[go: up one dir, main page]

TNSN05298A1 - Derives de pyrazolo-quinazoline, procede pour leur preparation et leur utilisation comme inhibiteurs de kinases - Google Patents

Derives de pyrazolo-quinazoline, procede pour leur preparation et leur utilisation comme inhibiteurs de kinases

Info

Publication number
TNSN05298A1
TNSN05298A1 TNP2005000298A TNSN05298A TNSN05298A1 TN SN05298 A1 TNSN05298 A1 TN SN05298A1 TN P2005000298 A TNP2005000298 A TN P2005000298A TN SN05298 A TNSN05298 A TN SN05298A TN SN05298 A1 TNSN05298 A1 TN SN05298A1
Authority
TN
Tunisia
Prior art keywords
pyrazolo
preparation
quinazoline derivatives
kinase inhibitors
deregulation
Prior art date
Application number
TNP2005000298A
Other languages
English (en)
Inventor
Gabriella Traquandi
Maria Gabriella Brasca
Roberto D'alessio
Paolo Polucci
Fulvia Roletto
Anna Vulpetti
Paolo Pevarello
Achille Panzeri
Francesca Quartieri
Ron Ferguson
Paola Vianello
Daniele Fancelli
Original Assignee
Nerviano Medical Sciences S R I
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=33476970&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TNSN05298(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Nerviano Medical Sciences S R I filed Critical Nerviano Medical Sciences S R I
Publication of TNSN05298A1 publication Critical patent/TNSN05298A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14Ortho-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
    • A61K31/495Heterocyclic 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • 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
    • C07D401/10Heterocyclic 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 carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Neurology (AREA)
  • Virology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Communicable Diseases (AREA)
  • Dermatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Hematology (AREA)
  • Hospice & Palliative Care (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Molecular Biology (AREA)
  • Pulmonology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Transplantation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Des dérivés de pyrazolo-quinazoline de formule (Ia) ou (Ib), répondant à la définition figurant dans le présent mémoire, et leurs sels pharmaceutiquement acceptables, un procédé pour leur préparation et des compositions pharmaceutiques les comprenant sont décrits ; Les composés de la présente invention peuvent être utiles, en thérapeutique, dans le traitement de maladies associées à une dérégulation d'activité de protéine-kinase, telles que le cancer.
TNP2005000298A 2003-05-22 2005-11-21 Derives de pyrazolo-quinazoline, procede pour leur preparation et leur utilisation comme inhibiteurs de kinases TNSN05298A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US47266103P 2003-05-22 2003-05-22
PCT/EP2004/050612 WO2004104007A1 (fr) 2003-05-22 2004-04-27 Derives de pyrazolo-quinazoline, procede de preparation associe et leur utilisation en tant qu'inhibiteurs de kinase

Publications (1)

Publication Number Publication Date
TNSN05298A1 true TNSN05298A1 (fr) 2007-07-10

Family

ID=33476970

Family Applications (1)

Application Number Title Priority Date Filing Date
TNP2005000298A TNSN05298A1 (fr) 2003-05-22 2005-11-21 Derives de pyrazolo-quinazoline, procede pour leur preparation et leur utilisation comme inhibiteurs de kinases

Country Status (36)

Country Link
US (9) US7482354B2 (fr)
EP (1) EP1636236B1 (fr)
JP (1) JP5043432B2 (fr)
KR (1) KR101084871B1 (fr)
CN (2) CN1826343A (fr)
AP (1) AP2064A (fr)
AR (2) AR044543A1 (fr)
AU (1) AU2004240772B2 (fr)
BR (2) BR122019010200B8 (fr)
CA (1) CA2526578C (fr)
CO (1) CO5721006A2 (fr)
CR (1) CR8102A (fr)
CY (1) CY1114708T1 (fr)
DK (1) DK1636236T3 (fr)
EA (1) EA010904B1 (fr)
EC (1) ECSP056194A (fr)
ES (1) ES2436524T3 (fr)
GE (1) GEP20094664B (fr)
HR (1) HRP20050967B8 (fr)
IL (1) IL172046A (fr)
IS (1) IS2939B (fr)
ME (1) ME00142B (fr)
MX (1) MXPA05012573A (fr)
MY (1) MY142019A (fr)
NO (1) NO334992B1 (fr)
NZ (1) NZ543661A (fr)
OA (1) OA13170A (fr)
PL (1) PL1636236T3 (fr)
PT (1) PT1636236E (fr)
RS (2) RS20050944A (fr)
SI (1) SI1636236T1 (fr)
TN (1) TNSN05298A1 (fr)
TW (1) TWI349672B (fr)
UA (1) UA80763C2 (fr)
WO (1) WO2004104007A1 (fr)
ZA (1) ZA200509486B (fr)

Families Citing this family (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RS20050944A (sr) 2003-05-22 2008-06-05 Nerviano Medical Sciences S.R.L., Derivati pirazolo- hinazolina,postupci za njihovo dobijanje i njihova upotreba kao inhibitora kinaze
CN1897950A (zh) 2003-10-14 2007-01-17 惠氏公司 稠合芳基和杂芳基衍生物及其使用方法
EP1694686A1 (fr) 2003-12-19 2006-08-30 Takeda San Diego, Inc. Inhibiteurs de kinase
US7772232B2 (en) 2004-04-15 2010-08-10 Bristol-Myers Squibb Company Quinazolinyl compounds as inhibitors of potassium channel function
ITMI20041033A1 (it) 2004-05-24 2004-08-24 Neuroscienze S C A R L Composti farmaceutici
JP2008510734A (ja) 2004-08-18 2008-04-10 タケダ サン ディエゴ インコーポレイテッド キナーゼ阻害剤
EP1812439B2 (fr) 2004-10-15 2017-12-06 Takeda Pharmaceutical Company Limited Inhibiteurs de kinase
US8119655B2 (en) 2005-10-07 2012-02-21 Takeda Pharmaceutical Company Limited Kinase inhibitors
EP1986632B1 (fr) * 2006-02-10 2012-08-15 Nerviano Medical Sciences S.R.L. Combinaisons comprenant un inhibiteur de cdk et un anticorps anti-facteur de croissance ou un antimitotique
EP2026800A1 (fr) * 2006-05-09 2009-02-25 Novartis AG Combinaison comprenant un chélatant du fer et un agent antinéoplasique et ses applications
US20080015193A1 (en) * 2006-06-20 2008-01-17 Mendoza Jose S Certain azoles exhibiting ATP-utilizing enzyme inhibitory activity, compositions, and uses thereof
US7517882B2 (en) * 2006-09-18 2009-04-14 Polaris Group Protein kinase inhibitors
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
UA102219C2 (ru) * 2006-12-21 2013-06-25 НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. Замещенные пиразолохиназолиновые производные, способ их получения и их применения как ингибиторов киназы
SI2125822T1 (sl) * 2006-12-21 2015-01-30 Nerviano Medical Sciences S.R.L. Substituirani pirazolo-kinazolinski derivati, postopek za njihovo pripravo in njihova uporaba kot inhibitorji kinaze
EP2213673B1 (fr) 2007-10-23 2013-06-05 Msd K.K. Dérivé de dihydropyrazolopyrimidinone substitué par pyridone
US8841312B2 (en) * 2007-12-19 2014-09-23 Amgen Inc. Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors
JP5530422B2 (ja) * 2008-04-07 2014-06-25 アムジエン・インコーポレーテツド 細胞周期阻害薬としてのgem−二置換およびスピロ環式アミノピリジン/ピリミジン
TWI426074B (zh) * 2008-04-30 2014-02-11 Nerviano Medical Sciences Srl 5-(2-胺基-嘧啶-4-基)-2-芳基-1h-吡咯-3-羧醯胺之製造方法
WO2009156315A1 (fr) * 2008-06-26 2009-12-30 Nerviano Medical Sciences S.R.L. Pyrazolo-quinazolines
CN102105152B (zh) 2008-07-29 2012-10-17 内尔维阿诺医学科学有限公司 包含cdks抑制剂和抗肿瘤剂的治疗组合
US8946226B2 (en) * 2008-07-29 2015-02-03 Nerviano Medical Sciences S.R.L. Use of CDK inhibitor for the treatment of glioma
US8653097B2 (en) * 2008-10-17 2014-02-18 Boehringer Ingelheim International Gmbh Tetra-aza-heterocycles as phosphatidylinositol-3-kinases (P13-kinases) inhibitor
US8912194B2 (en) * 2008-11-24 2014-12-16 Nerviano Medical Sciences S.R.L. CDK inhibitor for the treatment of mesothelioma
IT1395724B1 (it) * 2009-02-25 2012-10-19 Neuroscienze Pharmaness S C A R L Composti farmaceutici
JP5650193B2 (ja) * 2009-03-20 2015-01-07 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ 胸腺腫の治療のためのキナーゼ阻害剤の使用
US9243000B2 (en) 2009-04-22 2016-01-26 Boehringer Ingelheim International Gmbh Thia-triaza-indacenes
ES2660146T3 (es) 2009-04-29 2018-03-21 Nerviano Medical Sciences S.R.L. Sales del inhibidor de cdk
AR076784A1 (es) 2009-05-26 2011-07-06 Nerviano Medical Sciences Srl Combinacion terapeutica que comprende un inhibidor de plk1 y un agente antineoplasico
CN103626777B (zh) * 2009-07-29 2015-10-21 内尔维阿诺医学科学有限公司 Plk抑制剂的盐类
CN102844313B (zh) * 2010-01-28 2016-10-05 哈佛大学校长及研究员协会 提高蛋白酶体活性的组合物和方法
US8735386B2 (en) * 2010-07-23 2014-05-27 Boehringer Ingelheim International Gmbh Aminopyrazoloquinazolines
JP5997143B2 (ja) * 2010-07-30 2016-09-28 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ タンパク質キナーゼ活性の調整剤としてのイソオキサゾロ−キナゾリン
EP2619181A1 (fr) 2010-09-23 2013-07-31 Syngenta Participations AG Microbiocides inédits
HRP20161092T1 (hr) * 2010-10-25 2016-10-21 G1 Therapeutics, Inc. Cdk inhibitori
CA2812223C (fr) * 2010-12-17 2019-03-12 Nerviano Medical Sciences S.R.L. Derives de pyrazolo-quinazoline substitues a titre d'inhibiteurs de kinases
EP2668190B1 (fr) * 2011-01-26 2016-08-17 Nerviano Medical Sciences S.r.l. Dérivés pyrrolo tricycliques, leur procédé de préparation et leur utilisation à titre d'inhibiteurs de kinases
WO2012101029A1 (fr) * 2011-01-26 2012-08-02 Nerviano Medical Sciences S.R.L. Dérivés tricycliques, leur procédé de préparation et leur utilisation à titre d'inhibiteurs de kinases
WO2012117021A2 (fr) 2011-03-03 2012-09-07 Syngenta Participations Ag Nouveaux éthers d'oxime microbiocides
MY161199A (en) 2011-03-23 2017-04-14 Amgen Inc Fused tricyclic dual inhibitors of cdk 4/6 and flt3
US9556166B2 (en) 2011-05-12 2017-01-31 Proteostasis Therapeutics, Inc. Proteostasis regulators
WO2013092460A1 (fr) 2011-12-20 2013-06-27 Syngenta Participations Ag Microbicides bisoximes cycliques
JP6128133B2 (ja) * 2012-01-23 2017-05-17 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 Igf−1r/ir阻害剤としての5,8−ジヒドロ−6h−ピラゾロ[3,4−h]キナゾリン
EP2641901A1 (fr) 2012-03-22 2013-09-25 Syngenta Participations AG. Nouveaux microbicides bisoximes
ES2755772T3 (es) 2012-11-07 2020-04-23 Nerviano Medical Sciences Srl Pirimidinil y piridinilpirrolopiridinonas sustituidas, proceso para su preparación y su uso como inhibidores de cinasas
WO2014116228A1 (fr) 2013-01-25 2014-07-31 President And Fellows Of Harvard College Inhibiteurs de l'usp14 utilisables en vue du traitement ou de la prévention d'infections virales
CN105407723A (zh) 2013-03-15 2016-03-16 G1治疗公司 高效的抗赘生剂和抗增生剂
WO2014144326A1 (fr) 2013-03-15 2014-09-18 G1 Therapeutics, Inc. Protection transitoire de cellules normales pendant une chimiothérapie
WO2015073528A1 (fr) 2013-11-12 2015-05-21 Proteostasis Therapeutics, Inc. Composés renforçant l'activité des protéasomes
CA2944610C (fr) 2014-04-07 2024-01-09 Netherlands Translational Research Center B.V. (5,6-dihydro)pyrimido[4,5-e]indozilines
US20150297606A1 (en) 2014-04-17 2015-10-22 G1 Therapeutics, Inc. Tricyclic Lactams for Use in the Protection of Hematopoietic Stem and Progenitor Cells Against Ionizing Radiation
ES2873959T3 (es) 2014-05-28 2021-11-04 Piramal Entpr Ltd Combinación farmacéutica que comprende un inhibidor de CDK y un inhibidor de tiorredoxina reductasa para el tratamiento del cáncer
WO2016040848A1 (fr) 2014-09-12 2016-03-17 G1 Therapeutics, Inc. Traitement de tumeurs rb-négatives en utilisant des inhibiteurs de la topoisomérase en association avec des inhibiteurs des kinases cycline-dépendantes 4/6
WO2016040858A1 (fr) 2014-09-12 2016-03-17 G1 Therapeutics, Inc. Combinaisons et régimes posologiques pour traiter des tumeurs rb-positives
CA2992161A1 (fr) 2015-07-17 2017-01-26 Institut Pasteur Agent de stimulation du recepteur 1b de la 5-hydroxytryptamine destine a etre utilise comme promoteur de l'autorenouvellement et/ou de la differenciation des cellules satellites
WO2018011382A1 (fr) 2016-07-15 2018-01-18 Institut Pasteur Agent stimulant le récepteur de la 5-hydroxytryptamine 1b pour la réparation de la peau et/ou des cheveux.
DK3505519T3 (da) * 2016-11-11 2022-02-07 Yangtze River Pharm Group Co Pyridinamin-substituerede heterotricyclo-forbindelser, fremstilling deraf og anvendelse i medicin
US11117901B2 (en) 2017-07-11 2021-09-14 Nerviano Medical Sciences S.R.L. Substituted pyrazolo[4,3-h]quinazolines as choline kinase inhibitors
CN107383019B (zh) * 2017-07-28 2019-10-15 江苏艾凡生物医药有限公司 吡唑并[4,3-h]喹唑啉类化合物及其用途
KR102464677B1 (ko) * 2017-08-11 2022-11-10 셍커 파마슈티컬스 (지앙수) 엘티디. 단백질 인산화효소 억제제로 작용하는 1h-피라졸로[4,3-h]퀴나졸린 화합물
CA3140030A1 (fr) * 2019-06-06 2020-12-10 Arcus Biosciences, Inc. Procedes de preparation de composes aminopyrimidine
WO2021043190A1 (fr) * 2019-09-05 2021-03-11 成都赛诺希亚生物科技有限公司 Composés isoxazolo[5,4-h]quinazoline utilisés en tant qu'inhibiteurs de protéine kinase
WO2021084541A1 (fr) * 2019-10-31 2021-05-06 Sol-Gel Technologies Ltd. Traitement de troubles du type perte de cheveux avec un inhibiteur topique d'egfr
US10988479B1 (en) 2020-06-15 2021-04-27 G1 Therapeutics, Inc. Morphic forms of trilaciclib and methods of manufacture thereof
CN116547280A (zh) * 2020-10-08 2023-08-04 雷多纳治疗公司 用于治疗癌症的苯并[h]喹唑啉-4-胺和噻吩并[3,2-h]喹唑啉-4-胺衍生物
WO2022111634A1 (fr) * 2020-11-26 2022-06-02 成都赛璟生物医药科技有限公司 Composés d'hétéroaryle quinazoline utilisés comme inhibiteurs de protéine kinase
CN114685520B (zh) * 2020-12-25 2024-08-30 武汉誉祥医药科技有限公司 三并环化合物及其药物组合物和应用
CN116528871A (zh) * 2020-12-31 2023-08-01 恒元生物医药科技(苏州)有限公司 一种吡唑并喹唑啉类化合物、其制备方法及应用
CN116761806B (zh) * 2021-02-08 2025-10-10 上海复星医药产业发展有限公司 5,6-二氢噻吩并[3,4-h]喹唑啉类化合物
MX2024000022A (es) * 2021-06-22 2024-03-15 Taxis Pharmaceuticals Inc Compuestos terapeuticos.
CN113527310B (zh) * 2021-07-30 2022-09-23 上海市肺科医院 用于减轻自身免疫性疾病患者不良炎性反应的小分子化合物及其应用
WO2023104178A1 (fr) * 2021-12-10 2023-06-15 山东绿叶制药有限公司 Inhibiteur de protéine kinase, son procédé de préparation et son application
EP4653443A1 (fr) * 2023-01-17 2025-11-26 Phil Rivers Technology Co., Ltd Stéréoisomère et dérivé deutéré de composé pyrazoloquinazoline et utilisation
WO2024251230A1 (fr) * 2023-06-08 2024-12-12 山东绿叶制药有限公司 Forme saline et forme cristalline d'un inhibiteur de kinase plk1, son procédé de préparation et son utilisation

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2119975A (en) * 1936-08-26 1938-06-07 Beatrice S Nazel Fluid pressure hammer
JP3907220B2 (ja) * 1994-06-30 2007-04-18 エーザイ・アール・アンド・ディー・マネジメント株式会社 複素環含有化合物
JP3290666B2 (ja) 1995-06-07 2002-06-10 ファイザー・インコーポレーテッド 複素環式の縮合環ピリミジン誘導体
JP2001507349A (ja) 1996-12-23 2001-06-05 セルテック セラピューティックス リミテッド 縮合多環式2−アミノピリミジン誘導体、それらの製造およびたんぱく質チロシンキナーゼ抑制因子としてのそれらの使用
GB9713087D0 (en) 1997-06-20 1997-08-27 Celltech Therapeutics Ltd Chemical compounds
GB9911053D0 (en) 1999-05-12 1999-07-14 Pharmacia & Upjohn Spa 4,5,6,7-tetrahydroindazole derivatives process for their preparation and their use as antitumour agents
US6387900B1 (en) 1999-08-12 2002-05-14 Pharmacia & Upjohn S.P.A. 3(5)-ureido-pyrazole derivatives process for their preparation and their use as antitumor agents
BR0013143A (pt) 1999-08-12 2002-06-11 Pharmacia Italia Spa Derivados de 3 (5) amino pirazol, processo para sua preparação e uso dos mesmos como agentes antitumorais
CA2416527C (fr) 2000-08-10 2009-12-22 Pharmacia Italia S.P.A. Bicyclo-pyrazoles actifs en tant qu'inhibiteurs de kinase, leur procede de preparation et compositions pharmaceutiques les contenant
EP1309596B1 (fr) * 2000-08-11 2008-02-06 Boehringer Ingelheim Pharmaceuticals Inc. Composes heterocycliques utiles en tant qu'inhibiteurs de tyrosine kinases
WO2002048114A1 (fr) 2000-11-27 2002-06-20 Pharmacia Italia S.P.A. Derives phenylacetamido-pyrazole et leur utilisation comme agents antitumoraux
WO2002070515A2 (fr) 2001-01-26 2002-09-12 Pharmacia Italia Spa Derives de chromane, procede de preparation et d'utilisation de ces derives en tant qu'agents antitumoraux
CA2456939A1 (fr) * 2001-08-10 2003-02-20 Pharmacia Corporation Inhibiteur d'anhydrase carbonique
US20030100594A1 (en) 2001-08-10 2003-05-29 Pharmacia Corporation Carbonic anhydrase inhibitor
DE60238999D1 (de) 2001-09-26 2011-03-03 Pfizer Italia Srl Aminoindazolderivate mit kinaseinhibierender wirkung, verfahren zu deren herstellung und diese enthaltende pharmazeutische zusammensetzungen
MXPA04008130A (es) * 2002-02-19 2004-11-26 Pharmacia Corp Derivados triciclicos de pirazol para el tratamiento de la inflamacion.
RS20050944A (sr) 2003-05-22 2008-06-05 Nerviano Medical Sciences S.R.L., Derivati pirazolo- hinazolina,postupci za njihovo dobijanje i njihova upotreba kao inhibitora kinaze
SI2125822T1 (sl) * 2006-12-21 2015-01-30 Nerviano Medical Sciences S.R.L. Substituirani pirazolo-kinazolinski derivati, postopek za njihovo pripravo in njihova uporaba kot inhibitorji kinaze

Also Published As

Publication number Publication date
NO20055496L (no) 2006-02-14
BRPI0410563B1 (pt) 2020-12-01
JP2007502851A (ja) 2007-02-15
EP1636236A1 (fr) 2006-03-22
CA2526578C (fr) 2012-01-24
TWI349672B (en) 2011-10-01
AP2005003452A0 (en) 2005-12-31
US20150158876A1 (en) 2015-06-11
ZA200509486B (en) 2008-09-25
CN1826343A (zh) 2006-08-30
BR122019010200B8 (pt) 2021-07-27
US20190194214A1 (en) 2019-06-27
PT1636236E (pt) 2013-12-16
EP1636236B1 (fr) 2013-10-09
HRP20050967B8 (hr) 2014-04-25
US20170050972A1 (en) 2017-02-23
US20170190714A1 (en) 2017-07-06
RS52899B (sr) 2014-02-28
MXPA05012573A (es) 2006-02-22
CY1114708T1 (el) 2016-10-05
US8981089B2 (en) 2015-03-17
UA80763C2 (en) 2007-10-25
NO334992B1 (no) 2014-08-18
AU2004240772B2 (en) 2011-04-28
RS20050944A (sr) 2008-06-05
CA2526578A1 (fr) 2004-12-02
US9637497B2 (en) 2017-05-02
KR101084871B1 (ko) 2011-11-21
IL172046A (en) 2017-03-30
IS2939B (is) 2016-03-15
HRP20050967B1 (hr) 2014-03-28
EA200501849A1 (ru) 2006-06-30
BRPI0410563A (pt) 2006-06-20
EA010904B1 (ru) 2008-12-30
MY142019A (en) 2010-08-16
US8541429B2 (en) 2013-09-24
IS8132A (is) 2005-11-18
AR044543A1 (es) 2005-09-21
US10280176B2 (en) 2019-05-07
MEP25908A (bs) 2010-06-10
US20090124605A1 (en) 2009-05-14
OA13170A (en) 2006-12-13
US9464090B2 (en) 2016-10-11
JP5043432B2 (ja) 2012-10-10
GEP20094664B (en) 2009-04-10
US20070185143A1 (en) 2007-08-09
CR8102A (es) 2006-08-09
AP2064A (en) 2009-10-30
HRP20050967A2 (en) 2007-05-31
NO20055496D0 (no) 2005-11-21
US20130338148A1 (en) 2013-12-19
DK1636236T3 (da) 2013-12-09
BRPI0410563B8 (pt) 2021-05-25
US20210300935A1 (en) 2021-09-30
SI1636236T1 (sl) 2014-01-31
KR20060015294A (ko) 2006-02-16
PL1636236T3 (pl) 2014-02-28
WO2004104007A1 (fr) 2004-12-02
AR102722A2 (es) 2017-03-22
ECSP056194A (es) 2006-04-19
ES2436524T3 (es) 2014-01-02
CN102079746A (zh) 2011-06-01
US20250011333A1 (en) 2025-01-09
NZ543661A (en) 2009-05-31
ME00142B (me) 2010-10-10
BR122019010200B1 (pt) 2020-12-15
TW200505924A (en) 2005-02-16
US7482354B2 (en) 2009-01-27
AU2004240772A1 (en) 2004-12-02
CO5721006A2 (es) 2007-01-31

Similar Documents

Publication Publication Date Title
TNSN05298A1 (fr) Derives de pyrazolo-quinazoline, procede pour leur preparation et leur utilisation comme inhibiteurs de kinases
MA28064A1 (fr) Dérivés de pyrrolo [3,4-c] pyrazole actifs comme inhibiteurs de kinases
MA27711A1 (fr) Derives de pyrazolo [1,5-a] pyrimidine
MA27703A1 (fr) Derives de diazepino-indole servant d'inhibiteurs de kinases
MA29713B1 (fr) Derives de tetrahydroindolone et de tetrahydroindazolone
MA52360B1 (fr) Dérivés de 2-amino-pyridine ou de 2-amino-pyrimidine utilisés en tant qu'inhibiteurs de kinases dépendantes des cyclines
TNSN07476A1 (fr) Derives de n-(pyridine -2- yl) - sulfonamide
MA27569A1 (fr) Derives de pyrrolo-pyrazole substitues servant d'inhibiteurs de kinases
MA27389A1 (fr) Derives de benzimidazole nouveaux utiles comme agents antiproliferatifs.
MA54608B1 (fr) Inhibiteurs aza-hétérobicycliques de mat2a et procédés d'utilisation pour le traitement du cancer
MA32306B1 (fr) Derives de quinoleines et de quinoxalines en tant qu'inhibiteurs de proteine tyrosine kinases
TNSN05250A1 (fr) Pyrimidinones substituees
MA31766B1 (fr) Composés organiques
MA27093A1 (fr) Derives de sulfonamides, leur preparation et leur application comme medicaments.
MA31949B1 (fr) Dérivés d'aminotriazole comme agonistes d'alx
MA28429B1 (fr) Dérivés de 1H-thiéno [2,3-c] pyrazole utiles comme inhibiteurs de kinases
MA33502B1 (fr) Composés pyrazolopyrimidine inhibiteurs des jak et procédés
MXPA03011484A (es) Heteroarilos multiciclicos sustituidos con quinuclidinas para el tratamiento de enfermedades.
MA31952B1 (fr) Pyrrolopyrimidines et pyrrolopyridines
MA30142B1 (fr) Agonistes du recepteur de neuropeptide-2
MA56883B1 (fr) Dérivés de 2-hydroxycycloalcane-1-carbamoyle
MXPA06000302A (es) Derivados de pirazolil-indol activos como inhibidores de cinasa, procedimientos para su preparacion y composiciones farmaceuticas que los comprenden.
DE60206911D1 (de) Imidazol-2-carbonsäureamid derivate als raf-kinase-inhibitoren
ATE396986T1 (de) Pyrimidylpyrrolderivate, die als kinaseinhibitoren wirken
IL184116A0 (en) Use of thiazolidinone derivatives as antiangiogenic agents