JP5913126B2 - キナーゼ阻害剤としての使用のための三環式化合物 - Google Patents

キナーゼ阻害剤としての使用のための三環式化合物 Download PDF

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JP5913126B2
JP5913126B2 JP2012546501A JP2012546501A JP5913126B2 JP 5913126 B2 JP5913126 B2 JP 5913126B2 JP 2012546501 A JP2012546501 A JP 2012546501A JP 2012546501 A JP2012546501 A JP 2012546501A JP 5913126 B2 JP5913126 B2 JP 5913126B2
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methyl
cyclopenta
phenyl
dihydro
oxa
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JP2013516399A (ja
JP2013516399A5 (enExample
Inventor
フェルナンデス, ホアキン パストル
フェルナンデス, ホアキン パストル
リーマ, フランシスコ ハビエル ラモス
リーマ, フランシスコ ハビエル ラモス
イゲラス, アナ イサベル エルナンデス
イゲラス, アナ イサベル エルナンデス
ゴンサレス, ソニア マルティネス
ゴンサレス, ソニア マルティネス
エルナンド, ホセ イグナシオ マルティン
エルナンド, ホセ イグナシオ マルティン
カール−グスタベ ピエーレ サルステ,
カール−グスタベ ピエーレ サルステ,
カンタラピエドラ, エステール ゴンザレス
カンタラピエドラ, エステール ゴンザレス
アパリシオ, カルメン ブランコ
アパリシオ, カルメン ブランコ
エルゲタ, アントニオ ロドリゲス
エルゲタ, アントニオ ロドリゲス
コリャソ, アナ マリア ガルシア
コリャソ, アナ マリア ガルシア
セラーノ, アントニオ サルガド
セラーノ, アントニオ サルガド
マリーニョ, ベアトリス ノーヤ
マリーニョ, ベアトリス ノーヤ
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Spanish National Cancer Research Centre
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Spanish National Cancer Research Centre
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
    • C07D491/14—Ortho-condensed systems
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14—Ortho-condensed systems

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  • Orthopedic Medicine & Surgery (AREA)
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JP2012546501A 2009-12-31 2010-12-31 キナーゼ阻害剤としての使用のための三環式化合物 Active JP5913126B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP09380202.3 2009-12-31
EP09380202 2009-12-31
PCT/GB2010/002348 WO2011080510A1 (en) 2009-12-31 2010-12-31 Tricyclic compounds for use as kinase inhibitors

Publications (3)

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JP2013516399A JP2013516399A (ja) 2013-05-13
JP2013516399A5 JP2013516399A5 (enExample) 2015-04-23
JP5913126B2 true JP5913126B2 (ja) 2016-04-27

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JP2012546501A Active JP5913126B2 (ja) 2009-12-31 2010-12-31 キナーゼ阻害剤としての使用のための三環式化合物

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US (1) US9682991B2 (enExample)
EP (1) EP2519526B1 (enExample)
JP (1) JP5913126B2 (enExample)
KR (1) KR20120111739A (enExample)
CN (1) CN102791715B (enExample)
AU (1) AU2010338038B2 (enExample)
CA (1) CA2786002C (enExample)
IL (1) IL220701A0 (enExample)
NZ (1) NZ601033A (enExample)
PH (1) PH12012501361A1 (enExample)
SG (1) SG182297A1 (enExample)
WO (1) WO2011080510A1 (enExample)

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US9682991B2 (en) 2017-06-20
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