SG11201903801YA - Pyridone compound as c-met inhibitor - Google Patents

Pyridone compound as c-met inhibitor

Info

Publication number
SG11201903801YA
SG11201903801YA SG11201903801YA SG11201903801YA SG11201903801YA SG 11201903801Y A SG11201903801Y A SG 11201903801YA SG 11201903801Y A SG11201903801Y A SG 11201903801YA SG 11201903801Y A SG11201903801Y A SG 11201903801YA SG 11201903801Y A SG11201903801Y A SG 11201903801YA
Authority
SG
Singapore
Prior art keywords
met inhibitor
pyridone compound
met
pyridone
compound
Prior art date
Application number
SG11201903801YA
Inventor
Xiongbin Xu
Gang Li
Charles Z Ding
Lihong Hu
Guoping Hu
Jian Li
Shuhui Chen
Zhigang Chi
Kun Wang
Original Assignee
Fujian Cosunter Pharmaceutical 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=62024383&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201903801Y(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Fujian Cosunter Pharmaceutical Co Ltd filed Critical Fujian Cosunter Pharmaceutical Co Ltd
Publication of SG11201903801YA publication Critical patent/SG11201903801YA/en

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
    • A61K31/435Heterocyclic 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
    • 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
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • 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
    • A61K31/495Heterocyclic 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
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • 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
    • 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
    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Abstract

PyridoneCompound as C-MET Inhibitor Disclosed in the present invention is a type of pyridone specifically disclosed is a compound as shown in formula (I) thereof. compounds as c-met or a pharmaceutically acceptable inhibitors, and salt R 0 0 (I) A' N N <-.- R 2 N.„.... - - --.. 0 -..„,..N., 39
SG11201903801YA 2016-10-27 2017-10-27 Pyridone compound as c-met inhibitor SG11201903801YA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201610954377 2016-10-27
PCT/CN2017/107964 WO2018077227A1 (en) 2016-10-27 2017-10-27 Pyridone compound as c-met inhibitor

Publications (1)

Publication Number Publication Date
SG11201903801YA true SG11201903801YA (en) 2019-05-30

Family

ID=62024383

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201903801YA SG11201903801YA (en) 2016-10-27 2017-10-27 Pyridone compound as c-met inhibitor

Country Status (28)

Country Link
US (1) US10501443B2 (en)
EP (1) EP3533787B1 (en)
JP (1) JP6719679B2 (en)
KR (1) KR102070748B1 (en)
CN (1) CN109311812B (en)
AU (1) AU2017348810B2 (en)
BR (1) BR112019008415B1 (en)
CA (1) CA3041164C (en)
CO (1) CO2019005165A2 (en)
DK (1) DK3533787T3 (en)
EA (1) EA038108B1 (en)
ES (1) ES2835301T3 (en)
HR (1) HRP20201985T1 (en)
HU (1) HUE051734T2 (en)
IL (1) IL266126B (en)
LT (1) LT3533787T (en)
MX (1) MX2019004626A (en)
MY (1) MY189557A (en)
PE (1) PE20190912A1 (en)
PH (1) PH12019500875A1 (en)
PL (1) PL3533787T3 (en)
PT (1) PT3533787T (en)
RS (1) RS61126B1 (en)
SG (1) SG11201903801YA (en)
SI (1) SI3533787T1 (en)
UA (1) UA122737C2 (en)
WO (1) WO2018077227A1 (en)
ZA (1) ZA201903074B (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102374933B1 (en) * 2018-04-26 2022-03-15 푸젠 코선터 파마슈티컬 컴퍼니 리미티드 Crystalline form of c-Met inhibitor, salt form thereof and preparation method
JP7214879B2 (en) * 2019-02-01 2023-01-30 メッドシャイン ディスカバリー インコーポレイテッド Tricyclyl compounds containing pyrimidinyls as c-Met inhibitors
WO2022063869A2 (en) 2020-09-24 2022-03-31 Merck Patent Gmbh Compounds for the treatment of viral infections
EP4346829A1 (en) 2021-06-04 2024-04-10 Merck Patent GmbH Compounds for the treatment of glioblastoma

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002002519A2 (en) 2000-06-29 2002-01-10 Bristol-Myers Squibb Pharma Company THROMBIN OR FACTOR Xa INHIBITORS
US7732456B2 (en) 2004-03-05 2010-06-08 Banyu Pharmaceutical Co., Ltd. Pyridone derivative
US8314087B2 (en) * 2007-02-16 2012-11-20 Amgen Inc. Nitrogen-containing heterocyclyl ketones and methods of use
DE102007032507A1 (en) 2007-07-12 2009-04-02 Merck Patent Gmbh pyridazinone derivatives
DE102008062826A1 (en) * 2008-12-23 2010-07-01 Merck Patent Gmbh pyridazinone derivatives
EP2768826A1 (en) 2011-10-17 2014-08-27 Bayer Intellectual Property GmbH Substituted oxadiazolyl pyridinones and oxadiazolyl pyridazinones as hif inhibitors
KR20140138984A (en) * 2012-03-19 2014-12-04 메르크 파텐트 게엠베하 Combination of a 6-oxo-1,6-dihydro-pyridazine derivative having anti-cancer activity with other anti-tumor compounds
RU2684407C2 (en) * 2012-10-11 2019-04-09 Мерк Патент Гмбх Combination of 6-oxo-1,6-dihydro-pyridazine derivative having anticolic activity, with mek inhibitor
BR112017010232A2 (en) * 2014-12-11 2018-01-02 Merck Patent Gmbh COMBINATION OF A 6-OXO-1,6-DI-HYDRO-PYRIDAZINE DERIVATIVE HAVING ANTICANCER ACTIVITY WITH A QUINAZOLIN DERIVATIVE

Also Published As

Publication number Publication date
WO2018077227A1 (en) 2018-05-03
PE20190912A1 (en) 2019-06-26
MX2019004626A (en) 2019-11-08
HUE051734T2 (en) 2021-03-29
US10501443B2 (en) 2019-12-10
ZA201903074B (en) 2020-01-29
CA3041164C (en) 2019-12-17
BR112019008415B1 (en) 2020-09-29
MY189557A (en) 2022-02-16
AU2017348810B2 (en) 2020-05-07
JP2019535806A (en) 2019-12-12
EA201990952A1 (en) 2019-11-29
PT3533787T (en) 2020-11-20
CO2019005165A2 (en) 2019-05-31
CA3041164A1 (en) 2018-05-03
IL266126A (en) 2019-06-30
ES2835301T3 (en) 2021-06-22
PH12019500875A1 (en) 2019-06-17
KR20190058678A (en) 2019-05-29
US20190248763A1 (en) 2019-08-15
BR112019008415A2 (en) 2019-07-09
CN109311812B (en) 2020-03-17
RS61126B1 (en) 2020-12-31
EA038108B1 (en) 2021-07-07
EP3533787B1 (en) 2020-09-30
UA122737C2 (en) 2020-12-28
DK3533787T3 (en) 2020-11-30
HRP20201985T1 (en) 2021-02-05
EP3533787A4 (en) 2019-11-13
PL3533787T3 (en) 2021-03-08
NZ753020A (en) 2021-08-27
LT3533787T (en) 2020-11-25
SI3533787T1 (en) 2021-01-29
AU2017348810A1 (en) 2019-05-23
EP3533787A1 (en) 2019-09-04
JP6719679B2 (en) 2020-07-08
CN109311812A (en) 2019-02-05
IL266126B (en) 2020-07-30
KR102070748B1 (en) 2020-01-29

Similar Documents

Publication Publication Date Title
MX2022014864A (en) Bisamide sarcomere activating compounds and uses thereof.
NZ729005A (en) Aminopyrimidinyl compounds as jak inhibitors
PH12016500467A1 (en) Aminoheteroarlyl benzamides as kinase inhibitors
MX2021014531A (en) Substituted aminopurine compounds, compositions thereof, and methods of treatment therewith.
MX2014012454A (en) Imidazothiadiazole derivatives as protease activated receptor 4 (par4) inhibitors for treating platelet aggregation.
PH12017501523A1 (en) Selective bace1 inhibitors
MY180083A (en) Tetrahydropyrrolothiazine compounds
MA40059A (en) Phosphatidylinositol 3-kinase inhibitors
MY194116A (en) Pharmaceutical compounds
MX2016000675A (en) Aminomethyl-biaryl derivatives as complement factor d inhibitors and uses thereof.
PH12019500875A1 (en) Pyridone compound as c-met inhibitor
PH12019500839A1 (en) Therapeutic compounds and methods of use thereof
EA201991253A1 (en) BENZODIAZOLIUM COMPOUNDS AS ENAC INHIBITORS
JO3318B1 (en) Bace inhibitors
MX2022006783A (en) New methylquinazolinone derivatives.
PH12016502246B1 (en) Carboxamide derivatives
MX2018014813A (en) Antibacterial compositions.
MY193239A (en) Novel b-lactamase inhibitors
MX368496B (en) Analogues of 4h-pyrazolo[1,5-a]benzimidazole compound as parp inhibitors.
WO2018039077A8 (en) Therapeutic compounds
PH12019500370A1 (en) Triazolopyrazinone derivative useful as a human pde1 inhibitor