JP5089681B2 - c−fmsキナーゼの阻害剤としての複素環式化合物 - Google Patents

c−fmsキナーゼの阻害剤としての複素環式化合物 Download PDF

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JP5089681B2
JP5089681B2 JP2009506739A JP2009506739A JP5089681B2 JP 5089681 B2 JP5089681 B2 JP 5089681B2 JP 2009506739 A JP2009506739 A JP 2009506739A JP 2009506739 A JP2009506739 A JP 2009506739A JP 5089681 B2 JP5089681 B2 JP 5089681B2
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phenyl
mmol
alkyl
enyl
imidazole
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JP2009534403A (ja
JP2009534403A5 (enExample
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イリグ,カール・アール
バレンタイン,シエリー・ケイ
チエン,ジンシエング
デスジヤーレイス,レネー・ルイーズ
メーガラ,サナス・ケイ
ウオール,マーク
ウイルソン,ケネス
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Janssen Pharmaceutica NV
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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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
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JP2009506739A 2006-04-20 2007-04-18 c−fmsキナーゼの阻害剤としての複素環式化合物 Expired - Fee Related JP5089681B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US79369706P 2006-04-20 2006-04-20
US60/793,697 2006-04-20
US88353907P 2007-01-05 2007-01-05
US60/883,539 2007-01-05
PCT/US2007/066860 WO2007124316A1 (en) 2006-04-20 2007-04-18 Heterocyclic compounds as inhibitors of c-fms kinase

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Publication Number Publication Date
JP2009534403A JP2009534403A (ja) 2009-09-24
JP2009534403A5 JP2009534403A5 (enExample) 2010-05-13
JP5089681B2 true JP5089681B2 (ja) 2012-12-05

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JP2009506739A Expired - Fee Related JP5089681B2 (ja) 2006-04-20 2007-04-18 c−fmsキナーゼの阻害剤としての複素環式化合物

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US (6) US7414050B2 (enExample)
EP (1) EP2021335B1 (enExample)
JP (1) JP5089681B2 (enExample)
KR (1) KR101367645B1 (enExample)
AR (1) AR060608A1 (enExample)
AT (1) ATE510832T1 (enExample)
AU (1) AU2007240437B2 (enExample)
CA (1) CA2649736C (enExample)
CY (1) CY1111749T1 (enExample)
DK (1) DK2021335T3 (enExample)
MX (1) MX2008013533A (enExample)
NZ (1) NZ572073A (enExample)
PL (1) PL2021335T3 (enExample)
PT (1) PT2021335E (enExample)
SI (1) SI2021335T1 (enExample)
TW (1) TW200811162A (enExample)
WO (1) WO2007124316A1 (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009534418A (ja) * 2006-04-20 2009-09-24 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ C−kitキナーゼ阻害法

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US20060281788A1 (en) * 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor
AU2006307314C1 (en) 2005-10-25 2011-08-25 Shionogi & Co., Ltd. Aminodihydrothiazine derivative
US8697716B2 (en) 2006-04-20 2014-04-15 Janssen Pharmaceutica Nv Method of inhibiting C-KIT kinase
AU2007240439B2 (en) * 2006-04-20 2012-10-11 Janssen Pharmaceutica N.V. Inhibitors of c-fms kinase
KR101367645B1 (ko) * 2006-04-20 2014-02-27 얀센 파마슈티카 엔.브이. C-fms 키나제의 저해제로서의 복소환식 화합물
KR101367646B1 (ko) 2006-04-20 2014-02-27 얀센 파마슈티카 엔.브이. C-fms 키나제의 저해제
JP5383483B2 (ja) 2007-04-24 2014-01-08 塩野義製薬株式会社 アルツハイマー症治療用医薬組成物
ES2476605T3 (es) 2007-04-24 2014-07-15 Shionogi & Co., Ltd. Derivados de aminohidrotiazina sustituidos con grupos cíclicos
JO3240B1 (ar) * 2007-10-17 2018-03-08 Janssen Pharmaceutica Nv c-fms مثبطات كيناز
AU2009258496B8 (en) * 2008-06-13 2014-06-26 Shionogi & Co., Ltd. Sulfur-containing heterocyclic derivative having beta-secretase-inhibiting activity
WO2010047372A1 (ja) * 2008-10-22 2010-04-29 塩野義製薬株式会社 Bace1阻害活性を有する2-アミノピリミジン-4-オンおよび2-アミノピリジン誘導体
UA110467C2 (uk) 2009-12-11 2016-01-12 Шионогі Енд Ко., Лтд. Похідні оксазину
JP5766198B2 (ja) 2010-10-29 2015-08-19 塩野義製薬株式会社 縮合アミノジヒドロピリミジン誘導体
CN103261199A (zh) 2010-10-29 2013-08-21 盐野义制药株式会社 萘啶衍生物
CN103608345A (zh) 2011-04-26 2014-02-26 盐野义制药株式会社 噁嗪衍生物和含有该噁嗪衍生物的bace1抑制剂
PL2840080T3 (pl) * 2012-04-17 2018-06-29 Fujifilm Corporation Zawierający azot związek heterocykliczny lub jego sól
US9303046B2 (en) 2012-08-07 2016-04-05 Janssen Pharmaceutica Nv Process for the preparation of heterocyclic ester derivatives
JOP20180012A1 (ar) 2012-08-07 2019-01-30 Janssen Pharmaceutica Nv عملية السلفنة باستخدام نونافلوروبوتانيسولفونيل فلوريد
EP2912035A4 (en) 2012-10-24 2016-06-15 Shionogi & Co DERIVATIVES OF DIHYDROOXAZINE OR OXAZEPINE HAVING BACE1 INHIBITING ACTIVITY
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CN109776512A (zh) * 2018-01-30 2019-05-21 成都安诺晨创医药科技有限公司 一种n-取代咪唑甲酸酯类衍生物及其用途
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