JP2010518125A - C型肝炎ウイルス複製の新規な阻害剤 - Google Patents

C型肝炎ウイルス複製の新規な阻害剤 Download PDF

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JP2010518125A
JP2010518125A JP2009549295A JP2009549295A JP2010518125A JP 2010518125 A JP2010518125 A JP 2010518125A JP 2009549295 A JP2009549295 A JP 2009549295A JP 2009549295 A JP2009549295 A JP 2009549295A JP 2010518125 A JP2010518125 A JP 2010518125A
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ifn
optionally substituted
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aralkyl
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JP2010518125A5 (OSRAM
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レオニード・ビーゲルマン
ブラッド・バックマン
グアンギ・ワン
ジャセンカ・マトゥリック−アダミック
アンティッサ・ディミトロヴァ・ストイチェヴァ
スティーヴン・ダブリュー・アンドリューズ
ショーン・モーリス・ミシャレク
ピーティー・ラヴィ・ラジャゴパラン
アンドリュー・エム・フライヤー
インドラニ・グナワーダナ
ジュリア・ハース
リリー・ファン
マチェンダー・アール・マッドゥル
ガン・ザン
カール・コッセン
ヴラディミール・セレブリャニー
ローレンス・エム・ブラット
スコット・シーワート
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インターミューン・インコーポレーテッド
アレイ・バイオファーマ・インコーポレーテッド
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JP2009549295A 2007-02-12 2008-02-11 C型肝炎ウイルス複製の新規な阻害剤 Pending JP2010518125A (ja)

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Application Number Priority Date Filing Date Title
US88943307P 2007-02-12 2007-02-12
PCT/US2008/053617 WO2008100867A2 (en) 2007-02-12 2008-02-11 Novel inhibitors hepatitis c virus replication

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JP2010518125A true JP2010518125A (ja) 2010-05-27
JP2010518125A5 JP2010518125A5 (OSRAM) 2011-03-31

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US (1) US20090047246A1 (OSRAM)
EP (1) EP2134683A2 (OSRAM)
JP (1) JP2010518125A (OSRAM)
CN (1) CN101687789A (OSRAM)
AU (1) AU2008216382A1 (OSRAM)
CA (1) CA2676906A1 (OSRAM)
MX (1) MX2009008439A (OSRAM)
WO (1) WO2008100867A2 (OSRAM)

Cited By (5)

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JP2011503195A (ja) * 2007-11-16 2011-01-27 シェーリング コーポレイション ヘテロ環の3位が置換されたインドール誘導体およびその使用
JP2014513074A (ja) * 2011-04-07 2014-05-29 ラボラトワール ビオディム ウィルス複製の阻害剤、それらの調製方法及びそれらの治療的使用
JP2014514362A (ja) * 2011-05-12 2014-06-19 プロテオステイシス セラピューティクス,インコーポレイテッド プロテオスタシス調節因子
JP2020516664A (ja) * 2017-04-11 2020-06-11 セージ ファーマ, エルエルシー カルバゾール化合物及びその使用法
JP2023532996A (ja) * 2020-07-06 2023-08-01 クレセンタ バイオサイエンシズ Fabp4調節化合物の抗ウイルス的使用

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JP2010525032A (ja) * 2007-05-02 2010-07-22 ノバルティス アーゲー ヘテロ環化合物及び殺有害生物剤としてのそれらの使用
US8022085B2 (en) 2007-05-07 2011-09-20 Amgen Inc. Pyrazolo-pyridinone and pyrazolo-pyrazinone compounds as P38 modulators and methods of use thereof
MX2007009796A (es) 2007-08-14 2009-02-25 Cell Therapy And Technology S Gel conteniendo pirfenidona.
CN101910145A (zh) * 2008-02-14 2010-12-08 弗·哈夫曼-拉罗切有限公司 抗病毒的杂环化合物
WO2009117156A1 (en) 2008-03-21 2009-09-24 Amgen Inc. Pyrazolo-pyrazinone compounds and methods of use thereof
US8198449B2 (en) * 2008-09-11 2012-06-12 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
US8048887B2 (en) * 2008-09-11 2011-11-01 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
JP5854841B2 (ja) * 2009-02-27 2016-02-09 シガ・テクノロジーズ・インコーポレーテッド デングウイルス感染を治療及び予防するためのチエノピリジン誘導体類
RU2571662C2 (ru) 2009-03-25 2015-12-20 Эббви Инк. Противовирусные соединения и их применения
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ME01838B (me) 2009-06-29 2014-12-20 Lncyte Holdings Corp Pirimidinoni kao inhibitori pi3k
CN102574787B (zh) 2009-07-30 2014-12-31 新加坡国立大学 具有潜在的抗癌活性的小分子异戊二烯基半胱氨酸羧基甲基转移酶抑制剂
PL2462119T3 (pl) * 2009-08-03 2014-10-31 Acraf Sposób wytwarzania 1-benzylo-3-hydroksymetylo-1H-indazolu i jego pochodnych oraz potrzebnych magnezowych związków pośrednich
WO2011049988A2 (en) * 2009-10-20 2011-04-28 Eiger Biopharmaceuticals, Inc. Indazoles to treat flaviviridae virus infection
US8759359B2 (en) 2009-12-18 2014-06-24 Incyte Corporation Substituted heteroaryl fused derivatives as PI3K inhibitors
CA2787785C (en) 2010-01-28 2018-03-06 President And Fellows Of Harvard College Compositions and methods for enhancing proteasome activity
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CN103601683B (zh) * 2010-04-16 2016-03-30 中国科学院上海药物研究所 苯并杂环类化合物及其制备方法和用途
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BR112013009789A2 (pt) 2010-10-26 2016-07-19 Presidio Pharmaceuticals Inc inibidores do vírus da hepatite c
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