BR0212716A - Inibidores de liberação extracelular de citocinas inflamatórias e composição farmacêutica - Google Patents

Inibidores de liberação extracelular de citocinas inflamatórias e composição farmacêutica

Info

Publication number
BR0212716A
BR0212716A BR0212716-4A BR0212716A BR0212716A BR 0212716 A BR0212716 A BR 0212716A BR 0212716 A BR0212716 A BR 0212716A BR 0212716 A BR0212716 A BR 0212716A
Authority
BR
Brazil
Prior art keywords
extracellular release
pharmaceutical composition
taken together
hydrogen
release inhibitors
Prior art date
Application number
BR0212716-4A
Other languages
English (en)
Inventor
Michael Phillip Clark
Matthew John Laufersweiler
Jane Far-Jine Djung
Michael George Natchus
Biswanath De
Original Assignee
Procter & Gamble
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 Procter & Gamble filed Critical Procter & Gamble
Publication of BR0212716A publication Critical patent/BR0212716A/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/12Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
    • C07D491/20Spiro-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/12Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D495/20Spiro-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Cardiology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

"INIBIDORES DE LIBERAçãO EXTRACELULAR DE CITOCINAS INFLAMATóRIAS E COMPOSIçãO FARMACêUTICA". A presente invenção refere-se a compostos que são capazes de evitar a liberação extracelular de citocinas inflamatória, sendo que os ditos compostos incluindo todas as suas formas enantioméricas e diasterioméricas e os sais farmaceuticamente aceitáveis dessas substâncias, tendo a seguinte fórmula (I): sendo que R compreende éteres ou aminas; R^ 1^ é: a) arila substituída ou não-substituída; ou b) heteroarila substituída ou não-substituída; cada unidade R^ 2^ é independentemente selecionada a partir do grupo consistindo em: a) hidrogênio; b) -(CH~ 2~)~ j~O(CH~ 2~)~ n~R^ 8^; c) -(CH~ 2~)~ j~,NR^ 9a^R^ 9b^; d) -(CH~ 2~)~ j~CO~ 2~R^ 10^, e) -(CH~ 2~)~ j~OCO~ 2~R^ 10^; F) -(CH~ 2~)~ j~CON(R^ 10^)~ 2~; g) -(CH~ 2~)~ j~OCON(R^ 10^)~ 2~; h) duas unidades R^ 2^ podem ser tomadas em conjunto para formar uma unidade carbonila; i) e misturas dessas substâncias; cada um de R^ 8^, R^ 9a^, R^ 9b^ e R^ 10^ são, independentemente, hidrogênio, C~ 1~-C~ 4~ alquila e misturas dessas substâncias; R^ 9a^ e R^ 9b^ podem ser tomados em conjunto para formar um anel carbocíclico ou heterocíclico que contém de 3 a 7 átomos; duas unidades R^ 10^ podem ser tomadas em conjunto para formar um anel carbocíclico ou heterocíclico que contém de 3 a 7 átomos; j é um índice de 0 a 5, n é um índice de 0 a 5; Z é O, S, NR^ 11^ ou NOR^ 11^, R^ 11^ é hidrogênio ou C~ 1~-C~ 4~ alquila.
BR0212716-4A 2001-09-20 2002-09-20 Inibidores de liberação extracelular de citocinas inflamatórias e composição farmacêutica BR0212716A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32362501P 2001-09-20 2001-09-20
PCT/US2002/030135 WO2003024971A1 (en) 2001-09-20 2002-09-20 6,7-dihydro-5h-pyrazolo[1,2-a]pyrazol-1-ones which control inflammatory cytokines

Publications (1)

Publication Number Publication Date
BR0212716A true BR0212716A (pt) 2004-08-03

Family

ID=23259997

Family Applications (3)

Application Number Title Priority Date Filing Date
BR0212905-1A BR0212905A (pt) 2001-09-20 2002-09-20 Inibidores de liberação de citocinas inflamatórias e composição farmacêutica
BR0212673-7A BR0212673A (pt) 2001-09-20 2002-09-20 Espirocìclicas-6,7-dihidro-5h-pirazolo[1,2a]pirazol-1- onas e composição farmacêutica compreendendo as mesmas
BR0212716-4A BR0212716A (pt) 2001-09-20 2002-09-20 Inibidores de liberação extracelular de citocinas inflamatórias e composição farmacêutica

Family Applications Before (2)

Application Number Title Priority Date Filing Date
BR0212905-1A BR0212905A (pt) 2001-09-20 2002-09-20 Inibidores de liberação de citocinas inflamatórias e composição farmacêutica
BR0212673-7A BR0212673A (pt) 2001-09-20 2002-09-20 Espirocìclicas-6,7-dihidro-5h-pirazolo[1,2a]pirazol-1- onas e composição farmacêutica compreendendo as mesmas

Country Status (33)

Country Link
US (2) US6821971B2 (pt)
EP (3) EP1427732B1 (pt)
JP (3) JP2005504082A (pt)
KR (4) KR100623879B1 (pt)
CN (3) CN1250551C (pt)
AR (3) AR037237A1 (pt)
AT (3) ATE287887T1 (pt)
AU (2) AU2002327690B2 (pt)
BR (3) BR0212905A (pt)
CA (3) CA2461073A1 (pt)
CO (3) CO5560590A2 (pt)
CY (1) CY1106398T1 (pt)
CZ (3) CZ2004361A3 (pt)
DE (3) DE60202782T2 (pt)
DK (2) DK1427728T3 (pt)
EG (2) EG24413A (pt)
ES (3) ES2282459T3 (pt)
HK (2) HK1071366A1 (pt)
HU (3) HUP0402378A3 (pt)
IL (3) IL160741A0 (pt)
MA (3) MA27065A1 (pt)
MX (3) MXPA04002569A (pt)
MY (2) MY129069A (pt)
NO (2) NO20041594L (pt)
NZ (3) NZ531063A (pt)
PE (3) PE20030430A1 (pt)
PL (3) PL370351A1 (pt)
PT (3) PT1427732E (pt)
RU (3) RU2299885C2 (pt)
SA (1) SA03230529B1 (pt)
SK (3) SK1482004A3 (pt)
WO (3) WO2003024970A1 (pt)
ZA (3) ZA200401260B (pt)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6730668B2 (en) * 2001-09-20 2004-05-04 The Procter & Gamble Company 6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-ones which control inflammatory cytokines
US7087615B2 (en) 2001-09-20 2006-08-08 The Procter & Gamble Company 6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-ones which provide analgesia
US6849627B2 (en) 2001-09-20 2005-02-01 The Procter & Gamble Company 6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-ones which control inflammatory cytokines
US7473695B2 (en) * 2001-10-22 2009-01-06 Mitsubishi Tanabe Pharma Corporation 4-imidazolin-2-one compounds
US6677337B2 (en) * 2002-03-19 2004-01-13 The Procter & Gamble Company 1,2-dihydropyrazol-3-ones which controls inflammatory cytokines
CA2497007A1 (en) * 2002-09-09 2004-03-18 Amgen Inc. 1, 4, 5-substituted 1, 2-dihydro-pyrazol-3-one and 3-alkoxy-1h-pyrazole derivatives s tnf-alpha and interleukin lowering agents for the treatment of inflammations
JP4624982B2 (ja) * 2003-04-03 2011-02-02 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング 血栓症の処置のための凝固因子Xa阻害剤としての1−N−(フェニル)−2−N−(フェニル)ピラゾリジン−1,2−ジカルボキサミド誘導体
GB0308466D0 (en) * 2003-04-11 2003-05-21 Novartis Ag Organic compounds
US7482356B2 (en) * 2003-11-10 2009-01-27 The Procter & Gamble Company Bicyclic pyrazolone cytokine inhibitors
RU2450006C2 (ru) * 2006-04-18 2012-05-10 Эбботт Лэборетриз Антагонисты ванилоидного рецептора подтипа 1(vr1) и их применение
DE102008060549A1 (de) 2008-12-04 2010-06-10 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Wirkstoff-Peptid-Konstrukt zur extrazellulären Anreicherung
CA2760911A1 (en) * 2009-05-19 2010-11-25 George E. Davis Compounds and methods for controlling fungi
WO2016205284A1 (en) 2015-06-15 2016-12-22 Cummins Inc. Combustion chamber elasticity device
WO2017151409A1 (en) 2016-02-29 2017-09-08 University Of Florida Research Foundation, Incorporated Chemotherapeutic methods
CN107033090B (zh) * 2017-05-16 2019-05-07 无锡捷化医药科技有限公司 一种1,2,3,4-四氢噌啉的制备方法
RU2721684C1 (ru) * 2019-09-06 2020-05-21 Федеральное государственное бюджетное образовательное учреждение высшего образования "Пермский государственный национальный исследовательский университет" Метил 2,3,8-триоксо-4-фенилтетрагидро-6Н-пиразоло[1,2-а]пирроло[2,3-c]пиразол-9а(1Н)-карбоксилаты
WO2023076133A1 (en) * 2021-10-27 2023-05-04 Merck Sharp & Dohme Llc Spirotricycle ripk1 inhibitors and methods of uses thereof

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GB1054291A (pt) * 1963-02-26
GB1124982A (en) * 1965-02-09 1968-08-21 Lepetit Spa Diazabicyclo octanes and derivatives thereof
CH529153A (fr) 1969-10-27 1972-10-15 Lepetit Spa Procédé de préparation de pyrazolo (1,2-b) phtalazine-1,5 (10H)-diones
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US6730668B2 (en) * 2001-09-20 2004-05-04 The Procter & Gamble Company 6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-1-ones which control inflammatory cytokines

Also Published As

Publication number Publication date
PL370351A1 (en) 2005-05-16
NO20041605L (no) 2004-06-21
NZ531122A (en) 2005-09-30
CO5560589A2 (es) 2005-09-30
KR20040035836A (ko) 2004-04-29
RU2004111806A (ru) 2005-03-27
CN1556811A (zh) 2004-12-22
IL160742A0 (en) 2004-08-31
PE20030430A1 (es) 2003-06-24
MY129069A (en) 2007-03-30
DK1427728T3 (da) 2007-07-09
HK1071565A1 (en) 2005-07-22
BR0212673A (pt) 2004-08-24
CA2461072A1 (en) 2003-03-27
AU2002327690B2 (en) 2006-07-20
DE60213108D1 (de) 2006-08-24
CZ2004345A3 (cs) 2004-06-16
ES2282459T3 (es) 2007-10-16
MA27064A1 (fr) 2004-12-20
RU2278864C2 (ru) 2006-06-27
EP1427728A1 (en) 2004-06-16
DK1427732T3 (da) 2006-10-30
AR037145A1 (es) 2004-10-27
CZ2004358A3 (cs) 2004-07-14
ATE332901T1 (de) 2006-08-15
CN1249066C (zh) 2006-04-05
RU2299885C2 (ru) 2007-05-27
EP1427727A1 (en) 2004-06-16
CO5560590A2 (es) 2005-09-30
IL160741A0 (en) 2004-08-31
PT1427728E (pt) 2007-05-31
JP2005504083A (ja) 2005-02-10
WO2003024973A1 (en) 2003-03-27
KR100656126B1 (ko) 2006-12-12
HUP0402500A3 (en) 2008-10-28
AU2002334641B2 (en) 2007-03-29
EP1427728B1 (en) 2007-03-07
PE20030446A1 (es) 2003-07-21
KR20060036125A (ko) 2006-04-27
ZA200401260B (en) 2004-08-30
CA2461071A1 (en) 2003-03-27
MXPA04002569A (es) 2004-05-31
ZA200401402B (en) 2004-08-27
ES2268154T3 (es) 2007-03-16
IL160682A0 (en) 2004-08-31
MXPA04002574A (es) 2004-06-18
RU2004111803A (ru) 2005-10-10
CZ2004361A3 (cs) 2004-07-14
EG24363A (en) 2009-03-04
DE60218704T2 (de) 2007-11-08
DE60202782D1 (de) 2005-03-03
SK1492004A3 (en) 2004-11-03
NZ531063A (en) 2007-08-31
DE60218704D1 (de) 2007-04-19
JP2005504081A (ja) 2005-02-10
HUP0402378A2 (hu) 2005-02-28
US6566357B1 (en) 2003-05-20
CN1250551C (zh) 2006-04-12
PL370362A1 (en) 2005-05-16
HUP0500752A2 (en) 2006-01-30
EP1427732A1 (en) 2004-06-16
JP2005504082A (ja) 2005-02-10
CO5560579A2 (es) 2005-09-30
HUP0402378A3 (en) 2008-10-28
CN1257905C (zh) 2006-05-31
SK1482004A3 (en) 2004-08-03
CN1555379A (zh) 2004-12-15
SK1502004A3 (en) 2004-09-08
ES2237691T3 (es) 2005-08-01
MXPA04002570A (es) 2004-05-31
KR20040035837A (ko) 2004-04-29
MA27065A1 (fr) 2004-12-20
PE20030474A1 (es) 2003-07-22
PT1427732E (pt) 2006-12-29
HUP0402500A2 (hu) 2005-03-29
EP1427727B1 (en) 2005-01-26
DE60213108T2 (de) 2007-02-08
KR20040035835A (ko) 2004-04-29
ATE287887T1 (de) 2005-02-15
CY1106398T1 (el) 2011-10-12
MA27066A1 (fr) 2004-12-20
RU2004111805A (ru) 2005-04-10
NZ531123A (en) 2006-08-31
MY129329A (en) 2007-03-30
US20030105084A1 (en) 2003-06-05
NO20041594L (no) 2004-06-21
WO2003024971A1 (en) 2003-03-27
ZA200401403B (en) 2004-08-30
KR100623879B1 (ko) 2006-09-19
DE60202782T2 (de) 2006-01-19
AR037502A1 (es) 2004-11-17
PT1427727E (pt) 2005-06-30
CN1555375A (zh) 2004-12-15
SA03230529B1 (ar) 2008-06-21
PL370415A1 (en) 2005-05-30
BR0212905A (pt) 2004-10-13
EP1427732B1 (en) 2006-07-12
WO2003024970A1 (en) 2003-03-27
RU2272040C2 (ru) 2006-03-20
ATE356126T1 (de) 2007-03-15
US6821971B2 (en) 2004-11-23
CA2461073A1 (en) 2003-03-27
HK1071366A1 (en) 2005-07-15
EG24413A (en) 2009-05-25
AR037237A1 (es) 2004-11-03

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Legal Events

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B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 9A ANUIDADE(S).

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 2144 DE 07/02/2012.