SI2152701T1 - Spojine fenil amino pirimidina in njihova uporaba - Google Patents

Spojine fenil amino pirimidina in njihova uporaba

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Publication number
SI2152701T1
SI2152701T1 SI200831536T SI200831536T SI2152701T1 SI 2152701 T1 SI2152701 T1 SI 2152701T1 SI 200831536 T SI200831536 T SI 200831536T SI 200831536 T SI200831536 T SI 200831536T SI 2152701 T1 SI2152701 T1 SI 2152701T1
Authority
SI
Slovenia
Prior art keywords
phenyl amino
pyrimidine compounds
amino pyrimidine
compounds
phenyl
Prior art date
Application number
SI200831536T
Other languages
English (en)
Inventor
Christopher John Burns
Andrew Craig Donohue
John Thomas Feutrill
Thao Lien Thi Nguyen
Andrew Frederick Wilks
Jun Zeng
Original Assignee
Ym Biosciences Australia Pty 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 Ym Biosciences Australia Pty Ltd filed Critical Ym Biosciences Australia Pty Ltd
Publication of SI2152701T1 publication Critical patent/SI2152701T1/sl

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • 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
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    • C07D295/02Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
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    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
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SI200831536T 2007-03-12 2008-03-12 Spojine fenil amino pirimidina in njihova uporaba SI2152701T1 (sl)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US89426407P 2007-03-12 2007-03-12
US1625207P 2007-12-21 2007-12-21
EP08714386.3A EP2152701B1 (en) 2007-03-12 2008-03-12 Phenyl amino pyrimidine compounds and uses thereof
PCT/AU2008/000339 WO2008109943A1 (en) 2007-03-12 2008-03-12 Phenyl amino pyrimidine compounds and uses thereof

Publications (1)

Publication Number Publication Date
SI2152701T1 true SI2152701T1 (sl) 2016-03-31

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SI200831536T SI2152701T1 (sl) 2007-03-12 2008-03-12 Spojine fenil amino pirimidina in njihova uporaba

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US (5) US8486941B2 (sl)
EP (2) EP3023422A1 (sl)
JP (5) JP2010520892A (sl)
KR (3) KR101566840B1 (sl)
CN (2) CN101861313B (sl)
AU (1) AU2008226327B2 (sl)
BR (2) BR122020010759B1 (sl)
CA (1) CA2702650C (sl)
CY (1) CY1117180T1 (sl)
DK (1) DK2152701T3 (sl)
ES (1) ES2557930T3 (sl)
HK (1) HK1149749A1 (sl)
HR (1) HRP20151386T1 (sl)
HU (1) HUE029188T2 (sl)
MX (1) MX2009009792A (sl)
PL (1) PL2152701T3 (sl)
PT (1) PT2152701E (sl)
RS (1) RS54533B1 (sl)
RU (1) RU2498983C2 (sl)
SI (1) SI2152701T1 (sl)
WO (1) WO2008109943A1 (sl)
ZA (1) ZA200906848B (sl)

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PL2152701T3 (pl) 2007-03-12 2016-10-31 Związki fenyloaminopirymidyny i ich zastosowania
US8530480B2 (en) 2007-09-04 2013-09-10 The Scripps Research Institute Substituted pyrimidinyl-amines as protein kinase inhibitors
WO2009103032A1 (en) * 2008-02-15 2009-08-20 Rigel Pharmaceuticals, Inc. Pyrimidine-2-amine compounds and their use as inhibitors of jak kinases
CA2713716A1 (en) * 2008-02-22 2009-08-27 F. Hoffmann-La Roche Ag Modulators for amyloid beta
CN102791697A (zh) * 2009-10-12 2012-11-21 瑞科西有限公司 作为TBKL和/或IKKε抑制剂的氨基-嘧啶化合物
GB201012105D0 (en) 2010-07-19 2010-09-01 Domainex Ltd Novel pyrimidine compounds
JP2014500254A (ja) 2010-11-09 2014-01-09 セルゾーム リミティッド Tyk2阻害剤としてのピリジン化合物およびそのアザ類似体
MX2013006261A (es) * 2010-12-03 2013-10-01 Ym Biosciences Australia Pty Tratamiento de condiciones mediadas por jak2.
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
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