[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

SG11201602783SA - Salt and crystal forms of plk-4 inhibitor - Google Patents

Salt and crystal forms of plk-4 inhibitor

Info

Publication number
SG11201602783SA
SG11201602783SA SG11201602783SA SG11201602783SA SG11201602783SA SG 11201602783S A SG11201602783S A SG 11201602783SA SG 11201602783S A SG11201602783S A SG 11201602783SA SG 11201602783S A SG11201602783S A SG 11201602783SA SG 11201602783S A SG11201602783S A SG 11201602783SA
Authority
SG
Singapore
Prior art keywords
plk
inhibitor
salt
crystal forms
crystal
Prior art date
Application number
SG11201602783SA
Inventor
Peter Brent Sampson
Miklos Feher
Heinz W Pauls
Original Assignee
Univ Health Network
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 Univ Health Network filed Critical Univ Health Network
Publication of SG11201602783SA publication Critical patent/SG11201602783SA/en

Links

Classifications

    • 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
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Pulmonology (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SG11201602783SA 2013-10-18 2014-10-17 Salt and crystal forms of plk-4 inhibitor SG11201602783SA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361892564P 2013-10-18 2013-10-18
PCT/CA2014/051001 WO2015054793A1 (en) 2013-10-18 2014-10-17 Salt and crystal forms of plk-4 inhibitor

Publications (1)

Publication Number Publication Date
SG11201602783SA true SG11201602783SA (en) 2016-05-30

Family

ID=52827507

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201602783SA SG11201602783SA (en) 2013-10-18 2014-10-17 Salt and crystal forms of plk-4 inhibitor

Country Status (26)

Country Link
US (5) US9884855B2 (en)
EP (1) EP3057965B1 (en)
JP (1) JP6492072B2 (en)
KR (3) KR20220063299A (en)
CN (2) CN105764899B (en)
AU (1) AU2014336929B9 (en)
CA (1) CA2926845C (en)
CY (1) CY1121484T1 (en)
DK (1) DK3057965T3 (en)
EA (1) EA031569B1 (en)
ES (1) ES2718603T3 (en)
HR (1) HRP20190564T1 (en)
HU (1) HUE043194T2 (en)
IL (1) IL245038B (en)
LT (1) LT3057965T (en)
ME (1) ME03377B (en)
MX (1) MX359069B (en)
NZ (1) NZ718744A (en)
PL (1) PL3057965T3 (en)
PT (1) PT3057965T (en)
RS (1) RS58413B1 (en)
SG (1) SG11201602783SA (en)
SI (1) SI3057965T1 (en)
TR (1) TR201902875T4 (en)
TW (1) TWI659952B (en)
WO (1) WO2015054793A1 (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010115279A1 (en) 2009-04-06 2010-10-14 University Health Network Kinase inhibitors and method of treating cancer with same
PL2556071T3 (en) 2010-04-06 2017-02-28 University Health Network Kinase inhibitors and their use in treating cancer
KR20220063299A (en) 2013-10-18 2022-05-17 유니버시티 헬스 네트워크 Salt and crystal forms of plk-4 inhibitor
EP3678669A4 (en) * 2017-09-08 2021-06-09 University Health Network Combination therapies for inhibition of polo-like kinase 4
EP3959209A4 (en) * 2019-04-24 2022-12-28 University Health Network Crystal form s4 of the plk4 inhibitor (1r,2s)-(e)-2-(3-(4-((cis-2,6-dimethylmorpholino)methyl)styryl)- 1 h-imidazol-6- yl)-5'-methoxyspiro[cyclopropane-1,3'-indolin]-2'-one fumarate
EP4069246A4 (en) * 2019-12-06 2023-12-06 University Health Network Treatment for acute myeloid leukemia or myelodysplastic syndrome
CA3217983A1 (en) 2021-05-11 2022-11-17 Chudi Ndubaku Polo like kinase 4 inhibitors

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2483323A (en) * 1945-08-01 1949-09-27 Kay Fries Chemicals Inc Method of preparing phenyl ethyl alcohol
US7205328B2 (en) 2002-10-21 2007-04-17 Irm Llc Oxindoles with anti-HIV activity
DE102005005395A1 (en) * 2005-02-03 2006-08-10 Schering Aktiengesellschaft New thiazolidinone compounds are polo-like kinase inhibitors, useful for treating e.g. cancer, autoimmune diseases, cardiovascular diseases, infectious diseases, nephrological diseases and viral diseases
GB0606234D0 (en) * 2006-03-29 2006-05-10 Pliva Istrazivanje I Razvoj D Pharmaceutically acceptable salts and polymorphic forms
JP2010522078A (en) * 2007-03-23 2010-07-01 エージェンシー フォー サイエンス,テクノロジー アンド リサーチ Palladium catalyst
JP5372939B2 (en) * 2007-09-25 2013-12-18 武田薬品工業株式会社 Polo-like kinase inhibitor
JP2011506494A (en) * 2007-12-21 2011-03-03 ユニバーシティ・ヘルス・ネットワーク Indazolyl, benzimidazolyl, and benzotriazolyl substituted indolmon derivatives as kinase inhibitors useful in the treatment of cancer
WO2010115279A1 (en) 2009-04-06 2010-10-14 University Health Network Kinase inhibitors and method of treating cancer with same
JP5801285B2 (en) * 2009-04-29 2015-10-28 ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ CDK inhibitor salt
PL2556071T3 (en) 2010-04-06 2017-02-28 University Health Network Kinase inhibitors and their use in treating cancer
WO2012000103A1 (en) * 2010-07-02 2012-01-05 University Health Network Methods of targeting pten mutant diseases and compositions therefor
WO2012048411A1 (en) * 2010-10-13 2012-04-19 University Health Network Plk-4 inhibitors and method of treating cancer with same
KR20130105675A (en) * 2010-11-25 2013-09-25 라티오팜 게엠베하 Novel salts and polymorphic forms of afatinib
CA2850394C (en) * 2011-10-12 2019-05-21 University Health Network Indazole compounds as kinase inhibitors and method of treating cancer with same
KR20220063299A (en) 2013-10-18 2022-05-17 유니버시티 헬스 네트워크 Salt and crystal forms of plk-4 inhibitor
EP3057593B1 (en) 2013-10-18 2021-12-08 University Health Network Treatment for pancreatic cancer

Also Published As

Publication number Publication date
HUE043194T2 (en) 2019-08-28
IL245038B (en) 2019-11-28
KR102395737B1 (en) 2022-05-10
MX2016004963A (en) 2016-06-28
LT3057965T (en) 2019-03-12
WO2015054793A1 (en) 2015-04-23
AU2014336929B9 (en) 2019-03-21
JP6492072B2 (en) 2019-03-27
EP3057965A4 (en) 2017-05-24
CY1121484T1 (en) 2020-05-29
ES2718603T3 (en) 2019-07-03
KR20220063299A (en) 2022-05-17
AU2014336929B2 (en) 2018-11-22
US20200140428A1 (en) 2020-05-07
DK3057965T3 (en) 2019-04-01
ME03377B (en) 2020-01-20
PT3057965T (en) 2019-04-23
US9884855B2 (en) 2018-02-06
TW201609717A (en) 2016-03-16
KR20160070106A (en) 2016-06-17
CN113248486A (en) 2021-08-13
US20190248775A1 (en) 2019-08-15
US20180155335A1 (en) 2018-06-07
TR201902875T4 (en) 2019-03-21
IL245038A0 (en) 2016-05-31
TWI659952B (en) 2019-05-21
US20160264559A1 (en) 2016-09-15
RS58413B1 (en) 2019-04-30
EP3057965B1 (en) 2019-01-02
KR20210137251A (en) 2021-11-17
CN105764899B (en) 2021-06-01
CN105764899A (en) 2016-07-13
NZ718744A (en) 2021-07-30
EA201690755A1 (en) 2016-09-30
CA2926845C (en) 2023-06-13
US20210269428A1 (en) 2021-09-02
MX359069B (en) 2018-09-12
PL3057965T3 (en) 2019-08-30
US11667627B2 (en) 2023-06-06
SI3057965T1 (en) 2019-04-30
US10472353B2 (en) 2019-11-12
JP2016537326A (en) 2016-12-01
US10392374B2 (en) 2019-08-27
HRP20190564T1 (en) 2019-05-17
EA031569B1 (en) 2019-01-31
EP3057965A1 (en) 2016-08-24
CA2926845A1 (en) 2015-04-23
US10919886B2 (en) 2021-02-16

Similar Documents

Publication Publication Date Title
HK1221224A1 (en) Crystal modifications of elobixibat
HK1213889A1 (en) Glutaminase inhibitors and method of use
EP2964651A4 (en) Bmp inhibitors and methods of use thereof
HRP20190564T1 (en) Salt and crystal forms of plk-4 inhibitor
EP2970311A4 (en) Bmp inhibitors and methods of use thereof
IL250391A0 (en) Crystal forms of glutaminase inhibitors
HRP20181291T1 (en) Heterobicycloaryl rorc2 inhibitors and methods of use thereof
PT3293176T (en) Crystal form of a pde4 inhibitor
SG11201507897SA (en) Salt of pyrazoloquinoline derivative, and crystal thereof
IL244268A0 (en) Heterocyclic compounds and methods of use
PL3019477T3 (en) Heterocyclic compounds and methods of their use
HK1222339A1 (en) Inhibitors of metallo-ss-lactamase-enzymes --
IL240763A0 (en) Halogenopyrazoles as inhibitors of therombin
GB201312311D0 (en) Uses of enzyme inhibitors