SG10201710578TA - Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt - Google Patents

Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt

Info

Publication number
SG10201710578TA
SG10201710578TA SG10201710578TA SG10201710578TA SG10201710578TA SG 10201710578T A SG10201710578T A SG 10201710578TA SG 10201710578T A SG10201710578T A SG 10201710578TA SG 10201710578T A SG10201710578T A SG 10201710578TA SG 10201710578T A SG10201710578T A SG 10201710578TA
Authority
SG
Singapore
Prior art keywords
phthalazin
pyrido
triazol
fluorophenyl
dihydro
Prior art date
Application number
SG10201710578TA
Other languages
English (en)
Inventor
Bing Wang
Daniel Chu
Yongbo Liu
Shichun Peng
Original Assignee
Medivation Technologies Inc
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=44903424&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG10201710578T(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Medivation Technologies Inc filed Critical Medivation Technologies Inc
Publication of SG10201710578TA publication Critical patent/SG10201710578TA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/06Peri-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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
SG10201710578TA 2010-10-21 2011-10-20 Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt SG10201710578TA (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US40547610P 2010-10-21 2010-10-21

Publications (1)

Publication Number Publication Date
SG10201710578TA true SG10201710578TA (en) 2018-02-27

Family

ID=44903424

Family Applications (2)

Application Number Title Priority Date Filing Date
SG10201710578TA SG10201710578TA (en) 2010-10-21 2011-10-20 Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt
SG2013029731A SG189939A1 (en) 2010-10-21 2011-10-20 Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt

Family Applications After (1)

Application Number Title Priority Date Filing Date
SG2013029731A SG189939A1 (en) 2010-10-21 2011-10-20 Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt

Country Status (24)

Country Link
US (3) US8735392B2 (ja)
EP (2) EP3757106A1 (ja)
JP (5) JP2013540158A (ja)
KR (4) KR20210028747A (ja)
CN (1) CN103282365B (ja)
AR (1) AR083502A1 (ja)
AU (2) AU2011317040B2 (ja)
BR (1) BR112013009117A2 (ja)
CA (1) CA2814581C (ja)
CY (1) CY1123356T1 (ja)
DK (1) DK2630146T3 (ja)
ES (1) ES2816600T3 (ja)
HU (1) HUE051535T2 (ja)
IL (2) IL225789B (ja)
MX (1) MX362563B (ja)
NZ (1) NZ609490A (ja)
PL (1) PL2630146T3 (ja)
PT (1) PT2630146T (ja)
RU (1) RU2598606C3 (ja)
SG (2) SG10201710578TA (ja)
SI (1) SI2630146T1 (ja)
TW (2) TWI643858B (ja)
WO (1) WO2012054698A1 (ja)
ZA (1) ZA201302810B (ja)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL2326650T3 (pl) 2008-08-06 2014-07-31 Biomarin Pharm Inc Dihydropirydoftalazynonowe inhibitory polimerazy poli-(ADP-rybozy) (PARP)
EP2406389B1 (en) 2009-03-13 2019-05-08 Agios Pharmaceuticals, Inc. Methods and compositions for cell-proliferation-related disorders
DK2448582T3 (en) 2009-06-29 2017-07-17 Agios Pharmaceuticals Inc QUINOLIN-8 SULPHONAMIDE DERIVATIVES WITH ANTICANCER ACTIVITY
EP3561077B1 (en) 2009-10-21 2022-12-21 Les Laboratoires Servier Methods for cell-proliferation-related disorders
CN102869258A (zh) 2010-02-03 2013-01-09 生物马林药物股份有限公司 用于pten基因缺失相关疾病的治疗的聚(adp-核糖)聚合酶(parp)的二氢吡啶并酞嗪酮抑制剂
HUE030794T2 (en) * 2010-02-08 2017-06-28 Medivation Technologies Inc Synthesis Processes of Dihydro-Pyrido-Phthalazinone Derivatives
TWI643858B (zh) 2010-10-21 2018-12-11 美商梅迪維新技術有限責任公司 結晶型(8S,9R)-5-氟-8-(4-氟苯基)-9-(1-甲基-1H-1,2,4-三唑-5-基)-8,9-二氫-2H-吡啶并[4,3,2-de]呔-3(7H)-酮甲苯磺酸鹽
SI3406251T1 (sl) 2011-05-03 2024-05-31 Agios Pharmaceuticals, Inc. Aktivatorji piruvat kinaze za uporabo v terapiji
CN102827073A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
CN102827170A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
WO2013021044A1 (de) * 2011-08-11 2013-02-14 Bayer Intellectual Property Gmbh 1,2,4-triazolyl-substituierte ketoenole
WO2013028495A1 (en) * 2011-08-19 2013-02-28 Biomarin Pharmaceutical Inc. Dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) for the treatment of multiple myeloma
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
AU2013331626B2 (en) 2012-10-15 2018-08-02 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
JP6529492B2 (ja) 2013-07-11 2019-06-12 アジオス ファーマシューティカルズ, インコーポレイテッド 癌の処置のためのidh2突然変異体阻害剤としての2,4−または4,6−ジアミノピリミジン化合物
WO2015003360A2 (en) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
WO2015003355A2 (en) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US20150031627A1 (en) 2013-07-25 2015-01-29 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
CN106164066B (zh) 2014-02-13 2020-01-17 因赛特公司 作为lsd1抑制剂的环丙胺
WO2015123424A1 (en) 2014-02-13 2015-08-20 Incyte Corporation Cyclopropylamines as lsd1 inhibitors
MA39726A (fr) * 2014-03-14 2017-01-18 Agios Pharmaceuticals Inc Compositions pharmaceutiques de composés thérapeutiquement actifs
MX2016011865A (es) * 2014-03-14 2017-04-13 Agios Pharmaceuticals Inc Composiciones farmaceuticas de compuestos terapeuticamente activos.
US9695167B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors
EP3174855B1 (en) * 2014-07-31 2023-05-10 Medivation Technologies LLC Coformer salts of (2s,3s)-methyl 7-fluoro-2-(4-fluorophenyl)-3-(1-methyl-1h-1,2,4-triazol-5-yl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate and methods of preparing them
ES2757948T3 (es) 2015-04-03 2020-04-30 Incyte Corp Compuestos heterocíclicos como inhibidores LSD1
ES2959690T3 (es) 2015-06-11 2024-02-27 Agios Pharmaceuticals Inc Procedimientos de uso de activadores de piruvato cinasa
CR20180152A (es) 2015-08-12 2018-08-09 Incyte Corp Sales de un inhibidor de lsd1
MX2018004587A (es) 2015-10-15 2018-08-14 Agios Pharmaceuticals Inc Terapia de combinacion para tratar tumores malignos.
WO2017066571A1 (en) 2015-10-15 2017-04-20 Agios Pharmaceuticals, Inc. Combination therapy for treating malignancies
RU2018119128A (ru) * 2015-10-26 2019-11-28 МЕДИВЭЙШН ТЕКНОЛОДЖИЗ ЭлЭлСи Лечение мелкоклеточного рака легких ингибитором parp
CA3236518A1 (en) 2016-02-29 2017-09-08 F. Hoffmann-La Roche Ag Dosage form compositions comprising an inhibitor of bruton's tyrosine kinase
MX2020003361A (es) 2017-10-13 2020-07-29 Merck Patent Gmbh Combinacion de un inhibidor parp y un antagonista de union al eje pd-1.
TW201938165A (zh) 2017-12-18 2019-10-01 美商輝瑞股份有限公司 治療癌症的方法及組合療法
WO2019235822A1 (ko) 2018-06-04 2019-12-12 엘지전자 주식회사 어파인 움직임 예측을 이용하여 비디오 신호를 처리하는 방법 및 장치
US10980788B2 (en) 2018-06-08 2021-04-20 Agios Pharmaceuticals, Inc. Therapy for treating malignancies
US10942500B2 (en) * 2018-06-11 2021-03-09 Purdue Research Foundation System architecture and method of processing data therein
US10284866B1 (en) * 2018-07-02 2019-05-07 Tencent America LLC Method and apparatus for video coding
CN112424671B (zh) 2018-07-13 2023-10-27 奇跃公司 用于显示双目变形补偿的系统和方法
US10968200B2 (en) 2018-08-31 2021-04-06 Incyte Corporation Salts of an LSD1 inhibitor and processes for preparing the same
EP3876940A1 (en) 2018-11-05 2021-09-15 Pfizer Inc. Combinations for treating cancer
WO2021181233A2 (en) 2020-03-09 2021-09-16 Pfizer Inc. Fusion proteins and uses thereof
IL302889A (en) 2020-11-13 2023-07-01 Pfizer Gelatin capsules containing talazofrib
WO2022123427A1 (en) 2020-12-07 2022-06-16 Pfizer Inc. Methods of identifying a tumor that is sensitive to treatment with talazoparib and methods of treatment thereof
AU2022244439A1 (en) 2021-03-24 2023-09-28 Astellas Pharma Inc. Combination of talazoparib and an anti-androgen for the treatment of ddr gene mutated metastatic castration-sensitive prostate cancer
WO2023131894A1 (en) 2022-01-08 2023-07-13 Pfizer Inc. Genomic loss of heterozygosity as a predictive biomarker for treatment with talazoparib and methods of treatment thereof
WO2023201338A1 (en) 2022-04-15 2023-10-19 Ideaya Biosciences, Inc. Combination therapy comprising a mat2a inhibitor and a parp inhibitor
WO2023233295A1 (en) 2022-06-01 2023-12-07 Ideaya Biosciences, Inc. Thiadiazolyl derivatives as dna polymerase theta inhibitors and uses thereof
WO2024074959A1 (en) 2022-10-02 2024-04-11 Pfizer Inc. Combination of talazoparib and enzalutamide in the treatment of metastatic castration-resistant prostate cancer
WO2024127140A1 (en) 2022-12-17 2024-06-20 Pfizer Inc. Combination of talazoparib and enzalutamide in the treatment of metastatic castration-resistant prostate cancer

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4415504A (en) 1981-09-21 1983-11-15 Tanabe Seiyaku Co., Ltd. p-Hydroxyphenylglycine.α-phenylethanesulfonate, process for production thereof and utilization thereof in resolution of p-hydroxyphenylglycine
JPS58225065A (ja) 1982-06-21 1983-12-27 Nippon Shinyaku Co Ltd 2−キノロン誘導体
US5328905A (en) 1987-07-20 1994-07-12 Duphar International Research B.V. 8,9-anellated-1,2,3,4-tetrahydro-β-carboline derivatives
GB9505538D0 (en) 1995-03-18 1995-05-03 Ciba Geigy Ag New compounds
ID19155A (id) 1996-12-13 1998-06-18 Tanabe Seiyaku Co Turunan-turunan piridin, pembuatannya dan intermediet untuk pembuatannya
DE19727410A1 (de) 1997-06-27 1999-01-07 Hoechst Schering Agrevo Gmbh 3-(5-Tetrazolylcarbonyl)-2-chinolone und diese enthaltende nutzpflanzenschützende Mittel
US6514983B1 (en) 1997-09-03 2003-02-04 Guilford Pharmaceuticals Inc. Compounds, methods and pharmaceutical compositions for treating neural or cardiovascular tissue damage
TW430656B (en) 1997-12-03 2001-04-21 Dainippon Ink & Chemicals Quinolinone derivative, method for preparing the same, and anti-allergic agent
JP2002515490A (ja) 1998-05-15 2002-05-28 ギルフォード ファーマシューティカルズ インコーポレイテッド Parp活性を抑制する縮合三環化合物
DE19921567A1 (de) 1999-05-11 2000-11-16 Basf Ag Verwendung von Phthalazine-Derivaten
JP2001302669A (ja) 2000-04-18 2001-10-31 Meiji Seika Kaisha Ltd 三環性フタラジノン誘導体
JP2002284699A (ja) 2001-03-28 2002-10-03 Sumitomo Pharmaceut Co Ltd 視細胞変性疾患治療剤
AR036081A1 (es) 2001-06-07 2004-08-11 Smithkline Beecham Corp Compuesto de 1,2-dihidroquinolina, su uso para preparar una composicion farmaceutica, metodos para prepararlo y compuestos del acido 2-aminobenzoico n-alquilado de utilidad como intermediarios en dichos metodos
SE0102315D0 (sv) 2001-06-28 2001-06-28 Astrazeneca Ab Compounds
EP1477175B1 (en) * 2002-02-19 2011-04-27 Ono Pharmaceutical Co., Ltd. Fused pyridazine derivative compounds and drugs containing the compounds as the active ingredient
EP1340819A1 (en) 2002-02-28 2003-09-03 Institut National De La Sante Et De La Recherche Medicale (Inserm) Microsatellite markers
GB0221443D0 (en) 2002-09-16 2002-10-23 Glaxo Group Ltd Pyridine derivates
EP1400244A1 (en) 2002-09-17 2004-03-24 Warner-Lambert Company LLC New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors
WO2004043959A1 (ja) 2002-11-12 2004-05-27 Mochida Pharmaceutical Co., Ltd. 新規parp阻害剤
JP4027406B2 (ja) * 2003-03-12 2007-12-26 クドス ファーマシューティカルズ リミテッド フタラジノン誘導体
EP1633362B1 (en) 2003-05-28 2012-09-26 Eisai Inc. Compounds, methods and pharmaceutical compositions for inhibiting parp
BRPI0507498A (pt) 2004-02-18 2007-07-10 Astrazeneca Ab composto, composição farmacêutica, uso do composto, e, métodos para tratar distúrbios mediados por mglur 5 e para inibir ativação de receptores de mglur 5
GB0612971D0 (en) 2006-06-30 2006-08-09 Angeletti P Ist Richerche Bio Therapeutic compounds
US8198448B2 (en) 2006-07-14 2012-06-12 Amgen Inc. Fused heterocyclic derivatives and methods of use
AU2008247102B2 (en) 2007-05-03 2011-11-24 Pfizer Limited 2 -pyridine carboxamide derivatives as sodium channel modulators
WO2010017850A1 (de) 2008-08-12 2010-02-18 Boehringer Ingelheim International Gmbh Verfahren zur herstellung von cycloalkyl-substituierten piperazinverbindungen
WO2009024190A1 (en) 2007-08-22 2009-02-26 4Sc Ag Indolopyridines as inhibitors of the kinesin spindle protein (eg5 )
CN101998959B (zh) 2008-02-06 2013-08-28 生物马林药物股份有限公司 聚(adp-核糖)聚合酶(parp)的苯并噁唑甲酰胺抑制剂
PL2326650T3 (pl) 2008-08-06 2014-07-31 Biomarin Pharm Inc Dihydropirydoftalazynonowe inhibitory polimerazy poli-(ADP-rybozy) (PARP)
CN102869258A (zh) 2010-02-03 2013-01-09 生物马林药物股份有限公司 用于pten基因缺失相关疾病的治疗的聚(adp-核糖)聚合酶(parp)的二氢吡啶并酞嗪酮抑制剂
US20110190266A1 (en) 2010-02-04 2011-08-04 Daniel Chu 5,6,6a,7,8,9-HEXAHYDRO-2H-PYRIDOPHTHALAZINONE INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE (PARP)
HUE030794T2 (en) 2010-02-08 2017-06-28 Medivation Technologies Inc Synthesis Processes of Dihydro-Pyrido-Phthalazinone Derivatives
WO2011130661A1 (en) 2010-04-16 2011-10-20 Biomarin Pharmaceutical Inc. Methods of using dihydropyridophthalazinone inhibitors of poly (adp-ribose)polymerase (parp)
WO2011140009A1 (en) 2010-05-04 2011-11-10 Biomarin Pharmaceutical Inc. Methods of using semi-synthetic glycopeptides as antibacterial agents
TWI643858B (zh) 2010-10-21 2018-12-11 美商梅迪維新技術有限責任公司 結晶型(8S,9R)-5-氟-8-(4-氟苯基)-9-(1-甲基-1H-1,2,4-三唑-5-基)-8,9-二氫-2H-吡啶并[4,3,2-de]呔-3(7H)-酮甲苯磺酸鹽
WO2012166151A1 (en) 2011-06-03 2012-12-06 Biomarin Pharmaceutical Inc. Use of dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) in the treatment of myelodysplastic syndrome (mds) and acute myeloid leukaemia (aml)
WO2013028495A1 (en) 2011-08-19 2013-02-28 Biomarin Pharmaceutical Inc. Dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) for the treatment of multiple myeloma
US20130053365A1 (en) 2011-08-30 2013-02-28 Biomarin Pharmaceutical, Inc. Dihydropyridophthalazinone inhibitors of poly(adp-ribose)polymerase (parp)
CN105916846A (zh) 2013-11-07 2016-08-31 麦迪韦逊科技有限公司 用于合成经保护的n-烷基三唑甲醛的三唑中间体
EP3174855B1 (en) 2014-07-31 2023-05-10 Medivation Technologies LLC Coformer salts of (2s,3s)-methyl 7-fluoro-2-(4-fluorophenyl)-3-(1-methyl-1h-1,2,4-triazol-5-yl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate and methods of preparing them

Also Published As

Publication number Publication date
TW201713656A (en) 2017-04-16
US20180009806A1 (en) 2018-01-11
KR20180069132A (ko) 2018-06-22
JP2017061526A (ja) 2017-03-30
US20120129865A1 (en) 2012-05-24
KR20140009181A (ko) 2014-01-22
TWI557123B (zh) 2016-11-11
AU2011317040A1 (en) 2013-05-09
US20140228369A1 (en) 2014-08-14
ES2816600T3 (es) 2021-04-05
AU2017201564A1 (en) 2017-03-23
SG189939A1 (en) 2013-06-28
US8735392B2 (en) 2014-05-27
TW201307345A (zh) 2013-02-16
CA2814581A1 (en) 2012-04-26
KR20210028747A (ko) 2021-03-12
AU2011317040B2 (en) 2016-12-08
RU2598606C2 (ru) 2016-09-27
CA2814581C (en) 2019-02-12
IL225789A0 (en) 2013-06-27
CN103282365A (zh) 2013-09-04
EP2630146A1 (en) 2013-08-28
PL2630146T3 (pl) 2020-11-02
NZ609490A (en) 2015-06-26
WO2012054698A1 (en) 2012-04-26
RU2013123036A (ru) 2014-11-27
DK2630146T3 (da) 2020-08-10
MX362563B (es) 2019-01-25
US10189837B2 (en) 2019-01-29
JP2022140637A (ja) 2022-09-26
JP2013540158A (ja) 2013-10-31
MX2013004195A (es) 2013-07-22
CN103282365B (zh) 2017-12-29
AR083502A1 (es) 2013-02-27
TWI643858B (zh) 2018-12-11
JP2019034951A (ja) 2019-03-07
IL225789B (en) 2019-12-31
CY1123356T1 (el) 2021-12-31
EP2630146B1 (en) 2020-07-01
IL271497A (en) 2020-02-27
AU2017201564B2 (en) 2019-05-09
JP2020169209A (ja) 2020-10-15
HUE051535T2 (hu) 2021-03-01
EP3757106A1 (en) 2020-12-30
PT2630146T (pt) 2020-07-20
ZA201302810B (en) 2014-06-25
RU2598606C3 (ru) 2021-12-20
KR20190120458A (ko) 2019-10-23
SI2630146T1 (sl) 2020-12-31
BR112013009117A2 (pt) 2016-07-19

Similar Documents

Publication Publication Date Title
IL271497A (en) Tosylate salt of (S8, R9)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-H1- 4,2,1-triazol-5-yl)-9,8-dihydro-H2 -Crystalline pyrido[2,3,4-de]phthalazine-3(H3)-one
ZA201209632B (en) Imidazopyridine derivatives, process for the preparation thereof and therapeutic use thereof
EP2477648A4 (en) SYNERGISTIC ANTI-CD47 THERAPY FOR HEMATOLOGICAL CANCER
ZA201300100B (en) Indolizine derivatives,process for the preparation thereof and therapeutic use thereof
EP2549947A4 (en) COMPOSITE THREE DIMENSIONAL SURGICAL IMPLANT
ZA201107350B (en) Imidazo [2 1 b] [1, 3, 4] thiadiazole derivatives
IL229993A (en) 8 - Alkoxy [1,2,4] triazolo [5,1 – c] pyrimidine– 2
HK1175776A1 (en) 8-azabicyclo[3.2.1]octane-8-carboxamide derivative 8-[321]-8-
IL224450B (en) Crystalline forms of pyrimido[6,1-a] isoquinolin-4-one compounds
IL222080B (en) 6-alkyl-thieno[2,3-c]quinolin-4(5h)-one derivatives
IL246247A0 (en) Use of an anti-human prolactin receptor in the preparation of a drug to inhibit the growth of cancer
IL220448A (en) Pyridine [3,2 - d] Pyrimidine - 7 (8h) - Their medical uses and uses
IL222351A (en) Process for making derivatives 4,1-diethylene-di (3-pyroline) -tetrone
EP2565194A4 (en) Imidazo [1,2-A] pyridine
EP2511276A4 (en) PYRROLO [2,3-D] PYRIMIDINE DERIVATIVE
HK1185882A1 (en) Pyrazino[2,3-d]isoxazole derivative [23-d]
ZA201303580B (en) Oxazolo [5,4-b]pyridin-5-yl compounds and their use for the treatment of cancer
EP2623053A4 (en) CLAMP FOR A SURGICAL MILLING AND CUTTING TOOL
SI2477990T1 (sl) 5-fenil-pirazolopiridinski derivati, njihova priprava in terapevtska uporaba
EP2651937B8 (en) Imidazo[4,5-c]quinolin-1-yl derivative useful in therapy
AU2011246168A1 (en) Imidazo[1,2-a]pyridine derivative