JP2009534458A - アミノ−エチル−アミノ−アリール（ａｅａａ）化合物およびそれらの使用 - Google Patents

アミノ−エチル−アミノ−アリール（ａｅａａ）化合物およびそれらの使用 Download PDF

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JP2009534458A
JP2009534458A JP2009507166A JP2009507166A JP2009534458A JP 2009534458 A JP2009534458 A JP 2009534458A JP 2009507166 A JP2009507166 A JP 2009507166A JP 2009507166 A JP2009507166 A JP 2009507166A JP 2009534458 A JP2009534458 A JP 2009534458A
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JP2009534458A5 (enExample
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レインハム，トニー，マイケル
ハモンズ，ティモシー，ロビン
ジリアット，ジュリア，ヘレン
チャールズ，マーク，デヴィッド
アレクサンドル ペイブ，グレゴワール
フォクストン，キャロライン，ヘザー
カール，ジェイムズ，リンゼイ
ミストリー，ニーラ，スミト
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Cancer Research Technology Ltd
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Cancer Research Technology Ltd
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Priority claimed from GB0608269A external-priority patent/GB0608269D0/en
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JP2009507166A 2006-04-26 2007-04-26 アミノ−エチル−アミノ−アリール（ａｅａａ）化合物およびそれらの使用 Withdrawn JP2009534458A (ja)

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US74563006P 2006-04-26 2006-04-26
GB0608269A GB0608269D0 (en) 2006-04-26 2006-04-26 Therapeutic compounds
PCT/GB2007/001537 WO2007125331A2 (en) 2006-04-26 2007-04-26 Amino-ethyl-amino-aryl (aeaa) compounds and their use

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JP2009534458A true JP2009534458A (ja) 2009-09-24
JP2009534458A5 JP2009534458A5 (enExample) 2010-06-17

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US (1) US20090247519A1 (enExample)
EP (1) EP2024333A2 (enExample)
JP (1) JP2009534458A (enExample)
AU (1) AU2007245496A1 (enExample)
CA (1) CA2649995A1 (enExample)
IL (1) IL194899A0 (enExample)
MX (1) MX2008013718A (enExample)
WO (1) WO2007125331A2 (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013505909A (ja) * 2009-09-24 2013-02-21 ビーエーエスエフ ソシエタス・ヨーロピア 無脊椎動物害虫を駆除するためのアミノキナゾリン化合物
JP2022544700A (ja) * 2019-08-22 2022-10-20 バイオヘイブン・セラピューティクス・リミテッド 筋萎縮性側索硬化症および関連障害の治療のためにｔｄｐ－４３に結合する分子

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EP2099458A4 (en) * 2006-12-01 2011-05-11 Harvard College COMPOUNDS AND METHODS FOR ENZYME-MEDIATED TUMOR PRESENTATION AND THERAPY
CN101778825A (zh) * 2007-03-22 2010-07-14 沃泰克斯药物股份有限公司 适用作詹纳斯激酶抑制剂的n-杂环类化合物
ES2535736T3 (es) 2008-06-10 2015-05-14 Novartis Ag Derivados de pirazina como bloqueadores de los canales de sodio epitelial
CN102137856A (zh) * 2008-06-13 2011-07-27 诺瓦提斯公司 作为蛋白激酶d抑制剂的可用于治疗ia心力衰竭和癌症的2,4’-联吡啶化合物
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