SG11201408052WA - IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AS KINASE INHIBITORS - Google Patents

IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AS KINASE INHIBITORS

Info

Publication number
SG11201408052WA
SG11201408052WA SG11201408052WA SG11201408052WA SG11201408052WA SG 11201408052W A SG11201408052W A SG 11201408052WA SG 11201408052W A SG11201408052W A SG 11201408052WA SG 11201408052W A SG11201408052W A SG 11201408052WA SG 11201408052W A SG11201408052W A SG 11201408052WA
Authority
SG
Singapore
Prior art keywords
imidazo
compound
kinase inhibitors
pyridazine derivatives
acceptable salt
Prior art date
Application number
SG11201408052WA
Inventor
Yasuyuki Takeda
Kenji Yoshikawa
Yoshiko Kagoshima
Yuko Yamamoto
Ryoichi Tanaka
Yuichi Tominaga
Masaki Kiga
Yoshito Hamada
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 SG11201408052WA publication Critical patent/SG11201408052WA/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed 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
    • 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
    • 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

Abstract

- 285 - Abstract The present invention is intended to provide a compound or a pharmacologically acceptable salt thereof which is useful in the treatment of a tumor through its ROS1 kinase enzyme activity inhibitory effect and NTRK kinase enzyme inhibitory effect. The present invention provides a compound having an imidazo[1,2-b]pyridazine structure represented by the general formula (I) or a pharmacologically acceptable salt thereof, and a pharmaceutical composition comprising the compound. In the formula, R , G, T, Y , Y , Y , and Y are as defined 1 1 2 3 4 herein.
SG11201408052WA 2012-06-04 2013-06-03 IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AS KINASE INHIBITORS SG11201408052WA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2012127079 2012-06-04
PCT/JP2013/065328 WO2013183578A1 (en) 2012-06-04 2013-06-03 IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVE AS KINASE INHIBITOR

Publications (1)

Publication Number Publication Date
SG11201408052WA true SG11201408052WA (en) 2015-01-29

Family

ID=49711970

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201408052WA SG11201408052WA (en) 2012-06-04 2013-06-03 IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AS KINASE INHIBITORS

Country Status (32)

Country Link
US (2) US9187489B2 (en)
EP (1) EP2857404B1 (en)
JP (1) JP5814467B2 (en)
KR (1) KR101781255B1 (en)
CN (1) CN104520300B (en)
AU (1) AU2013272701B2 (en)
BR (1) BR112014029851B1 (en)
CA (1) CA2874819C (en)
CO (1) CO7160119A2 (en)
CY (1) CY1119607T1 (en)
DK (1) DK2857404T3 (en)
ES (1) ES2648228T3 (en)
HK (1) HK1207374A1 (en)
HR (1) HRP20171724T1 (en)
HU (1) HUE037221T2 (en)
IL (1) IL236075A (en)
IN (1) IN2014MN02497A (en)
LT (1) LT2857404T (en)
MX (1) MX357021B (en)
MY (1) MY170326A (en)
NO (1) NO2857404T3 (en)
NZ (1) NZ702574A (en)
PH (1) PH12014502721B1 (en)
PL (1) PL2857404T3 (en)
PT (1) PT2857404T (en)
RS (1) RS56625B1 (en)
RU (1) RU2635917C2 (en)
SG (1) SG11201408052WA (en)
SI (1) SI2857404T1 (en)
TW (1) TWI585088B (en)
WO (1) WO2013183578A1 (en)
ZA (1) ZA201408843B (en)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5503655B2 (en) 2008-09-22 2014-05-28 アレイ バイオファーマ、インコーポレイテッド Substituted imidazo [1,2B] pyridazine compounds as TRK kinase inhibitors
KR101784798B1 (en) 2008-10-22 2017-10-16 어레이 바이오파마 인크. SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS TRK KINASE INHIBITORS
AR077468A1 (en) 2009-07-09 2011-08-31 Array Biopharma Inc PIRAZOLO COMPOUNDS (1,5-A) PYRIMIDINE SUBSTITUTED AS TRK-QUINASA INHIBITORS
WO2011146336A1 (en) 2010-05-20 2011-11-24 Array Biopharma Inc. Macrocyclic compounds as trk kinase inhibitors
CA2872645A1 (en) 2012-05-30 2013-12-05 Nippon Shinyaku Co., Ltd. Aromatic heterocyclic derivative and pharmaceutical
EA032255B1 (en) * 2014-03-27 2019-04-30 Янссен Фармацевтика Нв SUBSTITUTED 4,5,6,7-TETRAHYDRO-PYRAZOLO[1,5-α]PYRAZINE DERIVATIVES AND 5,6,7,8-TETRAHYDRO-4H-PYRAZOLO[1,5-α][1,4]DIAZEPINE DERIVATIVES AS ROS1 INHIBITORS
CA2941206C (en) * 2014-03-27 2022-09-20 Janssen Pharmaceutica Nv Substituted 4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrimidine derivatives and 2,3-dihydro-1h-imidazo[1,2-b]pyrazole derivatives as ros1 inhibitors
MX2016013600A (en) * 2014-04-25 2017-04-27 Exelixis Inc Method of treating lung adenocarcinoma.
RS64122B1 (en) 2014-11-16 2023-05-31 Array Biopharma Inc Crystalline form of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate
EP3303631A1 (en) 2015-06-01 2018-04-11 Loxo Oncology Inc. Methods of diagnosing and treating cancer
MX2017016669A (en) 2015-06-18 2018-04-13 Cephalon Inc 1, 4-substituted piperidine derivatives.
US10919875B2 (en) 2015-06-18 2021-02-16 89Bio Ltd Substituted 4-benzyl and 4-benzoyl piperidine derivatives
TN2018000027A1 (en) 2015-07-16 2019-07-08 Array Biopharma Inc Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
BR112018008357A2 (en) 2015-10-26 2018-11-27 Array Biopharma Inc dot mutations in trk inhibitor resistant cancer and related methods
CN106854174A (en) * 2015-12-08 2017-06-16 湖南华腾制药有限公司 A kind of preparation method of 4 substituted piperidine derivatives
CR20180501A (en) 2016-04-04 2019-04-05 Loxo Oncology Inc Liquid formulations of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide
US10045991B2 (en) 2016-04-04 2018-08-14 Loxo Oncology, Inc. Methods of treating pediatric cancers
KR20180129911A (en) 2016-04-04 2018-12-05 록쏘 온콜로지, 인코포레이티드 How to treat pediatric cancer
PT3800189T (en) 2016-05-18 2023-07-27 Array Biopharma Inc Preparation of (s)-n-(5-((r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide
CN107400082A (en) * 2016-05-19 2017-11-28 湖南华腾制药有限公司 A kind of preparation method of substituted piperidine derivative
TWI704148B (en) 2016-10-10 2020-09-11 美商亞雷生物製藥股份有限公司 Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
JOP20190077A1 (en) 2016-10-10 2019-04-09 Array Biopharma Inc Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors
JOP20190072A1 (en) * 2016-10-13 2019-04-07 Glaxosmithkline Ip Dev Ltd 1,3 di-substituted cyclobutane or azetidine derivatives as hematopoietic prostaglandin d synthase inhibitors
JOP20190092A1 (en) 2016-10-26 2019-04-25 Array Biopharma Inc PROCESS FOR THE PREPARATION OF PYRAZOLO[1,5-a]PYRIMIDINES AND SALTS THEREOF
CN110267960B (en) 2017-01-18 2022-04-26 阿雷生物药品公司 Substituted pyrazolo [1,5-a ] pyrazine compounds as RET kinase inhibitors
WO2018136663A1 (en) 2017-01-18 2018-07-26 Array Biopharma, Inc. Ret inhibitors
EP3597648B1 (en) 2017-03-14 2023-06-07 Daiichi Sankyo Company, Limited METHOD FOR PRODUCING 3, 6-DISUBSTITUTED IMIDAZO[1, 2-b]PYRIDAZINE DERIVATIVE
JOP20190213A1 (en) 2017-03-16 2019-09-16 Array Biopharma Inc Macrocyclic compounds as ros1 kinase inhibitors
US10180422B1 (en) 2017-08-22 2019-01-15 Scripps Health Methods of treating a neuroendocrine tumor
TWI791053B (en) 2017-10-10 2023-02-01 美商亞雷生物製藥股份有限公司 Crystalline forms of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile and pharmaceutical composition thereof
TWI812649B (en) 2017-10-10 2023-08-21 美商絡速藥業公司 Formulations of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile
US20190247398A1 (en) 2017-10-26 2019-08-15 Array Biopharma Inc. Formulations of a macrocyclic trk kinase inhibitor
CN109748902B (en) * 2017-11-02 2020-11-06 杭州科巢生物科技有限公司 Preparation method of erlotinib hydrochloride
US20230242670A1 (en) * 2017-11-29 2023-08-03 Seoul National University R&Db Foundation Anti-ros1 antibody and use thereof
CN108129288B (en) * 2017-12-27 2021-01-22 上海毕得医药科技股份有限公司 Synthesis method of trans-3-hydroxycyclobutylformic acid
TW201938169A (en) 2018-01-18 2019-10-01 美商亞雷生物製藥股份有限公司 Substituted pyrazolo[3,4-d]pyrimidine compounds as RET kinase inhibitors
CN111615514B (en) 2018-01-18 2022-10-11 奥瑞生物药品公司 Substituted pyrazolo [4,3-C ] pyridine compounds as RET kinase inhibitors
WO2019143977A1 (en) 2018-01-18 2019-07-25 Array Biopharma Inc. Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors
EP3773725A1 (en) 2018-03-29 2021-02-17 Loxo Oncology Inc. Treatment of trk-associated cancers
JP7286755B2 (en) 2018-07-31 2023-06-05 ロクソ オンコロジー, インコーポレイテッド (S)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1H-pyrazole - Spray-dried dispersions and formulations of 4-carboxamides
ES2922314T3 (en) 2018-09-10 2022-09-13 Array Biopharma Inc Fused Heterocyclic Compounds as RET Kinase Inhibitors
CN113490666A (en) 2018-12-19 2021-10-08 奥瑞生物药品公司 Substituted pyrazolo [1,5-A ] pyridine compounds as inhibitors of FGFR tyrosine kinases
WO2020131674A1 (en) 2018-12-19 2020-06-25 Array Biopharma Inc. 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer
TW202100526A (en) * 2019-03-06 2021-01-01 日商第一三共股份有限公司 Pyrrolopyrazole derivative
CN114364798A (en) 2019-03-21 2022-04-15 欧恩科斯欧公司 Combination of Dbait molecules with kinase inhibitors for the treatment of cancer
CA3142088C (en) * 2019-05-08 2023-02-28 Tyk Medicines, Inc. Compound used as kinase inhibitor and application thereof
CN114761006A (en) 2019-11-08 2022-07-15 Inserm(法国国家健康医学研究院) Methods of treating cancer resistant to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
AR122159A1 (en) * 2020-05-28 2022-08-17 Novartis Ag MLL1 INHIBITORS AND ANTINEOPLASTIC AGENTS
CN114957259A (en) * 2021-02-25 2022-08-30 南京明德新药研发有限公司 Cyano-substituted aromatic bicyclic compound and application thereof
WO2023272701A1 (en) * 2021-07-01 2023-01-05 Anheart Therapeutics (Hangzhou) Co., Ltd. Crystalline forms of 3-{4-[(2r)-2-aminopropoxy]phenyl}-n-[(1r)- 1-(3-fluorophenyl) ethyl]imidazo[1,2-b]pyridazin-6-amine and salts thereof
WO2023220967A1 (en) * 2022-05-18 2023-11-23 Anheart Therapeutics (Hangzhou) Co., Ltd. Method for producing 3,6-disubstituted-imidazo[1,2-b]pyridazine compounds
CN114989176A (en) * 2022-07-08 2022-09-02 深圳市新樾生物科技有限公司 Imidazopyridazine derivative and application thereof
CN115197115A (en) * 2022-08-25 2022-10-18 成都金博汇康医药科技有限公司 Preparation method and application of chiral 5-oxopyrrolidine-3-formic acid

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6399780B1 (en) 1999-08-20 2002-06-04 Cephalon, Inc. Isomeric fused pyrrolocarbazoles and isoindolones
EP1317446A1 (en) 2000-09-01 2003-06-11 Glaxo Group Limited Oxindole derivatives
EP1339680A1 (en) 2000-09-01 2003-09-03 Glaxo Group Limited Substituted oxindole derivatives as tyrosine kinase inhibitors
JP2003231687A (en) 2002-02-04 2003-08-19 Japan Tobacco Inc Pyrazolyl condensed ring compound and pharmaceutical use thereof
MY141220A (en) 2003-11-17 2010-03-31 Astrazeneca Ab Pyrazole derivatives as inhibitors of receptor tyrosine kinases
WO2005103010A2 (en) 2004-04-21 2005-11-03 Astrazeneca Ab Pyrazole derivatives useful for the treatment of cancer
EP1832588A4 (en) 2004-12-28 2009-09-02 Takeda Pharmaceutical Condensed imidazole compound and use thereof
KR101302945B1 (en) 2005-02-04 2013-09-06 아스트라제네카 아베 Pyrazolylaminopyridine derivatives useful as kinase inhibitors
SI1853588T1 (en) 2005-02-16 2008-10-31 Astrazeneca Ab Chemical compounds
MX2007009842A (en) 2005-02-16 2007-08-23 Astrazeneca Ab Chemical compounds.
WO2007013673A1 (en) 2005-07-29 2007-02-01 Astellas Pharma Inc. Fused heterocycles as lck inhibitors
WO2007014707A1 (en) * 2005-08-01 2007-02-08 F. Hoffmann-La Roche Ag Heterocyclic benzylamino derivatives, their manufacture and use as pharmaceutical agents
DE102005042742A1 (en) 2005-09-02 2007-03-08 Schering Ag Substituted imidazo [1,2b] pyridazines as kinase inhibitors, their production and use as pharmaceuticals
DE102006029447A1 (en) * 2006-06-21 2007-12-27 Bayer Schering Pharma Ag Oxo-substituted imidazo [1,2b] pyridazines, their preparation and use as pharmaceuticals
AU2007315234A1 (en) 2006-10-30 2008-05-08 Novartis Ag Heterocyclic compounds as antiinflammatory agents
BRPI0718029A2 (en) * 2006-11-06 2013-11-26 Supergen Inc IMIDAZO (1,2-B) PYRIDAZINE AND PIRAZOLE (1,5-A) PYRIMIDINE DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS
WO2008072682A1 (en) * 2006-12-15 2008-06-19 Daiichi Sankyo Company, Limited Imidazo[1,2-b]pyridazine derivative
JP2009227599A (en) * 2008-03-21 2009-10-08 Daiichi Sankyo Co Ltd Imidazopyridazine derivative
WO2009140128A2 (en) 2008-05-13 2009-11-19 Irm Llc Compounds and compositions as kinase inhibitors
JP5503655B2 (en) * 2008-09-22 2014-05-28 アレイ バイオファーマ、インコーポレイテッド Substituted imidazo [1,2B] pyridazine compounds as TRK kinase inhibitors
KR101147550B1 (en) * 2009-10-22 2012-05-17 한국과학기술연구원 2,7-Substituted thieno[3,2-d]pyrimidine compounds as protein kinase inhibitors
WO2012005299A1 (en) 2010-07-07 2012-01-12 日本新薬株式会社 Ros tyrosine kinase inhibitor
WO2012125667A1 (en) 2011-03-17 2012-09-20 Merck Sharp & Dohme Corp. TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF

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EP2857404A1 (en) 2015-04-08
AU2013272701A1 (en) 2015-01-15
HRP20171724T1 (en) 2018-01-12
US9751887B2 (en) 2017-09-05
IL236075A0 (en) 2015-02-01
AU2013272701A2 (en) 2015-01-22
IL236075A (en) 2017-10-31
CA2874819C (en) 2017-06-20
CA2874819A1 (en) 2013-12-12
US9187489B2 (en) 2015-11-17
HUE037221T2 (en) 2018-08-28
AU2013272701B2 (en) 2017-12-21
CY1119607T1 (en) 2018-04-04
LT2857404T (en) 2017-11-10
DK2857404T3 (en) 2017-12-04
ZA201408843B (en) 2016-01-27
EP2857404B1 (en) 2017-08-23
BR112014029851B1 (en) 2023-01-03
ES2648228T3 (en) 2017-12-29
MX357021B (en) 2018-06-25
HK1207374A1 (en) 2016-01-29
KR101781255B1 (en) 2017-09-22
RS56625B1 (en) 2018-03-30
CN104520300A (en) 2015-04-15
SI2857404T1 (en) 2017-11-30
JP5814467B2 (en) 2015-11-17
US20160046639A1 (en) 2016-02-18
IN2014MN02497A (en) 2015-07-17
WO2013183578A1 (en) 2013-12-12
PT2857404T (en) 2017-11-23
CO7160119A2 (en) 2015-01-15
TWI585088B (en) 2017-06-01
NZ702574A (en) 2016-07-29
PH12014502721A1 (en) 2015-02-02
MY170326A (en) 2019-07-17
MX2014014803A (en) 2015-02-12
JPWO2013183578A1 (en) 2016-01-28
US20150051190A1 (en) 2015-02-19
RU2014153627A (en) 2016-08-10
KR20150014942A (en) 2015-02-09
TW201400486A (en) 2014-01-01
PH12014502721B1 (en) 2015-02-02
NO2857404T3 (en) 2018-01-20
RU2635917C2 (en) 2017-11-17
EP2857404A4 (en) 2016-01-20
CN104520300B (en) 2016-12-21
PL2857404T3 (en) 2018-04-30
BR112014029851A2 (en) 2017-06-27

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