ME01860B - Jedinjenja i preparati protein kinaznih inhibitora - Google Patents

Jedinjenja i preparati protein kinaznih inhibitora

Info

Publication number
ME01860B
ME01860B MEP-2014-94A MEP9414A ME01860B ME 01860 B ME01860 B ME 01860B ME P9414 A MEP9414 A ME P9414A ME 01860 B ME01860 B ME 01860B
Authority
ME
Montenegro
Prior art keywords
propan
pyrazol
pyrimidin
amino
carbamate
Prior art date
Application number
MEP-2014-94A
Other languages
English (en)
Unknown language (me)
Inventor
Shenlin Huang
Xianming Jin
Zuosheng Liu
Daniel Poon
John TELLEW
Yongqin Wan
Xing Wang
Yongping Xie
Original Assignee
Novartis Ag
Irm Llc
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=42782253&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ME01860(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag, Irm Llc filed Critical Novartis Ag
Publication of ME01860B publication Critical patent/ME01860B/me

Links

Classifications

    • 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
    • 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
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physiology (AREA)
  • Nutrition Science (AREA)
  • Hospice & Palliative Care (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Otolaryngology (AREA)
  • Psychiatry (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
MEP-2014-94A 2009-08-28 2010-08-27 Jedinjenja i preparati protein kinaznih inhibitora ME01860B (me)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US23807309P 2009-08-28 2009-08-28
US31303910P 2010-03-11 2010-03-11
EP10748211.9A EP2470526B1 (en) 2009-08-28 2010-08-27 Compounds and compositions as protein kinase inhibitors
PCT/US2010/046930 WO2011025927A1 (en) 2009-08-28 2010-08-27 Compounds and compositions as protein kinase inhibitors

Publications (1)

Publication Number Publication Date
ME01860B true ME01860B (me) 2014-12-20

Family

ID=42782253

Family Applications (2)

Application Number Title Priority Date Filing Date
MEP-2014-94A ME01860B (me) 2009-08-28 2010-08-27 Jedinjenja i preparati protein kinaznih inhibitora
MEP-2017-6A ME02684B (me) 2009-08-28 2010-08-27 Jedinjenja i preparati protein kinaznih inhibitora

Family Applications After (1)

Application Number Title Priority Date Filing Date
MEP-2017-6A ME02684B (me) 2009-08-28 2010-08-27 Jedinjenja i preparati protein kinaznih inhibitora

Country Status (49)

Country Link
US (12) US8501758B2 (en, 2012)
EP (2) EP2470526B1 (en, 2012)
JP (2) JP5475888B2 (en, 2012)
KR (1) KR101413392B1 (en, 2012)
CN (2) CN102725283B (en, 2012)
AR (1) AR077975A1 (en, 2012)
AU (1) AU2010286569C1 (en, 2012)
BR (1) BR112012004453B1 (en, 2012)
CA (1) CA2771775C (en, 2012)
CL (1) CL2012000340A1 (en, 2012)
CO (1) CO6612222A2 (en, 2012)
CR (1) CR20120102A (en, 2012)
CU (1) CU24110B1 (en, 2012)
CY (3) CY1118452T1 (en, 2012)
DK (2) DK2470526T3 (en, 2012)
DO (1) DOP2012000051A (en, 2012)
EA (2) EA025222B1 (en, 2012)
EC (2) ECSP12011700A (en, 2012)
ES (2) ES2492499T3 (en, 2012)
GE (1) GEP20146102B (en, 2012)
GT (1) GT201200053A (en, 2012)
HN (1) HN2012000441A (en, 2012)
HR (2) HRP20140799T1 (en, 2012)
HU (3) HUE032847T2 (en, 2012)
IL (1) IL218084A (en, 2012)
IN (1) IN2012DN02469A (en, 2012)
JO (1) JO3002B1 (en, 2012)
LT (3) LT2727918T (en, 2012)
LU (2) LUC00101I2 (en, 2012)
MA (1) MA33604B1 (en, 2012)
ME (2) ME01860B (en, 2012)
MX (1) MX2012002546A (en, 2012)
MY (1) MY156259A (en, 2012)
NI (1) NI201200029A (en, 2012)
NL (1) NL300973I2 (en, 2012)
NO (2) NO2019012I1 (en, 2012)
NZ (1) NZ598924A (en, 2012)
PE (1) PE20120861A1 (en, 2012)
PL (2) PL2727918T3 (en, 2012)
PT (2) PT2470526E (en, 2012)
RS (2) RS53489B1 (en, 2012)
SG (2) SG178351A1 (en, 2012)
SI (2) SI2470526T1 (en, 2012)
SM (3) SMT201700036T1 (en, 2012)
TN (1) TN2012000081A1 (en, 2012)
UA (1) UA112285C2 (en, 2012)
UY (1) UY32860A (en, 2012)
WO (1) WO2011025927A1 (en, 2012)
ZA (1) ZA201202020B (en, 2012)

Families Citing this family (67)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR077975A1 (es) 2009-08-28 2011-10-05 Irm Llc Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina
AU2011221227B2 (en) 2010-02-25 2015-07-09 Dana-Farber Cancer Institute, Inc. BRAF mutations conferring resistance to BRAF inhibitors
US8907270B2 (en) 2010-06-30 2014-12-09 Schlumberger Technology Corporation Method and apparatus for gain regulation in a gamma detector
CN108542906A (zh) * 2011-11-11 2018-09-18 诺华股份有限公司 治疗增生性疾病的方法
UA115039C2 (uk) * 2011-11-23 2017-09-11 Еррей Біофарма Інк. Фармацевтичні композиції
US9408885B2 (en) 2011-12-01 2016-08-09 Vib Vzw Combinations of therapeutic agents for treating melanoma
CN103159736B (zh) * 2011-12-10 2015-05-13 通化济达医药有限公司 取代的吡唑激酶抑制剂
TW201332989A (zh) * 2011-12-23 2013-08-16 Millennium Pharm Inc 雜芳基化合物及其用途
MX351945B (es) 2012-03-28 2017-11-03 Dana Farber Cancer Inst Inc Mutantes c-raf que confieren resistencia a inhibidores raf.
CN104640857B (zh) 2012-07-18 2017-07-04 圣路易斯大学 作为整合素拮抗剂的β氨基酸衍生物
US8716226B2 (en) 2012-07-18 2014-05-06 Saint Louis University 3,5 phenyl-substituted beta amino acid derivatives as integrin antagonists
AR091876A1 (es) * 2012-07-26 2015-03-04 Novartis Ag Combinaciones farmaceuticas para el tratamiento de enfermedades proliferativas
NZ703940A (en) * 2012-08-07 2018-04-27 Novartis Ag Pharmaceutical combinations comprising a b-raf inhibitor, an egfr inhibitor and optionally a pi3k-alpha inhibitor
CN110251512A (zh) 2012-08-17 2019-09-20 霍夫曼-拉罗奇有限公司 包括给药cobimetinib和威罗菲尼的黑色素瘤的组合疗法
US20150232452A1 (en) * 2012-09-19 2015-08-20 Ruga Corporation Novel raf kinase inhibitors
CA2890663A1 (en) 2012-11-08 2014-05-15 Novartis Ag Pharmaceutical combination comprising a b-raf inhibitor and a histone deacetylase inhibitor and their use in the treatment of proliferative diseases
SG10201906270VA (en) * 2013-03-21 2019-08-27 Novartis Ag Combination therapy comprising a b-raf inhibitor and a second inhibitor
TWI634114B (zh) 2013-05-08 2018-09-01 永恒生物科技公司 作為激酶抑制劑之呋喃酮化合物
CN105228983A (zh) * 2013-05-30 2016-01-06 普莱希科公司 用于激酶调节的化合物及其适应症
EP3757130A1 (en) 2013-09-26 2020-12-30 Costim Pharmaceuticals Inc. Methods for treating hematologic cancers
TW201605450A (zh) 2013-12-03 2016-02-16 諾華公司 Mdm2抑制劑與BRAF抑制劑之組合及其用途
AU2014368906B2 (en) * 2013-12-20 2020-04-30 Biomed Valley Discoveries, Inc. Cancer treatment using combinations of ERK and RAF inhibitors
KR20160100975A (ko) * 2013-12-23 2016-08-24 노파르티스 아게 제약 조합물
JOP20200094A1 (ar) 2014-01-24 2017-06-16 Dana Farber Cancer Inst Inc جزيئات جسم مضاد لـ pd-1 واستخداماتها
JOP20200096A1 (ar) 2014-01-31 2017-06-16 Children’S Medical Center Corp جزيئات جسم مضاد لـ tim-3 واستخداماتها
DE102015103158A1 (de) 2014-03-04 2015-09-10 Bergische Universität Wuppertal Verbindungen für die Behandlung des Melanoms
TWI852057B (zh) 2014-03-14 2024-08-11 瑞士商諾華公司 針對lag-3之抗體分子及其用途
WO2015145388A2 (en) 2014-03-27 2015-10-01 Novartis Ag Methods of treating colorectal cancers harboring upstream wnt pathway mutations
US10428387B2 (en) 2014-05-16 2019-10-01 University Of Massachusetts Treating chronic myelogenous leukemia (CML)
WO2015196072A2 (en) 2014-06-19 2015-12-23 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
WO2016038582A1 (en) * 2014-09-12 2016-03-17 Novartis Ag Compounds and compositions as raf kinase inhibitors
EP3659621A1 (en) 2014-09-13 2020-06-03 Novartis AG Combination therapies for cancer
BR112017006664A2 (pt) 2014-10-03 2017-12-26 Novartis Ag terapias de combinação
MA41044A (fr) 2014-10-08 2017-08-15 Novartis Ag Compositions et procédés d'utilisation pour une réponse immunitaire accrue et traitement contre le cancer
ES2952717T3 (es) 2014-10-14 2023-11-03 Novartis Ag Moléculas de anticuerpos contra PD-L1 y usos de las mismas
BR112017018908A2 (pt) 2015-03-10 2018-04-17 Aduro Biotech, Inc. composições e métodos para ativar a sinalização dependente do "estimulador do gene de interferon
HRP20211058T8 (hr) 2015-07-29 2021-11-26 Novartis Ag Kombinirane terapije koje sadrže molekule antitijela protiv lag-3
EP3316902A1 (en) 2015-07-29 2018-05-09 Novartis AG Combination therapies comprising antibody molecules to tim-3
US20180222982A1 (en) 2015-07-29 2018-08-09 Novartis Ag Combination therapies comprising antibody molecules to pd-1
LT3370768T (lt) 2015-11-03 2022-05-25 Janssen Biotech, Inc. Antikūnai, specifiškai surišantys pd-1, ir jų panaudojimas
WO2017106656A1 (en) 2015-12-17 2017-06-22 Novartis Ag Antibody molecules to pd-1 and uses thereof
WO2017117538A1 (en) 2015-12-30 2017-07-06 Saint Louis University Meta-azacyclic amino benzoic acid derivatives as pan integrin antagonists
RU2615986C1 (ru) * 2016-02-25 2017-04-12 Закрытое акционерное общество "Р-Фарм" (ЗАО "Р-Фарм") Замещенные метил (2-{ 4-[3-(3-метансульфониламино-2-фтор-5-хлор-фенил)-1Н-пиразол-4-ил]пиримидин-2-иламино} -этил)карбаматы, способ их получения и применения
PT3463345T (pt) * 2016-06-03 2023-01-06 Array Biopharma Inc Combinações farmacêuticas
US11098077B2 (en) 2016-07-05 2021-08-24 Chinook Therapeutics, Inc. Locked nucleic acid cyclic dinucleotide compounds and uses thereof
CA3048376A1 (en) * 2016-12-27 2018-07-05 Riken Bmp-signal-inhibiting compound
JP7341060B2 (ja) 2017-02-10 2023-09-08 アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル Mapk経路の活性化に関連付けられる癌の処置のための方法及び医薬組成物
UY37695A (es) 2017-04-28 2018-11-30 Novartis Ag Compuesto dinucleótido cíclico bis 2’-5’-rr-(3’f-a)(3’f-a) y usos del mismo
CN107540699A (zh) * 2017-10-16 2018-01-05 康化(上海)新药研发有限公司 一种2‑氨基‑3‑氟吡啶‑4‑硼酸盐酸盐的合成方法
JP7416716B2 (ja) 2017-12-28 2024-01-17 トラクト ファーマシューティカルズ インコーポレイテッド 円柱上皮幹細胞のための幹細胞培養系およびそれに関連した使用法
US12398209B2 (en) 2018-01-22 2025-08-26 Janssen Biotech, Inc. Methods of treating cancers with antagonistic anti-PD-1 antibodies
WO2020011141A1 (zh) * 2018-07-12 2020-01-16 深圳市塔吉瑞生物医药有限公司 一种二芳基吡唑化合物及包含该化合物的组合物及其用途
WO2020124397A1 (en) * 2018-12-19 2020-06-25 Inventisbio Shanghai Ltd. C-terminal src kinase inhibitors
KR20210107069A (ko) 2018-12-21 2021-08-31 다이이찌 산쿄 가부시키가이샤 항체-약물 컨쥬게이트와 키나아제 저해제의 조합
US20220168250A1 (en) 2019-05-16 2022-06-02 Eli Lilly And Company TRIPLE COMBINATION OF AN ERK1/2 INHIBITOR WITH A BRAF INHIBITOR AND AN EGFR INHIBITOR FOR USE IN THE TREATMENT OF BRAFv6ooE COLORECTAL CANCER
US20230036867A1 (en) 2019-12-05 2023-02-02 INSERM (Institut National de la Santé et de la Recherche Médicale) N-(3-(5-(pyrimidin-4-yl)thiazol-4-yl)phenyl)sulfonamide compounds and their uses as braf inhibitors
WO2021250521A1 (en) 2020-06-09 2021-12-16 Array Biopharma Inc. 4-oxo-3,4-dihydroquinazolinon compounds for the treatment of braf-associated diseases and disorders
EP4196228A1 (en) 2020-08-13 2023-06-21 Albert Einstein College of Medicine N-cyclyl-sulfonamides useful for inhibiting raf
WO2022074011A1 (en) 2020-10-05 2022-04-14 Pierre Fabre Medicament Combination of encorafenib and binimetinib as adjuvant treatment for resected stage ii melanoma
JP2024511373A (ja) 2021-03-18 2024-03-13 ノバルティス アーゲー がんのためのバイオマーカーおよびその使用
US12371667B2 (en) 2021-05-13 2025-07-29 Washington University Enhanced methods for inducing and maintaining naive human pluripotent stem cells
TW202313046A (zh) 2021-06-09 2023-04-01 瑞士商赫孚孟拉羅股份公司 用於癌症治療之組合療法
CN114557977A (zh) * 2022-02-16 2022-05-31 北京康立生医药技术开发有限公司 一种治疗肠癌的药物的制备方法、制剂及纯度分析方法
WO2023230554A1 (en) 2022-05-25 2023-11-30 Pfizer Inc. Combination of a braf inhibitor, an egfr inhibitor, and a pd-1 antagonist for the treatment of braf v600e-mutant, msi-h/dmmr colorectal cancer
WO2024163166A1 (en) * 2023-01-30 2024-08-08 5Metis, Inc. Boron containing compounds and their uses
CN116396222A (zh) * 2023-04-10 2023-07-07 上海睿腾医药科技有限公司 一种康奈非尼中间体1-(3-氨基-1-异丙基-1h-吡唑-4-基)乙-1-酮的合成方法
WO2025003956A1 (en) 2023-06-30 2025-01-02 Pfizer Inc. High drug loading formulations of encorafenib

Family Cites Families (72)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4104250A (en) * 1976-08-11 1978-08-01 Borg-Warner Corporation Flame-retardant polymers with 1,3,5-triazines having halo- and halo-aryl substitutents
JPS5475888A (en) 1977-11-29 1979-06-18 Jiyasuko Kk Surgical laser
DE3571974D1 (en) 1984-12-06 1989-09-07 Pfizer Substituted dihydroquinolone carboxylic acids, anti-bacterial compositions containing them
US6391636B1 (en) 1994-05-31 2002-05-21 Isis Pharmaceuticals, Inc. Antisense oligonucleotide modulation of raf gene expression
US6358932B1 (en) 1994-05-31 2002-03-19 Isis Pharmaceticals, Inc. Antisense oligonucleotide inhibition of raf gene expression
US6037136A (en) 1994-10-24 2000-03-14 Cold Spring Harbor Laboratory Interactions between RaF proto-oncogenes and CDC25 phosphatases, and uses related thereto
WO1997008950A1 (en) 1995-09-07 1997-03-13 Fuisz Technologies, Ltd. System for rendering substantially non-dissoluble bio-affecting agents bio-available
US5717100A (en) 1995-10-06 1998-02-10 Merck & Co., Inc. Substituted imidazoles having anti-cancer and cytokine inhibitory activity
WO1997044058A1 (en) 1996-05-23 1997-11-27 Applied Research Systems Ars Holding N.V. Compounds that inhibit the binding of raf-1 or 14-3-3 proteins to the beta chain of il-2 receptor, and pharmaceutical compositions containing same
AR012634A1 (es) 1997-05-02 2000-11-08 Sugen Inc Compuesto basado en quinazolina, composicion famaceutica que lo comprende, metodo para sintetizarlo, su uso, metodos de modulacion de la funcion deserina/treonina proteinaquinasa con dicho compuesto y metodo in vitro para identificar compuestos que modulan dicha funcion
US6514977B1 (en) 1997-05-22 2003-02-04 G.D. Searle & Company Substituted pyrazoles as p38 kinase inhibitors
BR9809147A (pt) 1997-05-22 2000-08-01 Searle & Co Composto pirazol substituìdo, composição farmacêutica, processos para tratar um distúrbio mediado por tnf, um distúrbio mediado por quinase p38, inflamação e artrite, e, para preparar pirazóis
US6187799B1 (en) 1997-05-23 2001-02-13 Onyx Pharmaceuticals Inhibition of raf kinase activity using aryl ureas
GB9716557D0 (en) 1997-08-06 1997-10-08 Glaxo Group Ltd Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity
US6022884A (en) 1997-11-07 2000-02-08 Amgen Inc. Substituted pyridine compounds and methods of use
US6204467B1 (en) 1998-03-24 2001-03-20 Ford Global Technologies, Inc. Method and apparatus for resistive welding
RU2319693C9 (ru) 1999-01-13 2008-08-20 Байер Копэрейшн Производные мочевины (варианты), фармацевтическая композиция (варианты) и способ лечения заболевания, связанного с ростом раковых клеток (варианты)
US6316435B2 (en) 1999-02-24 2001-11-13 Supergen, Inc. Combination therapy for lymphoproliferative diseases
AU2331801A (en) 1999-12-23 2001-07-09 F.H. Faulding & Co. Limited Improved pharmaceutical compositions for poorly soluble drugs
US6756410B2 (en) 2000-08-30 2004-06-29 Kamal D. Mehta Induction of LDL receptor expression by extracellular-signal regulated kinase, ERK-1/2
PE20020354A1 (es) 2000-09-01 2002-06-12 Novartis Ag Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
PT1441714E (pt) 2001-10-25 2008-03-10 Novartis Ag Combinações compreendendo um inibidor selectivo da ciclo-oxigenase 2
WO2003055860A1 (en) 2001-12-21 2003-07-10 Vernalis (Cambridge) Limited 3,4-diarylpyrazoles and their use in the therapy of cancer
HUE025767T2 (en) 2002-03-13 2016-05-30 Array Biopharma Inc N3 alkylated benzimidazole derivatives as MEK inhibitors
KR20060097000A (ko) 2003-09-23 2006-09-13 노파르티스 아게 화학요법제와 vegf 수용체 저해제의 배합물
CA2545942C (en) 2003-11-14 2012-07-10 Lorus Therapeutics Inc. Aryl imidazoles and their use as anti-cancer agents
KR20060127032A (ko) 2004-01-09 2006-12-11 노파르티스 아게 Igf―ir 억제제로서의페닐-[4-(3-페닐-1h-피라졸-4-일)-피리미딘-2-일]-아민유도체
ES2396135T3 (es) 2004-06-10 2013-02-19 Irm Llc Compuestos y composiciones como inhibidores de proteínas cinasas
US20060058311A1 (en) 2004-08-14 2006-03-16 Boehringer Ingelheim International Gmbh Combinations for the treatment of diseases involving cell proliferation
BRPI0606281A2 (pt) 2005-03-17 2009-06-09 Novartis Ag compostos orgánicos
US20070099856A1 (en) 2005-05-13 2007-05-03 Gumerlock Paul H Combined treatment with docetaxel and an epidermal growth factor receptor kinase inhibitor using an intermittent dosing regimen
CA2618377A1 (en) 2005-08-12 2007-02-22 Synta Pharmaceuticals Corp. Pyrazole compounds that modulate hsp90 activity
US20090214645A1 (en) 2005-08-22 2009-08-27 Andrea Kramer Pharmaceutical compositions comprising a ph-dependent drug, a ph modifier and a retarding agent
EP1917258A2 (en) 2005-08-26 2008-05-07 SmithKline Beecham Corporation Pyrimidinyl-pyrazole inhibitors of aurora kinases
PE20070335A1 (es) 2005-08-30 2007-04-21 Novartis Ag Benzimidazoles sustituidos y metodos para su preparacion
CA2643066A1 (en) * 2006-03-16 2007-09-20 Pfizer Products Inc. Pyrazole compounds
CN101415411A (zh) 2006-04-05 2009-04-22 诺瓦提斯公司 用于治疗癌症的治疗剂组合
US7501430B2 (en) * 2006-04-17 2009-03-10 Arqule, Inc. RAF inhibitors and their uses
EP2061772A4 (en) 2006-09-11 2011-06-29 Curis Inc MULTIFUNCTIONAL SMALL MOLECULES AS PROLIFERATION-ACTIVE ACTIVE SUBSTANCES
BRPI0717586A2 (pt) 2006-09-18 2013-10-29 Boehringer Ingelheim Int Método para tratar câncer apresentando mutações do egfr
EA015751B1 (ru) 2006-10-02 2011-12-30 АйАрЭм ЭлЭлСи Соединения и композиции в качестве ингибиторов протеинкиназ
BRPI0717805A2 (pt) * 2006-10-06 2013-10-29 Irm Llc Inibidores de proteína quinase e métodos de uso dos mesmos
CA2677651A1 (en) 2007-02-15 2008-08-21 Novartis Ag Combinations of therapeutic agents for treating cancer
US20090022789A1 (en) 2007-07-18 2009-01-22 Supernus Pharmaceuticals, Inc. Enhanced formulations of lamotrigine
EA201000113A1 (ru) * 2007-08-01 2010-08-30 Пфайзер Инк. Пиразольные соединения
CA2699301A1 (en) 2007-10-19 2009-04-23 Abbott Gmbh & Co. Kg Solid dispersion product of n-aryl urea-based drugs
MX2010005110A (es) * 2007-11-14 2010-09-09 Ortho Mcneil Janssen Pharm Derivados de imidazo[1,2-a]piridina y su uso como moduladores alostericos positivos de los receptores de glutamato metabotropico 2.
AU2009227013B2 (en) 2008-03-21 2013-01-10 Novartis Ag Novel heterocyclic compounds and uses therof
UA103319C2 (en) * 2008-05-06 2013-10-10 Глаксосмитклайн Ллк Thiazole- and oxazole-benzene sulfonamide compounds
CN102105459B (zh) * 2008-07-24 2014-09-10 内尔维阿诺医学科学有限公司 作为蛋白激酶抑制剂的3,4-二芳基吡唑类
WO2010014611A1 (en) 2008-07-28 2010-02-04 Gilead Colorado, Inc. Cycloalkylidene and heterocycloalkylidene histone deacetylase inhibitor compounds
UY32146A (es) 2008-09-29 2010-04-30 Boehringer Ingelheim Int Derivados de las 5-[4-(1,5-dimetil-1h-pirazol-4-il)-1,2,3-triazol-1-il]-6-metil-nicotinamidas n-(sustituidas) y de las n-{5-[4-(1,5-dimetil-1h-pirazol-4-il)-1,2,3-triazol-1-il]-6-metil-piridin-3-il}-benzamidas sustituidas y composiciones conteniéndolos
MY160340A (en) 2008-10-07 2017-02-28 Astrazeneca Uk Ltd Pharmaceutical formulation 514
US20110293750A1 (en) * 2008-11-11 2011-12-01 Yale University Activated wnt-beta-catenin signaling in melanoma
ES2422263T3 (es) 2008-12-19 2013-09-10 Nerviano Medical Sciences Srl Pirazoles bicíclicos como inhibidores de la proteinquinasa
AR075180A1 (es) 2009-01-29 2011-03-16 Novartis Ag Formulaciones orales solidas de una pirido-pirimidinona
RU2402602C1 (ru) 2009-02-12 2010-10-27 Государственное учреждение Российский онкологический научный центр им. Н.Н. Блохина РАМН КЛЕТОЧНАЯ ЛИНИЯ МЕЛАНОМЫ ЧЕЛОВЕКА mel Rac, ИСПОЛЬЗУЕМАЯ ДЛЯ ПОЛУЧЕНИЯ ПРОТИВООПУХОЛЕВЫХ ВАКЦИН
WO2010100127A1 (en) * 2009-03-04 2010-09-10 Novartis Ag Disubstituted imidazole derivatives as modulators of raf kinase
TWI532484B (zh) 2009-06-08 2016-05-11 艾伯維有限公司 包含凋亡促進劑之固態分散劑
EP3045457B1 (en) * 2009-06-15 2018-05-09 Nerviano Medical Sciences S.r.l. Substituted pyrimidinylpyrrolopyridinone derivatives, process for their preparation and their use as kinase inhibitors
KR101256018B1 (ko) * 2009-08-20 2013-04-18 한국과학기술연구원 단백질 키나아제 저해활성을 갖는 1,3,6-치환된 인돌 화합물
AR077975A1 (es) 2009-08-28 2011-10-05 Irm Llc Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina
US8242260B2 (en) 2009-08-28 2012-08-14 Novartis Ag Compounds and compositions as protein kinase inhibitors
EA023942B1 (ru) 2010-01-27 2016-07-29 НЕРВИАНО МЕДИКАЛ САЙЕНСИЗ С.р.л. Сульфонамидные производные 3,4-диарилпиразолов в качестве ингибиторов протеинкиназы
SG10201502484SA (en) 2010-03-30 2015-05-28 Verseon Corp Multisubstituted aromatic compounds as inhibitors of thrombin
CN103153980B (zh) 2010-08-03 2015-12-16 内尔维安诺医学科学有限公司 吡唑并苯基苯磺酰胺化合物的衍生物及其作为抗肿瘤药的用途
US20140093565A1 (en) 2011-03-21 2014-04-03 Valcuria Ab A pharmaceutical composition comprising a hdac inhibitor and a steroid and the use thereof
KR20140056212A (ko) 2011-06-14 2014-05-09 노파르티스 아게 골수성증식 신생물과 같은 암 치료에서의 파노비노스타트와 룩소리티닙의 조합물
CN108542906A (zh) 2011-11-11 2018-09-18 诺华股份有限公司 治疗增生性疾病的方法
UA115039C2 (uk) 2011-11-23 2017-09-11 Еррей Біофарма Інк. Фармацевтичні композиції
CA2890663A1 (en) 2012-11-08 2014-05-15 Novartis Ag Pharmaceutical combination comprising a b-raf inhibitor and a histone deacetylase inhibitor and their use in the treatment of proliferative diseases
US10576680B2 (en) 2015-11-19 2020-03-03 The Boeing Company Modular thermoforming system

Also Published As

Publication number Publication date
CR20120102A (es) 2012-05-02
US20160122324A1 (en) 2016-05-05
BR112012004453A8 (pt) 2021-06-08
CN103896921B (zh) 2016-02-24
JP6045519B2 (ja) 2016-12-14
US10005761B2 (en) 2018-06-26
US20160120866A1 (en) 2016-05-05
US20180297985A1 (en) 2018-10-18
EA025222B1 (ru) 2016-12-30
US10576080B2 (en) 2020-03-03
NI201200029A (es) 2012-05-29
SMT201700036B (it) 2017-03-08
KR101413392B1 (ko) 2014-06-27
US20160280686A1 (en) 2016-09-29
ECSP12011700A (es) 2012-03-30
LTC2470526I2 (lt) 2020-04-27
WO2011025927A1 (en) 2011-03-03
DOP2012000051A (es) 2012-05-31
US8501758B2 (en) 2013-08-06
HUS1900013I1 (hu) 2019-04-29
AU2010286569B2 (en) 2013-10-10
US9593100B2 (en) 2017-03-14
BR112012004453A2 (pt) 2021-03-09
HUE032847T2 (hu) 2017-11-28
HRP20140799T1 (hr) 2014-11-07
CY1118452T1 (el) 2017-07-12
PT2727918T (pt) 2017-01-20
UY32860A (es) 2011-03-31
NO2019011I1 (no) 2019-03-05
US20130296318A1 (en) 2013-11-07
SMT201400133B (it) 2014-11-10
EA201200373A1 (ru) 2012-09-28
IL218084A0 (en) 2012-04-30
US10568884B2 (en) 2020-02-25
ES2492499T3 (es) 2014-09-09
PL2470526T3 (pl) 2014-10-31
RS55568B1 (sr) 2017-05-31
US20160263113A1 (en) 2016-09-15
ME02684B (me) 2017-06-20
CA2771775A1 (en) 2011-03-03
SI2470526T1 (sl) 2014-09-30
SG178351A1 (en) 2012-03-29
CY2019013I1 (el) 2019-11-27
US9314464B2 (en) 2016-04-19
UA112285C2 (uk) 2016-08-25
CY2019013I2 (el) 2019-11-27
AR077975A1 (es) 2011-10-05
NZ598924A (en) 2013-07-26
EP2727918B1 (en) 2016-10-12
IL218084A (en) 2016-11-30
CN103896921A (zh) 2014-07-02
ECSP23004573A (es) 2023-04-28
SG10201405311TA (en) 2014-09-26
PL2727918T3 (pl) 2017-06-30
MY156259A (en) 2016-01-29
BR112012004453B1 (pt) 2022-04-26
CY2019014I2 (el) 2019-11-27
LUC00101I1 (en, 2012) 2019-02-13
DK2470526T3 (da) 2014-08-25
US20160280687A1 (en) 2016-09-29
US20230116233A1 (en) 2023-04-13
TN2012000081A1 (en) 2013-09-19
US9850230B2 (en) 2017-12-26
US9593099B2 (en) 2017-03-14
LT2727918T (lt) 2017-01-25
JP5475888B2 (ja) 2014-04-16
US20110306625A1 (en) 2011-12-15
SI2727918T1 (sl) 2017-02-28
RS53489B1 (en) 2015-02-27
CA2771775C (en) 2015-01-20
US9850229B2 (en) 2017-12-26
EP2727918A1 (en) 2014-05-07
AU2010286569A1 (en) 2012-04-12
NL300973I1 (en, 2012) 2019-03-27
MX2012002546A (es) 2012-04-11
ES2610825T3 (es) 2017-05-03
CL2012000340A1 (es) 2012-08-17
ZA201202020B (en) 2012-12-27
LTPA2019005I1 (lt) 2019-03-25
HUS1900012I1 (hu) 2019-04-29
PT2470526E (pt) 2014-09-01
JO3002B1 (ar) 2016-09-05
CU24110B1 (es) 2015-07-30
US20180297986A1 (en) 2018-10-18
USRE49556E1 (en) 2023-06-20
HK1167390A1 (en) 2012-11-30
GEP20146102B (en) 2014-05-27
CN102725283A (zh) 2012-10-10
LUC00102I2 (en, 2012) 2024-05-21
CU20120034A7 (es) 2012-06-21
CN102725283B (zh) 2014-02-26
JP2014098022A (ja) 2014-05-29
CY2019014I1 (el) 2019-11-27
KR20120062839A (ko) 2012-06-14
US20200323852A1 (en) 2020-10-15
NO2019012I1 (no) 2019-03-05
HRP20170005T1 (hr) 2017-03-10
EA201500175A1 (ru) 2015-05-29
PE20120861A1 (es) 2012-07-14
LUC00101I2 (en, 2012) 2020-01-23
GT201200053A (es) 2014-03-27
JP2013503186A (ja) 2013-01-31
MA33604B1 (fr) 2012-09-01
LTPA2019006I1 (lt) 2019-03-25
HN2012000441A (es) 2015-01-05
CO6612222A2 (es) 2013-02-01
NL300973I2 (nl) 2022-05-05
EP2470526B1 (en) 2014-05-28
DK2727918T3 (da) 2017-01-23
AU2010286569C1 (en) 2019-11-28
IN2012DN02469A (en, 2012) 2015-08-21
SMT201700036T1 (it) 2017-03-08
EP2470526A1 (en) 2012-07-04

Similar Documents

Publication Publication Date Title
ME01860B (me) Jedinjenja i preparati protein kinaznih inhibitora
CN1151789C (zh) 芳基(或杂芳基)吡咯基甲醇的衍生物的应用
KR101708538B1 (ko) 심혈관 질환의 치료 방법
CN102223884B (zh) 固体药物组合物
HK1209318A1 (en) Pharmaceutical compositions of (r)-1-(2,2-diflurorbenzo[d][1,3]dioxol-5-yl)-n-(1-(2,3-dihydroxypropyl)-6-fluoro-2-(1-hydroxy-2-methylpropan-2-yl)-1h-indol-5-yl) cyclopropanecarboxamide and administration thereof
EA201270221A1 (ru) Лечение болезни крона с применением лаквинимода
WO2012027247A3 (en) Pharmaceutical composition of (r)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-n-(1-(2,3-dihydroxy propyl)-6-fluoro-2-(1-hydroxy-2-methylpropan-2-yl)-1h-indol-5-yl) cyclopropanecarboxamide and administration therof
EA201070167A1 (ru) Замещенные производные индазола, активные как ингибиторы киназы
EA200900155A1 (ru) Модуляторы фармакокинетических свойств лекарственных средств
FI2498756T4 (fi) Neratinibimaleaatin tablettiformulaatiot
NZ593295A (en) Preparation method of dihydroindene amide compounds, their pharmaceutical compositions containing compounds thereof and use as protein kinase inhibitor
SG10201407409WA (en) Inhibitors of jun n-terminal kinase
MX2010004501A (es) Inhibidor de la proteina de activacion de 5-lipoxigenasa (plap).
NZ597375A (en) Tofa analogs useful in treating dermatological disorders or conditions
AU2006321907A1 (en) Use of a CB1 antagonist for treating negative symptoms of schizophrenia
MY144132A (en) Polymorph forms of (2s)-(4e)-n-methyl-5-[3-(5-isoproproxypyridin)yl]-4-penten-2-amine
MX2011010732A (es) Pirimidinas sustituidas por imidazol utiles en el tratamiento de trastornos relacionados con glucogeno sintasa cinasa 3 como la enfermedad de alzheimer.
UA86621C2 (ru) Антагонисты рецептора глюкагона, их получение и терапевтическое применение
CL2009000491A1 (es) Compuestos derivados de 3-(4-(2-oxoindol)-piperidin)-pirrolidinas y 3-(4-benzo[b]imidazol)-piperidin)-pirrolidinas sustituidas proceso de preparacion; composicion farmaceutica; compuestos intermediarios; utiles en el tratamiento de la terapia del dolor, de enfermedades tales como alzheimer, ansiedad, depresion y glaucoma.
US20060178348A1 (en) Compositions and therapeutic methods utilizing a combination of a protein extravasation inhibitor and an NSAID
Asmar Targeting effective blood pressure control with angiotensin receptor blockers
RU2009139186A (ru) Применение гиалуронидазы для профилактики или лечения артериальной гипертензии или сердечной недостаточности
MX2021000349A (es) Administracion de un inhibidor de la enzima activadora de sumo y anticuerpos anti-cd20.
MY147474A (en) 1-[(4-[benzoyl(methyl)amino]-3-(phenyl)butyl]azetidine derivatives for the treatment of gastrointestinal disorders 1
Wallace et al. New pharmacologic therapies in gastrointestinal disease