BRPI0520554A2 - uso de uma benzodiazepina ou um sal farmaceuticamente aceitável do mesmo, método para tratar ou prevenir uma infecção por hcv em um paciente, derivado de benzodiazepina ou um sal famaceuticamente aceitável do mesmo, e, composição farmacêutica - Google Patents
uso de uma benzodiazepina ou um sal farmaceuticamente aceitável do mesmo, método para tratar ou prevenir uma infecção por hcv em um paciente, derivado de benzodiazepina ou um sal famaceuticamente aceitável do mesmo, e, composição farmacêuticaInfo
- Publication number
- BRPI0520554A2 BRPI0520554A2 BRPI0520554-9A BRPI0520554A BRPI0520554A2 BR PI0520554 A2 BRPI0520554 A2 BR PI0520554A2 BR PI0520554 A BRPI0520554 A BR PI0520554A BR PI0520554 A2 BRPI0520554 A2 BR PI0520554A2
- Authority
- BR
- Brazil
- Prior art keywords
- alkyl
- aryl
- pharmaceutically acceptable
- heterocyclyl
- heteroaryl
- Prior art date
Links
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1h-1,2-benzodiazepine Chemical compound N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 title abstract 4
- 150000003839 salts Chemical class 0.000 title abstract 4
- 229940049706 benzodiazepine Drugs 0.000 title abstract 2
- 208000015181 infectious disease Diseases 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000001072 heteroaryl group Chemical group 0.000 abstract 9
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000004452 carbocyclyl group Chemical group 0.000 abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000004001 thioalkyl group Chemical group 0.000 abstract 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 208000005176 Hepatitis C Diseases 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 208000010710 hepatitis C virus infection Diseases 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
- C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
- C07D243/18—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals substituted in position 2 by nitrogen, oxygen or sulfur atoms
- C07D243/24—Oxygen atoms
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
USO DE UMA BENZODIAZEPINA OU UM SAL FARMACEUTICAMENTE ACEITáVEL DO MESMO, MéTODO PARA TRATAR OU PREVENIR UMA INFECçãO POR HCV EM UM PACIENTE, DERIVADO DE BENZODIAZEPINA OU UM SAL FARMACEUTICAMENTE ACEITáVEL DO MESMO, E, COMPOSIçãO FARMACêUTICA. O uso de uma benzodiazepina da fórmula (1), ou um sal desta farmaceuticamente aceitável, na fabricação de um medicamento para o uso no tratamento ou prevenção de uma infecção por hepatite C, em que: - R representa alquila C~ 1-6~, arila ou heteroarila; - R^ 2^ representa hidrogénio ou alquila C~ 1-6~; - cada R é o mesmo ou diferente e representa halogênio, hidróxi, alquila C~ 1-6~, alcóxi C~ 1-6~, tioalquila C~ 1-6~, haloalquila C~ 1-6~, haloalcóxi C~ 1-6~, amino, mono(alquila C~ 1-6~)amino, di(alquila C~ 1-6~)amino, nitro, ciano, -CO~ 2~R', -CONR'R", -NH-CO-R', S(O)R', -S(O)~ 2~R', -NH-S(O)~ 2~R', -S(O)NR'R" ou .-S(O)~ 2~NR'R", em que cada R' e R" é o mesmo ou diferente e representa hidrogênio ou alquila C~ 1-6~; - n é de O a 3; - representa hidrogênio ou alquila C~ 1-6~; - R^ 5^ representa alquila C~ 1-6~, arila, heteroarila, carbociclila, heterociclila, aril-(alquila C~ 1-6~)-, heteroaril-(alquilaC~ 1-6~)-, carbociclil-(heterociclila C~ 1-6~-(alquila C~ 1-6~)-, aril-(hidroxialquila C~1-6~)-, heteroaril-(hidroxialquila C~ 1-6~)-, carbociclil-(hidroxialquila C~ 1-6~)-, heterociclil-(hidroxialquila C~ 1-6~)-, aril-C(O)-C(O)-, heteroaril-C(O)-C(O)-, carbociclil-C(O)-C(O)-, heterociclil-C(O)-C(O)- ou -XR; - X representa -CO-, -S(0)- ou -S(O)~ 2~-; e R^ 6^ representa alquila C~ 1-6~, hidróxi, alcóxi C~ 1-6~, tioalquila C~ 1-6~, arila, heteroarila, carbociclila, heterociclila, aril-(alquila C~ 1-6~)-, heteroaril -(alquilaC~ 1-6~)-, carbociclil-(alquila C~ 1-6~)-, heterocielil-(alquila C~ 1-6~)-, aril-(alquila C~ 1-6~)- O-, heteroaril-(alquila C~ 1-6~)-O-, carbociclil-(alquila C~ 1-6~)-O-, heterocielil(alquila C~ 1-6~)-O- ou -NTR'R" em que cada R' e R" é o mesmo ou diferente e representa hidrogênio, alquila C~ 1-6~, carbocielila, heterociclila, arila, heteroarila, aril-(heteroarila C~ 1-6~-(earbocielila C~ 1-6~-(alquila C~ 1-6~)- ou heterociclil-(alquila C~ 1-6~)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/GB2005/003597 WO2007034127A1 (en) | 2005-09-19 | 2005-09-19 | Benzodiazepine derivatives for treating hepatitis c infection |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0520554A2 true BRPI0520554A2 (pt) | 2009-06-13 |
Family
ID=36481315
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0520554-9A BRPI0520554A2 (pt) | 2005-09-19 | 2005-09-19 | uso de uma benzodiazepina ou um sal farmaceuticamente aceitável do mesmo, método para tratar ou prevenir uma infecção por hcv em um paciente, derivado de benzodiazepina ou um sal famaceuticamente aceitável do mesmo, e, composição farmacêutica |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8039616B2 (pt) |
| EP (1) | EP1928465A1 (pt) |
| JP (1) | JP4980358B2 (pt) |
| CN (1) | CN101267825B (pt) |
| AU (1) | AU2005336627A1 (pt) |
| BR (1) | BRPI0520554A2 (pt) |
| CA (1) | CA2622592A1 (pt) |
| IL (1) | IL189792A0 (pt) |
| MX (1) | MX2008003369A (pt) |
| NO (1) | NO20081861L (pt) |
| WO (1) | WO2007034127A1 (pt) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2381410T3 (es) | 2007-05-04 | 2012-05-28 | Vertex Pharmceuticals Incorporated | Terapia de combinación paa el tratamiento de infecciones por VHC |
| EP2234977A4 (en) | 2007-12-19 | 2011-04-13 | Boehringer Ingelheim Int | VIRAL POLYMERASE INHIBITORS |
| CN102271699A (zh) | 2009-01-07 | 2011-12-07 | 西尼克斯公司 | 用于治疗hcv和hiv感染的环孢菌素衍生物 |
| US20110059043A1 (en) | 2009-09-03 | 2011-03-10 | Arrow Therapeutics Limited | Chemical compounds |
| CN101824037B (zh) * | 2010-03-18 | 2012-02-22 | 苏州市立德化学有限公司 | 一种西他列汀游离碱的制备方法 |
| WO2011151651A1 (en) | 2010-06-03 | 2011-12-08 | Arrow Therapeutics Limited | Benzodiazepine compounds useful for the treatment of hepatitis c |
| WO2011151652A1 (en) | 2010-06-03 | 2011-12-08 | Arrow Therapeutics Limited | Benzodiazepine compounds useful for the treatment of hepatitis c |
| KR101317656B1 (ko) | 2011-06-30 | 2013-10-15 | 연세대학교 산학협력단 | 복제효소 인산화를 조절하는 신규 c형 간염 예방 또는 치료용 조성물 |
| GB201506448D0 (en) * | 2015-04-16 | 2015-06-03 | Univ Durham | An antimicrobial compound |
| GB201613942D0 (en) * | 2016-08-15 | 2016-09-28 | Univ Of Durham The | An antimicrobial compound |
| GB201911944D0 (en) * | 2019-08-20 | 2019-10-02 | Reviral Ltd | Pharmaceutical compounds |
| GB201915273D0 (en) * | 2019-10-22 | 2019-12-04 | Reviral Ltd | Pharmaceutical compounds |
| GB201915932D0 (en) * | 2019-11-01 | 2019-12-18 | Reviral Ltd | Pharmaceutical compounds |
| CA3171651A1 (en) * | 2020-02-16 | 2021-08-19 | Ayala Pharmaceuticals Inc. | Methods of preparing chiral benzodiazepinone derivatives |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL134421C (pt) * | 1963-12-03 | |||
| US4820834A (en) * | 1984-06-26 | 1989-04-11 | Merck & Co., Inc. | Benzodiazepine analogs |
| CA1332410C (en) | 1984-06-26 | 1994-10-11 | Roger M. Freidinger | Benzodiazepine analogs |
| US4628084A (en) * | 1986-01-02 | 1986-12-09 | Merck & Co., Inc. | Process for 3-acylamino benzodiazepines |
| EP0491218A1 (en) | 1990-12-17 | 1992-06-24 | F. Hoffmann-La Roche Ag | Benzodiazepinones |
| GB9203790D0 (en) | 1992-02-21 | 1992-04-08 | Merck Sharp & Dohme | Therapeutic agents |
| US5426185A (en) | 1993-11-22 | 1995-06-20 | Merck & Co., Inc. | Antiarrhythmic benzodiazepines |
| JP2840454B2 (ja) | 1993-11-22 | 1998-12-24 | メルク エンド カンパニー インコーポレーテッド | ベンゾジアゼピン類 |
| JP2000504306A (ja) * | 1994-08-18 | 2000-04-11 | メルク エンド カンパニー インコーポレーテッド | N―2,3―ジヒドロ―1―(2―プロピル)―2―オキソ―5―フェニル―1h―1,4―ベンゾジアゼピン |
| US5852010A (en) * | 1996-04-03 | 1998-12-22 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| JP2000507587A (ja) * | 1996-04-03 | 2000-06-20 | メルク エンド カンパニー インコーポレーテッド | ファルネシルタンパク質トランスフェラーゼ阻害剤 |
| ATE290545T1 (de) * | 1996-12-06 | 2005-03-15 | Vertex Pharma | Inhibitoren des interleukin-1beta konvertierenden enzyms |
| AU741946B2 (en) | 1998-07-20 | 2001-12-13 | Bristol-Myers Squibb Company | Substituted benzimidazole antiviral agents |
| JP2002525289A (ja) | 1998-09-01 | 2002-08-13 | イノジェネティックス・ナムローゼ・フェンノートシャップ | アネキシンに結合するベンゾジアゼピンおよびベンゾチアゼピン誘導体ならびにhsbsagペプチド、それらの組成物ならびに使用 |
| EP2359831A3 (en) * | 1999-04-30 | 2012-02-01 | The Regents of the University of Michigan | Therapeutic applications of pro-apoptotic benzodiazepines |
| SG122814A1 (en) | 1999-06-28 | 2006-06-29 | Janssen Pharmaceutica Nv | Respiratory syncytial virus replication inhibitors |
| CN1436175A (zh) | 2000-04-03 | 2003-08-13 | 布里斯托尔-迈尔斯斯奎布药品公司 | 作为Aβ-蛋白生产抑制剂的环状内酰胺 |
| GB0012671D0 (en) | 2000-05-24 | 2000-07-19 | Merck Sharp & Dohme | Therapeutic agents |
| EP1268450A1 (en) | 2000-06-01 | 2003-01-02 | Bristol-Myers Squibb Pharma Company | Lactams substituted by cyclic succinates as inhibitors of a-beta protein production |
| US20020142940A1 (en) * | 2000-10-17 | 2002-10-03 | Graham Barney Scott | Method of inhibiting viral infection using HMG-COA reductase inhibitors and isoprenylation inhibitors |
| EP1423122A4 (en) | 2001-08-15 | 2008-12-10 | Univ Michigan | COMPOSITIONS AND METHODS RELATED TO NEW BENZODIAZEPINE COMPOUNDS AND THEIR OBJECTIVES |
| GB0201367D0 (en) | 2002-01-22 | 2002-03-13 | Ml Lab Plc | Composition |
| BR0314595A (pt) * | 2002-09-20 | 2005-08-09 | Arrow Therapeutics Ltd | Uso de um derivado de benzodiazepina ou um sal farmaceuticamente aceitável deste, inalador ou nebulisador, produto, usos de um produto e de um composto ou sal farmaceuticamente aceitável deste, derivado de benzodiazepina, composto, e, composição farmacêutica |
| GB0406280D0 (en) | 2004-03-19 | 2004-04-21 | Arrow Therapeutics Ltd | Chemical compounds |
| US20070293482A1 (en) | 2004-03-19 | 2007-12-20 | Novartis Pharmaceuticals Corporation | Process for Preparing Benzodiazepines |
-
2005
- 2005-09-19 BR BRPI0520554-9A patent/BRPI0520554A2/pt not_active IP Right Cessation
- 2005-09-19 MX MX2008003369A patent/MX2008003369A/es not_active Application Discontinuation
- 2005-09-19 AU AU2005336627A patent/AU2005336627A1/en not_active Abandoned
- 2005-09-19 US US12/067,318 patent/US8039616B2/en not_active Expired - Fee Related
- 2005-09-19 CA CA002622592A patent/CA2622592A1/en not_active Abandoned
- 2005-09-19 JP JP2008530590A patent/JP4980358B2/ja not_active Expired - Fee Related
- 2005-09-19 CN CN2005800516090A patent/CN101267825B/zh not_active Expired - Fee Related
- 2005-09-19 EP EP05784102A patent/EP1928465A1/en not_active Withdrawn
- 2005-09-19 WO PCT/GB2005/003597 patent/WO2007034127A1/en not_active Ceased
-
2008
- 2008-02-26 IL IL189792A patent/IL189792A0/en unknown
- 2008-04-17 NO NO20081861A patent/NO20081861L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP4980358B2 (ja) | 2012-07-18 |
| AU2005336627A1 (en) | 2007-03-29 |
| IL189792A0 (en) | 2008-08-07 |
| CA2622592A1 (en) | 2007-03-29 |
| EP1928465A1 (en) | 2008-06-11 |
| US20090318427A1 (en) | 2009-12-24 |
| MX2008003369A (es) | 2008-03-27 |
| CN101267825B (zh) | 2011-12-28 |
| WO2007034127A1 (en) | 2007-03-29 |
| JP2009508830A (ja) | 2009-03-05 |
| NO20081861L (no) | 2008-06-04 |
| CN101267825A (zh) | 2008-09-17 |
| US8039616B2 (en) | 2011-10-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BRPI0520554A2 (pt) | uso de uma benzodiazepina ou um sal farmaceuticamente aceitável do mesmo, método para tratar ou prevenir uma infecção por hcv em um paciente, derivado de benzodiazepina ou um sal famaceuticamente aceitável do mesmo, e, composição farmacêutica | |
| BR0312286A (pt) | pró-medicamentos de 2' e 3' - nucleosìdeo modificado para tratamento de infecções por flaviviridae | |
| NO20084199L (no) | Formuleringer for modifisert frigjoring og fremgangsmater for behandling av inflammatorisk tarmsykdom | |
| TN2013000421A1 (en) | 2'-substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases | |
| EA201101704A1 (ru) | ПРОИЗВОДНЫЕ 1H-ИМИДАЗО[4,5-c]ХИНОЛИНОНА | |
| MX2024001581A (es) | Derivados de ribosa modificados con 1'-alquilo y metodos de uso. | |
| BRPI0419345B8 (pt) | uso do (2r)-2-desoxi-2-flúor-2-c-metil nucleosídeo e de uma composição farmacêutica que o compreende | |
| BRPI0412343A (pt) | derivados de piridazina e seu uso como agentes terapêuticos | |
| WO2005020884A3 (en) | Nucleosides for treatment of infection by corona viruses, toga viruses and picorna viruses | |
| ATE514699T1 (de) | Substituierte pyrrolopyrazolderivate als kinaseinhibitoren | |
| WO2012142093A3 (en) | 2'-cyano substituted nucleoside derivatives and methods of use thereof for the treatment of viral diseases | |
| WO2008100447A3 (en) | Nucleoside analogs for antiviral treatment | |
| BR0016935A (pt) | Uso de derivados de ácido fumárico para tratamento de doenças mitocondriais | |
| BRPI0408999A (pt) | comprimidos prensados de multiparticulados de liberação oral prolongada | |
| IL207468A (en) | HCV inhibitors and their use in the preparation of medicines for the treatment of HCV infections | |
| UY28084A1 (es) | Derivados antivirales de nucleosidos | |
| BRPI0416212A (pt) | derivado de piridazinona, composição farmacêutica, uso do derivado, método para o tratamento de um sujeito afligido com uma condição ou doença susceptìvel de melhora pela inibição de fosfodiesterase 4 e produto de combinação | |
| BRPI0507984A (pt) | composto ou um sal do mesmo, processo para produzir um composto, medicamento, métodos para antagonizar angiotensina ii em um mamìfero, para melhorar a resistência de insulina em um mamìfero e para prevenir ou tratar doenças circulatórias em um mamìfero, e, uso do composto | |
| BRPI0416656A (pt) | compostos de pirrolopirimidina úteis no tratamento do cáncer | |
| DE60222137D1 (de) | Zuckerderivate von hydromorphon, dihydromorphin und dihydroisomorphin, zusammensetzungen davon und verwendung zur vorbeugung und behandlung von schmerzen | |
| MY141939A (en) | Pyridazine derivatives and their use as therapeutic agents | |
| BRPI0507966A (pt) | uso de meloxicam para o tratamento de doenças respiratórias em porcos | |
| BRPI0411098A (pt) | benzofuranocarboxamidas, com atividade pi3k, como agentes terapêuticos | |
| BRPI0417268A (pt) | benzimidazóis que contêm morfolinila, como inibidores da replicação de vìrus sinciciais respiratórios | |
| BRPI0509512A (pt) | método de tratar esquizofrenia e/ou anormalidades glicorregulatórias |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B06G | Technical and formal requirements: other requirements [chapter 6.7 patent gazette] |
Free format text: SOLICITA-SE A REGULARIZACAO DA PROCURACAO, UMA VEZ QUE BASEADO NO ARTIGO 216 1O DA LPI, O DOCUMENTO DE PROCURACAO DEVE SER APRESENTADO EM SUA FORMA AUTENTICADA; OU SEGUNDO PARECER DA PROCURADORIA NO 074/93, DEVE CONSTAR UMA DECLARACAO DE VERACIDADE, A QUAL DEVE SER ASSINADA POR UMA PESSOA DEVIDAMENTE AUTORIZADA A REPRESENTAR O INTERESSADO, DEVENDO A MESMA CONSTAR NO INSTRUMENTO DE PROCURACAO, OU NO SEU SUBSTABELECIMENTO. |
|
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 6A ANUIDADE. |
|
| 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 PUBLICADO NA RPI 2160 DE 29/05/2012. |