PE20090902A1 - Combinacion de un antimitotico e inhibidor de aurora quinasa como agentes anticancerigenos - Google Patents

Combinacion de un antimitotico e inhibidor de aurora quinasa como agentes anticancerigenos

Info

Publication number
PE20090902A1
PE20090902A1 PE2008001275A PE2008001275A PE20090902A1 PE 20090902 A1 PE20090902 A1 PE 20090902A1 PE 2008001275 A PE2008001275 A PE 2008001275A PE 2008001275 A PE2008001275 A PE 2008001275A PE 20090902 A1 PE20090902 A1 PE 20090902A1
Authority
PE
Peru
Prior art keywords
antimittic
combination
halo
alkyl
kinase inhibitor
Prior art date
Application number
PE2008001275A
Other languages
English (en)
Inventor
Andrea Dawn Basso
Original Assignee
Schering Corp
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40305124&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20090902(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Schering Corp filed Critical Schering Corp
Publication of PE20090902A1 publication Critical patent/PE20090902A1/es

Links

Classifications

    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Epoxy Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

REFERIDO A UNA COMPOSICION FARMACEUTICA QUE COMPRENDE: A) UN AGENTE ANTIMITOTICO SELECCIONADO DEL GRUPO QUE CONSISTE DE: TAXANO, PACLITAXEL, UN COMPUESTO DE FORMULA (A) ENTRE OTROS. DONDE EL ANILLO Y ES ARILO DE 5 A 6 MIEMBROS O UN HETEROARILO DE 5 O 6 MIEMBROS FUSIONADO COMO SE INDICA EN LA FORMULA A; W ES N O C(R12), DONDE R12 ES H, HALO, ALQUILO, ENTRE OTROS; X ES N O N-OXIDO; Z ES S, S(=O) O S(=O)2; R1 ES H, ALQUILO, HALO, ENTRE OTROS; R2 ES H, HALO, ARILO, ENTRE OTROS; R3 ES ALQUILO, CICLOALQUILO, HETEROCICLILO, ENTRE OTROS; Y B) UN INHIBIDOR DE AURORA QUINASA.TAL COMO (E), DONDE R ES H, CN, CICLOALQUILO, ENTRE OTROS; R1, R2 Y R3 SON H, ARILO, HETEROARILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: (i), (ii), (iii), ENTRE OTROS. TAMBIEN SE REFIERE A UN METODO DE PREPARACION. DICHO COMPUESTO ES INHIBIDOR DEL CRECIMIENTO CELULAR Y ES UTIL EN EL TRATAMIENTO DEL CANCER
PE2008001275A 2007-07-31 2008-07-30 Combinacion de un antimitotico e inhibidor de aurora quinasa como agentes anticancerigenos PE20090902A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US95308707P 2007-07-31 2007-07-31
US2398508P 2008-01-28 2008-01-28

Publications (1)

Publication Number Publication Date
PE20090902A1 true PE20090902A1 (es) 2009-07-25

Family

ID=40305124

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008001275A PE20090902A1 (es) 2007-07-31 2008-07-30 Combinacion de un antimitotico e inhibidor de aurora quinasa como agentes anticancerigenos

Country Status (17)

Country Link
US (1) US20100249030A1 (es)
EP (1) EP2182986A2 (es)
JP (1) JP2010535201A (es)
KR (1) KR20100042287A (es)
CN (1) CN101808666A (es)
AR (1) AR068048A1 (es)
AU (1) AU2008282885A1 (es)
BR (1) BRPI0814874A2 (es)
CA (1) CA2694218A1 (es)
CL (1) CL2008002224A1 (es)
CO (1) CO6331446A2 (es)
EC (1) ECSP109918A (es)
MX (1) MX2010001340A (es)
PE (1) PE20090902A1 (es)
RU (1) RU2010106878A (es)
TW (1) TW200911241A (es)
WO (1) WO2009017701A2 (es)

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EP2470183B1 (en) * 2009-08-26 2015-09-16 Merck Sharp & Dohme Corp. Heterocyclic amide compounds as protein kinase inhibitors
US8435976B2 (en) * 2009-09-08 2013-05-07 F. Hoffmann-La Roche 4-substituted pyridin-3-yl-carboxamide compounds and methods of use
NZ599597A (en) 2009-10-30 2013-05-31 Janssen Pharmaceutica Nv IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS
US8759535B2 (en) 2010-02-18 2014-06-24 High Point Pharmaceuticals, Llc Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof
AR080754A1 (es) 2010-03-09 2012-05-09 Janssen Pharmaceutica Nv Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10
EP2576560B1 (en) 2010-06-01 2015-09-30 Bayer Intellectual Property GmbH Substituted imidazopyrazines
US20140187548A1 (en) * 2010-12-17 2014-07-03 Bayer Intellectual Property Gmbh 6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders
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CN103204824B (zh) * 2012-01-12 2015-04-08 清华大学深圳研究生院 2-氨基噻唑-4-酰胺类衍生物及其制备方法与应用
US8940742B2 (en) 2012-04-10 2015-01-27 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
RU2657540C2 (ru) 2012-06-26 2018-06-14 Янссен Фармацевтика Нв Комбинации, содержащие ингибиторы pde 2, такие как 1-арил-4-метил-[1,2,4]триазоло[4,3-а]хиноксалиновые соединения, и ингибиторы pde 10, для применения в лечении неврологических или метаболических расстройств
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JP6437452B2 (ja) 2013-01-14 2018-12-12 インサイト・ホールディングス・コーポレイションＩｎｃｙｔｅ Ｈｏｌｄｉｎｇｓ Ｃｏｒｐｏｒａｔｉｏｎ Ｐｉｍキナーゼ阻害剤として有用な二環式芳香族カルボキサミド化合物
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AR097431A1 (es) 2013-08-23 2016-03-16 Incyte Corp Compuestos de carboxamida de furo y tienopiridina útiles como inhibidores de quinasas pim
JP6466924B2 (ja) 2013-10-04 2019-02-06 インフィニティー ファーマシューティカルズ， インコーポレイテッド 複素環式化合物及びその使用
WO2015051241A1 (en) 2013-10-04 2015-04-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
PL3105218T3 (pl) 2014-02-13 2020-03-31 Incyte Corporation Cyklopropyloaminy jako inhibitory lsd1
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Also Published As

Publication number Publication date
WO2009017701A2 (en) 2009-02-05
TW200911241A (en) 2009-03-16
CL2008002224A1 (es) 2009-07-17
MX2010001340A (es) 2010-06-02
EP2182986A2 (en) 2010-05-12
WO2009017701A3 (en) 2009-05-07
AR068048A1 (es) 2009-11-04
KR20100042287A (ko) 2010-04-23
CN101808666A (zh) 2010-08-18
RU2010106878A (ru) 2011-09-10
JP2010535201A (ja) 2010-11-18
CA2694218A1 (en) 2009-02-05
AU2008282885A1 (en) 2009-02-05
CO6331446A2 (es) 2011-10-20
BRPI0814874A2 (pt) 2019-09-24
US20100249030A1 (en) 2010-09-30
ECSP109918A (es) 2010-02-26

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