BRPI0512832A - composto ou um sal ou estereoisÈmero farmaceuticamente aceitável do mesmo, composição farmacêutica, e, método para usar um composto - Google Patents

composto ou um sal ou estereoisÈmero farmaceuticamente aceitável do mesmo, composição farmacêutica, e, método para usar um composto

Info

Publication number
BRPI0512832A
BRPI0512832A BRPI0512832-3A BRPI0512832A BRPI0512832A BR PI0512832 A BRPI0512832 A BR PI0512832A BR PI0512832 A BRPI0512832 A BR PI0512832A BR PI0512832 A BRPI0512832 A BR PI0512832A
Authority
BR
Brazil
Prior art keywords
compound
stereoisomer
pharmaceutically acceptable
pharmaceutical composition
acceptable salt
Prior art date
Application number
BRPI0512832-3A
Other languages
English (en)
Inventor
Jeffrey M Bergman
Paul J Coleman
Mark E Fraley
Robert M Garbaccio
George D Hartman
Chunze Li
Lou Anne Neilson
Christy M Olson
Edward S Tasber
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Publication of BRPI0512832A publication Critical patent/BRPI0512832A/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—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
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Abstract

COMPOSTO OU UM SAL OU ESTEREOISÈMERO FARMACEUTICAMENTE ACEITáVEL DO MESMO, COMPOSIçãO FARMACêUTICA, E, MéTODO PARA USAR UM COMPOSTO. A presente invenção se refere a pirazóis tricíclicos de acordo com Fórmula (I) que são úteis para tratar doenças de proliferação celular, para tratar distúrbios associados com atividade de cinesina KSP, e para inibir cinesina KSP. A invenção também se refere a composições que compreendem estes compostos, e métodos de usar elas para tratar câncer em mamíferos.
BRPI0512832-3A 2004-07-01 2005-06-27 composto ou um sal ou estereoisÈmero farmaceuticamente aceitável do mesmo, composição farmacêutica, e, método para usar um composto BRPI0512832A (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US58480804P 2004-07-01 2004-07-01
US60090104P 2004-08-12 2004-08-12
PCT/US2005/022730 WO2006007491A1 (en) 2004-07-01 2005-06-27 Mitotic kinesin inhibitors

Publications (1)

Publication Number Publication Date
BRPI0512832A true BRPI0512832A (pt) 2008-04-08

Family

ID=35149059

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0512832-3A BRPI0512832A (pt) 2004-07-01 2005-06-27 composto ou um sal ou estereoisÈmero farmaceuticamente aceitável do mesmo, composição farmacêutica, e, método para usar um composto

Country Status (15)

Country Link
US (1) US7632833B2 (pt)
EP (1) EP1765830B1 (pt)
JP (1) JP2008505085A (pt)
KR (1) KR20070039885A (pt)
CN (1) CN1980938B (pt)
AT (1) ATE482218T1 (pt)
AU (1) AU2005262373B2 (pt)
BR (1) BRPI0512832A (pt)
CA (1) CA2571807A1 (pt)
DE (1) DE602005023730D1 (pt)
IL (1) IL180328A0 (pt)
MX (1) MXPA06015275A (pt)
NO (1) NO20070589L (pt)
RU (1) RU2007103816A (pt)
WO (1) WO2006007491A1 (pt)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2220061B1 (en) 2007-10-19 2016-02-17 Merck Sharp & Dohme Corp. Spiro-condensed 1, 3, 4-thiadiazole derivatives for inhibiting ksp kinesin activity
SI2483278T1 (sl) * 2009-09-28 2014-03-31 F. Hoffmann-La Roche Ag Inhibitorske spojine benzoksazepina pi3k in njihova uporaba pri zdravljenju raka
US20140087309A1 (en) * 2011-04-01 2014-03-27 The Research Foundation Of State University Of New York Olefin-triggered acid amplifiers
US20140193752A1 (en) * 2011-04-01 2014-07-10 The Research Foundation Of State University Of New York Stabilized acid amplifiers
CA2864331C (en) 2012-02-14 2018-10-09 Children's Hospital Medical Center Use of small molecule inhibitors targeting the interaction between rac gtpase and p67(phox)
WO2014176268A1 (en) * 2013-04-22 2014-10-30 Abbvie Inc. Thiazoles and uses thereof
PL3419979T3 (pl) * 2016-02-23 2020-06-29 Pfizer Inc. Związki 6,7-dihydro-5h-pirazolo[5,1-b][1,3]oksazyno-2- karboksyamidowe

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990003378A1 (en) 1988-09-22 1990-04-05 E.I. Du Pont De Nemours And Company Substituted indazole arthropodicides
PH27357A (en) 1989-09-22 1993-06-21 Fujisawa Pharmaceutical Co Pyrazole derivatives and pharmaceutical compositions comprising the same
US5719147A (en) 1992-06-29 1998-02-17 Merck & Co., Inc. Morpholine and thiomorpholine tachykinin receptor antagonists
US5604260A (en) 1992-12-11 1997-02-18 Merck Frosst Canada Inc. 5-methanesulfonamido-1-indanones as an inhibitor of cyclooxygenase-2
CA2293952A1 (en) 1993-01-15 1994-07-21 David B. Reitz Preparation of esters and analogs thereof
US5409944A (en) 1993-03-12 1995-04-25 Merck Frosst Canada, Inc. Alkanesulfonamido-1-indanone derivatives as inhibitors of cyclooxygenase
US5380738A (en) 1993-05-21 1995-01-10 Monsanto Company 2-substituted oxazoles further substituted by 4-fluorophenyl and 4-methylsulfonylphenyl as antiinflammatory agents
US5474995A (en) 1993-06-24 1995-12-12 Merck Frosst Canada, Inc. Phenyl heterocycles as cox-2 inhibitors
GB9602877D0 (en) 1996-02-13 1996-04-10 Merck Frosst Canada Inc 3,4-Diaryl-2-hydroxy-2,5- dihydrofurans as prodrugs to cox-2 inhibitors
US5436265A (en) 1993-11-12 1995-07-25 Merck Frosst Canada, Inc. 1-aroyl-3-indolyl alkanoic acids and derivatives thereof useful as anti-inflammatory agents
US5344991A (en) 1993-10-29 1994-09-06 G.D. Searle & Co. 1,2 diarylcyclopentenyl compounds for the treatment of inflammation
US5466823A (en) 1993-11-30 1995-11-14 G.D. Searle & Co. Substituted pyrazolyl benzenesulfonamides
US5393790A (en) 1994-02-10 1995-02-28 G.D. Searle & Co. Substituted spiro compounds for the treatment of inflammation
US5633272A (en) 1995-02-13 1997-05-27 Talley; John J. Substituted isoxazoles for the treatment of inflammation
US6020343A (en) 1995-10-13 2000-02-01 Merck Frosst Canada, Inc. (Methylsulfonyl)phenyl-2-(5H)-furanones as COX-2 inhibitors
CA2249009C (en) 1996-04-12 2003-09-16 G.D. Searle & Co. Substituted benzenesulfonamide derivatives as prodrugs of cox-2 inhibitors
US5861419A (en) 1996-07-18 1999-01-19 Merck Frosst Canad, Inc. Substituted pyridines as selective cyclooxygenase-2 inhibitors
DE19805117A1 (de) 1998-02-09 1999-08-12 Bayer Ag Neue Oxazolidinone mit azolhaltigen Tricyclen
DE19905278A1 (de) 1999-02-09 2000-08-10 Bayer Ag Oxazolidinone und ihre Verwendung als antibakterielle Mittel
JP4597519B2 (ja) * 2001-12-06 2010-12-15 メルク・シャープ・エンド・ドーム・コーポレイション 有糸分裂キネシン阻害薬
DE60329990D1 (de) 2002-03-08 2009-12-24 Merck & Co Inc Mitotische kinesin-hemmer

Also Published As

Publication number Publication date
JP2008505085A (ja) 2008-02-21
ATE482218T1 (de) 2010-10-15
DE602005023730D1 (de) 2010-11-04
WO2006007491A1 (en) 2006-01-19
IL180328A0 (en) 2007-07-04
AU2005262373A1 (en) 2006-01-19
EP1765830B1 (en) 2010-09-22
AU2005262373B2 (en) 2011-03-17
MXPA06015275A (es) 2007-03-15
EP1765830A1 (en) 2007-03-28
CN1980938B (zh) 2010-11-03
KR20070039885A (ko) 2007-04-13
US7632833B2 (en) 2009-12-15
CN1980938A (zh) 2007-06-13
US20080287414A1 (en) 2008-11-20
RU2007103816A (ru) 2008-08-10
CA2571807A1 (en) 2006-01-19
NO20070589L (no) 2007-03-22

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Legal Events

Date Code Title Description
B11A Dismissal acc. art.33 of ipl - examination not requested within 36 months of filing
B11Y Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette]