CA2539320A1 - Use of chk1 inhibitors to control cell proliferation - Google Patents

Use of chk1 inhibitors to control cell proliferation Download PDF

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Publication number
CA2539320A1
CA2539320A1 CA002539320A CA2539320A CA2539320A1 CA 2539320 A1 CA2539320 A1 CA 2539320A1 CA 002539320 A CA002539320 A CA 002539320A CA 2539320 A CA2539320 A CA 2539320A CA 2539320 A1 CA2539320 A1 CA 2539320A1
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CA
Canada
Prior art keywords
substituted
unsubstituted
groups
alkyl
heterocyclyl
Prior art date
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Abandoned
Application number
CA002539320A
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English (en)
French (fr)
Inventor
Darcey Clark
Kathleen S. Keegan
Scott Peterson
Margaret Weidner
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Icos Corp
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Individual
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Publication of CA2539320A1 publication Critical patent/CA2539320A1/en
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    • 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
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
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    • A61K31/13—Amines
    • A61K31/15—Oximes (>C=N—O—); Hydrazines (>N—N<); Hydrazones (>N—N=) ; Imines (C—N=C)
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    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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    • 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
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    • A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
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    • A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
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  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Cardiology (AREA)
  • Inorganic Chemistry (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Vascular Medicine (AREA)
  • Transplantation (AREA)
  • Hematology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
CA002539320A 2003-09-17 2004-09-17 Use of chk1 inhibitors to control cell proliferation Abandoned CA2539320A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US50392503P 2003-09-17 2003-09-17
US60/503,925 2003-09-17
PCT/US2004/030806 WO2005027907A1 (en) 2003-09-17 2004-09-17 Use of chk1 inhibitors to control cell proliferation

Publications (1)

Publication Number Publication Date
CA2539320A1 true CA2539320A1 (en) 2005-03-31

Family

ID=34375418

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002539320A Abandoned CA2539320A1 (en) 2003-09-17 2004-09-17 Use of chk1 inhibitors to control cell proliferation

Country Status (12)

Country Link
US (1) US20070185013A1 (cg-RX-API-DMAC7.html)
EP (1) EP1667684A1 (cg-RX-API-DMAC7.html)
JP (1) JP2007519609A (cg-RX-API-DMAC7.html)
KR (1) KR20070064414A (cg-RX-API-DMAC7.html)
CN (1) CN1882342A (cg-RX-API-DMAC7.html)
AU (1) AU2004274013A1 (cg-RX-API-DMAC7.html)
CA (1) CA2539320A1 (cg-RX-API-DMAC7.html)
IL (1) IL174334A0 (cg-RX-API-DMAC7.html)
MX (1) MXPA06003110A (cg-RX-API-DMAC7.html)
NO (1) NO20061475L (cg-RX-API-DMAC7.html)
RU (1) RU2006112548A (cg-RX-API-DMAC7.html)
WO (1) WO2005027907A1 (cg-RX-API-DMAC7.html)

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USRE46379E1 (en) 2004-04-08 2017-04-25 Cornell Research Foundation, Inc. Functional immunohistochemical cell cycle analysis as a prognostic indicator for cancer
WO2006023931A2 (en) 2004-08-18 2006-03-02 Takeda San Diego, Inc. Kinase inhibitors
EP1778648A2 (en) * 2004-08-19 2007-05-02 ICOS Corporation Compounds useful for inhibiting chk1
EP1812439B2 (en) 2004-10-15 2017-12-06 Takeda Pharmaceutical Company Limited Kinase inhibitors
JP2008530575A (ja) * 2005-02-18 2008-08-07 アストラゼネカ アクチボラグ Chk1阻害薬に対する応答性を判定する方法
US8119655B2 (en) 2005-10-07 2012-02-21 Takeda Pharmaceutical Company Limited Kinase inhibitors
JP2009523149A (ja) * 2006-01-12 2009-06-18 ノバルティス アクチエンゲゼルシャフト mTOR阻害剤および抗葉酸化合物の組み合わせ
JP2010505962A (ja) 2006-10-09 2010-02-25 武田薬品工業株式会社 キナーゼ阻害剤
NZ575394A (en) * 2006-10-20 2012-01-12 Icos Corp Compositions of chk1 inhibitors and cyclodextrin
EP2086644A2 (en) * 2006-11-17 2009-08-12 Schering Corporation Combination of an inhibitor of dna polymerase-alpha and an inhibitor of a checkpoint kinase for proliferative disorders
CA2674075C (en) * 2006-12-29 2012-10-30 Charles P. Theuer Antifolate agent combinations in the treatment of cancer
WO2009099601A2 (en) * 2008-02-04 2009-08-13 Dana-Farber Cancer Institute, Inc. Chk1 suppresses a caspase-2 apoptotic response to dna damage that bypasses p53, bcl-2 and caspase-3
EP3563862B1 (en) * 2009-03-20 2021-05-05 The General Hospital Corporation d/b/a Massachusetts General Hospital D-arg-2'6'-dimethyltyrosine-lys-phe-nh2 for use in the prevention of secondary complications of burn injuries
KR101676062B1 (ko) * 2009-04-11 2016-11-14 어레이 바이오파마 인크. Dna 손상제를 강화시키기 위한 체크포인트 키나제 1 억제제
US8481557B2 (en) 2009-04-11 2013-07-09 Array Biopharma Inc. Method of treatment using checkpoint kinase 1 inhibitors
CN108721284A (zh) 2010-11-16 2018-11-02 阵列生物制药公司 检测点激酶1抑制剂和wee1激酶抑制剂的组合
WO2015036463A1 (en) * 2013-09-12 2015-03-19 Merz Pharma Gmbh & Co. Kgaa Topical application of vinca alkaloids for the treatment of actinic keratosis
CN105198790B (zh) * 2015-04-20 2018-02-16 范国煌 促进双阴性t细胞体外增殖的四环化合物
GB201703248D0 (en) * 2017-02-28 2017-04-12 Cancer Res Inst CHK 1 inhibition, synthetic lethality and cancer treatment

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US20070185013A1 (en) 2007-08-09
IL174334A0 (en) 2006-08-01
KR20070064414A (ko) 2007-06-20
EP1667684A1 (en) 2006-06-14
MXPA06003110A (es) 2006-06-20
JP2007519609A (ja) 2007-07-19
CN1882342A (zh) 2006-12-20
WO2005027907A1 (en) 2005-03-31
NO20061475L (no) 2006-06-13
RU2006112548A (ru) 2007-10-27
AU2004274013A1 (en) 2005-03-31

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