MX2023000008A - Inhibidor de fgfr y mutacion, metodo de preparacion y uso del mismo. - Google Patents

Inhibidor de fgfr y mutacion, metodo de preparacion y uso del mismo.

Info

Publication number
MX2023000008A
MX2023000008A MX2023000008A MX2023000008A MX2023000008A MX 2023000008 A MX2023000008 A MX 2023000008A MX 2023000008 A MX2023000008 A MX 2023000008A MX 2023000008 A MX2023000008 A MX 2023000008A MX 2023000008 A MX2023000008 A MX 2023000008A
Authority
MX
Mexico
Prior art keywords
fgfr
preparation
method therefor
inhibitor
mutation inhibitor
Prior art date
Application number
MX2023000008A
Other languages
English (en)
Inventor
Haibing Deng
Hongping Yu
Zhui Chen
Yaochang Xu
Haiyan Ying
Original Assignee
Abbisko Therapeutics 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 Abbisko Therapeutics Co Ltd filed Critical Abbisko Therapeutics Co Ltd
Publication of MX2023000008A publication Critical patent/MX2023000008A/es

Links

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
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring 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
    • 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
    • A61K31/52Purines, e.g. adenine
    • 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom
    • C07D473/34Nitrogen atom attached in position 6, e.g. adenine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

Se proporciona un inhibidor de FGFR y mutación del mismo, y un método de preparación y uso del mismo. En particular, se proporciona un inhibidor de FGFR y mutación que tiene una estructura de fórmula (I), un método de preparación del mismo, una composición farmacéutica que contiene el mismo, el uso del mismo como un inhibidor de FGFR y mutación del mismo y el uso del mismo en la preparación de un fármaco para tratar y/o prevenir un tumor o cáncer mediado, al menos en parte, por una cinasa de FGFR y para tratar a un paciente con un tumor que tiene resistencia a un inhibidor de FGFR, en particular, el uso del mismo en la preparación de un fármaco para tratar y/o prevenir un tumor en un paciente con mutaciones en V561, V565, N550, N540, V555, E566, K660 y/o V550 de una vía de señalización de FGFR. Cada sustituyente de fórmula (I) tiene la misma definición que en la descripción. (ver Fórmula).
MX2023000008A 2020-08-13 2021-08-11 Inhibidor de fgfr y mutacion, metodo de preparacion y uso del mismo. MX2023000008A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN202010811490 2020-08-13
PCT/CN2021/112121 WO2022033532A1 (zh) 2020-08-13 2021-08-11 一种fgfr及其突变抑制剂,其制备方法和应用

Publications (1)

Publication Number Publication Date
MX2023000008A true MX2023000008A (es) 2023-01-30

Family

ID=80246991

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2023000008A MX2023000008A (es) 2020-08-13 2021-08-11 Inhibidor de fgfr y mutacion, metodo de preparacion y uso del mismo.

Country Status (10)

Country Link
US (1) US20230303575A1 (es)
EP (1) EP4169922A4 (es)
KR (1) KR20230015419A (es)
CN (1) CN115485281B (es)
AU (1) AU2021323844B2 (es)
BR (1) BR112022026386A2 (es)
CA (1) CA3184247A1 (es)
MX (1) MX2023000008A (es)
TW (1) TWI797711B (es)
WO (1) WO2022033532A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116096707A (zh) * 2020-06-05 2023-05-09 金耐特生物制药公司 成纤维细胞生长因子受体激酶的抑制剂
CN115785103A (zh) * 2022-12-28 2023-03-14 北京康立生医药技术开发有限公司 一种治疗胆管癌药物福巴替尼的合成方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7659274B2 (en) * 2006-01-25 2010-02-09 Osi Pharmaceuticals, Inc. Unsaturated mTOR inhibitors
AU2013210403B2 (en) * 2012-01-19 2016-01-14 Taiho Pharmaceutical Co., Ltd. 3,5-disubstituted alkynylbenzene compound and salt thereof
DK3023100T3 (da) * 2013-07-18 2019-05-27 Taiho Pharmaceutical Co Ltd Antitumorlægemiddel til intermitterende administration af fgfr-hæmmer
ES2819398T3 (es) * 2013-07-18 2021-04-15 Taiho Pharmaceutical Co Ltd Agente terapéutico para el cáncer resistente al inhibidor de FGFR
CN105461720B (zh) * 2014-08-08 2019-08-06 南京圣和药业股份有限公司 吗啉类酪氨酸激酶抑制剂
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
CN109776544B (zh) * 2017-11-15 2022-02-01 上海医药工业研究院 吡唑并[3,4-d]嘧啶类化合物及其制备方法和用途
CN116096707A (zh) * 2020-06-05 2023-05-09 金耐特生物制药公司 成纤维细胞生长因子受体激酶的抑制剂

Also Published As

Publication number Publication date
WO2022033532A1 (zh) 2022-02-17
KR20230015419A (ko) 2023-01-31
CA3184247A1 (en) 2022-02-17
TWI797711B (zh) 2023-04-01
AU2021323844A1 (en) 2023-01-19
AU2021323844B2 (en) 2023-07-27
EP4169922A4 (en) 2024-03-13
CN115485281B (zh) 2023-11-21
EP4169922A1 (en) 2023-04-26
CN115485281A (zh) 2022-12-16
JP2023530768A (ja) 2023-07-19
TW202206433A (zh) 2022-02-16
BR112022026386A2 (pt) 2023-02-23
US20230303575A1 (en) 2023-09-28

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