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

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • 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
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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
    • C07D401/04—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 directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07—Optical 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 (zh) 2019-01-18 2020-01-16 作为布鲁顿酪氨酸激酶抑制剂的环状分子

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

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4087845A4 (en) * 2020-01-02 2024-01-24 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

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US6921763B2 (en) * 1999-09-17 2005-07-26 Abbott Laboratories Pyrazolopyrimidines as therapeutic agents
DK1212327T3 (da) * 1999-09-17 2003-12-15 Abbott Gmbh & Co Kg Pyrazolopyrimidiner som terapeutiske midler
US20060025383A1 (en) * 2004-02-03 2006-02-02 Neil Wishart Aminobenzoxazoles as therapeutic agents
EP1979002A2 (en) * 2005-12-19 2008-10-15 OSI Pharmaceuticals, Inc. Combination of igfr inhibitor and anti-cancer agent
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
EP2954900A1 (en) * 2007-03-28 2015-12-16 Pharmacyclics, Inc. Inhibitors of bruton's tyrosine kinase
EP2307025B1 (en) * 2008-07-16 2017-09-20 Pharmacyclics LLC Inhibitors of bruton's tyrosine kinase for the treatment of solid tumors
US7741330B1 (en) * 2009-10-12 2010-06-22 Pharmacyclics, Inc. Pyrazolo-pyrimidine inhibitors of Bruton's tyrosine kinase
EA201490265A1 (ru) * 2011-07-13 2014-12-30 Фармасайкликс, Инк. Ингибиторы тирозинкиназы брутона
EP2548877A1 (en) * 2011-07-19 2013-01-23 MSD Oss B.V. 4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
WO2013070976A1 (en) * 2011-11-08 2013-05-16 Intellikine, Llc Treatment regimens using multiple pharmaceutical agents
WO2013113097A1 (en) * 2012-01-31 2013-08-08 Beta Pharma Canada Inc. Cyclic molecules as bruton's tyrosine kinase inhibitors
CA2874211A1 (en) * 2012-05-31 2013-12-05 Pharmascience Inc. Protein kinase inhibitors
CA2874461C (en) * 2012-06-18 2021-10-12 Principia Biopharma Inc. Formulations containing reversible covalent compounds
WO2015132799A2 (en) * 2014-02-03 2015-09-11 Cadila Healthcare Limited Novel heterocyclic compounds
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
TW201613919A (en) * 2014-07-02 2016-04-16 Pharmacyclics Llc Inhibitors of Bruton's tyrosine kinase
TW201613926A (en) * 2014-08-01 2016-04-16 Pharmacyclics Llc Inhibitors of bruton's tyrosine kinase
US9533991B2 (en) * 2014-08-01 2017-01-03 Pharmacyclics Llc Inhibitors of Bruton's tyrosine kinase
CN108431007B (zh) * 2015-09-16 2022-06-07 洛克索肿瘤学股份有限公司 用于治疗癌症的作为btk抑制剂的吡唑并嘧啶衍生物
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
EP3481831B1 (en) * 2016-07-07 2023-09-06 Daewoong Pharmaceutical Co., Ltd. 4-aminopyrazolo[3,4-d]pyrimidinylazabicyclo derivatives and pharmaceutical composition comprising the same
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
JP2022523480A (ja) 2022-04-25
CA3129841C (en) 2023-09-26
CN111454268B (zh) 2023-09-08
CN113710671A (zh) 2021-11-26
MX2021008632A (es) 2021-10-26
KR20210135497A (ko) 2021-11-15
CA3129841A1 (en) 2020-07-23
EP3912980A4 (en) 2022-12-07
CN111454268A (zh) 2020-07-28
AU2020208128B2 (en) 2023-05-25
EA202191995A1 (ru) 2021-11-18
JP7436994B2 (ja) 2024-02-22
CN113710671B (zh) 2023-04-28
AU2020208128A1 (en) 2021-09-09
BR112021014100A2 (pt) 2021-09-21
WO2020147798A1 (zh) 2020-07-23
JP2023179562A (ja) 2023-12-19
IL284916A (en) 2021-09-30
US20220081445A1 (en) 2022-03-17
EP3912980A1 (en) 2021-11-24
CN116589465A (zh) 2023-08-15

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