BR0013792A - Derivados de amino-triazolopiridina - Google Patents
Derivados de amino-triazolopiridinaInfo
- Publication number
- BR0013792A BR0013792A BR0013792-8A BR0013792A BR0013792A BR 0013792 A BR0013792 A BR 0013792A BR 0013792 A BR0013792 A BR 0013792A BR 0013792 A BR0013792 A BR 0013792A
- Authority
- BR
- Brazil
- Prior art keywords
- phenyl
- lower alkyl
- optionally substituted
- halogen
- lower alkoxy
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
-
- 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
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/24—Antidepressants
-
- 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
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- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- 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
- A61P9/10—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Hospice & Palliative Care (AREA)
- Addiction (AREA)
- Immunology (AREA)
- Psychology (AREA)
- Vascular Medicine (AREA)
- Anesthesiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Patente de Invenção: "DERIVADOS DE AMINO-TRIAZOLOPIRIDINA". A invenção refere-se a compostos de fórmula (I) em que R^ 1^ é um grupo de heteroarila de 5 ou 6 membros, contendo de 1 a 3 heteroátomos, selecionados de N, O ou S, e cujos grupos são opcionalmente substituídos por um ou dois substituintes, que são alquila inferior, -(CH~ 2~)~ n~OH, halogeno ou alcóxi inferior, e em que os grupos de heteroarila podem ser opcionalmente ligados ao anel de pirazol através de um grupo alquileno ou alquenila, ou é fenila, opcionalmente substituída por um ou dois substituintes sendo alquila inferior, alquila inferior de hidróxi, halogeno, hidróxi ou alcóxi inferior ou é -O(CH~ 2~)~ n~fenila, benzofurila, indolila ou benzotiofenila, ou é alquila S-inferior; R^ 2^ e R^ 4^ são independentemente um do outro hidrogênio, ciano ou S(O)~ 2~-fenila; R^ 3^ é hidrogênio, halogeno ou é um grupo heteroarila de 5 ou 6 membros, contendo de 1 a 3 heteroátomos, selecionados de N, O ou S, e cujos grupos são opcionalmente substituídos por um ou dois substituintes, que são alquila inferior, -(CH~ 2~)~ n~-arila, hidróxi, halogeno, alcóxi inferior, morfolinila, amino, alquilamino inferior ou -C(O)NR'~ 2~, e em que R' é alquila inferior ou hidrogênio, ou é fenila, opcionalmente substituída por um ou dois substituintes sendo halogeno, alquila inferior, alcóxi inferior, amino, di-alquil amino inferior, CF~ 3~, -OCF~ 3~, -NHC(O)alquila inferior, ciano, -C(O)-alquila inferior, -C(O)O-alquila inferior, -S-alquila inferior, -S(0)~ 2~NH-fenila, -S(0)~ 2~-metilpiperazinila; ou é -NR'R", em que R' e R" são independentemente um do outro hidrogênio, -(CH~ 2~)~ n~fenila, cujo anel de fenila é opcionalmente substituído por halogeno ou alcóxi inferior, -CH(alquila inferior)-fenila, indan-1-ila, 1,2,3,4-tetraidro-naftaleno, ou cicloalquila; ou é -O-fenila, cujo anel de fenila é opcionalmente substituído por halogeno, alquila inferior ou alcóxi inferior, -O-tetraidronaftalenila ou -O-CH~ 2~-6-metil-piridin-2-ila; ou é benzo[1,3]dioxolila, 1 H-indol-5-ila, naftila, benzofuran-2-ila, 1,3,4,9-tetraidrob-carbolin-2-ila, piperidin-1-ila, pirrolidin-1-ila, piperazin-4-il-metila ou morfolinila; R^ 5^ é -NR~ 2~, em que R pode ser o mesmo ou diferente e é hidrogênio, alquila inferior, fenila, benzila, alquila -CO-inferior, -CO-alcóxi inferior, alquenila inferior, -CO(CH~ 2~)~ n~-fenila ou -COO(CH~ 2~)~ n~-fenila, em que o anel de fenila é opcionalmente substituído por CF~ 3~, alcóxi inferior, halogeno ou alquila inferior, -CO(CH~ 2~)~ 3~-NHCO-alcóxi inferior, -(CH~ 2~)~ n~-fenila, em que o anel de fenila é opcionalmente substituído por alcóxi inferior, CF~ 3~ ou halogeno, ou é ácido 4,5-diidro-1H-imidazol-2-il-benzóico, ácido 1,4,5,6-tetraldro-pirimidin-2-il-benzóico ou ácido 4,5,6,7-tetraidro-1H-[1,3]diazepin-2-il-benzóico; n é de 0 a 4 e seus sais farmaceuticamente aceitáveis.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99117578 | 1999-09-06 | ||
PCT/EP2000/008372 WO2001017999A2 (en) | 1999-09-06 | 2000-08-28 | Amino-triazolopyridine derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
BR0013792A true BR0013792A (pt) | 2002-05-14 |
Family
ID=8238933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR0013792-8A BR0013792A (pt) | 1999-09-06 | 2000-08-28 | Derivados de amino-triazolopiridina |
Country Status (22)
Country | Link |
---|---|
US (1) | US6355653B1 (pt) |
EP (1) | EP1214322A2 (pt) |
JP (1) | JP2003528811A (pt) |
KR (1) | KR20020027625A (pt) |
CN (1) | CN1379777A (pt) |
AR (1) | AR037484A1 (pt) |
AU (1) | AU7511000A (pt) |
BR (1) | BR0013792A (pt) |
CA (1) | CA2383998A1 (pt) |
CZ (1) | CZ20021220A3 (pt) |
HR (1) | HRP20020172A2 (pt) |
HU (1) | HUP0203316A3 (pt) |
IL (1) | IL148167A0 (pt) |
MA (1) | MA26816A1 (pt) |
MX (1) | MXPA02001748A (pt) |
NO (1) | NO20021077D0 (pt) |
PE (1) | PE20010629A1 (pt) |
PL (1) | PL354240A1 (pt) |
TR (1) | TR200200579T2 (pt) |
WO (1) | WO2001017999A2 (pt) |
YU (1) | YU13502A (pt) |
ZA (1) | ZA200201055B (pt) |
Families Citing this family (48)
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US6506772B1 (en) * | 2000-12-15 | 2003-01-14 | Hoffmann-La Roche Inc. | Substituted [1,2,4]triazolo[1,5a]pyridine derivatives with activity as adenosine receptor ligands |
US6514989B1 (en) | 2001-07-20 | 2003-02-04 | Hoffmann-La Roche Inc. | Aromatic and heteroaromatic substituted 1,2,4-triazolo pyridine derivatives |
BR0213172A (pt) * | 2001-10-08 | 2004-09-14 | Hoffmann La Roche | Amida do ácido 8-amino-[1,2,4]triazolo[1,5-a]piridina-6-carboxìlico |
US6693116B2 (en) * | 2001-10-08 | 2004-02-17 | Hoffmann-La Roche Inc. | Adenosine receptor ligands |
ES2283625T3 (es) | 2001-11-30 | 2007-11-01 | Schering Corporation | Antagonistas del receptopr a2a de adenosina de (1,2,4)-triazol biciclicos. |
HUP0105407A3 (en) * | 2001-12-21 | 2004-04-28 | Sanofi Aventis | Triazolo[1,5-a]quinolin derivatives, process for their preparation, pharmaceutical compositions thereof and intermediates |
PT2260850T (pt) | 2002-01-28 | 2018-10-24 | Kyowa Hakko Kogyo Kk | Antagonistas do recetor de a2a para utilização no tratamento de distúrbios de movimento |
MXPA04012566A (es) * | 2002-06-13 | 2005-04-19 | Pfizer | Agentes no peptidicos reguladores de la gnrh, composiciones farmaceuticas y procedimientos para su uso. |
WO2005070927A2 (en) * | 2004-01-26 | 2005-08-04 | Altana Pharma Ag | 1,2,4-triazolo[1,5-a] pyridines as gastric acid secretion inhibitors |
JP2008524330A (ja) | 2004-12-21 | 2008-07-10 | シェーリング コーポレイション | ピラゾロ[1,5−A]ピリミジンアデノシンA2a受容体アンタゴニスト |
ES2273599B1 (es) | 2005-10-14 | 2008-06-01 | Universidad De Barcelona | Compuestos para el tratamiento de la fibrilacion auricular. |
JP5448164B2 (ja) * | 2006-07-28 | 2014-03-19 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を変調する化合物 |
US7928123B2 (en) * | 2006-09-25 | 2011-04-19 | Boehringer Ingelheim International Gmbh | Compounds which modulate the CB2 receptor |
EP2096923B1 (en) * | 2006-11-27 | 2014-01-22 | H. Lundbeck A/S | Heteroaryl amide derivatives |
DE602007012133D1 (de) | 2006-12-01 | 2011-03-03 | Andrew Burritt | Triazolopyridinverbindungen zur behandlung von degenerations- und entzündungskrankheiten |
MY148461A (en) * | 2007-04-10 | 2013-04-30 | Lundbeck & Co As H | Heteroaryl amide analogues as p2x7 antagonists |
WO2009017954A1 (en) * | 2007-08-01 | 2009-02-05 | Phenomix Corporation | Inhibitors of jak2 kinase |
GB0719803D0 (en) | 2007-10-10 | 2007-11-21 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
WO2009061652A1 (en) * | 2007-11-07 | 2009-05-14 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
US20120015988A1 (en) * | 2008-05-13 | 2012-01-19 | Boehringer Ingelheim International Gmbh | Sulfone Compounds Which Modulate The CB2 Receptor |
WO2009155551A1 (en) * | 2008-06-20 | 2009-12-23 | Genentech, Inc. | Triazolopyridine jak inhibitor compounds and methods |
CN102131390A (zh) | 2008-06-20 | 2011-07-20 | 健泰科生物技术公司 | ***并吡啶jak抑制剂化合物和方法 |
JP5749162B2 (ja) * | 2008-07-10 | 2015-07-15 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を調節するスルホン化合物 |
TWI453207B (zh) * | 2008-09-08 | 2014-09-21 | Signal Pharm Llc | 胺基***并吡啶,其組合物及使用其之治療方法 |
AP2011005674A0 (en) | 2008-09-25 | 2011-04-30 | Boehringer Ingelheim Int | Sulfonyl compounds which selectively modulate the CB2 receptor. |
MY153913A (en) * | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
WO2010141796A2 (en) | 2009-06-05 | 2010-12-09 | Cephalon, Inc. | PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a] PYRIDINE DERIVATIVES |
US8299103B2 (en) * | 2009-06-15 | 2012-10-30 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the CB2 receptor |
WO2010147791A1 (en) | 2009-06-16 | 2010-12-23 | Boehringer Ingelheim International Gmbh | Azetidine 2 -carboxamide derivatives which modulate the cb2 receptor |
US8283465B2 (en) * | 2009-07-17 | 2012-10-09 | Japan Tobacco Inc. | Triazolopyridine compound, and action thereof as prolyl hydroxylase inhibitor or erythropoietin production-inducing agent |
WO2011037795A1 (en) * | 2009-09-22 | 2011-03-31 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the cb2 receptor |
EP2523936A1 (en) | 2010-01-15 | 2012-11-21 | Boehringer Ingelheim International GmbH | Compounds which modulate the cb2 receptor |
US8329735B2 (en) | 2010-03-05 | 2012-12-11 | Boehringer Ingelheim International Gmbh | Tetrazole compounds which selectively modulate the CB2 receptor |
EP2595959B1 (en) | 2010-07-22 | 2015-11-04 | Boehringer Ingelheim International GmbH | Sulfonyl compounds which modulate the cb2 receptor |
JP2014526533A (ja) * | 2011-09-19 | 2014-10-06 | エフ.ホフマン−ラ ロシュ アーゲー | Pde10a阻害剤としてのトリアゾロピリジン化合物 |
EP2757882B1 (en) | 2011-09-22 | 2020-11-04 | Merck Sharp & Dohme Corp. | Imidazopyridyl compounds as aldosterone synthase inhibitors |
US9193724B2 (en) * | 2011-09-22 | 2015-11-24 | Merck Sharp & Dohme Corp. | Triazolopyridyl compounds as aldosterone synthase inhibitors |
EP2803668A1 (en) | 2013-05-17 | 2014-11-19 | Boehringer Ingelheim International Gmbh | Novel (cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles |
TW201808906A (zh) | 2016-03-16 | 2018-03-16 | 拜耳作物科學股份有限公司 | 作為殺蟲劑之經取代吡啶化合物 |
CN106543175B (zh) * | 2016-10-28 | 2018-06-01 | 上海大学 | 三芳基[1,2,4]三氮唑[1,5-a]吡啶衍生物及其制备方法 |
JP7111733B2 (ja) * | 2017-03-16 | 2022-08-02 | 江蘇恒瑞医薬股▲ふん▼有限公司 | ヘテロアリール[4,3-c]ピリミジン-5-アミン誘導体、その製造方法、およびその医薬の使用 |
AU2019227607C1 (en) | 2018-02-27 | 2023-07-20 | Incyte Corporation | Imidazopyrimidines and triazolopyrimidines as A2A / A2B inhibitors |
CA3100731A1 (en) | 2018-05-18 | 2019-11-21 | Incyte Corporation | Fused pyrimidine derivatives as a2a / a2b inhibitors |
WO2020010197A1 (en) * | 2018-07-05 | 2020-01-09 | Incyte Corporation | Fused pyrazine derivatives as a2a / a2b inhibitors |
WO2020054712A1 (ja) * | 2018-09-12 | 2020-03-19 | 日本化薬株式会社 | 有害生物防除剤 |
PE20220277A1 (es) | 2018-12-20 | 2022-02-25 | Incyte Corp | Compuestos de imidazopiridazina e imidazopiridina como inhibidores de quinasa-2 de tipo receptor de activina |
TWI829857B (zh) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | 作為a2a / a2b抑制劑之吡唑并吡啶及***并吡啶 |
CN115867553A (zh) * | 2021-01-09 | 2023-03-28 | 巴格沃克斯研究有限公司 | 作为腺苷2A受体和腺苷2B受体拮抗剂的二氨基吡唑[1,5-a]并嘧啶-6-腈化合物 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9226735D0 (en) | 1992-12-22 | 1993-02-17 | Ici Plc | Azole derivatives |
WO1999043678A1 (fr) | 1998-02-24 | 1999-09-02 | Kyowa Hakko Kogyo Co., Ltd. | Medicaments et prophylaxie contre la maladie de parkinson |
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2000
- 2000-08-24 US US09/645,127 patent/US6355653B1/en not_active Expired - Fee Related
- 2000-08-28 CZ CZ20021220A patent/CZ20021220A3/cs unknown
- 2000-08-28 PL PL00354240A patent/PL354240A1/xx not_active Application Discontinuation
- 2000-08-28 EP EP00964043A patent/EP1214322A2/en not_active Withdrawn
- 2000-08-28 WO PCT/EP2000/008372 patent/WO2001017999A2/en not_active Application Discontinuation
- 2000-08-28 CN CN00812501A patent/CN1379777A/zh active Pending
- 2000-08-28 CA CA002383998A patent/CA2383998A1/en not_active Abandoned
- 2000-08-28 KR KR1020027002990A patent/KR20020027625A/ko not_active Application Discontinuation
- 2000-08-28 AU AU75110/00A patent/AU7511000A/en not_active Abandoned
- 2000-08-28 MX MXPA02001748A patent/MXPA02001748A/es unknown
- 2000-08-28 IL IL14816700A patent/IL148167A0/xx unknown
- 2000-08-28 JP JP2001522222A patent/JP2003528811A/ja active Pending
- 2000-08-28 HU HU0203316A patent/HUP0203316A3/hu unknown
- 2000-08-28 YU YU13502A patent/YU13502A/sh unknown
- 2000-08-28 BR BR0013792-8A patent/BR0013792A/pt not_active IP Right Cessation
- 2000-08-28 TR TR2002/00579T patent/TR200200579T2/xx unknown
- 2000-09-04 AR ARP000104612A patent/AR037484A1/es not_active Application Discontinuation
- 2000-09-04 PE PE2000000903A patent/PE20010629A1/es not_active Application Discontinuation
-
2002
- 2002-02-06 ZA ZA200201055A patent/ZA200201055B/xx unknown
- 2002-02-26 HR HR20020172A patent/HRP20020172A2/hr not_active Application Discontinuation
- 2002-03-05 NO NO20021077A patent/NO20021077D0/no not_active Application Discontinuation
- 2002-03-06 MA MA26540A patent/MA26816A1/fr unknown
Also Published As
Publication number | Publication date |
---|---|
HUP0203316A3 (en) | 2004-07-28 |
PE20010629A1 (es) | 2001-05-30 |
IL148167A0 (en) | 2002-09-12 |
ZA200201055B (en) | 2003-07-30 |
AR037484A1 (es) | 2004-11-17 |
EP1214322A2 (en) | 2002-06-19 |
MXPA02001748A (es) | 2002-08-06 |
US6355653B1 (en) | 2002-03-12 |
MA26816A1 (fr) | 2004-12-20 |
YU13502A (sh) | 2004-11-25 |
CA2383998A1 (en) | 2001-03-15 |
JP2003528811A (ja) | 2003-09-30 |
CN1379777A (zh) | 2002-11-13 |
CZ20021220A3 (cs) | 2002-10-16 |
WO2001017999A3 (en) | 2001-12-06 |
NO20021077L (no) | 2002-03-05 |
HRP20020172A2 (en) | 2003-10-31 |
TR200200579T2 (tr) | 2002-12-23 |
KR20020027625A (ko) | 2002-04-13 |
NO20021077D0 (no) | 2002-03-05 |
HUP0203316A2 (hu) | 2003-01-28 |
AU7511000A (en) | 2001-04-10 |
WO2001017999A2 (en) | 2001-03-15 |
PL354240A1 (en) | 2003-12-29 |
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