NZ700761A - Salt form of a human histone methyltransferase ezh2 inhibitor - Google Patents

Salt form of a human histone methyltransferase ezh2 inhibitor

Info

Publication number
NZ700761A
NZ700761A NZ700761A NZ70076113A NZ700761A NZ 700761 A NZ700761 A NZ 700761A NZ 700761 A NZ700761 A NZ 700761A NZ 70076113 A NZ70076113 A NZ 70076113A NZ 700761 A NZ700761 A NZ 700761A
Authority
NZ
New Zealand
Prior art keywords
salt form
histone methyltransferase
ezh2 inhibitor
human histone
methyltransferase ezh2
Prior art date
Application number
NZ700761A
Other languages
English (en)
Inventor
Kevin Wayne Kuntz
Kuan-Chun Huang
Hyeong Wook Choi
Kristen Sanders
Steven Mathieu
Arani Chanda
Frank Fang
Original Assignee
Epizyme Inc
Eisai R&D Man Co Ltd
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 Epizyme Inc, Eisai R&D Man Co Ltd filed Critical Epizyme Inc
Publication of NZ700761A publication Critical patent/NZ700761A/en

Links

Classifications

    • 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
    • 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
    • C07D405/02Heterocyclic 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
    • C07D405/12Heterocyclic 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
    • 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
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyridine Compounds (AREA)
NZ700761A 2012-04-13 2013-04-11 Salt form of a human histone methyltransferase ezh2 inhibitor NZ700761A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261624215P 2012-04-13 2012-04-13
PCT/US2013/036193 WO2013155317A1 (en) 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor

Publications (1)

Publication Number Publication Date
NZ700761A true NZ700761A (en) 2016-09-30

Family

ID=49328166

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ700761A NZ700761A (en) 2012-04-13 2013-04-11 Salt form of a human histone methyltransferase ezh2 inhibitor

Country Status (26)

Country Link
US (7) US9394283B2 (cg-RX-API-DMAC10.html)
EP (4) EP4190777A1 (cg-RX-API-DMAC10.html)
JP (3) JP6255382B2 (cg-RX-API-DMAC10.html)
KR (4) KR102438340B1 (cg-RX-API-DMAC10.html)
CN (2) CN108358899B (cg-RX-API-DMAC10.html)
AU (2) AU2013245878B2 (cg-RX-API-DMAC10.html)
BR (1) BR112014025508B1 (cg-RX-API-DMAC10.html)
CA (1) CA2870005C (cg-RX-API-DMAC10.html)
CY (2) CY1119383T1 (cg-RX-API-DMAC10.html)
DK (3) DK3184523T3 (cg-RX-API-DMAC10.html)
ES (3) ES2617379T3 (cg-RX-API-DMAC10.html)
HR (2) HRP20170295T1 (cg-RX-API-DMAC10.html)
HU (3) HUE060881T2 (cg-RX-API-DMAC10.html)
IL (4) IL282732B2 (cg-RX-API-DMAC10.html)
IN (1) IN2014DN09068A (cg-RX-API-DMAC10.html)
LT (2) LT2836491T (cg-RX-API-DMAC10.html)
MX (2) MX384641B (cg-RX-API-DMAC10.html)
NZ (1) NZ700761A (cg-RX-API-DMAC10.html)
PL (3) PL3184523T3 (cg-RX-API-DMAC10.html)
PT (3) PT3628670T (cg-RX-API-DMAC10.html)
RS (2) RS55690B1 (cg-RX-API-DMAC10.html)
RU (1) RU2658911C2 (cg-RX-API-DMAC10.html)
SG (3) SG10201912109QA (cg-RX-API-DMAC10.html)
SI (2) SI2836491T1 (cg-RX-API-DMAC10.html)
SM (2) SMT201700132T1 (cg-RX-API-DMAC10.html)
WO (1) WO2013155317A1 (cg-RX-API-DMAC10.html)

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Also Published As

Publication number Publication date
IL282732A (en) 2021-06-30
US9872862B2 (en) 2018-01-23
HUE060881T2 (hu) 2023-04-28
IL296199B2 (en) 2024-12-01
MX362339B (es) 2019-01-11
EP3628670B1 (en) 2022-10-12
RU2014145544A (ru) 2016-06-10
HRP20170295T1 (hr) 2017-04-21
AU2013245878B2 (en) 2017-10-12
PT2836491T (pt) 2017-02-08
DK3184523T3 (da) 2019-08-19
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