BR9813124A - Compostos indol 2,3-substituìdos como inibidores cox-2 - Google Patents

Compostos indol 2,3-substituìdos como inibidores cox-2

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Publication number
BR9813124A
BR9813124A BR9813124-9A BR9813124A BR9813124A BR 9813124 A BR9813124 A BR 9813124A BR 9813124 A BR9813124 A BR 9813124A BR 9813124 A BR9813124 A BR 9813124A
Authority
BR
Brazil
Prior art keywords
halo
alkoxy
alkyl
substituted
cox
Prior art date
Application number
BR9813124-9A
Other languages
English (en)
Inventor
Kazunari Nakao
Rodney William Stevens
Kiyoshi Kawamura
Chikara Uchida
Hiroki Koike
Stephane Caron
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of BR9813124A publication Critical patent/BR9813124A/pt

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/10Heterocyclic 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 aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/10Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/06Heterocyclic 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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/10Heterocyclic 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 two hetero rings linked by a carbon chain containing aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Patente de Invenção: <B>"COMPOSTOS INDOL 2,3-SUBSTITUìDOS COMO INIBIDORES COX-2"<D>. Este invenção proporciona um composto da fórmula seguinte: e os seus sais farmaceuticamente aceitáveis, em que <B>Z<D> representa OH, alcóxi C~ 1-6~, -NR²R³ ou heterociclo; <B>Q<D> é selecionado a partir dos seguintes: (a) fenila facultativamente substituída, (b) um grupo aromático monocíclico de 6 membros contendo um, dois, três ou quatro átomo(s) de nitrogênio, (c) um grupo aromático monocíclico de 5 membros contendo um heteroátomo selecionado a partir de O, S e N, e contendo, facultativamente, um, dois ou três átomo(s) de nitrogênio para além do referido heteroátomo, (d) uma cicloalquila C~ 3-7~ facultativamente substituída e (e) um heterociclo benzo-condensado facultativamente substituída; <B>R¹<D> representa hidrogênio, alquila C~ 1-4~ ou halo; <B>R² e R³<D> representam, independentemente H, OH, alcóxi C~ 1-4~ ou alquila C~ 1-4~ substituído com halo, OH, alcóxi C~ 1-4~, NH~ 2~ ou CN; <B>X<D> é selecionado, independentemente, a partir de halo, alquila C~ 1-4~, alquila C~ 1-4~ substituída com halo, OH, alcóxi C~ 1-4~, alcóxi C~ 1-4~ substituída com halo, alquiltio C~ 1-4~, NO~ 2~, NH~ 2~, di-(alquil C~ 1-4~)-amino e CN; e <B>n<D> representa 0, 1, 2, 3 ou 4. Esta invenção proporciona também uma composição farmacêutica, útil para o tratamento de um estado clínico em que se encontram implicadas, como patogênios, as prostaglandinas.
BR9813124-9A 1998-01-05 1998-12-18 Compostos indol 2,3-substituìdos como inibidores cox-2 BR9813124A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IB9800003 1998-01-05
PCT/IB1998/002065 WO1999035130A1 (en) 1998-01-05 1998-12-18 2,3-substituted indole compounds as cox-2 inhibitors

Publications (1)

Publication Number Publication Date
BR9813124A true BR9813124A (pt) 2000-10-10

Family

ID=11004645

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9813124-9A BR9813124A (pt) 1998-01-05 1998-12-18 Compostos indol 2,3-substituìdos como inibidores cox-2

Country Status (39)

Country Link
US (1) US6608070B1 (pt)
EP (1) EP1045833B1 (pt)
JP (1) JP3347136B2 (pt)
KR (1) KR100404054B1 (pt)
CN (1) CN1284064A (pt)
AP (1) AP869A (pt)
AR (1) AR016977A1 (pt)
AT (1) ATE308519T1 (pt)
AU (1) AU748107B2 (pt)
BG (1) BG104643A (pt)
BR (1) BR9813124A (pt)
CA (1) CA2316863A1 (pt)
CO (1) CO4970807A1 (pt)
DE (1) DE69832200T2 (pt)
DZ (1) DZ2700A1 (pt)
EA (1) EA200000614A1 (pt)
ES (1) ES2255190T3 (pt)
GT (1) GT199800205A (pt)
HN (1) HN1997000098A (pt)
HR (1) HRP20000454A2 (pt)
HU (1) HUP0102922A3 (pt)
ID (1) ID24876A (pt)
IL (1) IL136885A0 (pt)
IS (1) IS5532A (pt)
MA (1) MA24736A1 (pt)
NO (1) NO20003451L (pt)
OA (1) OA11441A (pt)
PA (1) PA8466201A1 (pt)
PE (1) PE20000055A1 (pt)
PL (1) PL341696A1 (pt)
SA (1) SA99191299A (pt)
SK (1) SK9912000A3 (pt)
TN (1) TNSN99001A1 (pt)
TR (1) TR200001906T2 (pt)
TW (1) TW436482B (pt)
UY (2) UY25332A1 (pt)
WO (1) WO1999035130A1 (pt)
YU (1) YU41600A (pt)
ZA (1) ZA9911B (pt)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6555540B1 (en) * 1999-06-30 2003-04-29 Pfizer Inc Combinations of aldose reductase inhibitors and selective cyclooxygenase-2 inhibitors
DE60000556T2 (de) * 1999-07-02 2003-02-13 Pfizer Tetrazolylalkyl-Indolderivate als entzündungshemmende und analgetische Mittel
MXPA00006605A (es) * 1999-07-02 2004-12-09 Pfizer Compuestos de carbonil-indol biciclicos como agentes antiinflamatorios/analgesicos.
CA2509881A1 (en) * 2002-12-19 2004-07-08 Elan Pharmaceuticals, Inc. Substituted n-phenyl sulfonamide bradykinin antagonists
US7098231B2 (en) * 2003-01-22 2006-08-29 Boehringer Ingelheim International Gmbh Viral polymerase inhibitors
US7223785B2 (en) 2003-01-22 2007-05-29 Boehringer Ingelheim International Gmbh Viral polymerase inhibitors
ATE342722T1 (de) 2003-05-07 2006-11-15 Osteologix As Behandlung von knorpel/knochen-erkrankungen mit wasserlöslichen strontiumsalzen
KR100795462B1 (ko) * 2006-09-27 2008-01-16 한국생명공학연구원 인돌 유도체, 이의 제조방법 및 이를 유효성분으로함유하는 대사성 질환 예방 및 치료용 약학적 조성물
KR101419965B1 (ko) 2006-10-17 2014-07-16 스티펠 래버러토리즈, 인코포레이티드 탈라로졸 대사물
US20120022121A1 (en) * 2007-11-29 2012-01-26 Dalton James T Indoles, derivatives and analogs thereof and uses therefor
HUE030263T2 (en) 2010-04-19 2017-04-28 Octeta Therapeutics Llc New synthesis for the preparation of thiazolidinedione compounds
WO2012006474A2 (en) 2010-07-07 2012-01-12 Ardelyx, Inc. Compounds and methods for inhibiting phosphate transport
JP5827328B2 (ja) 2010-07-07 2015-12-02 アーデリクス,インコーポレーテッド リン酸輸送を阻害する化合物及び方法
JP5827326B2 (ja) 2010-07-07 2015-12-02 アーデリクス,インコーポレーテッド リン酸輸送を阻害する化合物及び方法
JP5823514B2 (ja) 2010-07-07 2015-11-25 アーデリクス,インコーポレーテッド リン酸輸送を阻害する化合物及び方法
PL2603507T3 (pl) 2010-08-10 2016-12-30 Synteza związków tiazolidynodionu
EP2603498B1 (en) 2010-08-10 2016-11-09 Octeta Therapeutics, LLC Novel synthesis for thiazolidinedione compounds
US10266490B2 (en) * 2012-03-16 2019-04-23 Georgetown University Radioprotector compounds
US9808443B1 (en) 2016-11-28 2017-11-07 King Saud University Cyclooxygenase inhibitors
CN111004121A (zh) * 2019-12-09 2020-04-14 南京杰运医药科技有限公司 一种4-烷氧基乙酰乙酸酯类化合物的制备方法
CN112409281B (zh) * 2020-08-20 2022-11-18 上海大学 (e)-3-(3-氯-2-氟-6-(1h-四氮唑-1-基)苯基)丙烯酸的合成方法
CA3209491A1 (en) 2021-03-15 2022-09-22 Saul Yedgar Hyaluronic acid-conjugated dipalmitoyl phosphatidyl ethanolamine in combination with non-steroidal anti-inflammatory drugs (nsaids) for treating or alleviating inflammatory disease

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5604253A (en) * 1995-05-22 1997-02-18 Merck Frosst Canada, Inc. N-benzylindol-3-yl propanoic acid derivatives as cyclooxygenase inhibitors
US5510368A (en) * 1995-05-22 1996-04-23 Merck Frosst Canada, Inc. N-benzyl-3-indoleacetic acids as antiinflammatory drugs
CO5190664A1 (es) * 1999-06-30 2002-08-29 Pfizer Prod Inc Terapia de combinacion para el tratamiento de migrana administracion de un receptor 5ht, cafeina y un inhibidor de ciclooxigenasa-2

Also Published As

Publication number Publication date
AU748107B2 (en) 2002-05-30
CN1284064A (zh) 2001-02-14
ID24876A (id) 2000-08-31
NO20003451L (no) 2000-09-01
UY25332A1 (es) 2001-01-31
KR20010033859A (ko) 2001-04-25
EA200000614A1 (ru) 2001-02-26
EP1045833B1 (en) 2005-11-02
TNSN99001A1 (fr) 2005-11-10
HN1997000098A (es) 1998-12-28
SK9912000A3 (en) 2001-11-06
JP3347136B2 (ja) 2002-11-20
PA8466201A1 (es) 2000-09-29
OA11441A (en) 2004-04-27
DE69832200D1 (de) 2005-12-08
PE20000055A1 (es) 2000-02-08
HRP20000454A2 (en) 2001-04-30
KR100404054B1 (ko) 2003-11-01
AP869A (en) 2000-09-04
ATE308519T1 (de) 2005-11-15
CA2316863A1 (en) 1999-07-15
HUP0102922A3 (en) 2003-06-30
MA24736A1 (fr) 1999-10-01
CO4970807A1 (es) 2000-11-07
TW436482B (en) 2001-05-28
PL341696A1 (en) 2001-04-23
HUP0102922A2 (hu) 2001-12-28
IS5532A (is) 2000-06-13
AU1500599A (en) 1999-07-26
IL136885A0 (en) 2001-06-14
ES2255190T3 (es) 2006-06-16
AR016977A1 (es) 2001-08-01
DZ2700A1 (fr) 2003-09-01
BG104643A (bg) 2001-02-28
JP2002500217A (ja) 2002-01-08
NO20003451D0 (no) 2000-07-04
GT199800205A (es) 2000-06-21
UY25590A1 (es) 1999-09-27
SA99191299A (ar) 2005-12-03
YU41600A (sh) 2003-08-29
TR200001906T2 (tr) 2001-01-22
US6608070B1 (en) 2003-08-19
ZA9911B (en) 2000-07-04
EP1045833A1 (en) 2000-10-25
DE69832200T2 (de) 2006-04-20
AP9801423A0 (en) 1998-12-31
WO1999035130A1 (en) 1999-07-15

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B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

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