BR112014018702A8 - Composto, cristal, inibidor, medicamento, composição farmacêutica, e, uso de um composto ou sal - Google Patents

Composto, cristal, inibidor, medicamento, composição farmacêutica, e, uso de um composto ou sal

Info

Publication number
BR112014018702A8
BR112014018702A8 BR112014018702A BR112014018702A BR112014018702A8 BR 112014018702 A8 BR112014018702 A8 BR 112014018702A8 BR 112014018702 A BR112014018702 A BR 112014018702A BR 112014018702 A BR112014018702 A BR 112014018702A BR 112014018702 A8 BR112014018702 A8 BR 112014018702A8
Authority
BR
Brazil
Prior art keywords
compound
drug
inhibitor
salt
crystal
Prior art date
Application number
BR112014018702A
Other languages
English (en)
Other versions
BR112014018702B1 (pt
BR112014018702A2 (pt
Inventor
Ohki Hitoshi
Ota Masahiro
Takeuchi Kosuke
Watanabe Hideaki
Yamaguchi Akitake
Shibata Yoshihiro
Tominaga Yuichi
Jimbo Takeshi
Kobayashi Keijiro
Kobayashi Katsuhiro
Fukatsu Daisuke
Original Assignee
Daiichi Sankyo Co Ltd
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
Application filed by Daiichi Sankyo Co Ltd filed Critical Daiichi Sankyo Co Ltd
Publication of BR112014018702A2 publication Critical patent/BR112014018702A2/pt
Publication of BR112014018702A8 publication Critical patent/BR112014018702A8/pt
Publication of BR112014018702B1 publication Critical patent/BR112014018702B1/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • C07D213/82Amides; Imides in position 3
    • 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
    • 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 chain containing hetero atoms as chain links
    • 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
    • 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
    • C07D451/00Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine

Abstract

COMPOSTO, CRISTAL, INIBIDOR, MEDICAMENTO, COMPOSIÇÃO FARMACÊUTICA, MÉTODOS PARA O TRATAMENTO DE UMA DOENÇA, PARA A PREVENÇÃO DE METÁSTASES DO CÂNCER, E PARA SUPERAR A RESISTÊNCIA À DROGA, E, USO DE UM COMPOSTO OU SAL. São fornecidos novos compostos ou sais dos mesmos, ou cristais dos mesmos, que inibem Axl e são úteis para o tratamento de doenças causadas por hiperfunção de Axl, doenças associadas com hiperfunção de Axl e/ou doenças acompanhadas por hiperfunção de Axl. São fornecidos derivados de piridona representados pela fórmula (I) tendo vários substituintes ou sais dos mesmos, ou cristais dos mesmos (em que R1, R2, R3, R5, R6, A, W, X e n na fórmula (I) são como definidos no relatório descritivo, respectivamente).
BR112014018702-9A 2012-01-31 2013-01-30 Composto, cristal, inibidor, medicamento, composição farmacêutica, e, uso de um composto ou sal BR112014018702B1 (pt)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2012017971 2012-01-31
JP2012-017971 2012-01-31
US201261746039P 2012-12-26 2012-12-26
US61/746039 2012-12-26
PCT/JP2013/052111 WO2013115280A1 (ja) 2012-01-31 2013-01-30 ピリドン誘導体

Publications (3)

Publication Number Publication Date
BR112014018702A2 BR112014018702A2 (pt) 2017-06-20
BR112014018702A8 true BR112014018702A8 (pt) 2017-07-11
BR112014018702B1 BR112014018702B1 (pt) 2021-12-14

Family

ID=48905312

Family Applications (1)

Application Number Title Priority Date Filing Date
BR112014018702-9A BR112014018702B1 (pt) 2012-01-31 2013-01-30 Composto, cristal, inibidor, medicamento, composição farmacêutica, e, uso de um composto ou sal

Country Status (31)

Country Link
US (1) US8933103B2 (pt)
EP (1) EP2810937B1 (pt)
JP (1) JP6006241B2 (pt)
KR (1) KR102078530B1 (pt)
CN (1) CN104185627B (pt)
AU (1) AU2013216006B2 (pt)
BR (1) BR112014018702B1 (pt)
CA (1) CA2863515C (pt)
CO (1) CO7071126A2 (pt)
CY (1) CY1118656T1 (pt)
DK (1) DK2810937T3 (pt)
ES (1) ES2617484T3 (pt)
HK (1) HK1203504A1 (pt)
HR (1) HRP20170303T1 (pt)
HU (1) HUE031624T2 (pt)
IL (1) IL233863A (pt)
LT (1) LT2810937T (pt)
MX (1) MX351812B (pt)
MY (1) MY165215A (pt)
NZ (1) NZ627586A (pt)
PH (1) PH12014501719A1 (pt)
PL (1) PL2810937T3 (pt)
PT (1) PT2810937T (pt)
RS (1) RS55728B1 (pt)
RU (1) RU2632885C2 (pt)
SG (1) SG11201404505PA (pt)
SI (1) SI2810937T1 (pt)
SM (1) SMT201700065B (pt)
TW (1) TWI537259B (pt)
WO (1) WO2013115280A1 (pt)
ZA (1) ZA201405486B (pt)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013162061A1 (ja) * 2012-04-26 2013-10-31 第一三共株式会社 二環性ピリミジン化合物
WO2015068767A1 (ja) * 2013-11-08 2015-05-14 小野薬品工業株式会社 ピロロピリミジン誘導体
AU2014353006B2 (en) 2013-11-20 2019-04-04 Signalchem Life Sciences Corp. Quinazoline derivatives as TAM family kinase inhibitors
MX2016006815A (es) 2013-11-27 2016-12-02 Signalchem Lifesciences Corp Derivados de aminopiridina como inhibidores de cinasas de la familia de tyro3, axl y mer (tam).
CN106659765B (zh) 2014-04-04 2021-08-13 德玛医药 二脱水半乳糖醇及其类似物或衍生物用于治疗非小细胞肺癌和卵巢癌的用途
TWI723572B (zh) * 2014-07-07 2021-04-01 日商第一三共股份有限公司 具有四氫吡喃基甲基之吡啶酮衍生物及其用途
WO2016183071A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Hetero-tricyclic compounds and their use for the treatment of cancer
WO2017027717A1 (en) 2015-08-12 2017-02-16 Incyte Corporation Bicyclic fused pyrimidine compounds as tam inhibitors
WO2017035366A1 (en) 2015-08-26 2017-03-02 Incyte Corporation Pyrrolopyrimidine derivatives as tam inhibitors
ES2896079T3 (es) 2016-02-26 2022-02-23 Ono Pharmaceutical Co Fármaco para la terapia del cáncer, caracterizado por la administración de la combinación entre un inhibidor de Axl y un inhibidor del punto de control inmunitario
KR102558066B1 (ko) 2016-03-28 2023-07-25 인사이트 코포레이션 Tam 억제제로서 피롤로트리아진 화합물
CN108250200A (zh) * 2016-12-28 2018-07-06 中国科学院上海药物研究所 一种具有Axl抑制活性的化合物及其制备和应用
JP7156287B2 (ja) 2017-08-23 2022-10-19 小野薬品工業株式会社 Axl阻害剤を有効成分として含むがん治療剤
KR20200088308A (ko) 2017-09-27 2020-07-22 인사이트 코포레이션 Tam 억제제로서 유용한 피롤로트리아진 유도체의 염
JP7223998B2 (ja) 2017-10-13 2023-02-17 小野薬品工業株式会社 Axl阻害剤を有効成分として含む固形がん治療剤
MX2020007956A (es) * 2018-01-29 2021-01-08 Capulus Therapeutics Llc Inhibidores de la proteína de unión al elemento regulador de esterol (srebp) que comprenden un anillo central de 6 miembros.
IL277071B1 (en) 2018-03-08 2024-03-01 Incyte Corp Aminopyrizine diol compounds as PI3K–y inhibitors
MA53010A (fr) 2018-06-29 2021-05-05 Incyte Corp Formulations d'un inhibiteur de axl/mer
US11046658B2 (en) 2018-07-02 2021-06-29 Incyte Corporation Aminopyrazine derivatives as PI3K-γ inhibitors
IL279070B1 (en) * 2018-07-04 2024-01-01 Daiichi Sankyo Co Ltd A method for the production of diarylpyridine derivatives
US20220143049A1 (en) 2019-03-21 2022-05-12 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
US11718612B2 (en) 2019-09-06 2023-08-08 Board Of Regents, The University Of Texas System Inhibitors of receptor interacting protein kinase I for the treatment of disease
CN112625026B (zh) * 2019-09-24 2022-09-09 药捷安康(南京)科技股份有限公司 Tam家族激酶抑制剂的喹啉衍生物
AU2020353663A1 (en) 2019-09-27 2022-04-07 Board Of Regents, The University Of Texas System Inhibitors of Receptor Interacting Protein Kinase I for the treatment of disease
JP2023500906A (ja) 2019-11-08 2023-01-11 インサーム(インスティテュ ナシオナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシェ メディカル) キナーゼ阻害剤に対する獲得抵抗性を有するがんの処置方法
AU2020391425A1 (en) * 2019-11-26 2022-06-16 Board Of Regents, The University Of Texas System Inhibitors of Receptor Interacting Protein Kinase 1 for the treatment of disease
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
WO2022220227A1 (ja) * 2021-04-14 2022-10-20 エーザイ・アール・アンド・ディー・マネジメント株式会社 テトラヒドロピリドピリミジン化合物

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL205322B1 (pl) * 1999-05-07 2010-04-30 Encysive Pharmaceuticals Inc Pochodne kwasu propionowego, środek farmaceutyczny i zastosowanie pochodnych kwasu propionowego
EP1136485A1 (en) * 2000-03-23 2001-09-26 Sanofi-Synthelabo Aminophenyl pyrimidone derivatives
EP1483400A4 (en) 2002-02-12 2007-07-11 Quark Biotech Inc USE OF THE AXL RECEPTOR FOR THE DIAGNOSIS AND TREATMENT OF A KIDNEY DISEASE
WO2007030680A2 (en) 2005-09-07 2007-03-15 Rigel Pharmaceuticals, Inc. Triazole derivatives useful as axl inhibitors
WO2007057399A2 (en) 2005-11-15 2007-05-24 Boehringer Ingelheim International Gmbh Treatment of cancer with indole derivatives
SI1959955T1 (sl) 2005-12-05 2011-02-28 Pfizer Prod Inc Postopek zdravljenja abnormalne celične rasti
WO2007070872A1 (en) 2005-12-15 2007-06-21 Rigel Pharmaceuticals, Inc. Kinase inhibitors and their uses
EP1900727A1 (en) 2006-08-30 2008-03-19 Cellzome Ag Aminopyridine derivatives as kinase inhibitors
US8097630B2 (en) 2006-10-10 2012-01-17 Rigel Pharmaceuticals, Inc. Pinane-substituted pyrimidinediamine derivatives useful as Axl inhibitors
GB0625659D0 (en) 2006-12-21 2007-01-31 Cancer Rec Tech Ltd Therapeutic compounds and their use
DK2078010T3 (da) 2006-12-29 2014-04-28 Rigel Pharmaceuticals Inc Polycyklisk heteroaryl-substituerede triazoler, der er anvendelige som axl-hæmmere
EP2074115B1 (en) 2006-12-29 2018-03-07 Rigel Pharmaceuticals, Inc. N3-heteroaryl substituted triazoles and n5-heteroaryl substituted triazoles useful as axl inhibitors
CA2710043C (en) 2006-12-29 2016-02-09 Rigel Pharmaceuticals, Inc. Bicyclic aryl and bicyclic heteroaryl substituted triazoles useful as axl inhibitors
US8906922B2 (en) 2006-12-29 2014-12-09 Rigel Pharmaceuticals, Inc. Substituted triazoles useful as AXl inhibitors
PL2114955T3 (pl) 2006-12-29 2013-06-28 Rigel Pharmaceuticals Inc Triazole podstawione mostkowanym bicyklicznym arylem oraz mostkowanym bicyklicznym heteroarylem użyteczne jako inhibitory Axl
EP2139869A2 (en) 2007-04-13 2010-01-06 SuperGen, Inc. Axl kinase inhibitors useful for the treatment of cancer or hyperproliferative disorders
WO2009007749A2 (en) * 2007-07-09 2009-01-15 Astrazeneca Ab Trisubstituted pyrimidine derivatives for the treatment of proliferative diseases
GB0713259D0 (en) 2007-07-09 2007-08-15 Astrazeneca Ab Pyrazine derivatives 954
WO2009024825A1 (en) 2007-08-21 2009-02-26 Astrazeneca Ab 2-pyrazinylbenzimidazole derivatives as receptor tyrosine kinase inhibitors
GB0719803D0 (en) * 2007-10-10 2007-11-21 Cancer Rec Tech Ltd Therapeutic compounds and their use
AU2008315746A1 (en) 2007-10-25 2009-04-30 Astrazeneca Ab Pyridine and pyrazine derivatives useful in the treatment of cell proliferative disorders
RU2010120536A (ru) * 2007-10-25 2011-11-27 Астразенека Аб (Se) Производные пиридина и пиразина, полезные для лечения клеточных проферативных расстройств
ES2424259T3 (es) * 2007-10-26 2013-09-30 Rigel Pharmaceuticals, Inc. Triazoles sustituidos con arilo policíclico y heteroarilo policíclico, útiles como agentes inhibidores del Axl
WO2009058801A1 (en) 2007-11-02 2009-05-07 Janssen Pharmaceutica, N.V. Use of cfms inhibitor for treating or preventing bone cancer and the bone loss and bone pain associated with bone cancer
DK2235002T3 (da) 2008-01-23 2013-03-11 Bristol Myers Squibb Co 4-pyridinonforbindelser og anvendelse heraf til behandling af cancer
ES2531396T3 (es) 2008-01-23 2015-03-13 Bristol Myers Squibb Co Proceso para preparar compuestos de piridinona
RU2010146474A (ru) 2008-04-16 2012-05-27 Макс-Планк-Гезелльшафт Цур Фердерунг Дер Виссеншафтен Е.Ф. (De) Производные хинолина в качестве ингибиторов axl киназ
UY31800A (es) 2008-05-05 2009-11-10 Smithkline Beckman Corp Metodo de tratamiento de cancer usando un inhibidor de cmet y axl y un inhibidor de erbb
WO2009138799A1 (en) 2008-05-14 2009-11-19 Astex Therapeutics Limited Therapeutic uses of 1-cycl0pr0pyl-3 - [3- ( 5 -morpholin- 4 -ylmethyl- 1h-benz0imidaz0l- 2 -yl) -lh-pyrazol-4-yl] -urea
WO2010005876A2 (en) 2008-07-09 2010-01-14 Rigel Pharmaceuticals, Inc. Polycyclic heteroaryl substituted triazoles useful as axl inhibitors
US8431594B2 (en) 2008-07-09 2013-04-30 Rigel Pharmaceuticals, Inc. Bridged bicyclic heteroaryl substituted triazoles useful as AXL inhibitors
CA2748943A1 (en) 2009-02-09 2010-08-12 Supergen, Inc. Pyrrolopyrimidinyl axl kinase inhibitors
US8367836B2 (en) * 2009-04-27 2013-02-05 Elan Pharmaceuticals, Inc. Pyridinone antagonists of alpha-4 integrins
EP2311809A1 (en) 2009-10-16 2011-04-20 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Quinolinyloxyphenylsulfonamides
US8962623B2 (en) 2011-03-04 2015-02-24 Locus Pharmaceuticals, Inc. Aminopyrazine compounds

Also Published As

Publication number Publication date
WO2013115280A1 (ja) 2013-08-08
DK2810937T3 (en) 2017-03-13
BR112014018702B1 (pt) 2021-12-14
HRP20170303T1 (hr) 2017-04-21
CY1118656T1 (el) 2017-07-12
RU2632885C2 (ru) 2017-10-11
LT2810937T (lt) 2017-02-10
TWI537259B (zh) 2016-06-11
SMT201700065B (it) 2017-03-08
SG11201404505PA (en) 2014-10-30
IL233863A (en) 2017-08-31
CN104185627A (zh) 2014-12-03
HK1203504A1 (en) 2015-10-30
MX2014009246A (es) 2014-10-14
CN104185627B (zh) 2018-01-12
KR20140117439A (ko) 2014-10-07
US20130281428A1 (en) 2013-10-24
NZ627586A (en) 2016-08-26
JPWO2013115280A1 (ja) 2015-05-11
TW201335148A (zh) 2013-09-01
EP2810937A4 (en) 2015-07-22
MX351812B (es) 2017-10-27
PH12014501719B1 (en) 2014-11-10
PT2810937T (pt) 2017-03-03
AU2013216006B2 (en) 2017-06-08
EP2810937B1 (en) 2016-11-30
BR112014018702A2 (pt) 2017-06-20
AU2013216006A1 (en) 2014-08-28
PL2810937T3 (pl) 2017-07-31
US8933103B2 (en) 2015-01-13
KR102078530B1 (ko) 2020-02-18
JP6006241B2 (ja) 2016-10-12
CA2863515A1 (en) 2013-08-08
PH12014501719A1 (en) 2014-11-10
ES2617484T3 (es) 2017-06-19
CO7071126A2 (es) 2014-09-30
IL233863A0 (en) 2014-09-30
RS55728B1 (sr) 2017-07-31
EP2810937A1 (en) 2014-12-10
SI2810937T1 (sl) 2017-01-31
ZA201405486B (en) 2015-11-25
CA2863515C (en) 2018-02-27
HUE031624T2 (en) 2017-07-28
MY165215A (en) 2018-03-09
RU2014135401A (ru) 2016-03-20

Similar Documents

Publication Publication Date Title
BR112014018702A8 (pt) Composto, cristal, inibidor, medicamento, composição farmacêutica, e, uso de um composto ou sal
BR112015021983A8 (pt) compostos heterocíclicos, composições e usos dos mesmos
BR112018005497A2 (pt) compostos heterocíclicos e usos dos mesmos
BR112015022643A2 (pt) inibidores diidro-pirrolpiridinona
BR112015020772A2 (pt) compostos de pirimidina e piridina e seu uso
BR112015018738A8 (pt) compostos de tetra-hidropirrolotiazina, seus usos, e composição farmacêutica
BR112016024545A2 (pt) derivados de pirazolo pirimidina e seu uso como inibidores de malt1
BR112015003188A2 (pt) Composto, composição farmacêutica, uso do composto e método para tratar uma doença ou condição mediada por rorgammat em um paciente
BR112018008397A2 (pt) derivados de di-hidroimidazopirazinona úteis no tratamento do câncer
BR112014007193A2 (pt) derivados de pirazoloquinolinona, preparação dos mesmos e uso terapêutico dos mesmos
BR112015016911A2 (pt) tiadiazol, análogos dos mesmos e métodos de tratamento de condições relacionadas à deficiência de smn
BR112015022077A2 (pt) composto de pirazol-amida e usos medicinais do mesmo
BR112016007396A2 (pt) derivados de cetona pirídicos, método de preparação dos mesmos e aplicação farmacêutica dos mesmos
BR112015020350A2 (pt) derivados de 6-(5-hidroxi-1h-pirazol-1-il)nicotinamida e seu uso como inibidores de phd
BR112014005468A2 (pt) derivados de aminopiridina para uso como moduladores de atividade quinase
BR112017000242A2 (pt) composto, cristal, inibidor de axl, medicamento, composição farmacêutica, métodos para tratamento de uma doença, para prevenção de metástases de câncer, para superar a resistência a drogas de um câncer e para inibir a aquisição de resistência a drogas de um câncer, e, uso de um composto
BR112012007322A2 (pt) composto de 2-piridona usados como inibidores de neutrófilo elastase
BR112014003587A2 (pt) derivados de 5-flúor-4-imino-3-(substituído)-3,4-di-hidropirimidin-2(1h)ona
BR112014022214A2 (pt) fenólicos antibacterianos
UA109290C2 (uk) Спільні кристали і солі інгібіторів ccr3
BR112015017331A2 (pt) compostos químicos
BR112015016325A2 (pt) Composto, composição farmacêutica, e, usos de uma composição, composto, pró-droga ou sal farmaceuticamente aceitável do mesmo
BR112015012825A2 (pt) piridopirazinas substituídas como inibidores de syk
BR112018001035A2 (pt) compostos de fenoxiacetamidas aneladas, sal farmaceuticamente aceitável, seu método de síntese, combinação de medicamento e uso dos mesmos
BR112014007578A2 (pt) derivados de carbamato/ureia contendo anéis piperidina e piperazina como inibidores do receptor de h3

Legal Events

Date Code Title Description
B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]
B07E Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette]

Free format text: NOTIFICACAO DE ANUENCIA RELACIONADA COM O ART 229 DA LPI

B06U Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]

Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 30/01/2013, OBSERVADAS AS CONDICOES LEGAIS.