JP2024533975A - Pi3kアイソフォームアルファを阻害する化合物及びがんを処置するための方法 - Google Patents

Pi3kアイソフォームアルファを阻害する化合物及びがんを処置するための方法 Download PDF

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JP2024533975A
JP2024533975A JP2024506896A JP2024506896A JP2024533975A JP 2024533975 A JP2024533975 A JP 2024533975A JP 2024506896 A JP2024506896 A JP 2024506896A JP 2024506896 A JP2024506896 A JP 2024506896A JP 2024533975 A JP2024533975 A JP 2024533975A
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compound
pi3kα
alkyl
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cancer
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JP2024533975A5 (enExample
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ジーン, デイビッド ジュニア セント
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Scorpion Therapeutics Inc
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Scorpion Therapeutics Inc
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32—Nitrogen atom
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/4353—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/52—Purines, e.g. adenine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • 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
    • C07D405/02—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 two hetero rings
    • C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
JP2024506896A 2021-08-09 2022-08-08 Pi3kアイソフォームアルファを阻害する化合物及びがんを処置するための方法 Pending JP2024533975A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202163231156P 2021-08-09 2021-08-09
US63/231,156 2021-08-09
PCT/US2022/039674 WO2023018636A1 (en) 2021-08-09 2022-08-08 Compounds that inhibit pi3k isoform alpha and methods for treating cancer

Publications (2)

Publication Number Publication Date
JP2024533975A true JP2024533975A (ja) 2024-09-18
JP2024533975A5 JP2024533975A5 (enExample) 2025-07-28

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JP2024506896A Pending JP2024533975A (ja) 2021-08-09 2022-08-08 Pi3kアイソフォームアルファを阻害する化合物及びがんを処置するための方法

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US (1) US20240343728A1 (enExample)
EP (1) EP4363414A1 (enExample)
JP (1) JP2024533975A (enExample)
KR (1) KR20240051953A (enExample)
CN (1) CN118159534A (enExample)
AU (1) AU2022325819A1 (enExample)
CA (1) CA3227902A1 (enExample)
CL (1) CL2024000327A1 (enExample)
CO (1) CO2024000448A2 (enExample)
CR (1) CR20240045A (enExample)
DO (1) DOP2024000019A (enExample)
EC (1) ECSP24008488A (enExample)
GE (1) GEAP202416449A (enExample)
IL (1) IL310588A (enExample)
JO (1) JOP20240020A1 (enExample)
MA (1) MA63885B1 (enExample)
MX (1) MX2024000708A (enExample)
PE (1) PE20240652A1 (enExample)
UA (1) UA130857C2 (enExample)
WO (1) WO2023018636A1 (enExample)
ZA (1) ZA202401094B (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2025538147A (ja) 2022-11-02 2025-11-26 ペトラ・ファーマ・コーポレイション 疾患の治療のためのホスホイノシチド3-キナーゼ(pi3k)のアロステリックポケット及びオルソステリックポケットの標的化
WO2024233256A1 (en) 2023-05-05 2024-11-14 Eli Lilly And Company Imlunestrant or salts thereof for use in treating and preventing central nervous system (cns) metastases in subjects having er+ breast cancer
WO2025036439A1 (en) * 2023-08-16 2025-02-20 Laekna Pharmaceutical Ningbo Co., Ltd. Multicyclic compounds and their use as pi3k alpha inhibitors
IL330261A (en) * 2023-12-27 2026-08-01 Genesis Molecular Ai Inc Cancer treatment methods
WO2025201503A1 (en) * 2024-03-28 2025-10-02 InventisBio Co., Ltd. Compounds, preparation methods and uses thereof
WO2026060099A1 (en) * 2024-09-12 2026-03-19 Kymathera, Inc. Selective pi3k inhibitors

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009501749A (ja) * 2005-07-21 2009-01-22 ノバルティス アクチエンゲゼルシャフト 炎症性疾患の処置のためのベンゾイミダゾール誘導体
JP2011504164A (ja) * 2007-06-26 2011-02-03 ユセベ ファルマ ソシエテ アノニム キナーゼ阻害剤としての縮合チアゾール誘導体
US20110312979A1 (en) * 2010-06-21 2011-12-22 Yun-Long Li Fused pyrrole derivatives as pi3k inhibitors
JP2017519786A (ja) * 2014-07-04 2017-07-20 ルピン・リミテッド Pi3k阻害剤としてのキノリジノン誘導体

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2755285C (en) * 2009-03-20 2014-02-11 Yunxin Y. Bo Inhibitors of pi3 kinase
DE102009043260A1 (de) * 2009-09-28 2011-04-28 Merck Patent Gmbh Pyridinyl-imidazolonderivate
CN111909173B (zh) * 2015-07-02 2025-03-04 豪夫迈·罗氏有限公司 苯并氧氮杂䓬噁唑烷酮化合物及其使用方法
WO2017221272A1 (en) * 2016-06-23 2017-12-28 Sun Pharmaceutical Industries Limited Process for the preparation of idelalisib
WO2021001431A1 (en) * 2019-07-02 2021-01-07 INSERM (Institut National de la Santé et de la Recherche Médicale) Use of pi3ka-selective inhibitors for treating metastatic disease in patients suffering from pancreatic cancer

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009501749A (ja) * 2005-07-21 2009-01-22 ノバルティス アクチエンゲゼルシャフト 炎症性疾患の処置のためのベンゾイミダゾール誘導体
JP2011504164A (ja) * 2007-06-26 2011-02-03 ユセベ ファルマ ソシエテ アノニム キナーゼ阻害剤としての縮合チアゾール誘導体
US20110312979A1 (en) * 2010-06-21 2011-12-22 Yun-Long Li Fused pyrrole derivatives as pi3k inhibitors
JP2017519786A (ja) * 2014-07-04 2017-07-20 ルピン・リミテッド Pi3k阻害剤としてのキノリジノン誘導体

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CL2024000327A1 (es) 2024-08-09
ZA202401094B (en) 2025-05-28
IL310588A (en) 2024-04-01
ECSP24008488A (es) 2024-05-31
EP4363414A1 (en) 2024-05-08
CN118159534A (zh) 2024-06-07
JOP20240020A1 (ar) 2024-02-01
UA130857C2 (uk) 2026-05-27
CA3227902A1 (en) 2023-02-16
CR20240045A (es) 2024-02-20
KR20240051953A (ko) 2024-04-22
PE20240652A1 (es) 2024-04-04
WO2023018636A1 (en) 2023-02-16
CO2024000448A2 (es) 2024-02-15
DOP2024000019A (es) 2024-03-15
MA63885B1 (fr) 2025-01-31
AU2022325819A1 (en) 2024-02-29
GEAP202416449A (en) 2024-04-25
MA63885A1 (fr) 2024-09-30
US20240343728A1 (en) 2024-10-17
MX2024000708A (es) 2024-02-08

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