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TW200738689A - Salts and polymorphs of a VEGF-R inhibitor - Google Patents

Salts and polymorphs of a VEGF-R inhibitor

Info

Publication number
TW200738689A
TW200738689A TW095128889A TW95128889A TW200738689A TW 200738689 A TW200738689 A TW 200738689A TW 095128889 A TW095128889 A TW 095128889A TW 95128889 A TW95128889 A TW 95128889A TW 200738689 A TW200738689 A TW 200738689A
Authority
TW
Taiwan
Prior art keywords
salts
polymorphs
vegf
inhibitor
free base
Prior art date
Application number
TW095128889A
Other languages
English (en)
Inventor
Yi Li
Jia Liu
Anand Sistla
Bruce Joseph Elder
Yufeng Hong
Paul Kenneth Isbester
Grant Jackson Palmer
Jonathon Stuart Salsbury
Luckner Gerard Ulysse
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of TW200738689A publication Critical patent/TW200738689A/zh

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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Plural Heterocyclic Compounds (AREA)
TW095128889A 2005-08-08 2006-08-07 Salts and polymorphs of a VEGF-R inhibitor TW200738689A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US70633205P 2005-08-08 2005-08-08
US75018905P 2005-12-14 2005-12-14

Publications (1)

Publication Number Publication Date
TW200738689A true TW200738689A (en) 2007-10-16

Family

ID=37320417

Family Applications (1)

Application Number Title Priority Date Filing Date
TW095128889A TW200738689A (en) 2005-08-08 2006-08-07 Salts and polymorphs of a VEGF-R inhibitor

Country Status (13)

Country Link
US (1) US7928226B2 (zh)
EP (1) EP1915368A1 (zh)
JP (1) JP4536688B2 (zh)
KR (1) KR20080027923A (zh)
AR (1) AR055600A1 (zh)
AU (1) AU2006277742B2 (zh)
BR (1) BRPI0614115A2 (zh)
CA (1) CA2615760A1 (zh)
IL (1) IL188851A0 (zh)
MX (1) MX2008001838A (zh)
RU (1) RU2369607C1 (zh)
TW (1) TW200738689A (zh)
WO (1) WO2007017740A1 (zh)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20080027923A (ko) 2005-08-08 2008-03-28 화이자 인코포레이티드 Vegf-r 억제제의 염 및 다형체
TWI384986B (zh) * 2007-01-17 2013-02-11 Lg Life Sciences Ltd 抗病毒劑之順丁烯二酸單鹽以及含有該單鹽之醫藥組成物
US8211911B2 (en) 2008-08-19 2012-07-03 Guoqing Paul Chen Compounds as kinase inhibitors
CA2770545C (en) * 2009-08-21 2015-11-03 F. Hoffmann-La Roche Ag Use of a bis-maleic anhydride cross-linking agent for fixation of a cell or tissue sample
WO2012042421A1 (en) 2010-09-29 2012-04-05 Pfizer Inc. Method of treating abnormal cell growth

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT772610E (pt) * 1994-07-22 2001-03-30 Byk Gulden Lomberg Chem Fab Di-hidrobenzofuranos
NZ505362A (en) * 1997-12-22 2004-12-24 Upjohn Co 4-hydroxyquinoline-3-carboxamides and -hydrazides useful as antiviral agents
CN1165532C (zh) 1998-09-29 2004-09-08 惠氏控股有限公司 作为蛋白质酪氨酸激酶抑制剂的取代的3-氰基喹啉
WO2001040192A1 (en) * 1999-12-03 2001-06-07 Kyoto Pharmaceutical Industries, Ltd. Novel heterocyclic compounds and salts thereof and medicinal use of the same
GB0008269D0 (en) 2000-04-05 2000-05-24 Astrazeneca Ab Combination chemotherapy
MXPA03000252A (es) 2000-08-09 2003-06-06 Astrazeneca Ab Derivados de quinolina que tienen actividad de inhibicion de fcev.
CA2478050A1 (en) 2002-03-01 2003-09-12 Pfizer Inc. Indolyl-urea derivatives of thienopyridines useful as anti-angiogenic agents
UA82577C2 (en) * 2003-12-23 2008-04-25 Пфайзер Инк. Quinoline derivatives
US8091987B2 (en) 2005-07-07 2012-01-10 Xaar Plc Ink jet print head with improved reliability
KR20080027923A (ko) 2005-08-08 2008-03-28 화이자 인코포레이티드 Vegf-r 억제제의 염 및 다형체

Also Published As

Publication number Publication date
US20090048254A1 (en) 2009-02-19
RU2008104776A (ru) 2009-08-20
AU2006277742A1 (en) 2007-02-15
BRPI0614115A2 (pt) 2011-03-09
US7928226B2 (en) 2011-04-19
AU2006277742B2 (en) 2010-08-26
AR055600A1 (es) 2007-08-29
JP4536688B2 (ja) 2010-09-01
EP1915368A1 (en) 2008-04-30
CA2615760A1 (en) 2007-02-15
IL188851A0 (en) 2008-04-13
RU2369607C1 (ru) 2009-10-10
MX2008001838A (es) 2008-04-09
JP2007045822A (ja) 2007-02-22
WO2007017740A1 (en) 2007-02-15
KR20080027923A (ko) 2008-03-28

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