SG11201901251SA - Aminopyrimidines as alk inhibitors - Google Patents

Aminopyrimidines as alk inhibitors

Info

Publication number
SG11201901251SA
SG11201901251SA SG11201901251SA SG11201901251SA SG11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA SG 11201901251S A SG11201901251S A SG 11201901251SA
Authority
SG
Singapore
Prior art keywords
international
pct
co7d
english
august
Prior art date
Application number
SG11201901251SA
Other languages
English (en)
Inventor
Shaomeng Wang
Jianyong Chen
Original Assignee
Univ Michigan Regents
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 Univ Michigan Regents filed Critical Univ Michigan Regents
Publication of SG11201901251SA publication Critical patent/SG11201901251SA/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic 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
    • C07D405/14—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/12—Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SG11201901251SA 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors SG11201901251SA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662380818P 2016-08-29 2016-08-29
PCT/US2017/048845 WO2018044767A2 (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors

Publications (1)

Publication Number Publication Date
SG11201901251SA true SG11201901251SA (en) 2019-03-28

Family

ID=59846649

Family Applications (2)

Application Number Title Priority Date Filing Date
SG11201901251SA SG11201901251SA (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors
SG10201914030UA SG10201914030UA (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors

Family Applications After (1)

Application Number Title Priority Date Filing Date
SG10201914030UA SG10201914030UA (en) 2016-08-29 2017-08-28 Aminopyrimidines as alk inhibitors

Country Status (11)

Country Link
US (2) US10709705B2 (OSRAM)
EP (2) EP4001273A3 (OSRAM)
JP (2) JP7094566B2 (OSRAM)
KR (1) KR102530871B1 (OSRAM)
CN (2) CN115043821B (OSRAM)
AU (2) AU2017319135B2 (OSRAM)
IL (1) IL264638B (OSRAM)
MX (2) MX389265B (OSRAM)
NZ (1) NZ751713A (OSRAM)
SG (2) SG11201901251SA (OSRAM)
WO (1) WO2018044767A2 (OSRAM)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110772638B (zh) * 2018-07-31 2021-02-23 苏州亚盛药业有限公司 Alk抑制剂与egfr抑制剂在制备治疗癌症的药物中的用途
CN111171033B (zh) * 2018-11-09 2021-11-02 天津大学 一种嘧啶衍生物及其合成方法和应用
EP3942045A1 (en) 2019-03-21 2022-01-26 Onxeo A dbait molecule in combination with kinase inhibitor for the treatment of cancer
CN110143947B (zh) * 2019-05-29 2021-10-15 华东师范大学 一种色瑞替尼类似物的制备方法
WO2020259553A1 (en) * 2019-06-25 2020-12-30 Ascentage Pharma (Suzhou) Co., Ltd. Combination of fak inhibitor and btk inhibitor for treating a disease
EP4054579A1 (en) 2019-11-08 2022-09-14 Institut National de la Santé et de la Recherche Médicale (INSERM) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
WO2022063220A1 (en) * 2020-09-25 2022-03-31 Ascentage Pharma (Suzhou) Co., Ltd. A pharmaceutical composition and use thereof for treatment of cancer
US20240316051A1 (en) * 2021-04-19 2024-09-26 Ascentage Pharma (Suzhou) Co., Ltd. A pharmaceutical combination and use thereof
EP4446320A4 (en) * 2021-12-09 2025-11-26 Oncobix Co Ltd NEW HETEROCYCLIC SUBSTITUTION PYRIMIDINE DERIVATIVE WITH CANCER CELL GROWTH INHIBITORY EFFECT, AND PHARMACEUTICAL COMPOSITION CONTAINING IT
CN116332919B (zh) * 2022-03-30 2025-08-26 苏州亚盛药业有限公司 一种alk抑制剂化合物及其中间体的制备方法
TWI885708B (zh) * 2023-01-20 2025-06-01 大陸商蘇州亞盛藥業有限公司 Alk抑制劑或其鹽、溶劑合物的結晶形式及其製備方法和應用
JP2026511009A (ja) * 2023-03-22 2026-04-10 アセンテージ ファーマ(スーチョウ)カンパニー,リミティド 医薬組合せ及びその使用
WO2025232723A1 (en) * 2024-05-06 2025-11-13 Ascentage Pharma (Suzhou) Co., Ltd. Treatment method with focal adhesion kinase inhibitor

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5093330A (en) 1987-06-15 1992-03-03 Ciba-Geigy Corporation Staurosporine derivatives substituted at methylamino nitrogen
GB0004888D0 (en) 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
GB0305929D0 (en) * 2003-03-14 2003-04-23 Novartis Ag Organic compounds
TWI378923B (en) 2003-08-15 2012-12-11 Novartis Ag Pyrimidine derivatives
BRPI0414544A (pt) * 2003-09-18 2006-11-07 Novartis Ag 2,4-di-(fenilamino) pirimidinas úteis no tratamento de transtornos proliferativos
RS52545B (sr) * 2004-04-07 2013-04-30 Novartis Ag Inhibitori protein apoptoze (iap)
BRPI0722383A2 (pt) 2006-12-08 2012-06-05 Irm Llc compostos inibidores de proteìna quinase, composições contendo os mesmos bem como seus usos
US8592432B2 (en) 2008-04-07 2013-11-26 Bei Chen Compounds and compositions as protein kinase inhibitors
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
US20140024620A1 (en) 2010-10-14 2014-01-23 Ariad Pharmaceuticals, Inc. Methods for Inhibiting Cell Proliferation in EGFR-Driven Cancers
HUE025395T2 (en) 2011-02-02 2016-02-29 Novartis Ag Methods using ALK inhibitors
CN104672214B (zh) * 2013-12-03 2019-04-12 上海翰森生物医药科技有限公司 具有alk抑制活性的化合物及其制备与用途
KR101656382B1 (ko) * 2014-02-28 2016-09-09 한국화학연구원 피리미딘-2,4-디아민 유도체 및 이를 유효성분으로 함유하는 항암용 약학적 조성물

Also Published As

Publication number Publication date
KR102530871B1 (ko) 2023-05-09
WO2018044767A2 (en) 2018-03-08
US20190175595A1 (en) 2019-06-13
KR20190039760A (ko) 2019-04-15
MX2022000376A (es) 2022-02-10
AU2017319135A1 (en) 2019-04-04
US11110090B2 (en) 2021-09-07
AU2017319135B2 (en) 2021-03-18
EP4001273A2 (en) 2022-05-25
US10709705B2 (en) 2020-07-14
SG10201914030UA (en) 2020-03-30
MX389265B (es) 2025-03-20
WO2018044767A3 (en) 2018-04-12
AU2021203098A1 (en) 2021-06-10
BR112019003897A2 (pt) 2019-05-21
JP2019528307A (ja) 2019-10-10
AU2021203098B2 (en) 2023-05-25
MX2019002393A (es) 2019-07-08
CN109715620B (zh) 2022-05-06
EP3504203B1 (en) 2022-09-28
EP4001273A3 (en) 2022-08-24
NZ751713A (en) 2022-07-01
JP7094566B2 (ja) 2022-07-04
CA3033223A1 (en) 2018-03-08
EP3504203A2 (en) 2019-07-03
CN115043821A (zh) 2022-09-13
CN115043821B (zh) 2024-08-06
JP2022120151A (ja) 2022-08-17
US20200330464A1 (en) 2020-10-22
IL264638B (en) 2021-08-31
CN109715620A (zh) 2019-05-03

Similar Documents

Publication Publication Date Title
SG11201809714TA (en) Piperidines as menin inhibitors
SG11201900135YA (en) N-(phenylsulfonyl)benzamides and related compounds as bcl-2 inhibitors
SG11201901747VA (en) Inhibitors of cellular metabolic processes
SG11201804934PA (en) Novel Compounds
SG11201908532UA (en) Macrocyclic compounds as ros1 kinase inhibitors
SG11201907356SA (en) Piperidine-substituted mnk inhibitors and methods related thereto
SG11201908542QA (en) Gip receptor activating peptide
SG11201807301SA (en) Spiro-condensed pyrrolidine derivatives as deubiquitylating enzymes (dub) inhibitors
SG11201909083UA (en) Piperidines as covalent menin inhibitors
SG11201909710XA (en) Indole ahr inhibitors and uses thereof
SG11201909949XA (en) Targeted immunotolerance
SG11201906891RA (en) Methods for the administration of certain vmat2 inhibitors
SG11201909019SA (en) Methods of treatment using a jak inhibitor compound
SG11201804373VA (en) Compositions and methods for immunooncology
SG11201900163PA (en) Macrocycle kinase inhibitors
SG11201907744QA (en) Replacement of cytotoxic preconditioning before cellular immunotherapy
SG11201909825VA (en) Hsp90 inhibitor oral formulations and related methods
SG11201809064QA (en) Chimeric neurotoxins
SG11201808682XA (en) Silicone atoms containing ivacaftor analogues
SG11201908598PA (en) Compounds useful in the treatment or prevention of a prmt5-mediated disorder
SG11201805709RA (en) Anti-pro/latent myostatin antibodies and methods of use thereof
SG11201806583XA (en) Compositions containing tucaresol or its analogs
SG11201901658PA (en) Beta-lactamase inhibitor compounds
SG11201906386XA (en) Combination therapy involving diaryl macrocyclic compounds
SG11201907023UA (en) Method of reducing neutropenia