CA3162280A1 - 4,5-dihydro-1h-pyrazolyl compounds as repication protein a (rpa)-dna interaction inhibitors - Google Patents

4,5-dihydro-1h-pyrazolyl compounds as repication protein a (rpa)-dna interaction inhibitors

Info

Publication number
CA3162280A1
CA3162280A1 CA3162280A CA3162280A CA3162280A1 CA 3162280 A1 CA3162280 A1 CA 3162280A1 CA 3162280 A CA3162280 A CA 3162280A CA 3162280 A CA3162280 A CA 3162280A CA 3162280 A1 CA3162280 A1 CA 3162280A1
Authority
CA
Canada
Prior art keywords
compound
pharmaceutically acceptable
acceptable salt
chloro
acid
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
CA3162280A
Other languages
English (en)
French (fr)
Inventor
John J. Turchi
Navnath GAVANDE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Indiana University Bloomington
Original Assignee
Indiana University Bloomington
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 Indiana University Bloomington filed Critical Indiana University Bloomington
Publication of CA3162280A1 publication Critical patent/CA3162280A1/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (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)
CA3162280A 2019-12-10 2020-12-10 4,5-dihydro-1h-pyrazolyl compounds as repication protein a (rpa)-dna interaction inhibitors Pending CA3162280A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962946100P 2019-12-10 2019-12-10
US62/946,100 2019-12-10
PCT/US2020/064191 WO2021119242A1 (en) 2019-12-10 2020-12-10 Replication protein a (rpa)-dna interaction inhibitors

Publications (1)

Publication Number Publication Date
CA3162280A1 true CA3162280A1 (en) 2021-06-17

Family

ID=76330773

Family Applications (1)

Application Number Title Priority Date Filing Date
CA3162280A Pending CA3162280A1 (en) 2019-12-10 2020-12-10 4,5-dihydro-1h-pyrazolyl compounds as repication protein a (rpa)-dna interaction inhibitors

Country Status (6)

Country Link
US (1) US12486246B2 (https=)
EP (1) EP4073055A4 (https=)
JP (1) JP7677646B2 (https=)
BR (1) BR112022011372A2 (https=)
CA (1) CA3162280A1 (https=)
WO (1) WO2021119242A1 (https=)

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070196395A1 (en) 2003-12-12 2007-08-23 Mackerell Alexander Immunomodulatory compounds that target and inhibit the py'binding site of tyrosene kinase p56 lck sh2 domain
EP2402323A3 (en) * 2004-10-13 2012-05-30 PTC Therapeutics, Inc. Pyrazole or triazole compounds and their use for the manufacture of a medicament for treating somatic mutation-related diseases
EP1905762A1 (en) 2005-05-30 2008-04-02 Genecare Research Institute Co., Ltd Pyrazolone derivative
US20100055116A1 (en) 2006-04-13 2010-03-04 Liou Hsiou-Chi Methods and Compositions for Targeting c-Rel
WO2008045663A2 (en) * 2006-10-06 2008-04-17 Kalypsys, Inc. Aryl-substituted heterocyclic pde4 inhibitors as antiinflammatory agents
MY150697A (en) 2007-04-10 2014-02-28 Exelixis Inc Methods of treating cancer using pyridopyrimdinone inhibitors of p13k alpha
WO2008148747A2 (en) 2007-06-08 2008-12-11 University Of Copenhagen Pdz domain modulators
US8476458B2 (en) 2007-06-21 2013-07-02 The Wistar Institute Methods and compositions for modulating P300/CBP activity
HRP20161004T1 (hr) 2007-09-27 2016-10-21 Dow Agrosciences Llc Tehnološki konstruirani proteini cinkovi prsti koji imaju kao cilj gene za sintazu 5-enolpiruvilshikimat-3-fosfata
WO2009145829A1 (en) 2008-04-01 2009-12-03 University Of Massachusetts Type iii secretion inhibitors, analogs and uses thereof
WO2009146179A1 (en) 2008-04-15 2009-12-03 University Of Iowa Research Foundation Zinc finger nuclease for the cftr gene and methods of use thereof
US9005670B2 (en) 2010-01-05 2015-04-14 The Johns Hopkins University Use of histone acetyltransferase inhibitors as novel anti-cancer therapies
CA2825680C (en) 2010-02-05 2019-12-03 Indiana University Research And Technology Corporation Materials and method for inhibiting replication protein a and uses thereof
WO2012037573A1 (en) 2010-09-17 2012-03-22 Indiana University Research And Technology Corporation Small molecule inhibitors of replication protein a that also act synergistically with cisplatin
EP2840140B2 (en) 2012-12-12 2023-02-22 The Broad Institute, Inc. Crispr-Cas based method for mutation of prokaryotic cells
US8697359B1 (en) 2012-12-12 2014-04-15 The Broad Institute, Inc. CRISPR-Cas systems and methods for altering expression of gene products
US10227610B2 (en) 2013-02-25 2019-03-12 Sangamo Therapeutics, Inc. Methods and compositions for enhancing nuclease-mediated gene disruption
JP6482546B2 (ja) 2013-07-19 2019-03-13 ラリクス・バイオサイエンス・リミテッド・ライアビリティ・カンパニーLarix Bioscience, Llc 二重対立遺伝子ノックアウトを生成するための方法および組成物
WO2015021426A1 (en) 2013-08-09 2015-02-12 Sage Labs, Inc. A crispr/cas system-based novel fusion protein and its application in genome editing
ITMI20131410A1 (it) 2013-08-26 2015-02-27 Univ Degli Studi Modena E Reggio Emilia Composti e composizioni per l'uso nella inibizione dell' interazione lbc-rhoa
US9526784B2 (en) 2013-09-06 2016-12-27 President And Fellows Of Harvard College Delivery system for functional nucleases
WO2016077752A2 (en) * 2014-11-13 2016-05-19 Indiana University Research And Technology Corporation Materials and method for inhibiting replication protein a and uses thereof
WO2017205503A1 (en) 2016-05-24 2017-11-30 Indiana University Research And Technology Corporation Ku inhibitors and their use
CA3075734A1 (en) 2017-09-19 2019-03-28 Indiana University Research And Technology Corporation Xpa inhibitor compounds and their use

Also Published As

Publication number Publication date
US12486246B2 (en) 2025-12-02
JP7677646B2 (ja) 2025-05-15
EP4073055A1 (en) 2022-10-19
BR112022011372A2 (pt) 2022-08-23
US20230056729A1 (en) 2023-02-23
WO2021119242A1 (en) 2021-06-17
JP2023505690A (ja) 2023-02-10
EP4073055A4 (en) 2024-02-28

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