PL448716A1 - Kopolimer blokowy funkcjonalizowany fotoprzełącznikiem aryloazopirazolowym o fotoprzełączalnej aktywności antykoagulacyjnej i zastosowanie polimeru blokowego - Google Patents

Kopolimer blokowy funkcjonalizowany fotoprzełącznikiem aryloazopirazolowym o fotoprzełączalnej aktywności antykoagulacyjnej i zastosowanie polimeru blokowego

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Publication number
PL448716A1
PL448716A1 PL448716A PL44871624A PL448716A1 PL 448716 A1 PL448716 A1 PL 448716A1 PL 448716 A PL448716 A PL 448716A PL 44871624 A PL44871624 A PL 44871624A PL 448716 A1 PL448716 A1 PL 448716A1
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PL
Poland
Prior art keywords
application
arylazolyrazole
photoswitchable
photoswitch
block copolymer
Prior art date
Application number
PL448716A
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English (en)
Inventor
Nastassia Zhioba
Marta Stolarek
Krzysztof SZCZUBIAŁKA
Andrzej MOGIELNICKI
Bartłomiej Kałaska
Aleksandra FRĄCKIEWICZ
Dariusz PAWLAK
Original Assignee
Uniwersytet Jagielloński
Uniwersytet Medyczny W Białymstoku
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Application filed by Uniwersytet Jagielloński, Uniwersytet Medyczny W Białymstoku filed Critical Uniwersytet Jagielloński
Priority to PL448716A priority Critical patent/PL448716A1/pl
Priority to PCT/PL2025/050046 priority patent/WO2025250029A1/en
Publication of PL448716A1 publication Critical patent/PL448716A1/pl

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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F293/00Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
    • C08F293/005Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/14Esterification
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/74Synthetic polymeric materials
    • A61K31/795Polymers containing sulfur
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K41/00Medicinal preparations obtained by treating materials with wave energy or particle radiation ; Therapies using these preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K41/00Medicinal preparations obtained by treating materials with wave energy or particle radiation ; Therapies using these preparations
    • A61K41/10Inactivation or decontamination of a medicinal preparation prior to administration to an animal or a person
    • A61K41/17Inactivation or decontamination of a medicinal preparation prior to administration to an animal or a person by ultraviolet [UV] or infrared [IR] light, X-rays or gamma rays
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2438/00Living radical polymerisation
    • C08F2438/03Use of a di- or tri-thiocarbonylthio compound, e.g. di- or tri-thioester, di- or tri-thiocarbamate, or a xanthate as chain transfer agent, e.g . Reversible Addition Fragmentation chain Transfer [RAFT] or Macromolecular Design via Interchange of Xanthates [MADIX]
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Przedmiotem zgłoszenia jest kopolimer blokowy poli(sulfonianu styrenu) sodowego i kwasu poliakrylowego funkcjonalizowany podstawnikiem fenyloazopirazolowym określony wzorem (1). Zgłoszenie obejmuje również zastosowanie kopolimeru w farmacji, zwłaszcza do kontrolowania procesu krzepnięcia krwi oraz jego zastosowanie w leczeniu lub zapobieganiu chorób wymagających kontrolowania procesu krzepnięcia krwi.
PL448716A 2024-05-29 2024-05-29 Kopolimer blokowy funkcjonalizowany fotoprzełącznikiem aryloazopirazolowym o fotoprzełączalnej aktywności antykoagulacyjnej i zastosowanie polimeru blokowego PL448716A1 (pl)

Priority Applications (2)

Application Number Priority Date Filing Date Title
PL448716A PL448716A1 (pl) 2024-05-29 2024-05-29 Kopolimer blokowy funkcjonalizowany fotoprzełącznikiem aryloazopirazolowym o fotoprzełączalnej aktywności antykoagulacyjnej i zastosowanie polimeru blokowego
PCT/PL2025/050046 WO2025250029A1 (en) 2024-05-29 2025-05-29 A block copolymer functionalized with an arylazopyrazole photoswitch with photoswitchable anticoagulant activity and the use of the block polymer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL448716A PL448716A1 (pl) 2024-05-29 2024-05-29 Kopolimer blokowy funkcjonalizowany fotoprzełącznikiem aryloazopirazolowym o fotoprzełączalnej aktywności antykoagulacyjnej i zastosowanie polimeru blokowego

Publications (1)

Publication Number Publication Date
PL448716A1 true PL448716A1 (pl) 2025-12-01

Family

ID=96502829

Family Applications (1)

Application Number Title Priority Date Filing Date
PL448716A PL448716A1 (pl) 2024-05-29 2024-05-29 Kopolimer blokowy funkcjonalizowany fotoprzełącznikiem aryloazopirazolowym o fotoprzełączalnej aktywności antykoagulacyjnej i zastosowanie polimeru blokowego

Country Status (2)

Country Link
PL (1) PL448716A1 (pl)
WO (1) WO2025250029A1 (pl)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2098256B1 (en) * 2006-11-17 2016-06-08 National Cerebral and Cardiovascular Center Blood-coagulation inhibiting material, coating material and in vivo indwelling members made by using the material, and method of treatment
CA2964454A1 (en) * 2014-10-13 2016-04-21 Novabone Products, Llc Irrigation resistant compositions for regeneration of hard tissues and methods and kits of using the same

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
HENG PHO YAP ET AL.: "Langmuir 2008, 24, 16, 8981–8990; https://doi.org/10.1021/la8011074", SYNTHESIS, MULTILAYER FILM ASSEMBLY, AND CAPSULE FORMATION OF MACROMOLECULARLY ENGINEERED ACRYLIC ACID AND STYRENE SULFONATE BLOCK COPOLYMERS *
MARTA STOLAREK ET AL.: "J. Med. Chem. 2023, 66, 3, 1778–1789; https://doi.org/10.1021/acs.jmedchem.2c01616", BIOLOGICAL PROPERTIES OF HEPARINS MODIFIED WITH AN ARYLAZOPYRAZOLE-BASED PHOTOSWITCH *
NAHAIN, A. A. ET AL.: "Biomacromolecules, 21(2), 1009-1021, (2020); abstract; https://doi.org/10.1021/acs.biomac.9b01688", ANTICOAGULANT HEPARIN MIMETICS VIA RAFT POLYMERIZATION *
ZHAO-YANG ZHANG ET AL.: "Chem. Eur. J. 2019, 25, 13402 – 13410; DOI: 10.1002/chem.201902897", PYRAZOLYLAZOPHENYL ETHER-BASED PHOTOSWITCHES: FACILE SYNTHESIS, (NEAR-)QUANTITATIVE PHOTOCONVERSION, LONG THERMAL HALF-LIFE, EASY FUNCTIONALIZATION, AND VERSATILE APPLICATIONS IN LIGHT-RESPONSIVE SYSTEMS *

Also Published As

Publication number Publication date
WO2025250029A1 (en) 2025-12-04

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