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MA32900B1 - Compose d'aminopyrazole - Google Patents

Compose d'aminopyrazole

Info

Publication number
MA32900B1
MA32900B1 MA33943A MA33943A MA32900B1 MA 32900 B1 MA32900 B1 MA 32900B1 MA 33943 A MA33943 A MA 33943A MA 33943 A MA33943 A MA 33943A MA 32900 B1 MA32900 B1 MA 32900B1
Authority
MA
Morocco
Prior art keywords
aminoprazole
compound
glioblastoma
leukemia
treatment
Prior art date
Application number
MA33943A
Other languages
Arabic (ar)
English (en)
Inventor
Timothy Paul Burkholder
Joshua Ryan Clayton
Liandong Ma
Original Assignee
Lilly Co Eli
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=41630090&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA32900(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of MA32900B1 publication Critical patent/MA32900B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • 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
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (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)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La présente invention porte sur des composés amino pyrazole utiles dans le traitement de troubles myéloprolifératifs chroniques et de divers cancers, par exemple, un glioblastome, un cancer du sein, un myélome multiple, un cancer de la prostate et des leucémies.
MA33943A 2008-12-16 2011-06-14 Compose d'aminopyrazole MA32900B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12285408P 2008-12-16 2008-12-16
PCT/US2009/067056 WO2010074947A1 (fr) 2008-12-16 2009-12-08 Composé amino pyrazole

Publications (1)

Publication Number Publication Date
MA32900B1 true MA32900B1 (fr) 2011-12-01

Family

ID=41630090

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33943A MA32900B1 (fr) 2008-12-16 2011-06-14 Compose d'aminopyrazole

Country Status (38)

Country Link
US (2) US7897600B2 (fr)
EP (1) EP2379557B1 (fr)
JP (1) JP5509217B2 (fr)
KR (1) KR101300458B1 (fr)
CN (1) CN102232075B (fr)
AR (1) AR074240A1 (fr)
AU (1) AU2009330503B2 (fr)
BR (1) BRPI0923048A2 (fr)
CA (1) CA2744714C (fr)
CL (1) CL2011001445A1 (fr)
CO (1) CO6331442A2 (fr)
CR (1) CR20110341A (fr)
CY (1) CY1113637T1 (fr)
DK (1) DK2379557T3 (fr)
DO (1) DOP2011000190A (fr)
EA (1) EA019554B1 (fr)
EC (1) ECSP11011132A (fr)
ES (1) ES2396617T3 (fr)
HN (1) HN2011001697A (fr)
HR (1) HRP20120918T1 (fr)
IL (1) IL213065A0 (fr)
JO (1) JO2833B1 (fr)
MA (1) MA32900B1 (fr)
MX (1) MX2011006441A (fr)
MY (1) MY158691A (fr)
NZ (1) NZ592641A (fr)
PA (1) PA8851101A1 (fr)
PE (1) PE20110549A1 (fr)
PL (1) PL2379557T3 (fr)
PT (1) PT2379557E (fr)
SG (1) SG172202A1 (fr)
SI (1) SI2379557T1 (fr)
SV (1) SV2011003949A (fr)
TN (1) TN2011000292A1 (fr)
TW (1) TWI440640B (fr)
UA (1) UA104743C2 (fr)
WO (1) WO2010074947A1 (fr)
ZA (1) ZA201103942B (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2435646A (en) * 2006-03-01 2007-09-05 Spin Tec Engineering Gmbh Apparatus and method of extraction of an arthropod gland
US8105633B2 (en) * 2006-03-01 2012-01-31 Spintec Engineering Gmbh Method and apparatus for extraction of arthropod gland
US20110121485A1 (en) * 2006-10-30 2011-05-26 Spintec Engineering Gmbh Method and apparatus for the manufacture of a fiber
JP2014513925A (ja) * 2011-03-07 2014-06-19 フォンダッツィオーネ・テレソン Ｔｆｅｂ変異体およびその使用
US9573960B2 (en) * 2011-06-15 2017-02-21 Life & Brain Gmbh Glioblastoma inhibiting compounds and their use
JP6280546B2 (ja) 2012-06-26 2018-02-14 デル マー ファーマシューティカルズ ジアンヒドロガラクチトール、ジアセチルジアンヒドロガラクチトール、ジブロモズルシトール、又はこれらの類似体若しくは誘導体を用いた、遺伝子多型又はａｈｉ１の調節不全若しくは変異を有する患者におけるチロシンキナーゼインヒビター抵抗性悪性腫瘍を処置するための方法
PL400213A1 (pl) 2012-08-01 2014-02-03 Celon Pharma Spólka Z Ograniczona Odpowiedzialnoscia Pochodne imidazo[1,2-b]pirydazyno-6-aminy jako inhibitory kinazy JAK-2
LT3179991T (lt) 2014-08-11 2021-11-10 Acerta Pharma B.V. Terapiniai btk inhibitoriaus ir bcl-2 inhibitoriaus deriniai
US20170239351A1 (en) 2014-08-11 2017-08-24 Acerta Pharma B.V. Therapeutic Combinations of a BTK Inhibitor, a PI3K Inhibitor, a JAK-2 Inhibitor, a PD-1 Inhibitor, and/or a PD-L1 Inhibitor
WO2016024232A1 (fr) 2014-08-11 2016-02-18 Acerta Pharma B.V. Combinaisons thérapeutiques d'un inhibiteur de la btk, d'un inhibiteur de la pi3k, d'un inhibiteur de la jak-2 et/ou d'un inhibiteur de la cdk 4/6
ES2849974T3 (es) * 2016-11-17 2021-08-24 Bristol Myers Squibb Co Moduladores de imidazopiridazina de IL-12, IL-23 y/o IFNalfa
WO2018167283A1 (fr) 2017-03-17 2018-09-20 INSERM (Institut National de la Santé et de la Recherche Médicale) Procédés pour le diagnostic et le traitement d'un remodelage neuronal associé à un adénocarcinome canalaire pancréatique
WO2018189335A1 (fr) 2017-04-13 2018-10-18 INSERM (Institut National de la Santé et de la Recherche Médicale) Procédés de diagnostic et de traitement d'un adénocarcinome canalaire pancréatique
KR102328682B1 (ko) 2018-08-27 2021-11-18 주식회사 대웅제약 신규한 헤테로사이클릭아민 유도체 및 이를 포함하는 약학 조성물
WO2020092015A1 (fr) 2018-11-02 2020-05-07 University Of Rochester Atténuation thérapeutique d'une infection épithéliale
CN110305140B (zh) 2019-07-30 2020-08-04 上海勋和医药科技有限公司 二氢吡咯并嘧啶类选择性jak2抑制剂

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE354573T1 (de) 2000-12-21 2007-03-15 Vertex Pharma ßPYRAZOLVERBINDUNGEN, DIE SICH ALS PROTEINKINASEINHIBITOREN EIGNENß
JP2003137785A (ja) * 2001-08-23 2003-05-14 Takeda Chem Ind Ltd Ｊｎｋ活性化阻害剤
CN1596255A (zh) 2001-12-21 2005-03-16 阿诺麦德股份有限公司 具有强效的与趋化因子受体结合的杂环化合物
AU2006215386B2 (en) 2005-02-16 2009-06-11 Astrazeneca Ab Chemical compounds
WO2006087538A1 (fr) 2005-02-16 2006-08-24 Astrazeneca Ab Composés chimiques
MX2007016066A (es) * 2005-07-01 2008-03-10 Irm Llc Derivados de bencimidazol sustituidos por pirimidina como inhibidores de cinasa de proteina.
GB0515026D0 (en) * 2005-07-21 2005-08-31 Novartis Ag Organic compounds
WO2007044426A2 (fr) * 2005-10-06 2007-04-19 Schering Corporation Pyrazolopyrimidines utilisees comme inhibiteurs de proteines kinases
US7776865B2 (en) * 2005-10-06 2010-08-17 Schering Corporation Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors
MX2008007049A (es) 2005-11-30 2008-10-23 Vertex Pharma Inhibidores de c-met y usos de los mismos.
US7989459B2 (en) 2006-02-17 2011-08-02 Pharmacopeia, Llc Purinones and 1H-imidazopyridinones as PKC-theta inhibitors
WO2008030579A2 (fr) 2006-09-07 2008-03-13 Biogen Idec Ma Inc. Modulateurs de la kinase associée au récepteur de l'interleukine-1
US20100041662A1 (en) * 2006-10-30 2010-02-18 Sandrine Ferrand Heterocyclic compounds as antiinflammatory agents
WO2008129255A1 (fr) * 2007-04-18 2008-10-30 Astrazeneca Ab Dérivés de 5-aminopyrazol-3-yl-3h-imidazo[4,5-b]pyridine et leur utilisation pour le traitement du cancer
CN101679412A (zh) 2007-05-23 2010-03-24 药典有限责任公司 作为PKC-θ抑制剂的嘌呤酮类和1H-咪唑并吡啶酮类
WO2009062059A2 (fr) 2007-11-08 2009-05-14 Pharmacopeia, Inc. Purinones et 1h-imidazopyridinones isomères comme inhibiteurs de pkc-thêta

Also Published As

Publication number Publication date
MY158691A (en) 2016-10-31
KR20110084993A (ko) 2011-07-26
CO6331442A2 (es) 2011-10-20
AR074240A1 (es) 2011-01-05
HN2011001697A (es) 2013-11-26
US20100152181A1 (en) 2010-06-17
PT2379557E (pt) 2013-01-14
CA2744714C (fr) 2013-06-25
HK1160109A1 (en) 2012-08-10
CY1113637T1 (el) 2016-06-22
SV2011003949A (es) 2011-07-21
IL213065A0 (en) 2011-07-31
NZ592641A (en) 2013-01-25
DK2379557T3 (da) 2012-12-17
DOP2011000190A (es) 2011-07-31
SG172202A1 (en) 2011-07-28
JP5509217B2 (ja) 2014-06-04
AU2009330503B2 (en) 2012-06-07
KR101300458B1 (ko) 2013-08-30
MX2011006441A (es) 2011-07-19
PA8851101A1 (es) 2010-07-27
EP2379557B1 (fr) 2012-10-31
TWI440640B (zh) 2014-06-11
CA2744714A1 (fr) 2010-07-01
CR20110341A (es) 2011-07-13
US20100286139A1 (en) 2010-11-11
CN102232075A (zh) 2011-11-02
JO2833B1 (en) 2014-09-15
BRPI0923048A2 (pt) 2018-09-25
CN102232075B (zh) 2013-12-11
PE20110549A1 (es) 2011-08-04
ECSP11011132A (es) 2011-07-29
SI2379557T1 (sl) 2013-02-28
JP2012512158A (ja) 2012-05-31
EP2379557A1 (fr) 2011-10-26
ZA201103942B (en) 2012-08-29
TW201024301A (en) 2010-07-01
TN2011000292A1 (en) 2012-12-17
EA201170831A1 (ru) 2011-12-30
UA104743C2 (ru) 2014-03-11
AU2009330503A1 (en) 2010-07-01
HRP20120918T1 (hr) 2012-12-31
CL2011001445A1 (es) 2011-11-11
PL2379557T3 (pl) 2013-03-29
ES2396617T3 (es) 2013-02-22
US7897600B2 (en) 2011-03-01
WO2010074947A1 (fr) 2010-07-01
EA019554B1 (ru) 2014-04-30

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