[go: up one dir, main page]

PE20110365A1 - Diazacarbazoles como inhibidores de checkpoint quinasa 1 (chk1) - Google Patents

Diazacarbazoles como inhibidores de checkpoint quinasa 1 (chk1)

Info

Publication number
PE20110365A1
PE20110365A1 PE2010001127A PE2010001127A PE20110365A1 PE 20110365 A1 PE20110365 A1 PE 20110365A1 PE 2010001127 A PE2010001127 A PE 2010001127A PE 2010001127 A PE2010001127 A PE 2010001127A PE 20110365 A1 PE20110365 A1 PE 20110365A1
Authority
PE
Peru
Prior art keywords
halo
dipyrido
pyrrol
chk1
inhibitors
Prior art date
Application number
PE2010001127A
Other languages
English (en)
Inventor
Hazel Joan Dyke
Charles Ellwood
Emanuela Gancia
Lewis J Gazzard
Simon Charles Goodacre
Samuel S Kintz
Joseph P Lyssikatos
Calum Macleod
Karen Williams
Huifen Chen
Original Assignee
Genentech 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41066724&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20110365(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Genentech Inc filed Critical Genentech Inc
Publication of PE20110365A1 publication Critical patent/PE20110365A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/437Heterocyclic 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 nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/4375Heterocyclic 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 six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • 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
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Peptides Or Proteins (AREA)

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE 1,7-DIAZACARBAZOL DE FORMULAS (I), (I-a) Y (I-b) DONDE X ES CR2 O N, DONDE R2 ES H, HALO, CN, ENTRE OTROS; Y ES CR4 O N, DONDE R4 ES H, HALO, CF3, ENTRE OTROS; Z ES CR8 O N, DONDE R8 ES H, CN, NO2, ENTRE OTROS; R3 ES H, CN, HALO, ENTRE OTROS; R5 ES H, HALO, OCF3, OH, ENTRE OTROS; R6 ES H, CN, ALQUILO, ENTRE OTROS; R7 ES H, OH, O(ALQUILO C1-C3), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 3-[4-(1-METIL-PIPERIDIN-4-IL)-FENIL]-9H-DIPIRIDO[2,3-b;4',3'-d]PIRROL-6-CARBONITRILO; 3-(4-PIRROLIDIN-1-IL-FENIL)-9H-DIPIRIDO[2,3-b;4',3'-d]PIRROL-6-CARBONITRILO; N-{2-[4-(6-CIANO-9H-DIPIRIDO[2,3-b;4',3'-d]PIRROL-3-IL)-FENOXI]-ETIL}-METANSULFONAMIDA; ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA CON UN SEGUNDO COMPUESTO ACTIVO QUE ES UN AGENTE QUE DANA EL ADN. DICHOS COMPUESTOS SON INHIBIDORES DE CHECKPOINT QUINASA 1 (CHK1) SIENDO UTILES EN EL TRATAMIENTO DE CANCER DE MAMA, CANCER DE PULMON DE CELULAS NO PEQUENAS, SARCOMA, MELANOMA
PE2010001127A 2008-06-11 2009-06-10 Diazacarbazoles como inhibidores de checkpoint quinasa 1 (chk1) PE20110365A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US6074608P 2008-06-11 2008-06-11
US14800109P 2009-01-28 2009-01-28

Publications (1)

Publication Number Publication Date
PE20110365A1 true PE20110365A1 (es) 2011-07-11

Family

ID=41066724

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2010001127A PE20110365A1 (es) 2008-06-11 2009-06-10 Diazacarbazoles como inhibidores de checkpoint quinasa 1 (chk1)
PE2013002559A PE20140609A1 (es) 2008-06-11 2009-06-10 Diazacarbazoles y metodos de uso

Family Applications After (1)

Application Number Title Priority Date Filing Date
PE2013002559A PE20140609A1 (es) 2008-06-11 2009-06-10 Diazacarbazoles y metodos de uso

Country Status (20)

Country Link
US (3) US8501765B2 (es)
EP (2) EP2300475B1 (es)
JP (2) JP5599784B2 (es)
KR (1) KR101710732B1 (es)
CN (2) CN102119163A (es)
AR (1) AR072092A1 (es)
AU (1) AU2009258124C1 (es)
BR (1) BRPI0909954A2 (es)
CA (1) CA2725754C (es)
CL (1) CL2010001415A1 (es)
DK (1) DK2300475T3 (es)
ES (1) ES2529361T3 (es)
IL (1) IL209754A0 (es)
MX (1) MX2010013627A (es)
PE (2) PE20110365A1 (es)
PH (1) PH12013502369A1 (es)
RU (2) RU2515972C2 (es)
TW (2) TW201512199A (es)
WO (1) WO2009151598A1 (es)
ZA (1) ZA201008483B (es)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL1896040T3 (pl) 2005-06-29 2012-12-31 Threshold Pharmaceuticals Inc Proleki alkilatora fosforoamidowego
JP5599784B2 (ja) * 2008-06-11 2014-10-01 ジェネンテック, インコーポレイテッド ジアザカルバゾール類と使用方法
AR072084A1 (es) * 2008-06-12 2010-08-04 Sanofi Aventis Derivados de azacarbolinas, su preparacion y su utilizacion terapeutica como inhibidores de las quinasas pim
FR2950891B1 (fr) * 2009-10-06 2012-11-09 Sanofi Aventis Derives d'azacarbolines 9h-pyrrolo[2,3-b:5,4-c']dipyridine, leur preparation et leur utilisation therapeutique
CN102365282A (zh) * 2009-03-24 2012-02-29 赛诺菲 9H-吡咯并[2,3-b:5,4-c’]二吡啶氮杂咔啉衍生物、其制备方法及其治疗用途
US20110183938A1 (en) * 2009-12-16 2011-07-28 Genentech, Inc. 1,7-diazacarbazoles and methods of use
CN103442710B (zh) 2010-11-16 2018-05-29 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
CN102503959B (zh) * 2011-10-25 2015-04-08 南方医科大学 一种稠三环类化合物及其制备方法、以及含该类化合物的药物组合物及其应用
BR112014010938A2 (pt) * 2011-11-09 2017-05-16 Cancer Res Tech Ltd compostos de 5-(piridin-2-il-amino)-pirazina-2-carbonitrila e seu uso terapêutico
EP2793882A4 (en) 2011-12-22 2015-04-29 Threshold Pharmaceuticals Inc ADMINISTRATION OF HYPOXIA-ACTIVATED PRODRUGS IN COMBINATION WITH CHK1 INHIBITORS FOR THE TREATMENT OF CANCER
CA2869954C (en) 2012-04-20 2023-01-03 Advinus Therapeutics Limited Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof in medical conditions related to modulation of bruton's tyrosine kinase activity
EP2671881A1 (en) 2012-06-07 2013-12-11 Syngenta Participations AG. Pesticidally active pyridyl- and pyrimidyl- substituted thiazole derivatives
CN105764501A (zh) 2013-07-26 2016-07-13 现代化制药公司 改善比生群治疗效益的组合物
US10071109B2 (en) 2013-11-06 2018-09-11 Molecular Templates, Inc. Predictive biomarker for hypoxia-activated prodrug therapy
AU2015240465B2 (en) 2014-04-04 2020-02-27 Del Mar Pharmaceuticals Use of dianhydrogalactitol and analogs or derivatives thereof to treat non-small-cell carcinoma of the lung and ovarian cancer
CN107118207B (zh) * 2017-05-22 2020-10-02 苏州东南药业股份有限公司 一类cdk抑制剂的制备方法
CN112566912A (zh) 2018-05-04 2021-03-26 因赛特公司 Fgfr抑制剂的盐
WO2020061377A1 (en) * 2018-09-19 2020-03-26 Genentech, Inc. Spirocyclic 2,3-dihydro-7-azaindole compounds and uses thereof
WO2020072675A1 (en) 2018-10-02 2020-04-09 Northwestern University Beta-carbolines as positive allosteric modulators of the human serotonin receptor 2c (5-ht2c)
CA3122183A1 (en) * 2018-12-13 2020-06-18 Intervet International B.V. Process for preparing 1-[(3r,4s)-4-cyanotetrahydropyran-3-yl]-3-[(2-fluoro-6-methoxy-4-pyridyl)amino]p yrazole-4-carboxamide
EP4069695A1 (en) 2019-12-04 2022-10-12 Incyte Corporation Derivatives of an fgfr inhibitor
US12168662B1 (en) 2023-12-15 2024-12-17 King Faisal University Pyrido[4′,3′:4,5]pyrrolo[2,3-c][2,7]naphthyridines compounds as CK2 inhibitors
US12129252B1 (en) 2024-02-15 2024-10-29 King Faisal University Pyrrolo[2,3-c][2,6]naphthyridine-8-carboxylic acids as CK2 inhibitors

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60141895D1 (de) 2000-03-15 2010-06-02 Sanofi Aventis Deutschland Substituierte beta-carboline mit ikb-kinase hemmender wirkung
WO2001068648A1 (en) * 2000-03-15 2001-09-20 Aventis Pharma Deutschland Gmbh Substituted beta-carbolines with ikb-kinase inhibiting activity
GB0116966D0 (en) * 2001-07-11 2001-09-05 Pharma Mar Sa Anittumoral compounds
GB0121941D0 (en) 2001-09-11 2001-10-31 Astrazeneca Ab Chemical compounds
EP1443927B1 (en) * 2001-11-07 2007-01-10 Millennium Pharmaceuticals, Inc. Carboline derivatives as inhibitors of ikb in the treatment of multiple myeloma
EP1599202A1 (en) 2003-02-17 2005-11-30 Pharmacia Italia S.p.A. Tetracyclic pyrazole derivatives as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
SE0401655D0 (sv) 2004-06-24 2004-06-24 Astrazeneca Ab New compounds
JP2008542433A (ja) * 2005-06-09 2008-11-27 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング CDK−1インヒビターとしてのα−カルボリン
US8119655B2 (en) * 2005-10-07 2012-02-21 Takeda Pharmaceutical Company Limited Kinase inhibitors
EP2145877B1 (en) 2006-10-09 2012-10-03 Takeda Pharmaceutical Company Limited Aurora Kinase inhibitors
EP2081930A2 (en) 2006-10-09 2009-07-29 Takeda San Diego, Inc. Kinase inhibitors
US8618121B2 (en) 2007-07-02 2013-12-31 Cancer Research Technology Limited 9H-pyrimido[4,5-B]indoles, 9H-pyrido[4',3':4,5]pyrrolo[2,3-D]pyridines, and 9H 1,3,6,9 tetraaza-fluorenes as CHK1 kinase function inhibitors
US8133506B2 (en) 2008-03-12 2012-03-13 Aptalis Pharmatech, Inc. Drug delivery systems comprising weakly basic drugs and organic acids
WO2009129401A1 (en) 2008-04-16 2009-10-22 Takeda Pharmaceutical Company Limited Kinase inhibitors
JP5599784B2 (ja) * 2008-06-11 2014-10-01 ジェネンテック, インコーポレイテッド ジアザカルバゾール類と使用方法
AR072084A1 (es) 2008-06-12 2010-08-04 Sanofi Aventis Derivados de azacarbolinas, su preparacion y su utilizacion terapeutica como inhibidores de las quinasas pim
WO2010015589A1 (en) 2008-08-05 2010-02-11 Nycomed Gmbh Benzyl-substituted tetracyclic heterocyclic compounds as pde5 inhibitors
CN102365282A (zh) 2009-03-24 2012-02-29 赛诺菲 9H-吡咯并[2,3-b:5,4-c’]二吡啶氮杂咔啉衍生物、其制备方法及其治疗用途

Also Published As

Publication number Publication date
HK1149933A1 (en) 2011-10-21
CN104059066A (zh) 2014-09-24
JP5599784B2 (ja) 2014-10-01
AU2009258124B2 (en) 2015-01-29
RU2010154105A (ru) 2012-07-20
MX2010013627A (es) 2010-12-21
AU2009258124C1 (en) 2016-01-07
US20150087630A1 (en) 2015-03-26
ZA201008483B (en) 2012-03-28
TW201512199A (zh) 2015-04-01
CA2725754C (en) 2017-05-23
EP2706059A1 (en) 2014-03-12
US20130261104A1 (en) 2013-10-03
ES2529361T3 (es) 2015-02-19
TWI466886B (zh) 2015-01-01
JP2015028027A (ja) 2015-02-12
AR072092A1 (es) 2010-08-04
WO2009151598A8 (en) 2010-05-06
IL209754A0 (en) 2011-02-28
KR101710732B1 (ko) 2017-02-27
CL2010001415A1 (es) 2011-05-06
EP2300475B1 (en) 2014-11-05
AU2009258124A2 (en) 2011-01-20
EP2300475A1 (en) 2011-03-30
CN102119163A (zh) 2011-07-06
US8501765B2 (en) 2013-08-06
RU2013156074A (ru) 2015-06-27
WO2009151598A1 (en) 2009-12-17
CA2725754A1 (en) 2009-12-17
BRPI0909954A2 (pt) 2015-11-03
US9216980B2 (en) 2015-12-22
RU2515972C2 (ru) 2014-05-20
DK2300475T3 (en) 2014-12-08
PE20140609A1 (es) 2014-05-22
KR20110015697A (ko) 2011-02-16
TW201011023A (en) 2010-03-16
PH12013502369A1 (en) 2015-09-21
US20110118230A1 (en) 2011-05-19
JP2011522889A (ja) 2011-08-04
AU2009258124A1 (en) 2009-12-17

Similar Documents

Publication Publication Date Title
PE20110365A1 (es) Diazacarbazoles como inhibidores de checkpoint quinasa 1 (chk1)
PE20130038A1 (es) Derivados de piperidin-4-il azetidina como inhibidores de jak1
PE20090773A1 (es) Derivados de morfolina pirimidina
PE20091842A1 (es) Pirrolidinonas como activadores de glucoquinasa
CL2011000735A1 (es) N-[4-({4-[3-(3-terc-butil-1-p-tolil-1h-pirazol-5-il)ureido]naftalen-1-il-oxi}metil)piridin-2-il]-2-metoxiacetamida; procedimiento de preparacion; compuestos intermediarios; composicion farmaceutica; y uso en el tratamiento de epoc, asma, dermatitis de contacto, artritis, entre otros.
PE20090601A1 (es) Derivados de piridin-il-oxi-piridinas como inhibidores de alk5
AR081385A1 (es) Composiciones metodo y uso
PE20190175A1 (es) Compuestos de pirrolotriazina como inhibidores de tam
PE20090772A1 (es) Derivados de bencimidazol
PE20140826A1 (es) Compuestos sustituidos fungicidas de 2-[2-halogenalquil-4-(fenoxi)-fenil]-1-[1,2,4]triazol-1-il-etanol
EA201001358A1 (ru) Активаторы глюкокиназы
PE20081512A1 (es) Compuestos y composiciones como inhibidores de la actividad del receptor de canabinoide 1
PE20091656A1 (es) Compuestos heterociclicos como inhibidores de la cinasa raf
PE20091623A1 (es) DERIVADOS DE 1H-PIRAZOLO[3,4-b]PIRIDINA COMO INHIBIDORES DE RAF QUINASA
PE20060215A1 (es) 4-fenilamino-quinazolin-6-il-amidas
PE20140913A1 (es) Inhibidores de nampt y rock
PE20091943A1 (es) Compuestos triazina como inhibidores mtor y quinasa pi3
PE20141120A1 (es) Compuestos heterociclicos
CO6210776A2 (es) Diaminopirimidinas como fungicidas
PE20110424A1 (es) Isoindolonas que inhiben la cinasa mek
PE20091561A1 (es) Compuestos inhibidores de raf y metodos para su uso
GEP201706728B (en) Noxious organism control agent
PE20121480A1 (es) Aminopirimidinas como inhibidores de syk
PE20140934A1 (es) Derivados de pirazol
MX2010010135A (es) Derivados de hidroximoil-tetrazol fungicidas.

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed