[go: up one dir, main page]

MA34064B1 - Compose heterocyclique - Google Patents

Compose heterocyclique

Info

Publication number
MA34064B1
MA34064B1 MA35205A MA35205A MA34064B1 MA 34064 B1 MA34064 B1 MA 34064B1 MA 35205 A MA35205 A MA 35205A MA 35205 A MA35205 A MA 35205A MA 34064 B1 MA34064 B1 MA 34064B1
Authority
MA
Morocco
Prior art keywords
heterocyclic compound
component
salt
relates
useful
Prior art date
Application number
MA35205A
Other languages
Arabic (ar)
English (en)
Inventor
Misaki Homma
Toru Miyazaki
Yuya Oguro
Osamu Kurasawa
Original Assignee
Takeda Pharmaceutical
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=44482985&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA34064(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical
Publication of MA34064B1 publication Critical patent/MA34064B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/20Spiro-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

L'INVENTION PORTE SUR UN COMPOSÉ UTILE EN TANT QU'AGENT PROPHYLACTIQUE OU THÉRAPEUTIQUE POUR LE CANCER. PLUS PARTICULIÈREMENT, L'INVENTION PORTE SUR UN COMPOSÉ REPRÉSENTÉ PAR LA FORMULE (I) [CHAQUE SYMBOLE ÉTANT TEL QUE DÉFINI DANS LA DESCRIPTION] OU SUR UN SEL DE CELUI-CI, OU SUR UN PROMÉDICAMENT DU COMPOSÉ OU DU SEL DE CELUI-CI, UTILE POUR LA PRÉVENTION OU LE TRAITEMENT DU CANCER.
MA35205A 2010-02-17 2011-02-16 Compose heterocyclique MA34064B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2010031899 2010-02-17
JP2010131950 2010-06-09
PCT/JP2011/053303 WO2011102399A1 (fr) 2010-02-17 2011-02-16 Composé hétérocyclique

Publications (1)

Publication Number Publication Date
MA34064B1 true MA34064B1 (fr) 2013-03-05

Family

ID=44482985

Family Applications (1)

Application Number Title Priority Date Filing Date
MA35205A MA34064B1 (fr) 2010-02-17 2011-02-16 Compose heterocyclique

Country Status (37)

Country Link
US (6) US8722660B2 (fr)
EP (2) EP3533797B1 (fr)
JP (1) JP5689454B2 (fr)
KR (1) KR101735868B1 (fr)
CN (1) CN102844320B (fr)
AU (1) AU2011216404B2 (fr)
BR (1) BR112012020311B1 (fr)
CA (1) CA2790284C (fr)
CL (1) CL2012002250A1 (fr)
CO (1) CO6592104A2 (fr)
CR (1) CR20120448A (fr)
CY (1) CY1121792T1 (fr)
DK (1) DK2540728T3 (fr)
DO (1) DOP2012000224A (fr)
EA (1) EA020724B1 (fr)
EC (1) ECSP12012160A (fr)
ES (1) ES2733221T3 (fr)
GE (1) GEP20146202B (fr)
HR (1) HRP20190947T1 (fr)
HU (1) HUE043514T2 (fr)
IL (1) IL221442A0 (fr)
LT (1) LT2540728T (fr)
MA (1) MA34064B1 (fr)
ME (1) ME03410B (fr)
MX (1) MX353500B (fr)
MY (1) MY164776A (fr)
NZ (1) NZ602089A (fr)
PE (1) PE20130184A1 (fr)
PH (1) PH12012501650B1 (fr)
PL (1) PL2540728T3 (fr)
PT (1) PT2540728T (fr)
RS (1) RS58796B1 (fr)
SG (1) SG183304A1 (fr)
SI (1) SI2540728T1 (fr)
SM (1) SMT201900385T1 (fr)
TN (1) TN2012000401A1 (fr)
WO (1) WO2011102399A1 (fr)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH12013500274A1 (en) * 2010-08-11 2013-03-04 Millennium Pharm Inc Heteroaryls and uses thereof
US9974795B2 (en) 2014-01-31 2018-05-22 Carna Biosciences, Inc. Anticancer agent composition
TW201620879A (zh) 2014-04-28 2016-06-16 杜邦股份有限公司 除草性經取代之3-苯基-4-氟基苯甲醯基吡唑
US10174032B2 (en) * 2014-05-05 2019-01-08 Signalrx Pharmaceuticals, Inc. Heterocyclic compound classes for signaling modulation
KR102006320B1 (ko) 2015-12-07 2019-08-02 지머젠 인코포레이티드 Htp 게놈 공학 플랫폼에 의한 미생물 균주 개량
AU2016378723B2 (en) 2015-12-22 2021-09-30 SHY Therapeutics LLC Compounds for the treatment of cancer and inflammatory disease
WO2017172565A1 (fr) * 2016-03-28 2017-10-05 Takeda Pharmaceutical Company Limited Formes cristallines de 2-[(2s)-1-azabicyclo[2.2.2]oct-2-yl]-6-(3-méthyl-1h-pyrazol-4-yl)thiéno[3,2-d]pyrimidin-4(3h)-one hémihydratée
EA035560B1 (ru) * 2016-07-28 2020-07-07 Такеда Фармасьютикал Компани Лимитед Кристаллические формы гемигидрата 2-[(2s)-1-азабицикло[2.2.2]окт-2-ил]-6-(3-метил-1h-пиразол-4-ил)тиено[3,2- d]пиримидин-4(3h)-она
JP7071383B2 (ja) 2016-11-08 2022-05-18 キャンサー・リサーチ・テクノロジー・リミテッド cdc7阻害剤としてのピリミジノン誘導体
US11155879B2 (en) 2017-03-01 2021-10-26 Takeda Pharmaceutical Company Limited Method of predicting effects of CDC7 inhibitor
WO2018217439A1 (fr) * 2017-05-21 2018-11-29 Zhang Hai Jun [5,6]cyclique-4(3h)-pyrimidinones substitués en tant qu'agents anticancéreux
MX2019014875A (es) 2017-06-21 2021-01-29 SHY Therapeutics LLC Compuestos que interaccionan con la superfamilia ras para el tratamiento de cancer, enfermedades inflamatorias, rasopatias y enfermedad fibrotica.
CA3095264A1 (fr) * 2018-04-02 2019-10-10 Takeda Pharmaceutical Company Limited Procedes de synthese de 2-[(2s)-1-azabicyclo[2.2.2]oct-2-yl]-6- (3-methyl-1 h-pyrazol-4-yl)thieno[3,2-d]pyrimidin-4(3h)-one
TWI846703B (zh) 2018-06-19 2024-07-01 日商武田藥品工業股份有限公司 癌症治療方法
EP3823599B1 (fr) * 2018-07-19 2024-08-28 Takeda Pharmaceutical Company Limited Compositions pharmaceutiques comprenant un inhibiteur de cdc7
CA3113621A1 (fr) 2018-09-24 2020-04-02 Sierra Oncology, Inc. Methodes de traitement du cancer comprenant des inhibiteurs de cdc7
US12391705B2 (en) 2018-12-19 2025-08-19 Shy Therapeutics, Llc Compounds that interact with the Ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease
KR20220027883A (ko) * 2019-05-30 2022-03-08 치아타이 티안큉 파마수티컬 그룹 주식회사 Cdc7 억제제로서의 테트라사이클릭 화합물
BR112022000734A2 (pt) * 2019-07-19 2022-04-12 Takeda Pharmaceuticals Co Método para tratar câncer em um paciente, uso de composto 1, e, composto 1
US20220389026A1 (en) * 2019-08-20 2022-12-08 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Tetracyclic compound used as cdc7 inhibitor
US20230101747A1 (en) * 2019-12-06 2023-03-30 Schrödinger, Inc. Cyclic compounds and methods of using same
WO2022055963A1 (fr) * 2020-09-10 2022-03-17 Schrödinger, Inc. Inhibiteurs de kinase cdc7 péricondensés hétérocycliques utilisés dans le traitement du cancer
AU2021386437A1 (en) * 2020-11-30 2023-06-29 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Salt form used as cdc7 inhibitor and crystal form thereof
CN112661770B (zh) * 2020-12-24 2022-11-08 南京正济医药研究有限公司 一种化合物及利用其制备取代的[5,6]环-4(3h)-嘧啶酮化合物的方法
WO2022167999A1 (fr) 2021-02-08 2022-08-11 Takeda Pharmaceutical Company Limited Polythérapie pour le traitement du cancer
CN117120447A (zh) * 2021-03-18 2023-11-24 薛定谔公司 环状化合物和其使用方法
TW202300150A (zh) * 2021-03-18 2023-01-01 美商薛定諤公司 環狀化合物及其使用方法
TW202330552A (zh) * 2021-10-13 2023-08-01 美商雷密克斯醫療公司 調節剪接之化合物及方法
WO2025160538A1 (fr) * 2024-01-26 2025-07-31 The Board Of Regents Of The University Of Texas System Compositions et méthodes de traitement du grisonnement et de la chute des cheveux associés au vieillissement
WO2025168620A1 (fr) 2024-02-07 2025-08-14 Bayer Aktiengesellschaft 4,5-dihydro-1h-2,4,5-oxadiazines substituées par hétéroaryle utilisées en tant que nouveaux fongicides

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4196207A (en) * 1977-05-23 1980-04-01 Ici Australia Limited Process for controlling eradicating or preventing infestations of animals by Ixodid ticks
DE19644228A1 (de) * 1996-10-24 1998-04-30 Merck Patent Gmbh Thienopyrimidine
AUPO721997A0 (en) 1997-06-06 1997-07-03 Queensland Institute Of Medical Research, The Anticancer compounds
JP2002105081A (ja) 2000-07-28 2002-04-10 Nikken Chem Co Ltd 新規チオフェンニ環化合物
CN1458933A (zh) 2000-09-29 2003-11-26 日本曹达株式会社 噻吩并嘧啶化合物及其盐以及其制备方法
US6503914B1 (en) 2000-10-23 2003-01-07 Board Of Regents, The University Of Texas System Thienopyrimidine-based inhibitors of the Src family
US20030096813A1 (en) 2001-04-20 2003-05-22 Jingrong Cao Compositions useful as inhibitors of GSK-3
BR0313078A (pt) 2002-08-06 2005-07-12 Astrazeneca Ab Composto ou um sal deste farmaceuticamente aceitável, composição farmacêutica, e, uso do composto ou de um sal deste farmaceuticamente aceitável
EP1646615B1 (fr) 2003-06-06 2009-08-26 Vertex Pharmaceuticals Incorporated Derives de pyrimidne utilises en tant que modulateurs de transporteurs de cassette de liaison a l'atp
DE602004020070D1 (de) * 2003-06-11 2010-10-07 Xention Ltd Thienopyrimidin-derivate als kaliumkanal-inhibitoren
US20050032869A1 (en) * 2003-07-08 2005-02-10 Pharmacia Italia S.P.A. Pyrazolyl-indole derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
CA2534496A1 (fr) * 2003-08-08 2005-02-17 Ermes Vanotti Derives de pyrimidylpyrrole pouvant etre utilises comme inhibiteurs de kinases
US7279575B2 (en) 2003-08-08 2007-10-09 Pfizer Italia S.R.L. Pyrimidylpyrrole derivatives active as kinase inhibitors
CN1989131A (zh) * 2004-03-30 2007-06-27 希龙公司 取代的噻吩衍生物用作抗癌药
WO2005097189A1 (fr) 2004-04-09 2005-10-20 Genecare Research Institute Co., Ltd. Agent induisant une apoptose specifique aux cellules carcinomes ciblant un gene intervenant dans la stabilisation des chromosomes
JP4545196B2 (ja) 2005-01-19 2010-09-15 メルク・シャープ・エンド・ドーム・コーポレイション 有糸分裂キネシン阻害剤
JP2009501217A (ja) 2005-07-15 2009-01-15 アストラゼネカ アクチボラグ 治療薬
RU2376300C1 (ru) 2005-08-30 2009-12-20 Асахи Касеи Фарма Корпорэйшн Сульфонамидное соединение
FI20055498A0 (fi) 2005-09-16 2005-09-16 Biotie Therapies Corp Sulfonamidijohdannaisia
US20070142414A1 (en) * 2005-12-16 2007-06-21 Pharmacia Italia S.P.A. N-substituted pyrrolopyridinones active as kinase inhibitors
US7618982B2 (en) * 2005-12-19 2009-11-17 Nerviano Medical Sciences S.R.L. Heteroarylpyrrolopyridinones active as kinase inhibitors
WO2007102679A1 (fr) 2006-03-06 2007-09-13 Je Il Pharmaceutical Co., Ltd. Nouveaux dérivés de la thiénopyrimidine ou leurs sels pharmacocompatibles, leur procédé de préparation, et préparations pharmaceutiques les comprenant
WO2008082839A2 (fr) 2006-12-29 2008-07-10 Abbott Laboratories Inhibiteurs de la pim kinase comme agents chimiothérapeutiques destinés à lutter contre le cancer
US20090030196A1 (en) * 2006-12-29 2009-01-29 Abbott Laboratories Pim kinase inhibitors as cancer chemotherapeutics
CL2008000252A1 (es) 2007-01-29 2008-03-14 Xenon Pharmaceuticals Inc Compuestos derivados de quinazolinona o pirimidinona; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar enfermedades mediadas por los canales de calcio, tales como dolor, depresion, enfermedades cardiovasculares, respir
WO2009001214A2 (fr) 2007-06-28 2008-12-31 Pfizer Products Inc. Dérivés de thieno[2,3-d]pyrimidin-4(3h)-one, d'isoxazolo[5,4-d]pyrimidin-4(5h)-one et d'isothiazolo[5,4-d]pyrimidin-4(5h)-one utilisés comme antagonistes du récepteur du calcium
US20090118276A1 (en) 2007-11-02 2009-05-07 Wyeth Thienopyrimidines, thienopyridines, and pyrrolopyrimidines as b-raf inhibitors
WO2009112490A1 (fr) 2008-03-11 2009-09-17 Cellzome Limited Sulfonamides en tant qu'inhibiteurs de zap-70
PE20091928A1 (es) 2008-05-29 2009-12-31 Bristol Myers Squibb Co Tienopirimidinas hidroxisustituidas como antagonistas de receptor-1 de hormona concentradora de melanina no basicos
MX2010014280A (es) 2008-06-26 2011-05-23 Dana Farber Cancer Inst Inc Distintivos y determinantes asociados con metástasis y método para utilizarlos.
US8691828B2 (en) 2009-03-05 2014-04-08 Takeda Pharmaceutical Company Limited Thienopyrimidine as CDC7 kinase inhibitors
WO2010126002A1 (fr) 2009-04-28 2010-11-04 塩野義製薬株式会社 Produit pharmaceutique contenant un composé sulfonamide hétérocyclique
TW201111378A (en) 2009-09-11 2011-04-01 Bayer Schering Pharma Ag Substituted (heteroarylmethyl) thiohydantoins
CA2773615A1 (fr) 2009-09-11 2011-03-17 Arwed Cleve Thiohydantoines a substitution heteroarylmethyle, en tant que medicaments anticancer
AR079343A1 (es) 2009-12-21 2012-01-18 Lilly Co Eli Compuesto de acido 2-amino-4-(4h-1,2,4-triazol-3-ilsulfanil)biciclo[3.1.0]hexano-2,6-dicarboxilico, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para tratar un trastorno psiquiatrico

Also Published As

Publication number Publication date
LT2540728T (lt) 2019-06-25
US8933069B2 (en) 2015-01-13
DK2540728T3 (da) 2019-05-13
EP3533797B1 (fr) 2023-12-20
MX353500B (es) 2018-01-16
US20140235615A1 (en) 2014-08-21
WO2011102399A1 (fr) 2011-08-25
CL2012002250A1 (es) 2013-02-08
CA2790284C (fr) 2019-01-08
JPWO2011102399A1 (ja) 2013-06-17
TN2012000401A1 (en) 2014-01-30
PT2540728T (pt) 2019-07-11
ME03410B (fr) 2020-01-20
IL221442A0 (en) 2012-10-31
MX2012009602A (es) 2012-12-17
DOP2012000224A (es) 2013-01-31
EP2540728A1 (fr) 2013-01-02
US20140228352A1 (en) 2014-08-14
PH12012501650A1 (en) 2012-10-22
CN102844320B (zh) 2016-03-23
NZ602089A (en) 2014-05-30
PE20130184A1 (es) 2013-03-09
CA2790284A1 (fr) 2011-08-25
EA201290800A1 (ru) 2013-03-29
SI2540728T1 (sl) 2019-06-28
US20160310494A1 (en) 2016-10-27
CR20120448A (es) 2012-11-13
EP3533797A1 (fr) 2019-09-04
ES2733221T3 (es) 2019-11-28
KR20130001246A (ko) 2013-01-03
CN102844320A (zh) 2012-12-26
JP5689454B2 (ja) 2015-03-25
US8921354B2 (en) 2014-12-30
ECSP12012160A (es) 2013-03-28
CY1121792T1 (el) 2020-07-31
US9388195B2 (en) 2016-07-12
GEP20146202B (en) 2014-11-25
PL2540728T3 (pl) 2019-09-30
EP2540728B1 (fr) 2019-04-10
US8722660B2 (en) 2014-05-13
US20130029969A1 (en) 2013-01-31
US20170209452A1 (en) 2017-07-27
MY164776A (en) 2018-01-30
US9655900B2 (en) 2017-05-23
RS58796B1 (sr) 2019-07-31
SMT201900385T1 (it) 2019-09-09
HUE043514T2 (hu) 2019-08-28
HRP20190947T1 (hr) 2019-07-26
AU2011216404A1 (en) 2012-09-20
AU2011216404B2 (en) 2016-04-07
CO6592104A2 (es) 2013-01-02
US20150158882A1 (en) 2015-06-11
PH12012501650B1 (en) 2018-11-07
BR112012020311A2 (pt) 2017-03-01
SG183304A1 (en) 2012-09-27
BR112012020311B1 (pt) 2019-01-29
EP2540728A4 (fr) 2013-11-06
KR101735868B1 (ko) 2017-05-15
EA020724B1 (ru) 2015-01-30

Similar Documents

Publication Publication Date Title
MA34064B1 (fr) Compose heterocyclique
PH12017502141A1 (en) Compounds and their methods of use
EA201391626A1 (ru) Соединения для ингибирования клеточной пролиферации в egfr-стимулированных типах рака
EA201071032A1 (ru) Гетероциклическое соединение
MX352672B (es) Compuestos heterocíclicos como inhibidores de mdm2 para el tratamiento del cáncer.
MX374513B (es) Compuestos de morfolinona de ácido heteroarilo como inhibidores mdm2 para el tratamiento de cáncer.
MX2016000675A (es) Derivados de amino-metil-biarilo como inhibidores del factor de complemento d y usos de los mismos.
UA111161C2 (uk) Похідна фталазинонкетону, спосіб її одержання та її фармацевтичне застосування
PH12016500072B1 (en) Piperidinyl-indole derivatives complement factor b inhibitors and uses thereof
TN2012000559A1 (en) Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer
EA201590224A1 (ru) Имидазотриазинкарбонитрилы, используемые в качестве ингибиторов киназы
PH12015501316A1 (en) Heterocyclic compound
EA201690598A1 (ru) Аминогетероарил бензамиды в качестве ингибиторов киназы
GEP201706624B (en) Triazolopyrazine as brd4 inhibitors and usage thereof for cancer treatment
JO3148B1 (ar) مركب مثبط لإشارات مسار notch
TN2013000413A1 (en) Glycoside derivatives and their uses for the treatment of diabetes
MX2015010619A (es) Cis-morfolinona y otros compuestos como inhibidores de mdm2 para el tratamiento del cancer.
MX2013007937A (es) Nuevo derivado de indol o indazol o sal del mismo.
NZ700356A (en) Pyrazole compounds as sglt1 inhibitors
EA201270728A1 (ru) Пуриновые соединения
UA110834C2 (uk) Сполука-інгібітор сигнального шляху notch
TN2010000397A1 (en) Heterocyclic compounds
MX2011003390A (es) Compuestos y composiciones útiles en el tratamiento de enfermedades cardiacas con efectos secundarios reducidos.