JP2004526699A - 5−ht6受容体の拮抗薬としてのベンゼンスルホン酸インドール−5−イルエステル類 - Google Patents

5−ht6受容体の拮抗薬としてのベンゼンスルホン酸インドール−5−イルエステル類 Download PDF

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JP2004526699A
JP2004526699A JP2002561022A JP2002561022A JP2004526699A JP 2004526699 A JP2004526699 A JP 2004526699A JP 2002561022 A JP2002561022 A JP 2002561022A JP 2002561022 A JP2002561022 A JP 2002561022A JP 2004526699 A JP2004526699 A JP 2004526699A
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ester
indol
methylpiperidin
acid
mmol
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JP2004526699A5 (cg-RX-API-DMAC7.html
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サンドラ・アン・フィラ
マイケル・エドワード・フロー
ジェイムズ・ロナルド・ジリグ
ローレンス・ジョゼフ・ハインツ
ジョゼフ・ハーマン・クルシンスキー・ジュニア
リュー・ビン
マルタ・マリア・ピネイロ−ヌネス
ジョン・メーナート・ショース
ジョン・スタンリー・ウォード
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Eli Lilly and Co
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Eli Lilly and Co
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    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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  • Plural Heterocyclic Compounds (AREA)
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  • Nitrogen Condensed Heterocyclic Rings (AREA)
JP2002561022A 2001-01-30 2002-01-17 5−ht6受容体の拮抗薬としてのベンゼンスルホン酸インドール−5−イルエステル類 Pending JP2004526699A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US26499601P 2001-01-30 2001-01-30
PCT/US2002/000502 WO2002060871A2 (en) 2001-01-30 2002-01-17 Benzenesulfonic acid indol-5-yl esters as antagonists of the 5-ht6 receptor

Publications (2)

Publication Number Publication Date
JP2004526699A true JP2004526699A (ja) 2004-09-02
JP2004526699A5 JP2004526699A5 (cg-RX-API-DMAC7.html) 2005-12-22

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JP2002561022A Pending JP2004526699A (ja) 2001-01-30 2002-01-17 5−ht6受容体の拮抗薬としてのベンゼンスルホン酸インドール−5−イルエステル類

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US (2) US7230011B2 (cg-RX-API-DMAC7.html)
EP (1) EP1377580B1 (cg-RX-API-DMAC7.html)
JP (1) JP2004526699A (cg-RX-API-DMAC7.html)
CN (1) CN1275967C (cg-RX-API-DMAC7.html)
AT (1) ATE340795T1 (cg-RX-API-DMAC7.html)
AU (1) AU2002236730B2 (cg-RX-API-DMAC7.html)
BR (1) BR0206595A (cg-RX-API-DMAC7.html)
CA (1) CA2433351A1 (cg-RX-API-DMAC7.html)
DE (1) DE60214990T2 (cg-RX-API-DMAC7.html)
ES (1) ES2272667T3 (cg-RX-API-DMAC7.html)
MX (1) MXPA03006605A (cg-RX-API-DMAC7.html)
WO (1) WO2002060871A2 (cg-RX-API-DMAC7.html)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010507621A (ja) * 2006-10-27 2010-03-11 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規な置換ピペリジル−プロパン−チオール
JP2010507620A (ja) * 2006-10-27 2010-03-11 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング ピペリジル−プロパン−チオールccr3モジュレーター
JP2018510131A (ja) * 2015-01-30 2018-04-12 ファイザー・インク Rorc2のスルホンアミド置換インドールモジュレーターおよびその使用方法

Families Citing this family (23)

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ES2222827B1 (es) * 2003-07-30 2006-03-01 Laboratorios Del Dr. Esteve, S.A. Derivados de 5-indolilsulfonamidas, su preparacion y su aplicacion como medicamentos.
ES2222830B1 (es) 2003-07-30 2006-02-16 Laboratorios Del Dr. Esteve, S.A. Derivados de 7-indolilsulfonamidas, su preparacion y su aplicacion como medicamentos.
ES2222828B1 (es) * 2003-07-30 2006-04-16 Laboratorios Del Dr. Esteve, S.A. Derivados de 1-sulfonilindoles, su preparacion y su aplicacion como medicamentos.
ES2222832B1 (es) * 2003-07-30 2006-02-16 Laboratorios Del Dr. Esteve, S.A. Derivados de 6-indolilsulfonamidas, su preparacion y su aplicacion como medicamentos.
ES2222829B1 (es) * 2003-07-30 2006-03-01 Laboratorios Del Dr. Esteve, S.A. Derivados de 4-indolilsulfonamidas, su preparacion y su aplicacion como medicamentos.
PT1704154E (pt) * 2004-01-02 2009-08-05 Suven Life Sciences Ltd Novos indeno[2,1a]indenos e isoindol[2,1-a]indóis
JP2009501705A (ja) * 2005-07-05 2009-01-22 アストラゼネカ・アクチエボラーグ 新規化合物、その製造方法、中間体、医薬組成物、並びにアルツハイマー病、認知障害、統合失調症に伴う認識機能障害、肥満及びパーキンソン病のような5−ht6介在疾患の治療におけるそれらの使用
JP2009515833A (ja) * 2005-10-24 2009-04-16 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 3−ピペリジン−4−イル−インドールorl−1受容体モジュレーター
WO2007098418A1 (en) 2006-02-17 2007-08-30 Memory Pharmaceuticals Corporation Compounds having 5-ht6 receptor affinity
AR061637A1 (es) * 2006-06-26 2008-09-10 Epix Delaware Inc Composiciones y metodos de tratamiento de trastornos del snc
MX2009006077A (es) 2007-01-08 2009-06-17 Suven Life Sciences Ltd Compuestos de 5-(heterociclil)alquil-n-(arilsulfonil)indol y su uso como ligandos de la 5-hidroxitriptamina6.
ATE513810T1 (de) 2007-05-03 2011-07-15 Suven Life Sciences Ltd Aminoalkoxy-aryl-sulfonamidverbindungen und ihre verwendung als 5-ht6-liganden
JP5236001B2 (ja) 2007-10-26 2013-07-17 スヴェン・ライフ・サイエンシズ・リミテッド アミノアリールスルホンアミド化合物および5−ht6リガンドとしてのその使用
US8318725B2 (en) 2008-09-17 2012-11-27 Suven Life Sciences Limited Aryl indolyl sulfonamide compounds and their use as 5-HT6 ligands
CN102159564B (zh) 2008-09-17 2014-06-18 苏文生命科学有限公司 芳基磺酰胺胺化合物及它们作为5-ht6配体的用途
WO2011082266A2 (en) 2009-12-30 2011-07-07 Arqule, Inc. Substituted heterocyclic compounds
JP5628937B2 (ja) 2010-01-05 2014-11-19 スベン ライフ サイエンシズ リミティド 5−ht6受容体リガンドとしてのスルホン化合物
KR101250606B1 (ko) * 2011-01-24 2013-04-03 이화여자대학교 산학협력단 5-ht6 수용체 억제 작용을 갖는 신규한 벤조티아졸 및 벤즈이소티아졸유도체, 이의 제조 방법 및 이를 포함하는 약학적 조성물
CA2850707C (en) * 2011-10-03 2023-03-21 The University Of Utah Research Foundation Application of 5-ht6 receptor antagonists for the alleviation of cognitive deficits of down syndrome
EP3082802B1 (en) 2013-12-03 2020-02-26 Iomet Pharma Ltd. Tryptophan-2,3-dioxygenase (tdo) and/or indolamine-2,3-dioxygenase (ido) inhibitors and their use
US9974785B2 (en) 2014-07-08 2018-05-22 Sunshine Lake Pharma Co., Ltd. Aromatic heterocyclic derivatives and pharmaceutical applications thereof
EP3331530A4 (en) * 2015-08-03 2018-12-19 Raze Therapeutics Inc. Mthfd2 inhibitors and uses thereof
CN115521307B (zh) * 2022-09-30 2023-09-22 甘肃皓天医药科技有限责任公司 一种5-卤代-7-氮杂吲哚的制备方法

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ATE190608T1 (de) * 1991-11-25 2000-04-15 Pfizer 5-(hetero- oder carbocyclylamino)-indol derivate, deren herstellung und deren verwendung als 5-ht1 agonisten
US5521196A (en) 1994-10-05 1996-05-28 Eli Lilly And Company 5-HT1F agonists for the treatment of migraine
US5521197A (en) 1994-12-01 1996-05-28 Eli Lilly And Company 3-<1-alkylenearyl>-4-<1,2,3,6-tetrahydropyridinyl>-and 3-<1-alkylenearyl>-4-piperidinyl-1h-indoles: new 5-HT1F agonists
DE4444864A1 (de) * 1994-12-16 1996-06-20 Bayer Ag Verwendung von 5-Acyl-1,4-dihydropyridinen
TR199700993T1 (xx) 1995-03-20 1998-03-21 Eli Lilly And Company 5-ikameli-3-(1,2,3,6-tetrahidropridin-4-il)- ve 3-(piperidin-4-il)-1H-indoller: yeni 5-HT1F agonistler.
JPH11513666A (ja) 1995-10-10 1999-11-24 イーライ・リリー・アンド・カンパニー N−[2−置換−3−(2−アミノエチル)−1h−インドール−5−イル]−アミド:新規5−ht▲下1f▼作動剤
US5792763A (en) 1996-10-08 1998-08-11 Eli Lilly And Company Serotonin 5-HT1F agonists
US6133287A (en) 1998-03-24 2000-10-17 Allelix Biopharmaceuticals Inc. Piperidine-indole compounds having 5-HT6 affinity
CA2370147C (en) * 1999-04-21 2009-07-28 Allelix Biopharmaceuticals Inc. Piperidine-indole compounds having 5-ht6 affinity
AU6339200A (en) 1999-07-28 2001-02-19 Kirin Beer Kabushiki Kaisha Urea derivatives as inhibitors of ccr-3 receptor

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010507621A (ja) * 2006-10-27 2010-03-11 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 新規な置換ピペリジル−プロパン−チオール
JP2010507620A (ja) * 2006-10-27 2010-03-11 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング ピペリジル−プロパン−チオールccr3モジュレーター
JP2018510131A (ja) * 2015-01-30 2018-04-12 ファイザー・インク Rorc2のスルホンアミド置換インドールモジュレーターおよびその使用方法

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MXPA03006605A (es) 2003-09-22
US20040102481A1 (en) 2004-05-27
DE60214990T2 (de) 2007-04-05
ATE340795T1 (de) 2006-10-15
EP1377580A2 (en) 2004-01-07
WO2002060871A2 (en) 2002-08-08
BR0206595A (pt) 2004-07-13
EP1377580B1 (en) 2006-09-27
CN1275967C (zh) 2006-09-20
WO2002060871A8 (en) 2003-12-18
ES2272667T3 (es) 2007-05-01
CN1489591A (zh) 2004-04-14
AU2002236730B2 (en) 2006-06-15
DE60214990D1 (de) 2006-11-09
US20070135484A1 (en) 2007-06-14
US7230011B2 (en) 2007-06-12
CA2433351A1 (en) 2002-08-08
WO2002060871A3 (en) 2003-09-12

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