BR9915743A - Compostos de cefem contendo imidazo[4,5-b]piridiniometila possuindo amplo espectro antibactericida - Google Patents

Compostos de cefem contendo imidazo[4,5-b]piridiniometila possuindo amplo espectro antibactericida

Info

Publication number
BR9915743A
BR9915743A BR9915743-8A BR9915743A BR9915743A BR 9915743 A BR9915743 A BR 9915743A BR 9915743 A BR9915743 A BR 9915743A BR 9915743 A BR9915743 A BR 9915743A
Authority
BR
Brazil
Prior art keywords
hydrogen
compounds containing
optionally substituted
pyridiniomethyl
antibacterial spectrum
Prior art date
Application number
BR9915743-8A
Other languages
English (en)
Inventor
Yasuhiro Nishitani
Hikaru Itani
Tadashi Irie
Original Assignee
Shionogi & Co
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 Shionogi & Co filed Critical Shionogi & Co
Publication of BR9915743A publication Critical patent/BR9915743A/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/48—Methylene radicals, substituted by hetero rings
    • C07D501/56—Methylene radicals, substituted by hetero rings with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • 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
    • A61P31/04—Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Cephalosporin Compounds (AREA)

Abstract

Patente de Invenção: <B>"COMPOSTOS DE CEFEM CONTENDO IMIDAZO[4,5-b]PIRIDINIOMETILA POSSUINDO AMPLO ESPECTRO ANTIBACTERICIDA"<D>. A invenção refere-se a composto de cefem da fórmula (I) mostra amplo espectro bactericida contra várias bactérias patogênicas incluindo MRSA. onde X é N ou CY e Y é H ou halogênio; R é amino ou amino protegido; R é hidrogênio ou alquila inferior opcionalmente substituída, etc.; R é hidrogênio, etc.; R^ 4^ é hidrogênio, alquila inferior opcionalmente substituída ou grupo heterocíclico contendo N opcionalmente substituído, etc.; R^ 5^ é hidrogênio, etc. e uma linha ondulada significa sin ou anti-isomerismo ou misturas dos mesmos.
BR9915743-8A 1998-11-27 1999-11-25 Compostos de cefem contendo imidazo[4,5-b]piridiniometila possuindo amplo espectro antibactericida BR9915743A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP33670798 1998-11-27
PCT/JP1999/006562 WO2000032606A1 (fr) 1998-11-27 1999-11-25 COMPOSÉS DE CÉPHÈME À BASE D'IMIDAZO[4,5-b]PYRIDINIUMMÉTHYLE À LARGE SPECTRE ANTIBACTÉRIEN

Publications (1)

Publication Number Publication Date
BR9915743A true BR9915743A (pt) 2001-08-21

Family

ID=18301969

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9915743-8A BR9915743A (pt) 1998-11-27 1999-11-25 Compostos de cefem contendo imidazo[4,5-b]piridiniometila possuindo amplo espectro antibactericida

Country Status (23)

Country Link
US (2) US6518263B1 (pt)
EP (1) EP1134222B1 (pt)
JP (1) JP3636663B2 (pt)
KR (1) KR100692169B1 (pt)
CN (1) CN100436456C (pt)
AT (1) ATE293114T1 (pt)
AU (1) AU758662B2 (pt)
BR (1) BR9915743A (pt)
CA (1) CA2350905C (pt)
CZ (1) CZ20011719A3 (pt)
DE (1) DE69924751T2 (pt)
ES (1) ES2241374T3 (pt)
HU (1) HUP0200450A3 (pt)
ID (1) ID28740A (pt)
IL (1) IL143314A0 (pt)
NO (1) NO20012554L (pt)
NZ (1) NZ511619A (pt)
PL (1) PL347897A1 (pt)
RU (1) RU2223964C2 (pt)
TR (1) TR200101507T2 (pt)
TW (1) TW526202B (pt)
WO (1) WO2000032606A1 (pt)
ZA (1) ZA200103850B (pt)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW526202B (en) * 1998-11-27 2003-04-01 Shionogi & Amp Co Broad spectrum cephem having benzo[4,5-b]pyridium methyl group of antibiotic activity
CZ302015B6 (cs) 1999-10-08 2010-09-08 Affinium Pharmaceuticals, Inc. Inhibitory Fab I
JP2003012647A (ja) * 2000-10-04 2003-01-15 Shionogi & Co Ltd ２，３−ジアミノピリジンの製造方法
ATE420640T1 (de) * 2001-04-06 2009-01-15 Affinium Pharm Inc Fab-i-inhibitoren
RU2003132537A (ru) * 2001-04-23 2005-04-20 Шмоноги Энд Ко.,Лтд. (Jp) Сульфат цефема
AU2003211942A1 (en) * 2002-02-14 2003-09-04 Shionogi And Co., Ltd. Process for production of 2,3-diaminopyridine derivatives
PL205531B1 (pl) * 2002-03-13 2010-04-30 Janssen Pharmaceutica Nv Pochodna karbonyloaminowa, jej zastosowanie i sposób wytwarzania oraz kompozycja farmaceutyczna
WO2004000323A1 (ja) * 2002-06-21 2003-12-31 Shionogi & Co., Ltd. セフェム化合物の注射用医薬組成物
AU2003264462A1 (en) * 2002-09-20 2004-04-08 Shionogi And Co., Ltd. Process for the preparation of cephems
JPWO2004039816A1 (ja) * 2002-10-29 2006-03-02 塩野義製薬株式会社 セフェム化合物の無機酸塩の結晶
AU2002952355A0 (en) * 2002-10-30 2002-11-14 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
DK1556389T6 (da) 2002-10-30 2015-05-11 Astellas Pharma Inc Cephemforbindelser
DK1575951T3 (da) * 2002-12-06 2014-09-15 Debiopharm Int Sa Heterocykliske forbindelser, fremgangsmåder til fremstilling deraf og deres anvendelse i terapi
EP1608377B1 (en) * 2003-03-17 2008-10-01 Affinium Pharmaceuticals, Inc. Pharmaceutical compositions comprising inhibitors of fab i and further antibiotics
AU2003902380A0 (en) * 2003-05-16 2003-06-05 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
AR045768A1 (es) 2003-09-18 2005-11-09 Fujisawa Pharmaceutical Co Compuestos de cefem y sus sales farmaceuticamente aceptables
JP4535366B2 (ja) * 2003-12-03 2010-09-01 塩野義製薬株式会社 セフェム剤の製造方法
TW200530255A (en) * 2004-03-05 2005-09-16 Shionogi & Co 3-pyridiniummethylcefem compound
SI1828167T1 (sl) * 2004-06-04 2014-12-31 Debiopharm International Sa Forum "Apres-Demain" Akrilamidni derivati kot anitibiotična sredstva
JP2006206529A (ja) * 2005-01-31 2006-08-10 Shionogi & Co Ltd Ｎ−（４−ピリジル）エチレンジアミン誘導体
WO2007067416A2 (en) * 2005-12-05 2007-06-14 Affinium Pharmaceuticals, Inc. Heterocyclylacrylamide compounds as fabi inhibitors and antibacterial agents
EP2054422B1 (en) 2006-07-20 2017-06-14 Debiopharm International SA Acrylamide derivatives as fab i inhibitors
WO2008098374A1 (en) 2007-02-16 2008-08-21 Affinium Pharmaceuticals, Inc. Salts, prodrugs and polymorphs of fab i inhibitors
US8198434B2 (en) * 2008-05-07 2012-06-12 Idexx Laboratories, Inc. Process for preparing cefsulodin sodium
CN102443017B (zh) * 2010-10-13 2014-10-29 石药集团中奇制药技术（石家庄）有限公司 一种盐酸头孢唑兰的制备方法
EA028342B1 (ru) 2011-09-09 2017-11-30 Мерк Шарп И Доум Корп. Способы лечения пневмонии
MX356695B (es) 2012-06-19 2018-06-11 Debiopharm Int Sa Profarmacos derivados de (e)-n-metil-n-((3-metilbenzofuran-2-il)me til)-3-(7-oxo-5,6,7,8-tetrahidro-1,8-naftiridin-3-il) acrilamida.
US8809314B1 (en) 2012-09-07 2014-08-19 Cubist Pharmacueticals, Inc. Cephalosporin compound
US8476425B1 (en) 2012-09-27 2013-07-02 Cubist Pharmaceuticals, Inc. Tazobactam arginine compositions
PT2909204T (pt) 2012-10-12 2019-03-21 Dana Farber Cancer Inst Inc Inibidores de gsk3 e métodos de utilização dos mesmos
US20140274996A1 (en) 2013-03-15 2014-09-18 Cubist Pharmaceuticals, Inc. Tazobactam and ceftolozane antibiotic compositions
US20140274994A1 (en) 2013-03-15 2014-09-18 Cubist Pharmaceuticals, Inc. Stabilizing ceftolozane
US9872906B2 (en) 2013-03-15 2018-01-23 Merck Sharp & Dohme Corp. Ceftolozane antibiotic compositions
EP3043797B1 (en) 2013-09-09 2020-04-08 Merck Sharp & Dohme Corp. Treating infections with ceftolozane/tazobactam in subjects having impaired renal function
US20150094293A1 (en) 2013-09-27 2015-04-02 Calixa Therapeutics, Inc. Solid forms of ceftolozane
US10351533B2 (en) * 2015-06-29 2019-07-16 Sandoz Ag Process for the preparation of carbamoylamino pyrazole derivatives
CA3005779C (en) * 2015-12-10 2020-04-07 Naeja-Rgm Pharmaceuticals Ulc Cephem compounds, their production and use
KR20180114177A (ko) 2016-02-26 2018-10-17 데비오팜 인터네셔날 에스 에이 당뇨병성 족부 감염의 치료제
CN110958882B (zh) 2017-04-05 2023-08-29 布罗德研究所股份有限公司 作为糖原合酶激酶3(gsk3)抑制剂的三环化合物及其用途

Family Cites Families (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3585199A (en) * 1967-05-25 1971-06-15 Merck & Co Inc (4-(3-(polyazaheterocyclic)alkanoyl)phenoxy)alkanoic acids
US4002623A (en) * 1974-08-07 1977-01-11 Pfizer Inc. Anti-inflammatory 1-[3-(dialkylamino)propyl]-2-acylaminobenzimidazoles and 2-acylamino-3-[3-(dialkylamino)-propyl]imidazo[4,5-b]pyridines
GR75644B (pt) 1980-06-18 1984-08-02 Fujisawa Pharmaceutical Co
DE3279470D1 (en) 1981-04-03 1989-04-06 Fujisawa Pharmaceutical Co New cephem compounds, processes for their preparation, pharmaceutical compositions containing them and their starting compounds
GR76701B (pt) 1981-09-08 1984-08-29 Lilly Co Eli
US4406899A (en) 1982-03-04 1983-09-27 Bristol-Myers Company Cephalosporins
ZA838864B (en) * 1982-12-17 1984-11-28 Ici Pharma Process for the manufacture of cephalosporin derivatives
DE3248281A1 (de) 1982-12-28 1984-06-28 Hoechst Ag, 6230 Frankfurt Kristalisierte cephem-saeureadditionssalze und verfahren zu ihrer herstellung
US4525473A (en) 1983-03-30 1985-06-25 Bristol-Myers Company Cephalosporins
DE3336757A1 (de) 1983-10-08 1985-04-25 Hoechst Ag, 6230 Frankfurt Cephalosporinderivate und verfahren zu ihrer herstellung
DE3409431A1 (de) 1983-10-08 1985-04-18 Hoechst Ag, 6230 Frankfurt Cephalosporinderivate und verfahren zu ihrer herstellung
US4692443A (en) * 1983-10-17 1987-09-08 Eli Lilly And Company 3-bicyclicpyridinium-methyl cephalosporins
NZ209833A (en) 1983-10-17 1988-04-29 Lilly Co Eli 3-bicyclicpyridiniummethyl-cephalosporins and pharmaceutical compositions
JPS60120889A (ja) 1983-11-30 1985-06-28 Meiji Seika Kaisha Ltd 新規セファロスポリン化合物及びその製造法
US4547573A (en) 1983-12-02 1985-10-15 Ici Pharma Process for preparing cephalosporin derivatives
GB8401093D0 (en) 1984-01-16 1984-02-15 Fujisawa Pharmaceutical Co Cephem compounds
NO165842C (no) 1984-04-23 1991-04-17 Takeda Chemical Industries Ltd Analogifremgangsmaate for fremstilling av terapeutisk aktive cefem-forbindelser.
IL77458A (en) 1985-01-14 1990-07-26 Eisai Co Ltd Cephem derivatives,their production and antibacterial compositions containing them and certain novel intermediates therefor
ATE89826T1 (de) 1985-03-01 1993-06-15 Takeda Chemical Industries Ltd Antibakterielle verbindungen, ihre herstellung und verwendung.
NO166283C (no) 1985-03-01 1991-06-26 Takeda Chemical Industries Ltd Analogifremgangsmaate for fremstilling av terapeutisk aktive 7beta-(2-(5-amino-1,2,4-tiadiazol-3-yl)-2(z)-substituertoksyiminoacetamido)-3-(heterocyclylmetyl)-3-cefem-4-karboksylsyrederivater.
US4804658A (en) 1986-09-15 1989-02-14 G. D. Searle & Co. Imidazopyridine derivatives and pharmaceutical compositions
GB8712747D0 (en) * 1987-05-30 1987-07-01 Pfizer Ltd Therapeutic agents
JPH0248587A (ja) * 1988-08-10 1990-02-19 Yamanouchi Pharmaceut Co Ltd 複素環置換ビスフォスフォン酸誘導体及びその医薬
JPH02286679A (ja) * 1989-04-28 1990-11-26 Grelan Pharmaceut Co Ltd イミダゾピリジン誘導体
IL94390A (en) * 1989-05-30 1996-03-31 Merck & Co Inc The 6-membered trans-nitrogen-containing heterocycles are compressed with imidazo and pharmaceutical preparations containing them
US5332744A (en) 1989-05-30 1994-07-26 Merck & Co., Inc. Substituted imidazo-fused 6-membered heterocycles as angiotensin II antagonists
IE70593B1 (en) * 1989-09-29 1996-12-11 Eisai Co Ltd Biphenylmethane derivative the use of it and pharmacological compositions containing same
US5298518A (en) 1989-09-29 1994-03-29 Eisai Co., Ltd. Biphenylmethane derivative and pharmacological use
EP0434038A1 (en) * 1989-12-22 1991-06-26 Takeda Chemical Industries, Ltd. Fused imidazole derivatives, their production and use
FR2672052B1 (fr) 1991-01-28 1995-05-24 Esteve Labor Dr Derives d'aryl (ou heteroaryl)-piperazinyl-alkyl-azoles, leur preparation et leur application en tant que medicaments.
DE4005970A1 (de) * 1990-02-26 1991-08-29 Boehringer Mannheim Gmbh Neue trisubstituierte maleinimide, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten
AU653524B2 (en) * 1990-06-08 1994-10-06 Roussel-Uclaf New imidazole derivatives, their preparation process, the new intermediates obtained, their use as medicaments and the pharmaceutical compositions containing them
AU8506791A (en) 1990-10-01 1992-04-28 Janssen Pharmaceutica N.V. Novel 4-piperidinylcarbonyl derivatives
US5281589A (en) * 1991-06-15 1994-01-25 Cheil Foods & Chemicals, Inc. 3-fused pyridiniummethyl cephalosporins
JPH05201991A (ja) * 1991-07-10 1993-08-10 Dainippon Pharmaceut Co Ltd アミノ酸誘導体
JPH05222058A (ja) 1992-02-17 1993-08-31 Fujisawa Pharmaceut Co Ltd 新規セフェム化合物およびその塩
JPH0641149A (ja) * 1992-05-28 1994-02-15 Toyama Chem Co Ltd 新規なセファロスポリン誘導体およびその塩
JP3269658B2 (ja) * 1992-06-02 2002-03-25 エーザイ株式会社 フェノール誘導体
GB9216287D0 (en) 1992-07-31 1992-09-16 Fujisawa Pharmaceutical Co New cephem compounds
JPH07101958A (ja) 1992-10-16 1995-04-18 Takeda Chem Ind Ltd セフェム化合物、その製造法および抗菌組成物
US5334598A (en) 1993-03-19 1994-08-02 Merck & Co., Inc. Six-membered ring fused imidazoles substituted with phenoxyphenylacetic acid derivatives
DE4309969A1 (de) 1993-03-26 1994-09-29 Bayer Ag Substituierte heteroanellierte Imidazole
JPH07101960A (ja) 1993-10-05 1995-04-18 Takeda Chem Ind Ltd セフェム化合物、その製造法および抗菌組成物
US5486525A (en) 1993-12-16 1996-01-23 Abbott Laboratories Platelet activating factor antagonists: imidazopyridine indoles
FR2719587B1 (fr) * 1994-05-03 1996-07-12 Roussel Uclaf Nouveaux dérivés de l'érythromycine, leur procédé de préparation et leur application comme médicaments.
DE4416433A1 (de) 1994-05-10 1995-11-16 Hoechst Ag Cyclohexan-Derivate, Verfahren zu ihrer Herstellung und die Verwendung der Verbindungen zur Behandlung von Krankheiten
US5585492A (en) * 1994-10-11 1996-12-17 G. D. Searle & Co. LTA4 Hydrolase inhibitors
US5635514A (en) * 1994-10-25 1997-06-03 G. D. Searle & Company Heteroaralkyl and heteroarylthioalkyl thiophenolic compounds as 5-lipoxgenase inhibitors
US5846990A (en) * 1995-07-24 1998-12-08 Bristol-Myers Squibb Co. Substituted biphenyl isoxazole sulfonamides
JPH09165371A (ja) 1995-10-09 1997-06-24 Sankyo Co Ltd 複素環化合物を含有する医薬
JPH09110877A (ja) * 1995-10-17 1997-04-28 Katayama Seiyakushiyo:Kk セフェム化合物、その製造法及びそれを含有する抗菌剤
FR2742052B1 (fr) * 1995-12-12 1998-04-10 Esteve Labor Dr Utilisation des derives 1-(4-(4-aryl (ou heteroaryl)-1-piper azinyl)-buty)-1h-azole pour le traitement de la depression, des troubles obsessifs compulsifs, l'apnee du sommeil, les dysfonctions sexuelles, l'emese et le mal des transports
AUPN955596A0 (en) 1996-04-30 1996-05-23 Fujisawa Pharmaceutical Co., Ltd. New compound
JP4028894B2 (ja) * 1996-08-09 2007-12-26 エーザイ・アール・アンド・ディー・マネジメント株式会社 ベンゾピペリジン誘導体
TW526202B (en) * 1998-11-27 2003-04-01 Shionogi & Amp Co Broad spectrum cephem having benzo[4,5-b]pyridium methyl group of antibiotic activity

Also Published As

Publication number Publication date
TR200101507T2 (tr) 2001-09-21
NO20012554D0 (no) 2001-05-23
ID28740A (id) 2001-06-28
NZ511619A (en) 2002-11-26
US6518263B1 (en) 2003-02-11
RU2223964C2 (ru) 2004-02-20
HUP0200450A3 (en) 2004-04-28
US6800621B2 (en) 2004-10-05
CZ20011719A3 (cs) 2001-12-12
JP3636663B2 (ja) 2005-04-06
ATE293114T1 (de) 2005-04-15
AU758662B2 (en) 2003-03-27
DE69924751T2 (de) 2006-03-09
ZA200103850B (en) 2002-05-13
EP1134222A1 (en) 2001-09-19
KR100692169B1 (ko) 2007-03-12
EP1134222B1 (en) 2005-04-13
CA2350905A1 (en) 2000-06-08
CA2350905C (en) 2007-10-23
DE69924751D1 (de) 2005-05-19
TW526202B (en) 2003-04-01
AU1409000A (en) 2000-06-19
HUP0200450A2 (hu) 2002-07-29
CN100436456C (zh) 2008-11-26
PL347897A1 (en) 2002-04-22
WO2000032606A1 (fr) 2000-06-08
IL143314A0 (en) 2002-04-21
NO20012554L (no) 2001-07-27
ES2241374T3 (es) 2005-10-16
KR20010086058A (ko) 2001-09-07
CN1333776A (zh) 2002-01-30
EP1134222A4 (en) 2003-01-29
US20030149014A1 (en) 2003-08-07

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Legal Events

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B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B11B Dismissal acc. art. 36, par 1 of ipl - no reply within 90 days to fullfil the necessary requirements
B11N Dismissal: publication cancelled [chapter 11.14 patent gazette]

Free format text: PUBLICACAO ANULADA REFERENTE A RPI NO 2076 DE 19/10/2010.

B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]
B07E Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 13A ANUI DADE.

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 2199 DE 26/02/2013.

B11D Dismissal acc. art. 38, par 2 of ipl - failure to pay fee after grant in time