03-16 | Hohneker John A | Treatment of mesothelioma |
| GB0612721D0 (en) | 2006-06-27 | 2006-08-09 | Novartis Ag | Organic compounds |
| EP2137177B1 (en) | 2007-04-05 | 2014-05-07 | Amgen, Inc | Aurora kinase modulators and method of use |
| PL2167549T3 (pl) | 2007-06-19 | 2013-03-29 | Rynel Inc | Materiały zawierające cząstki polimeru rozpuszczalnego w wodzie oraz sposoby ich wytwarzania i stosowania |
| MX2010010151A (es) | 2008-03-20 | 2010-10-25 | Amgen Inc | Moduladores de cinasa aurora y metodo de uso. |
| AU2009279760B2 (en) * | 2008-08-04 | 2012-07-12 | Amgen Inc. | Aurora kinase modulators and methods of use |
| US9126935B2 (en) | 2008-08-14 | 2015-09-08 | Amgen Inc. | Aurora kinase modulators and methods of use |
| JP2024505256A (ja) * | 2021-01-28 | 2024-02-05 | ユニバーシティ オブ フロリダ リサーチファウンデーション インコーポレイティッド | 神経変性、変性及び代謝性障害の処置のための化合物並びにその使用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1293565A (en) * | 1969-05-03 | 1972-10-18 | Aspro Nicholas Ltd | Aminophthalazines and pharmaceutical compositions thereof |
| JPH03106875A (ja) * | 1989-09-20 | 1991-05-07 | Morishita Pharmaceut Co Ltd | 1―(3―ピリジルメチル)フタラジン誘導体 |
| JPH0673022A (ja) * | 1992-08-27 | 1994-03-15 | Kumiai Chem Ind Co Ltd | ピリミジンまたはトリアジン誘導体及び除草剤 |
| HU219864B (hu) * | 1994-08-09 | 2001-08-28 | Eisai Co., Ltd. | cGMP-PDE inhibitor kondenzált piridazinszármazékok és alkalmazásuk |
| JP3919835B2 (ja) * | 1994-08-09 | 2007-05-30 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 縮合ピリダジン系化合物 |
| CO4950519A1 (es) * | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
| DE60028740T2 (de) * | 1999-03-30 | 2007-05-24 | Novartis Ag | Phthalazinderivate zur behandlung von entzündlichen erkrankungen |
-
2000
- 2000-08-07 AR ARP000104073A patent/AR025068A1/es unknown
- 2000-08-08 NZ NZ517087A patent/NZ517087A/en unknown
- 2000-08-08 CO CO00059237A patent/CO5180637A1/es unknown
- 2000-08-08 ES ES00957317T patent/ES2219382T3/es not_active Expired - Lifetime
- 2000-08-08 JP JP2001515668A patent/JP2003506447A/ja active Pending
- 2000-08-08 EP EP00957317A patent/EP1208096B1/en not_active Expired - Lifetime
- 2000-08-08 DE DE60010280T patent/DE60010280T2/de not_active Expired - Lifetime
- 2000-08-08 AT AT00957317T patent/ATE265448T1/de not_active IP Right Cessation
- 2000-08-08 BR BR0013113-0A patent/BR0013113A/pt not_active IP Right Cessation
- 2000-08-08 AU AU68954/00A patent/AU775237B2/en not_active Ceased
- 2000-08-08 KR KR1020027001797A patent/KR20020019969A/ko not_active Ceased
- 2000-08-08 IL IL14788500A patent/IL147885A0/xx unknown
- 2000-08-08 WO PCT/US2000/021579 patent/WO2001010859A1/en not_active Ceased
- 2000-08-08 CN CN00814059A patent/CN1378543A/zh active Pending
- 2000-08-08 PE PE2000000799A patent/PE20010494A1/es not_active Application Discontinuation
- 2000-08-08 CA CA002381621A patent/CA2381621A1/en not_active Abandoned
- 2000-08-08 MX MXPA02001324A patent/MXPA02001324A/es active IP Right Grant
-
2002
- 2002-01-25 ZA ZA200200691A patent/ZA200200691B/en unknown
- 2002-02-05 NO NO20020569A patent/NO20020569L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20020569D0 (no) | 2002-02-05 |
| MXPA02001324A (es) | 2002-07-22 |
| EP1208096A1 (en) | 2002-05-29 |
| ES2219382T3 (es) | 2004-12-01 |
| DE60010280T2 (de) | 2009-10-15 |
| AU775237B2 (en) | 2004-07-22 |
| NO20020569L (no) | 2002-04-10 |
| IL147885A0 (en) | 2002-08-14 |
| WO2001010859A1 (en) | 2001-02-15 |
| ATE265448T1 (de) | 2004-05-15 |
| JP2003506447A (ja) | 2003-02-18 |
| AR025068A1 (es) | 2002-11-06 |
| KR20020019969A (ko) | 2002-03-13 |
| CO5180637A1 (es) | 2002-07-30 |
| CN1378543A (zh) | 2002-11-06 |
| ZA200200691B (en) | 2003-10-29 |
| CA2381621A1 (en) | 2001-02-15 |
| NZ517087A (en) | 2004-05-28 |
| AU6895400A (en) | 2001-03-05 |
| DE60010280D1 (de) | 2004-06-03 |
| EP1208096B1 (en) | 2004-04-28 |
| PE20010494A1 (es) | 2001-06-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BR0013113A (pt) | Piridazinas substituìdas e piridazinas fundidas com atividade inibidora da angiogênese | |
| BRPI0014382B8 (pt) | piridinas e piridazinas substituídas com atividade de inibição de angiogênese bem como composições farmacêuticas compreendendo os mesmos | |
| BR9810137A (pt) | Composto, composição farmacêutica e método de tratamento ou prevenção de uma desordem tromoboembólica | |
| WO2001019798A3 (en) | Inhibitors of factor xa | |
| WO2001019788A3 (en) | BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa | |
| WO2000071510A3 (en) | INHIBITORS OF FACTOR Xa | |
| NO953967L (no) | Indolderivater som 5-HT1A og/eller 5-HT2 ligander | |
| BR9803497A (pt) | Compostos, composições farmacêuticas, e processos para preparar os compostos e as composições e para tratar distúrbio do sistema nervoso central. | |
| FR2674856B1 (fr) | Nouveaux antihistaminiques non sedatifs, derives de benzimidazole, leur procede de preparation et leur utilisation en tant que medicaments. | |
| DE69118198D1 (de) | Substituierte tetrahydropyridine und hydroxypiperidine als mittel zur behandlung des zentralen nervensystems | |
| ES2196308T3 (es) | Derivado de 2-cianoiminoimidazol que inhiben la pde iv. | |
| DE69433148D1 (de) | Tricyclische kondensierte heterocyclische Verbindungen zur Behandlung von seniler Demenz | |
| BR9811557A (pt) | Derivados do 2-)4-aril ou heteroaril-piperazin-1-ilmetil)-1h-indol | |
| NO180780C (no) | Pyridonkarboksylsyrederivat | |
| DK0450420T3 (da) | Heterocyclisk substituerede dihydropyridiner, fremgangsmåde til deres fremstilling og deres anvendelse i lægemidler | |
| NO975681L (no) | Benzisoxazol- og indazol-derivater som antipsykotiske midler | |
| NO923686L (no) | Substituerte pyridinylamino-1h-indoler, 1h-indazoler, 2h-indazoler, benzo(b)-thiofener og 1,2-benzisotiazoler, en fremgangsmaate for deres fremstilling og deres anvendelse som legemidler | |
| RU93045711A (ru) | Нейролептические пергидро-1h-пиридо(1,2-a)пиразины, способ их получения, фармацевтическая композиция, способ лечения | |
| BR9814188A (pt) | "agonistas de 5-ht1f" | |
| FI964436A0 (fi) | Uudet hydroksiimijohdannaiset, niitä sisältävät farmaseuttiset koostumukset sekä menetelmä niiden valmistamiseksi | |
| ATE244258T1 (de) | Halo-derivate von 9-deoxo-9a-aza-9a- homerythromycin a | |
| CA2334012A1 (en) | 2-aminopyridines containing fused ring substituents as nitric oxide synthase inhibitors | |
| BR0010673A (pt) | Compostos substituìdos de benzolactamas | |
| DK164057C (da) | Oe5,6aa-cis-1,3-oxathianderivater og fremgangsmaade til deres fremstilling og farmaceutisk middel indeholdende et saadant derivat | |
| ATE190316T1 (de) | Peptid-aldehydderivate als antikoagulierende mittel |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 7A, 8A E 9A ANUIDADES |
|
| B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 DA RPI 2008 DE 30/06/2009. |