Nothing Special   »   [go: up one dir, main page]

CO5650252A2 - Inhibidores de quinesina mitotica - Google Patents

Inhibidores de quinesina mitotica

Info

Publication number
CO5650252A2
CO5650252A2 CO06013574A CO06013574A CO5650252A2 CO 5650252 A2 CO5650252 A2 CO 5650252A2 CO 06013574 A CO06013574 A CO 06013574A CO 06013574 A CO06013574 A CO 06013574A CO 5650252 A2 CO5650252 A2 CO 5650252A2
Authority
CO
Colombia
Prior art keywords
alkyl
alkynyl
cycloalkyl
alkenyl
quinesine
Prior art date
Application number
CO06013574A
Other languages
English (en)
Inventor
Paul J Coleman
Christopher D Cox
Robert M Garbaccio
George D Hartman
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 CO5650252A2 publication Critical patent/CO5650252A2/es

Links

Classifications

    • 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
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/626Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
    • C04B35/63Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
    • C04B35/632Organic additives
    • 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • 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
    • C07D417/14Heterocyclic 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 three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Structural Engineering (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)

Abstract

1.- Un compuesto de fórmula I: o una sal o estereoisómero farmacéuticamente aceptable del mismo,en la que: a es 0 ó 1; b es 0 ó 1; m es 0, 1, ó 2; n es 0, 1, 2 ó 3; r es 0 ó 1 ; s es 0 ó 1; t es 0, 1 ó 2;R1 y R2 se seleccionan independientemente de: H, alquilo C1-C6, arilo, heterociclilo y cicloalquilo C3-C6, opcionalmente sustituido con uno, dos o tres sustituyentes seleccionados de R7; R3 se selecciona de:1) hidrógeno;2) alquilo C1-C10;3) alquil C1-C10-O-Rd,4) alquenil C2-C10-O-Rd, 5) alquinil C2-C10-O-Rd, 6) (alquilen C1-C6)n-cicloalquil C3-C8-O-Rd,7) alquil C1-C10-(C=O)b-NRCRCAND#39, 8) alquenil C2-C10-(C=O)bNRCRCAND#39, 9) alquinil C2-C10-(C=O)bNRCRCAND#39, 10) (alquilen C1-C6)n-cicloalquil C3-C8-(C=O)bNRCRCAND#39, 11) alquil C1-C10-S(O)m-Rd, 12) alquenil C2-C10-S(O)m-Rd, 13) alquinil C2-C10-S(O)m-Rd, 14) (alquilen C1-C6)n-cicloalquil C3-C8-S(O)m-Rd, estando opcionalmente sustituidos dichos alquilo, alquenilo, alquinilo y cicloalquilo con uno o más sustituyentes seleccionados de R6;R4 se selecciona independientemente de:1) (C=O)aOb-alquilo C1-C10, 2) (C=O)aObarilo, 3) CO2H, 4) halo, ...
CO06013574A 2003-08-15 2006-02-10 Inhibidores de quinesina mitotica CO5650252A2 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US49563703P 2003-08-15 2003-08-15
US51268003P 2003-10-20 2003-10-20
US56358604P 2004-04-19 2004-04-19

Publications (1)

Publication Number Publication Date
CO5650252A2 true CO5650252A2 (es) 2006-06-30

Family

ID=34222358

Family Applications (1)

Application Number Title Priority Date Filing Date
CO06013574A CO5650252A2 (es) 2003-08-15 2006-02-10 Inhibidores de quinesina mitotica

Country Status (13)

Country Link
US (1) US20050038074A1 (es)
KR (1) KR20060058716A (es)
AR (1) AR045342A1 (es)
BR (1) BRPI0413580A (es)
CO (1) CO5650252A2 (es)
EC (1) ECSP066362A (es)
IL (1) IL173513A0 (es)
IS (1) IS8276A (es)
MA (1) MA27986A1 (es)
NO (1) NO20061194L (es)
PE (1) PE20050730A1 (es)
TW (1) TW200510380A (es)
WO (1) WO2005019205A1 (es)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2003276005B2 (en) 2002-06-14 2009-01-15 Merck Sharp & Dohme Corp. Mitotic kinesin inhibitors
CN100421665C (zh) 2002-06-14 2008-10-01 麦克公司 有丝分裂驱动蛋白抑制剂
CA2534729A1 (en) 2003-08-15 2005-02-24 Merck & Co., Inc. Mitotic kinesin inhibitors
SI1664026T1 (sl) * 2003-08-15 2009-04-30 Merck & Co Inc Inhibitorji mitotiäśnega kinezina
CN1835756A (zh) 2003-08-15 2006-09-20 默克公司 有丝分裂驱动蛋白抑制剂
JP2007533762A (ja) * 2004-04-19 2007-11-22 メルク エンド カムパニー インコーポレーテッド 2,2−二置換ピロールの調製方法
EP1888050B1 (en) 2005-05-17 2012-03-21 Merck Sharp & Dohme Ltd. cis-4-[(4-chlorophenyl)sulfonyl]-4-(2,5-difluorophenyl)cyclohexanepropanoic acid for the treatment of cancer
EP2001880A2 (en) * 2006-03-07 2008-12-17 Array Biopharma, Inc. Heterobicyclic pyrazole compounds and methods of use
BRPI0818605A2 (pt) 2007-10-19 2015-04-22 Schering Corp Derivados de 1,3,4-tiadiazl espiro-condensados para inibir a atividade de ksp cinesima
EP2413932A4 (en) 2009-04-01 2012-09-19 Merck Sharp & Dohme INHIBITORS OF AKT ACTIVITY
JP5099731B1 (ja) 2009-10-14 2012-12-19 メルク・シャープ・アンド・ドーム・コーポレーション p53活性を増大する置換ピペリジン及びその使用
US8999957B2 (en) 2010-06-24 2015-04-07 Merck Sharp & Dohme Corp. Heterocyclic compounds as ERK inhibitors
CN103068980B (zh) 2010-08-02 2017-04-05 瑟纳治疗公司 使用短干扰核酸(siNA)的RNA干扰介导的联蛋白(钙粘蛋白关联蛋白质),β1(CTNNB1)基因表达的抑制
WO2012024170A2 (en) 2010-08-17 2012-02-23 Merck Sharp & Dohme Corp. RNA INTERFERENCE MEDIATED INHIBITION OF HEPATITIS B VIRUS (HBV) GENE EXPRESSION USING SHORT INTERFERING NUCLEIC ACID (siNA)
WO2012030685A2 (en) 2010-09-01 2012-03-08 Schering Corporation Indazole derivatives useful as erk inhibitors
DK2632472T3 (en) 2010-10-29 2018-03-19 Sirna Therapeutics Inc RNA INTERFERENCE-MEDIATED INHIBITION OF GENE EXPRESSION USING SHORT INTERFERRING NUCLEIC ACIDS (SINA)
WO2012087772A1 (en) 2010-12-21 2012-06-28 Schering Corporation Indazole derivatives useful as erk inhibitors
WO2013063214A1 (en) 2011-10-27 2013-05-02 Merck Sharp & Dohme Corp. Novel compounds that are erk inhibitors
WO2013165816A2 (en) 2012-05-02 2013-11-07 Merck Sharp & Dohme Corp. SHORT INTERFERING NUCLEIC ACID (siNA) COMPOSITIONS
WO2014052563A2 (en) 2012-09-28 2014-04-03 Merck Sharp & Dohme Corp. Novel compounds that are erk inhibitors
RU2660349C2 (ru) 2012-11-28 2018-07-05 Мерк Шарп И Доум Корп. Композиции и способы для лечения злокачественной опухоли
EP2935263B1 (en) 2012-12-20 2018-12-05 Merck Sharp & Dohme Corp. Substituted imidazopyridines as hdm2 inhibitors
EP2951180B1 (en) 2013-01-30 2018-05-02 Merck Sharp & Dohme Corp. 2,6,7,8 substituted purines as hdm2 inhibitors
US20160194368A1 (en) 2013-09-03 2016-07-07 Moderna Therapeutics, Inc. Circular polynucleotides
JOP20190055A1 (ar) 2016-09-26 2019-03-24 Merck Sharp & Dohme أجسام مضادة ضد cd27
WO2018071283A1 (en) 2016-10-12 2018-04-19 Merck Sharp & Dohme Corp. Kdm5 inhibitors
MX2019012233A (es) 2017-04-13 2020-01-14 Aduro Biotech Holdings Europe Bv Anticuerpos anti-sirpa.
EP3706747A4 (en) 2017-11-08 2021-08-04 Merck Sharp & Dohme Corp. PRMT5 INHIBITORS
WO2019094311A1 (en) 2017-11-08 2019-05-16 Merck Sharp & Dohme Corp. Prmt5 inhibitors
WO2019148412A1 (en) 2018-02-01 2019-08-08 Merck Sharp & Dohme Corp. Anti-pd-1/lag3 bispecific antibodies
US11981701B2 (en) 2018-08-07 2024-05-14 Merck Sharp & Dohme Llc PRMT5 inhibitors
EP3833668A4 (en) 2018-08-07 2022-05-11 Merck Sharp & Dohme Corp. PRMT5 INHIBITORS
US20230108452A1 (en) 2019-12-17 2023-04-06 Merck Sharp & Dohme Llc Prmt5 inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6057342A (en) * 1996-08-16 2000-05-02 Dupont Pharmaceutical Co. Amidinophenyl-pyrrolidines, -pyrrolines, and -isoxazolidines and derivatives thereof
US6440686B1 (en) * 2000-06-15 2002-08-27 Cytokinetics, Inc. Methods for screening and therapeutic applications of kinesin modulators
EP1458726B1 (en) * 2001-12-06 2009-07-15 Merck & Co., Inc. Mitotic kinesin inhibitors
CN100421665C (zh) * 2002-06-14 2008-10-01 麦克公司 有丝分裂驱动蛋白抑制剂
AU2003276005B2 (en) * 2002-06-14 2009-01-15 Merck Sharp & Dohme Corp. Mitotic kinesin inhibitors
CA2500848A1 (en) * 2002-10-18 2004-05-06 Merck & Co., Inc. Mitotic kinesin inhibitors

Also Published As

Publication number Publication date
IL173513A0 (en) 2006-07-05
AR045342A1 (es) 2005-10-26
KR20060058716A (ko) 2006-05-30
IS8276A (is) 2006-01-31
NO20061194L (no) 2006-05-05
TW200510380A (en) 2005-03-16
US20050038074A1 (en) 2005-02-17
PE20050730A1 (es) 2005-09-20
MA27986A1 (fr) 2006-07-03
ECSP066362A (es) 2006-10-31
WO2005019205A1 (en) 2005-03-03
BRPI0413580A (pt) 2006-10-17

Similar Documents

Publication Publication Date Title
CO5650252A2 (es) Inhibidores de quinesina mitotica
RS52397B (en) PYRIDO / 2,1-A / ISOCHINOLINE DERIVATIVES AS DPP-IV INHIBITORS
AR047076A1 (es) Compuestos de pirrolotriazina como inhibidores de tirosina quinasas, composiciones farmaceuticas
MX2009005219A (es) Inhibidores macrociclicos del virus de hepatitis c.
RS51101B (sr) Inhibitori hcv ns3 proteaze
ECSP088150A (es) Inhibidores macrociclicos del virus de la hepatitis c
DE60217186D1 (de) Dpiv-inhibitoren auf glutaminbasis
HK1110868A1 (en) Heterocyclic compounds as ccr2b antagonists
TW200730501A (en) Heterocyclic derivatives as inhibitors of 11-β-hydroxysteroid dehydrogenase I
AR061008A1 (es) Inhibidores ns5b de vhc de indolobenzazepina fusionados a ciclopropilo
AR065810A1 (es) Derivados de isoindolina 4'-o-sustituidos,composiciones farmaceuticas que los comprenden y usos de los mismos en el tratamiento del cancer y en otros trastornos donde es necesario el control de la angiogenesis o la inhibicion de citoquinas, incluyendo tnf-alfa.
ES2476422T3 (es) Compuestos de piperidina 3,5-sustituida como inhibidores de renina
EA200501617A1 (ru) Новые гетероциклические соединения, применяемые для лечения нарушений аллергической или воспалительной природы: способы синтеза и содержащие их фармацевтические составы
HUP0201088A2 (hu) Új alfa-aminosav-szulfonil-vegyületek, eljárás előállításukra és ilyen vegyületeket tartalmazó gyógyászati készítmények
HRP20120523T1 (hr) Inhibitori virusa hepatitisa c
MY144718A (en) Viral polymerase inhibitors.
TN2009000012A1 (en) Amino-piperidine derivatives as cetp inhibitors
EA200601830A1 (ru) Ортозамещённые арильные или гетероарильные амидные соединения
BRPI0014526B8 (pt) compostos cíclicos de seis elementos contendo nitrogênio aromático, composição farmacêutica e uso do mesmo
PE20080209A1 (es) Derivados de glicina como inhibidores de prolil hidroxilasa
CO6270320A2 (es) Derivados de piperidina utiles como antagonistas del receptor orexina
PE20091573A1 (es) Derivados heterociclicos de urea como inhibidores de adn girasa y/o topoisomerasa
RS52978B (en) FUSIONED AMINO PIRIDIN AS HSP90 INHIBITORS
CO5320599A1 (es) Inhibidores no peptidilicos de la union a las celulas depen dientes de vla-4 utiles en el tratamiento de enfermedades inflamatorias, autoinmunes y respiratorias
MX2010000658A (es) Derivados de pirimidina 934.

Legal Events

Date Code Title Description
FC Application refused