EA202192903A1 - Кристаллическая форма ингибитора plk4 - Google Patents

Кристаллическая форма ингибитора plk4

Info

Publication number
EA202192903A1
EA202192903A1 EA202192903A EA202192903A EA202192903A1 EA 202192903 A1 EA202192903 A1 EA 202192903A1 EA 202192903 A EA202192903 A EA 202192903A EA 202192903 A EA202192903 A EA 202192903A EA 202192903 A1 EA202192903 A1 EA 202192903A1
Authority
EA
Eurasian Patent Office
Prior art keywords
crystalline form
plk4 inhibitor
compound
plk4
inhibitor
Prior art date
Application number
EA202192903A
Other languages
English (en)
Russian (ru)
Inventor
Сзе-Ван Ли
Марк Роберт Брей
Original Assignee
Юниверсити Хелс Нетуорк
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 Юниверсити Хелс Нетуорк filed Critical Юниверсити Хелс Нетуорк
Publication of EA202192903A1 publication Critical patent/EA202192903A1/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • 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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
EA202192903A 2019-04-24 2020-04-23 Кристаллическая форма ингибитора plk4 EA202192903A1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201962837858P 2019-04-24 2019-04-24
PCT/CA2020/050535 WO2020215155A1 (en) 2019-04-24 2020-04-23 Crystal form s4 of the plk4 inhibitor (lr,2s)-(e)-2-(3-(4-((cis-2,6-dimethylmorpholino)methyl)styryl)- 1 h-imidazol-6- yl)-5'-methoxyspiro[cyclopropane-l,3'-indolin]-2'-one fumarate

Publications (1)

Publication Number Publication Date
EA202192903A1 true EA202192903A1 (ru) 2022-02-09

Family

ID=72940551

Family Applications (1)

Application Number Title Priority Date Filing Date
EA202192903A EA202192903A1 (ru) 2019-04-24 2020-04-23 Кристаллическая форма ингибитора plk4

Country Status (16)

Country Link
US (1) US12325700B2 (https=)
EP (1) EP3959209A4 (https=)
JP (1) JP7705351B2 (https=)
KR (1) KR20220004102A (https=)
CN (1) CN113966330B (https=)
AU (1) AU2020264143A1 (https=)
BR (1) BR112021021106A2 (https=)
CA (1) CA3137191A1 (https=)
EA (1) EA202192903A1 (https=)
IL (1) IL287394A (https=)
MA (1) MA55767A (https=)
MX (1) MX2021012993A (https=)
SA (1) SA521430647B1 (https=)
SG (1) SG11202111003UA (https=)
TW (1) TWI862582B (https=)
WO (1) WO2020215155A1 (https=)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7717842B2 (ja) 2021-05-11 2025-08-04 オリック ファーマシューティカルズ,インク. ポロ様キナーゼ4阻害剤

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7205328B2 (en) 2002-10-21 2007-04-17 Irm Llc Oxindoles with anti-HIV activity
DE102005005395A1 (de) 2005-02-03 2006-08-10 Schering Aktiengesellschaft Thiazolidinone, deren Herstellung und Verwendung als Arzneimittel
GB0606234D0 (en) 2006-03-29 2006-05-10 Pliva Istrazivanje I Razvoj D Pharmaceutically acceptable salts and polymorphic forms
EP2205241B1 (en) 2007-09-25 2014-05-21 Takeda Pharmaceutical Company Limited Polo-like kinase inhibitors
EP2235004A4 (en) 2007-12-21 2011-05-04 Univ Health Network INDAZOLYL, BENZIMIDAZOLYL, BENZOTRIAZOLYL-SUBSTITUTED INDOLUND DERIVATIVES AS A KINASE-HEMMER FOR CANCER TREATMENT
ES2465971T3 (es) 2009-04-06 2014-06-09 University Health Network Inhibidores de quinasa y método para tratar cáncer con los mismos
US8586598B2 (en) 2009-04-29 2013-11-19 Nerviano Medical Sciences S.R.L. CDK inhibitor salts
SI2556071T1 (sl) 2010-04-06 2016-12-30 University Health Network Kinazni inhibitorji in njihova uporaba pri zdravljenju raka
ES2706066T3 (es) 2010-07-02 2019-03-27 Univ Health Network Procedimiento dirigido a enfermedades mutantes con PTEN y composiciones para las mismas
WO2012048411A1 (en) 2010-10-13 2012-04-19 University Health Network Plk-4 inhibitors and method of treating cancer with same
US9012464B2 (en) 2010-11-25 2015-04-21 Ratiopharm Gmbh Salts and polymorphic forms of Afatinib
US20140051679A1 (en) 2011-10-12 2014-02-20 Univeristy Health Networks Kinase inhibitors and method of treating cancer with same
WO2015054781A1 (en) 2013-10-18 2015-04-23 University Health Network Treatment for pancreatic cancer
HUE043194T2 (hu) * 2013-10-18 2019-08-28 Univ Health Network PLK-4 inhibitor sója és kristályformái

Also Published As

Publication number Publication date
BR112021021106A2 (pt) 2021-12-14
WO2020215155A8 (en) 2020-11-26
TW202104216A (zh) 2021-02-01
JP7705351B2 (ja) 2025-07-09
KR20220004102A (ko) 2022-01-11
TWI862582B (zh) 2024-11-21
SA521430647B1 (ar) 2024-01-27
MX2021012993A (es) 2021-12-10
MA55767A (fr) 2022-03-02
IL287394A (en) 2021-12-01
US12325700B2 (en) 2025-06-10
WO2020215155A1 (en) 2020-10-29
EP3959209A4 (en) 2022-12-28
AU2020264143A1 (en) 2021-10-28
CA3137191A1 (en) 2020-10-29
EP3959209A1 (en) 2022-03-02
SG11202111003UA (en) 2021-11-29
US20220204494A1 (en) 2022-06-30
CN113966330A (zh) 2022-01-21
JP2022530028A (ja) 2022-06-27
CN113966330B (zh) 2024-09-13

Similar Documents

Publication Publication Date Title
JOP20210001A1 (ar) مشتقات 3-(5- هيدروكسي -1- أوكسو أيزو إندولين -2- يل) بيبريدين -2، 6- دايون واستخدامها لمعالجة أمراض مرتبطة ببروتين ذات أصبع الزنك من عائلة (ikaros 2 (ikzf2
CR20220354A (es) Inhibidores de egfr
ZA202213152B (en) Novel acid secretion inhibitor and use thereof
ZA202308002B (en) Pyrimidopyran compound
MX2021000348A (es) 2-fluoro-3-nitrotolueno cristalino y procedimiento para la preparacion del mismo.
UA83720C2 (ru) Кристаллическая форма v агомелатина, способ ее получения и фармацевтическая композиция, которая ее содержит
EA200300107A1 (ru) Кристаллические формы трет-бутиламиновой соли периндоприла
EA200802119A1 (ru) Новая кристаллическая форма vi агомелатина, способ его получения и фармацевтические композиции, которые ее содержат
EA200601271A1 (ru) Новая кристаллическая форма iv агомелатина, способ её получения и фармацевтические композиции, которые её содержат
EA200601274A1 (ru) Новая кристаллическая форма iii агомелатина, способ её получения и фармацевтические композиции, которые её содержат
MX2021003427A (es) Nuevos oxadiazoles.
GEP20247655B (en) Crystalline salt forms of kinase inhibitor
JOP20210072A1 (ar) ملح جديد لمثبط bcl-2، صورة بلورية ذات صلة، طريقة تحضيره وتركيبات صيدلية تحتوي عليه
EA202190880A1 (ru) Кристаллическая форма морфолинохиназолинового соединения, способ ее получения и ее применение
EA202092393A1 (ru) Кристаллическое соединение оксазола
ZA202101487B (en) Novel compounds
MX2021001904A (es) Formas solidas de benzoxaborol sustituido y composiciones de las mismas.
EA202192903A1 (ru) Кристаллическая форма ингибитора plk4
SG11201810725WA (en) Novel β-lactamase inhibitors
WO2020003272A8 (en) An improved process for the preparation of venetoclax
CR20240173A (es) Compuestos de cd73
MY209356A (en) A xinafoate salt of a jak inhibiting compound
MY202100A (en) Crystal
MX2022005201A (es) Formulaciones de naftalimida dimerica.
WO2020251871A3 (en) Novel substituted tetrahydroquinolin compounds as indoleamine 2,3-dioxygenase (ido) inhibitors