NO20072489L - Inhibitorer av C-FMS-kinase - Google Patents

Inhibitorer av C-FMS-kinase

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Publication number
NO20072489L
NO20072489L NO20072489A NO20072489A NO20072489L NO 20072489 L NO20072489 L NO 20072489L NO 20072489 A NO20072489 A NO 20072489A NO 20072489 A NO20072489 A NO 20072489A NO 20072489 L NO20072489 L NO 20072489L
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NO
Norway
Prior art keywords
well
compounds
treatment
diseases
formula
Prior art date
Application number
NO20072489A
Other languages
English (en)
Other versions
NO339555B1 (no
Inventor
Jonathan M Rudolph
Shelley Ballentine
Sanath Meegalla
Mark Wall
Jinsheng Chen
Carl R Illig
Ken Wilson
Renee Desjarlais
Christopher Molloy
Carl Manthey
Christopher Flores
Original Assignee
Janssen Pharmaceutica Nv
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Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of NO20072489L publication Critical patent/NO20072489L/no
Publication of NO339555B1 publication Critical patent/NO339555B1/no

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    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/68Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
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    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

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Abstract

Det beskrives forbindelser med formel I: der A, X, R2 og W er som angitt i beskrivelsen, så vel som solvater, hydrater, tautomerer og farmasøytisk akseptable salter derav. De beskrevne forbindelser inhiberer proteintyrosinkinaser og særlig c-fms kinase. Det beskrives videre behandling av autoimmune sykdommer samt sykdommer med en inflammatorisk komponent; behandling av metastase fra ovarie-, uterin-, bryst-, kolon- eller mavecancer, hårcelleleukemi og ikke-små celle lungekarsinom; og det beskrives videre behandling av smerte, inkludert skjelettsmerte forårsaket av tumormetastase eller osteoartritt, eller viseral, inflammatorisk og neurogenisk smerte, så vel som osteoporose, Paget's sykdom og andre sykdommer der benresporsjon medierer morbiditet inkludert artritt, prostesesvikt, osteolytisk sarkom, myelom og tumormetastaser i ben, med forbindelsene med formel I.
NO20072489A 2004-10-22 2007-05-15 Inhibitorer av c-fms kinase NO339555B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US62121104P 2004-10-22 2004-10-22
PCT/US2005/037868 WO2006047277A2 (en) 2004-10-22 2005-10-20 Inhibitors of c-fms kinase

Publications (2)

Publication Number Publication Date
NO20072489L true NO20072489L (no) 2007-06-29
NO339555B1 NO339555B1 (no) 2017-01-02

Family

ID=36228272

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20072489A NO339555B1 (no) 2004-10-22 2007-05-15 Inhibitorer av c-fms kinase

Country Status (18)

Country Link
EP (1) EP1807077B1 (no)
JP (1) JP5046950B2 (no)
KR (1) KR101273434B1 (no)
CN (1) CN101437514B (no)
AU (1) AU2005299837A1 (no)
BR (1) BRPI0516947A (no)
CA (1) CA2585053C (no)
DK (1) DK1807077T3 (no)
EA (1) EA013250B1 (no)
ES (1) ES2611604T3 (no)
HU (1) HUE033089T2 (no)
MX (1) MX2007004784A (no)
NO (1) NO339555B1 (no)
PL (1) PL1807077T3 (no)
PT (1) PT1807077T (no)
UA (1) UA88648C2 (no)
WO (1) WO2006047277A2 (no)
ZA (1) ZA200704106B (no)

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NO342001B1 (no) * 2006-04-20 2018-03-12 Janssen Pharmaceutica Nv C-kit kinase inhibitor for anvendelse i terapeutisk behandling av gastrointestinal stromaltumor eller mastocytose.

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WO2006047277A3 (en) 2009-05-07
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NO339555B1 (no) 2017-01-02
EP1807077A2 (en) 2007-07-18
CA2585053C (en) 2011-07-12
PT1807077T (pt) 2017-01-06
CN101437514B (zh) 2012-04-25
JP5046950B2 (ja) 2012-10-10
ZA200704106B (en) 2009-09-30
CA2585053A1 (en) 2006-05-04
KR20070085382A (ko) 2007-08-27
KR101273434B1 (ko) 2013-06-11
PL1807077T3 (pl) 2017-05-31
EP1807077A4 (en) 2011-09-21
JP2008517926A (ja) 2008-05-29
MX2007004784A (es) 2007-09-11
EA200700918A1 (ru) 2008-06-30
AU2005299837A1 (en) 2006-05-04
BRPI0516947A (pt) 2008-09-23
WO2006047277A2 (en) 2006-05-04
EP1807077B1 (en) 2016-11-23
CN101437514A (zh) 2009-05-20
ES2611604T3 (es) 2017-05-09
HUE033089T2 (en) 2017-11-28
UA88648C2 (en) 2009-11-10

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