WO2008064265A3 - Compounds modulating c-fms and/or c-kit activity and uses therefor - Google Patents

Compounds modulating c-fms and/or c-kit activity and uses therefor Download PDF

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Publication number
WO2008064265A3
WO2008064265A3 PCT/US2007/085299 US2007085299W WO2008064265A3 WO 2008064265 A3 WO2008064265 A3 WO 2008064265A3 US 2007085299 W US2007085299 W US 2007085299W WO 2008064265 A3 WO2008064265 A3 WO 2008064265A3
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Prior art keywords
fms
uses therefor
kit activity
compounds modulating
kit
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PCT/US2007/085299
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French (fr)
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WO2008064265A2 (en
Inventor
Chao Zhang
Jiazhong Zhang
Prabha N Ibrahim
Dean R Artis
Ryan Bremer
Guoxian Wu
Hongyao Zhu
Marika Nespi
Original Assignee
Plexxikon Inc
Chao Zhang
Jiazhong Zhang
Prabha N Ibrahim
Dean R Artis
Ryan Bremer
Guoxian Wu
Hongyao Zhu
Marika Nespi
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39322825&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2008064265(A3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Plexxikon Inc, Chao Zhang, Jiazhong Zhang, Prabha N Ibrahim, Dean R Artis, Ryan Bremer, Guoxian Wu, Hongyao Zhu, Marika Nespi filed Critical Plexxikon Inc
Publication of WO2008064265A2 publication Critical patent/WO2008064265A2/en
Publication of WO2008064265A3 publication Critical patent/WO2008064265A3/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
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    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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    • A61K31/53751,4-Oxazines, e.g. morpholine
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Abstract

Compounds active on the receptor protein tyrosine kinases c-kit and/or c-fms are provided herewith. Also provided herewith are compositions useful for treatment of c-kit mediated diseases or conditions and/or c-fms-mediated diseases or conditions, and methods for the use thereof.
PCT/US2007/085299 2006-11-22 2007-11-20 Compounds modulating c-fms and/or c-kit activity and uses therefor WO2008064265A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US86074906P 2006-11-22 2006-11-22
US60/860,749 2006-11-22

Publications (2)

Publication Number Publication Date
WO2008064265A2 WO2008064265A2 (en) 2008-05-29
WO2008064265A3 true WO2008064265A3 (en) 2008-11-13

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ID=39322825

Family Applications (3)

Application Number Title Priority Date Filing Date
PCT/US2007/083910 WO2008063888A2 (en) 2006-11-22 2007-11-07 Compounds modulating c-fms and/or c-kit activity and uses therefor
PCT/US2007/085299 WO2008064265A2 (en) 2006-11-22 2007-11-20 Compounds modulating c-fms and/or c-kit activity and uses therefor
PCT/US2007/085289 WO2008064255A2 (en) 2006-11-22 2007-11-20 Compounds modulating c-fms and/or c-kit activity and uses therefor

Family Applications Before (1)

Application Number Title Priority Date Filing Date
PCT/US2007/083910 WO2008063888A2 (en) 2006-11-22 2007-11-07 Compounds modulating c-fms and/or c-kit activity and uses therefor

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/US2007/085289 WO2008064255A2 (en) 2006-11-22 2007-11-20 Compounds modulating c-fms and/or c-kit activity and uses therefor

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EP (1) EP2086972B1 (en)
JP (4) JP2010510321A (en)
KR (1) KR101506044B1 (en)
CN (2) CN103497188B (en)
AR (1) AR063878A1 (en)
AU (1) AU2007323644B2 (en)
BR (1) BRPI0721137B8 (en)
CA (1) CA2670362C (en)
CL (1) CL2007003326A1 (en)
CO (1) CO6180438A2 (en)
CR (1) CR10817A (en)
DK (1) DK2086972T3 (en)
EC (1) ECSP099357A (en)
ES (1) ES2447779T3 (en)
GT (1) GT200700101A (en)
HK (1) HK1133649A1 (en)
IL (1) IL198624A (en)
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UA (1) UA97816C2 (en)
UY (1) UY30732A1 (en)
WO (3) WO2008063888A2 (en)
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US8741920B2 (en) 2009-08-03 2014-06-03 Hoffmann-La Roche, Inc. Process for the manufacture of pharmaceutically active compounds
US9096593B2 (en) 2009-11-06 2015-08-04 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
US9150570B2 (en) 2012-05-31 2015-10-06 Plexxikon Inc. Synthesis of heterocyclic compounds
US9169250B2 (en) 2006-11-22 2015-10-27 Plexxikon Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor

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JP5138938B2 (en) 2003-12-19 2013-02-06 プレキシコン インコーポレーテッド Compounds and methods for the development of RET modulators
US7498342B2 (en) * 2004-06-17 2009-03-03 Plexxikon, Inc. Compounds modulating c-kit activity
ES2371397T3 (en) * 2005-06-22 2011-12-30 Plexxikon, Inc. PIRROLO DERIVATIVES [2,3-B] PIRIDINE AS INHIBITORS OF PROTEIN KINES.
WO2008079909A1 (en) * 2006-12-21 2008-07-03 Plexxikon, Inc. Pyrrolo [2,3-b] pyridines as kinase modulators
PE20121126A1 (en) * 2006-12-21 2012-08-24 Plexxikon Inc PIRROLO [2,3-B] PYRIDINES COMPOUNDS AS KINASE MODULATORS
AU2008276063B2 (en) 2007-07-17 2013-11-28 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
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WO2009106441A1 (en) * 2008-02-25 2009-09-03 F. Hoffmann-La Roche Ag Pyrrolopyrazine kinase inhibitors
PL2250172T3 (en) 2008-02-25 2012-01-31 Hoffmann La Roche Pyrrolopyrazine kinase inhibitors
CA2713718A1 (en) * 2008-02-25 2009-09-03 F. Hoffmann-La Roche Ag Pyrrolopyrazine kinase inhibitors
PT2247592E (en) * 2008-02-25 2011-11-03 Hoffmann La Roche Pyrrolopyrazine kinase inhibitors
WO2009143018A2 (en) 2008-05-19 2009-11-26 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
US8119637B2 (en) * 2008-06-10 2012-02-21 Plexxikon Inc. Substituted pyrrolo[2,3-b]pyrazines and methods for kinase modulation, and indications therefor
EP2356116A1 (en) * 2008-11-20 2011-08-17 OSI Pharmaceuticals, Inc. Substituted pyrroloý2,3-b¨-pyridines and-pyrazines
BR122013027950A2 (en) * 2008-12-24 2019-12-10 BIAL PORTELA & Cª S A pharmaceutical compounds
AR078033A1 (en) 2009-04-03 2011-10-12 Plexxikon Inc A SOLID DISPERSION, CONTAINING THE COMPOUND {3- [5- (4- (CHLORINE-PHENYL) -1H-PIRROLO [2,3-B] PIRIDINA-3-CARBONIL] -2,4-DIFLUOR-PHENIL} -AMIDA OF PROPANE-1-SULPHONIC ACID, COMPOSITIONS AND FORMULATIONS THAT INCLUDE SUCH SOLID DISPERSION; METHODS FOR MANUFACTURING SUCH SOLID DISPERSION, FORMS 1 AND 2
TW201041888A (en) 2009-05-06 2010-12-01 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
EA201290073A1 (en) 2009-08-24 2013-01-30 Эсэпиен Фармасьютикалз, Инк. UREA COMPOUNDS CONTAINING 5,6-BICYCLIC HETEROARYL AS KINAZ INHIBITORS
WO2011063159A1 (en) * 2009-11-18 2011-05-26 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
JP5815558B2 (en) 2009-12-23 2015-11-17 プレキシコン インコーポレーテッドPlexxikon Inc. Compounds and methods for kinase regulation and their indications
US9180127B2 (en) 2009-12-29 2015-11-10 Dana-Farber Cancer Institute, Inc. Type II Raf kinase inhibitors
US8518945B2 (en) 2010-03-22 2013-08-27 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
US8481541B2 (en) 2010-03-22 2013-07-09 Hoffmann-La Roche Inc. Pyrrolopyrazine kinase inhibitors
AU2011238616B2 (en) 2010-03-30 2016-08-04 Verseon Corporation Multisubstituted aromatic compounds as inhibitors of thrombin
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