SG11202107886RA - Cyclic molecules as bruton's tyrosine kinase inhibitor - Google Patents

Cyclic molecules as bruton's tyrosine kinase inhibitor

Info

Publication number
SG11202107886RA
SG11202107886RA SG11202107886RA SG11202107886RA SG11202107886RA SG 11202107886R A SG11202107886R A SG 11202107886RA SG 11202107886R A SG11202107886R A SG 11202107886RA SG 11202107886R A SG11202107886R A SG 11202107886RA SG 11202107886R A SG11202107886R A SG 11202107886RA
Authority
SG
Singapore
Prior art keywords
bruton
tyrosine kinase
kinase inhibitor
cyclic molecules
cyclic
Prior art date
Application number
SG11202107886RA
Other languages
English (en)
Inventor
Zhaoyin Wang
Bing Yao
Yuanshan Yao
Ao Li
Prabhakar Kondaji Jadhav
Guoqing Cao
Original Assignee
Minghui Pharmaceutical Shanghai Ltd
Minghui Pharmaceutical Hangzhou 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 Minghui Pharmaceutical Shanghai Ltd, Minghui Pharmaceutical Hangzhou Ltd filed Critical Minghui Pharmaceutical Shanghai Ltd
Publication of SG11202107886RA publication Critical patent/SG11202107886RA/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • 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
    • 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
    • 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
SG11202107886RA 2019-01-18 2020-01-16 Cyclic molecules as bruton's tyrosine kinase inhibitor SG11202107886RA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201910049183.9A CN111454268B (zh) 2019-01-18 2019-01-18 作为布鲁顿酪氨酸激酶抑制剂的环状分子
PCT/CN2020/072551 WO2020147798A1 (fr) 2019-01-18 2020-01-16 Molécules cycliques servant d'inhibiteur de la tyrosine kinase de bruton

Publications (1)

Publication Number Publication Date
SG11202107886RA true SG11202107886RA (en) 2021-08-30

Family

ID=71613532

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202107886RA SG11202107886RA (en) 2019-01-18 2020-01-16 Cyclic molecules as bruton's tyrosine kinase inhibitor

Country Status (13)

Country Link
US (1) US20220081445A1 (fr)
EP (1) EP3912980A4 (fr)
JP (2) JP7436994B2 (fr)
KR (1) KR20210135497A (fr)
CN (3) CN111454268B (fr)
AU (1) AU2020208128B2 (fr)
BR (1) BR112021014100A2 (fr)
CA (1) CA3129841C (fr)
EA (1) EA202191995A1 (fr)
IL (1) IL284916A (fr)
MX (1) MX2021008632A (fr)
SG (1) SG11202107886RA (fr)
WO (1) WO2020147798A1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2020419422A1 (en) * 2020-01-02 2022-06-02 Dizal (Jiangsu) Pharmaceutical Co., Ltd. BTK inhibitors
CN113943294A (zh) * 2020-07-15 2022-01-18 成都海博为药业有限公司 一种作为btk抑制剂的化合物及其制备方法与用途
CN114573586B (zh) * 2020-11-28 2023-11-03 杭州和正医药有限公司 一种抑制布鲁顿酪氨酸激酶活性的多环化合物、药物组合物及其应用

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6921763B2 (en) * 1999-09-17 2005-07-26 Abbott Laboratories Pyrazolopyrimidines as therapeutic agents
ATE247657T1 (de) * 1999-09-17 2003-09-15 Basf Ag Pyrazolopyrimidine als arzneimittel
JP2007520559A (ja) * 2004-02-03 2007-07-26 アボット・ラボラトリーズ 治療薬としてのアミノベンゾオキサゾール類
WO2007075554A2 (fr) * 2005-12-19 2007-07-05 Osi Pharmaceuticals, Inc. Traitement combine avec une composition d’inhibiteur de proteine kinase heterobicyclique a noyau 6,6-bicyclique et d'agents anticancereux
CN102887900B (zh) * 2006-09-22 2015-04-29 药品循环公司 布鲁顿酪氨酸激酶的抑制剂
SG10201508035TA (en) * 2007-03-28 2015-10-29 Pharmacyclics Inc Inhibitors of bruton's tyrosine kinase
EP3311818A3 (fr) * 2008-07-16 2018-07-18 Pharmacyclics, LLC Inhibiteurs de tyrosine-kinase de bruton pour le traitement de tumeurs solides
US7741330B1 (en) * 2009-10-12 2010-06-22 Pharmacyclics, Inc. Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase
JP2014520863A (ja) * 2011-07-13 2014-08-25 ファーマサイクリックス,インク. Bruton型チロシンキナーゼの阻害剤
EP2548877A1 (fr) * 2011-07-19 2013-01-23 MSD Oss B.V. Dérivés de 4-(pyridine condensée à 5 chaînons)benzamide comme inhibiteurs de BTK
JP6114296B2 (ja) * 2011-11-08 2017-04-12 インテリカイン, エルエルシー 複数の医薬品を使用した治療レジメン
CN104080789B (zh) * 2012-01-31 2016-05-11 南京奥昭生物科技有限公司 作为布鲁顿酪氨酸激酶抑制剂的环状分子
RU2678767C2 (ru) * 2012-05-31 2019-02-01 ГБ005, Инк. Ингибиторы протеинкиназ
AU2013277582B2 (en) * 2012-06-18 2017-11-30 Principia Biopharma Inc. Reversible covalent pyrrolo- or pyrazolopyrimidines useful for the treatment cancer and autoimmune diseases
CA2934989C (fr) * 2014-02-03 2017-08-08 Cadila Healthcare Limited Nouveaux composes heterocycliques
CN105017256A (zh) * 2014-04-29 2015-11-04 浙江导明医药科技有限公司 多氟化合物作为布鲁顿酪氨酸激酶抑制剂
US9580416B2 (en) * 2014-07-02 2017-02-28 Pharmacyclics Llc Inhibitors of Bruton's tyrosine kinase
CA2959602A1 (fr) * 2014-08-01 2016-02-04 Pharmacyclics Llc Inhibiteurs de la tyrosine kinase de bruton
TW201613926A (en) * 2014-08-01 2016-04-16 Pharmacyclics Llc Inhibitors of bruton's tyrosine kinase
CA2998796A1 (fr) * 2015-09-16 2017-03-23 Loxo Oncology, Inc. Derives de pyrazolopyrimidine comme inhibiteurs de btk pour le traitement du cancer
CN105732638B (zh) * 2016-01-22 2018-01-30 成都倍特药业有限公司 一种具有螺环或桥环结构的布鲁顿酪氨酸激酶抑制剂及其制备方法
CN107344940B (zh) * 2016-05-06 2020-04-21 广东东阳光药业有限公司 Btk抑制剂及其用途
CN109153680B (zh) * 2016-07-07 2021-04-23 株式会社大熊制药 4-氨基吡唑并[3,4-d]嘧啶基氮杂双环衍生物及含其的药物组合物
US10865208B2 (en) * 2016-11-11 2020-12-15 Millennium Pharmaceuticals, Inc. ATG7 inhibitors and the uses thereof
GB201705971D0 (en) * 2017-04-13 2017-05-31 Cancer Res Tech Ltd Inhibitor compounds
CN107827892A (zh) * 2017-10-27 2018-03-23 上海应用技术大学 一种非受体酪氨酸激酶小分子抑制剂及其应用

Also Published As

Publication number Publication date
EP3912980A4 (fr) 2022-12-07
JP2022523480A (ja) 2022-04-25
US20220081445A1 (en) 2022-03-17
MX2021008632A (es) 2021-10-26
EP3912980A1 (fr) 2021-11-24
JP7436994B2 (ja) 2024-02-22
KR20210135497A (ko) 2021-11-15
CA3129841C (fr) 2023-09-26
CN111454268A (zh) 2020-07-28
CN116589465A (zh) 2023-08-15
JP2023179562A (ja) 2023-12-19
CN111454268B (zh) 2023-09-08
BR112021014100A2 (pt) 2021-09-21
EA202191995A1 (ru) 2021-11-18
AU2020208128A1 (en) 2021-09-09
IL284916A (en) 2021-09-30
CN113710671A (zh) 2021-11-26
WO2020147798A1 (fr) 2020-07-23
CN113710671B (zh) 2023-04-28
CA3129841A1 (fr) 2020-07-23
AU2020208128B2 (en) 2023-05-25

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