RU2010109452A - Способы и композиции, предназначенные для лечения раковых заболеваний - Google Patents

Способы и композиции, предназначенные для лечения раковых заболеваний Download PDF

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RU2010109452A
RU2010109452A RU2010109452/15A RU2010109452A RU2010109452A RU 2010109452 A RU2010109452 A RU 2010109452A RU 2010109452/15 A RU2010109452/15 A RU 2010109452/15A RU 2010109452 A RU2010109452 A RU 2010109452A RU 2010109452 A RU2010109452 A RU 2010109452A
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Кристине ДИРКС (DE)
Кристине Диркс
Маркус ВАРМУТ (US)
Маркус Вармут
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Айрм Ллк (Bm)
Айрм Ллк
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    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/4355Heterocyclic 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 containing a five-membered ring having oxygen as a ring hetero atom
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    • A61K31/435Heterocyclic 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
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/33Heterocyclic compounds
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    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/33Heterocyclic compounds
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    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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

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  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

1. Композиция, содержащая первый агент, который обладает способностью ингибировать путь передачи сигнала hedgehog, и второй агент, который обладает способностью ингибировать BCR-ABL. ! 2. Композиция по п.1, в которой первый агент связывается с Smo. ! 3. Композиция по п.1, в которой первый агент представляет собой циклопамин или форсколин. ! 4. Композиция по п.1, в которой второй агент представляет собой ингибитор ABL, ингибитор ABL/Scr, ингибитор киназы Aurora или не-АТФ-конкурентный ингибитор BCR-ABL. ! 5. Композиция по п.1, в которой второй агент выбран из группы, включающей ! ! ! ! ! ! , , и . ! 6. Фармацевтическая композиция, содержащая в терапевтически эффективном количестве первый агент, который обладает способностью ингибировать путь передачи сигнала hedgehog, второй агент, который обладает способностью ингибировать BCR-ABL, и фармацевтически приемлемый носитель. ! 7. Применение композиции по одному из пп.1-6 для приготовления лекарственного средства, предназначенного для лечения BCR-ABL-позитивного лейкоза. ! 8. Применение по п.7, в котором BCR-ABL-позитивный лейкоз представляет собой хронический миелолейкоз или острый лимфолейкоз.

Claims (8)

1. Композиция, содержащая первый агент, который обладает способностью ингибировать путь передачи сигнала hedgehog, и второй агент, который обладает способностью ингибировать BCR-ABL.
2. Композиция по п.1, в которой первый агент связывается с Smo.
3. Композиция по п.1, в которой первый агент представляет собой циклопамин или форсколин.
4. Композиция по п.1, в которой второй агент представляет собой ингибитор ABL, ингибитор ABL/Scr, ингибитор киназы Aurora или не-АТФ-конкурентный ингибитор BCR-ABL.
5. Композиция по п.1, в которой второй агент выбран из группы, включающей
Figure 00000001
Figure 00000002
Figure 00000003
Figure 00000004
Figure 00000005
Figure 00000006
Figure 00000007
Figure 00000008
Figure 00000009
Figure 00000010
Figure 00000011
Figure 00000012
,
Figure 00000013
, и
Figure 00000014
.
6. Фармацевтическая композиция, содержащая в терапевтически эффективном количестве первый агент, который обладает способностью ингибировать путь передачи сигнала hedgehog, второй агент, который обладает способностью ингибировать BCR-ABL, и фармацевтически приемлемый носитель.
7. Применение композиции по одному из пп.1-6 для приготовления лекарственного средства, предназначенного для лечения BCR-ABL-позитивного лейкоза.
8. Применение по п.7, в котором BCR-ABL-позитивный лейкоз представляет собой хронический миелолейкоз или острый лимфолейкоз.
RU2010109452/15A 2007-08-16 2008-08-13 Способы и композиции, предназначенные для лечения раковых заболеваний RU2010109452A (ru)

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US60/956,295 2007-08-16

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US (3) US20100216828A1 (ru)
EP (1) EP2187967B1 (ru)
JP (1) JP2010536775A (ru)
KR (1) KR20100056525A (ru)
CN (1) CN101820915A (ru)
AU (1) AU2008289255B2 (ru)
BR (1) BRPI0815330A2 (ru)
CA (1) CA2699988A1 (ru)
DK (1) DK2187967T3 (ru)
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HR (1) HRP20130642T1 (ru)
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PL (1) PL2187967T3 (ru)
RU (1) RU2010109452A (ru)
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US20110117212A1 (en) * 2008-07-24 2011-05-19 Nerviano Medical Sciences S.R.L. Therapeutic combination comprising an aurora kinase inhibitor and an antineoplastic agent
US20110039850A1 (en) * 2009-08-12 2011-02-17 Mhairi Copland Leukemia Treatment
RU2012120901A (ru) * 2009-10-23 2013-12-10 Новартис Аг Способ лечения пролиферативных расстройств и других патологических состояний, опосредованных действием киназ bcr-abl, c-kit, ddr1, ddr2 или pdgf-r
WO2013187967A1 (en) 2012-06-15 2013-12-19 Institute For Cancer Research D/B/A The Research Institute Of Fox Case Cancer Center ("Fox Chase Cancer Center") Sensitization of cancer cells to dna damage by inhibiting kinases essential for dna damage checkpoint control
CN103768067A (zh) * 2012-10-23 2014-05-07 杨子娇 一类治疗房角狭窄的化合物及其用途
CN104262262B (zh) * 2014-08-29 2016-06-08 西安交通大学 一种N,6二苯基嘧啶-4-胺类Bcr-Abl抑制剂及其制备方法和应用
CN109744199A (zh) * 2017-11-08 2019-05-14 南京艾莫瑞生物科技有限公司 一种肿瘤细胞异种移植斑马鱼模型、其构建方法及应用
WO2018211007A1 (en) * 2017-05-18 2018-11-22 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of mast cell diseases
CN108721217B (zh) * 2018-08-21 2020-09-08 武汉轻工大学 抗肿瘤药物组合物及药物制剂和应用
US20200297725A1 (en) * 2019-03-22 2020-09-24 Yale University Allosteric bcr-abl proteolysis targeting chimeric compounds

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US5789650A (en) 1990-08-29 1998-08-04 Genpharm International, Inc. Transgenic non-human animals for producing heterologous antibodies
DE19541844C1 (de) 1995-11-09 1997-07-24 Gsf Forschungszentrum Umwelt Verfahren zur Herstellung von menschlichen Antikörpern und deren Verwendung
US6291516B1 (en) 1999-01-13 2001-09-18 Curis, Inc. Regulators of the hedgehog pathway, compositions and uses related thereto
ATE404200T1 (de) 2002-04-22 2008-08-15 Univ Johns Hopkins Med Modulatoren von hedgehog signalpfaden, zusammensetzungen und verwandte verwendungen
WO2004072266A2 (en) 2003-02-13 2004-08-26 Kalobios Inc. Antibody affinity engineering by serial epitope-guided complementarity replacement
CN102964294A (zh) 2004-09-02 2013-03-13 遗传技术研究公司 Hedgehog信号转导的吡啶基抑制剂
WO2006102611A2 (en) * 2005-03-24 2006-09-28 The Ohio State University Research Foundation Therapeutic agents for the treatment of leukemia

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CA2699988A1 (en) 2009-02-26
CN101820915A (zh) 2010-09-01
SI2187967T1 (sl) 2013-07-31
US20100216828A1 (en) 2010-08-26
AU2008289255B2 (en) 2012-02-02
EP2187967B1 (en) 2013-04-24
BRPI0815330A2 (pt) 2017-05-09
US20130210771A1 (en) 2013-08-15
PL2187967T3 (pl) 2013-09-30
ES2422285T3 (es) 2013-09-10
AU2008289255A1 (en) 2009-02-26
KR20100056525A (ko) 2010-05-27
DK2187967T3 (da) 2013-07-22
EP2187967A1 (en) 2010-05-26
US20120165355A1 (en) 2012-06-28
MX2010001813A (es) 2010-03-10
WO2009026075A1 (en) 2009-02-26
JP2010536775A (ja) 2010-12-02
HRP20130642T1 (en) 2013-08-31

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