JP7291145B2 - Tlr阻害剤として有効な置換されたインドール化合物 - Google Patents

Tlr阻害剤として有効な置換されたインドール化合物 Download PDF

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JP7291145B2
JP7291145B2 JP2020534224A JP2020534224A JP7291145B2 JP 7291145 B2 JP7291145 B2 JP 7291145B2 JP 2020534224 A JP2020534224 A JP 2020534224A JP 2020534224 A JP2020534224 A JP 2020534224A JP 7291145 B2 JP7291145 B2 JP 7291145B2
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isopropyl
indol
triazolo
pyridin
methoxy
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JP2021506889A (ja
JP2021506889A5 (https=
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アラリック・ジェイ・ディックマン
ダームパル・エス・ドッド
クリストファー・ピー・マッサリ
ジョン・エル・ギルモア
タシル・シャムスル・ハーク
トレバー・シー・シャーウッド
ブライアン・ケイ・ホワイトリー
ショシャナ・エル・ポージー
スリーカンタ・ラトナ・クマール
ラクスマン・パスヌーリ
スリニバサン・クンチタパタム・ドゥライサミー
スブラマニア・ヘグデ
ルシト・クマール・アヌムラ
ピタニ・ビーラ・ベンカタ・スリニバス
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Bristol Myers Squibb Co
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    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
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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
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • C07D491/02Heterocyclic 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 two hetero rings
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  • Pain & Pain Management (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Indole Compounds (AREA)
JP2020534224A 2017-12-19 2018-12-18 Tlr阻害剤として有効な置換されたインドール化合物 Active JP7291145B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762607472P 2017-12-19 2017-12-19
US62/607,472 2017-12-19
PCT/US2018/066149 WO2019126113A1 (en) 2017-12-19 2018-12-18 Substituted indole compounds useful as tlr inhibitors

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JP2021506889A JP2021506889A (ja) 2021-02-22
JP2021506889A5 JP2021506889A5 (https=) 2021-12-23
JP7291145B2 true JP7291145B2 (ja) 2023-06-14

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US (1) US11878975B2 (https=)
EP (1) EP3728225B1 (https=)
JP (1) JP7291145B2 (https=)
KR (1) KR102742178B1 (https=)
CN (1) CN111491930B (https=)
AU (1) AU2018390820A1 (https=)
BR (1) BR112020012084A2 (https=)
CA (1) CA3085590A1 (https=)
EA (1) EA202091474A1 (https=)
ES (1) ES2932361T3 (https=)
IL (1) IL275356A (https=)
MX (1) MX2020005462A (https=)
SG (1) SG11202005696YA (https=)
WO (1) WO2019126113A1 (https=)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022532145A (ja) * 2019-05-09 2022-07-13 ブリストル-マイヤーズ スクイブ カンパニー 置換ベンズイミダゾロン化合物

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10071079B2 (en) 2016-06-29 2018-09-11 Bristol-Myers Squibb Company [1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds
WO2019126082A1 (en) * 2017-12-19 2019-06-27 Bristol-Myers Squibb Company 6-azaindole compounds
BR112020011984A2 (pt) * 2017-12-20 2020-11-17 Bristol-Myers Squibb Company compostos de amino indol úteis como inibidores de tlr
CA3085942A1 (en) * 2017-12-20 2019-06-27 Bristol-Myers Squibb Company Aryl and heteroaryl substituted indole compounds
JP7328977B2 (ja) 2018-02-12 2023-08-17 エフ. ホフマン-ラ ロシュ アーゲー ウイルス感染の処置および予防のための新規のスルホン化合物および誘導体
KR20210018818A (ko) 2018-06-05 2021-02-18 에프. 호프만-라 로슈 아게 자가면역 질환의 치료를 위한 테트라하이드로-1H-피라지노[2,1-a]이소인돌릴퀴놀린 화합물
EP3807270B1 (en) 2018-06-12 2023-09-13 F. Hoffmann-La Roche AG Novel heteroaryl heterocyclyl compounds for the treatment of autoimmune disease
US11952363B2 (en) 2018-07-23 2024-04-09 Hoffmann-La Roche Inc. Piperazine compounds for the treatment of autoimmune disease
WO2020048583A1 (en) 2018-09-04 2020-03-12 F. Hoffmann-La Roche Ag Benzothiazole compounds for the treatment of autoimmune diseases
WO2020048595A1 (en) 2018-09-06 2020-03-12 F. Hoffmann-La Roche Ag Novel cyclic amidine compounds for the treatment of autoimmune disease
JP7367004B2 (ja) 2018-09-06 2023-10-23 エフ. ホフマン-ラ ロシュ アーゲー 自己免疫疾患の処置のための新規のピラゾロビリジン化合物
ES2963696T3 (es) * 2018-10-24 2024-04-01 Bristol Myers Squibb Co Compuestos diméricos de indol sustituidos
CN112955450A (zh) 2018-10-24 2021-06-11 百时美施贵宝公司 经取代的吲哚和吲唑化合物
CN114829350B (zh) * 2019-10-04 2024-05-28 百时美施贵宝公司 经取代的咔唑化合物
US12421240B2 (en) 2019-10-31 2025-09-23 Hoffmann-La Roche Inc. Hydropyrazino[1,2-d][1,4]diazepine compounds for the treatment of autoimmune disease
JP2023502087A (ja) 2019-11-19 2023-01-20 エフ.ホフマン-ラ ロシュ アーゲー 自己免疫疾患の処置のためのヒドロ-1H-ピロロ[1,2-a]ピラジン化合物
JP7649306B2 (ja) 2019-11-20 2025-03-19 エフ. ホフマン-ラ ロシュ アーゲー 自己免疫疾患の処置のためのスピロ(イソベンゾフラナゼチジン)化合物
CN115052860B (zh) * 2020-01-30 2024-06-21 艾尼莫生物科技公司 胶原蛋白1翻译抑制剂和其使用方法
AR123286A1 (es) 2020-08-19 2022-11-16 Bristol Myers Squibb Co Compuestos de benzimidazol sustituidos útiles como inhibidores de tlr9
AR123281A1 (es) 2020-08-19 2022-11-16 Bristol Myers Squibb Co Compuestos bicíclicos sustituidos útiles como inhibidores de tlr9
AU2021328577A1 (en) 2020-08-19 2023-03-23 Bristol-Myers Squibb Company 1H-pyrrolo[3,2-c]pyridine and 1H-pyrrolo[2,3-c]pyridine derivatives as TLR9 inhibitors for the treatment of fibrosis
TWI887510B (zh) * 2020-12-22 2025-06-21 美商基利科學股份有限公司 6-取代之吲哚化合物
CN116783202A (zh) * 2021-02-09 2023-09-19 吉利德科学公司 噻吩并吡咯化合物
KR20230171469A (ko) 2021-04-16 2023-12-20 길리애드 사이언시즈, 인코포레이티드 티에노피롤 화합물
EP4398989A1 (en) 2021-09-10 2024-07-17 Gilead Sciences, Inc. Thienopyrrole compounds
KR20240148414A (ko) * 2022-02-18 2024-10-11 브리스톨-마이어스 스큅 컴퍼니 Tlr9의 억제제로서 유용한 치환된 이미다조피리디닐 화합물
CN114591339B (zh) * 2022-05-10 2022-08-02 上海维申医药有限公司 一类Toll样受体抑制剂及其制备和应用
US20250214977A1 (en) * 2024-01-03 2025-07-03 Kymera Therapeutics, Inc. Stat6 inhibitors and uses thereof

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003512369A (ja) 1999-10-19 2003-04-02 メルク エンド カムパニー インコーポレーテッド チロシンキナーゼ阻害剤
JP2005524621A (ja) 2002-01-07 2005-08-18 エーザイ株式会社 デアザプリンおよびそれらの用途
WO2006113458A1 (en) 2005-04-15 2006-10-26 Bristol-Myers Squibb Company Heterocyclic inhibitors of protein arginine methyl transferases
JP2006526654A (ja) 2003-06-05 2006-11-24 メルク エンド カムパニー インコーポレーテッド 置換インドールおよび置換インドールの調製方法
JP2008534439A (ja) 2005-01-28 2008-08-28 メルク エンド カムパニー インコーポレーテッド チェックポイントキナーゼの阻害剤
WO2009042092A1 (en) 2007-09-25 2009-04-02 Merck & Co., Inc. 2-aryl or heteroaryl indole derivatives
JP2009526766A (ja) 2006-02-03 2009-07-23 メルク シャープ エンド ドーム リミテッド アルツハイマー病の治療のためのインダゾール誘導体
JP2012504133A (ja) 2008-09-26 2012-02-16 エーザイ・アール・アンド・ディー・マネジメント株式会社 ベンゾオキサゾール化合物および使用方法
JP2015523981A (ja) 2012-05-31 2015-08-20 エーザイ・アール・アンド・ディー・マネジメント株式会社 テトラヒドロピラゾロピリミジン化合物
WO2016151085A1 (en) 2015-03-24 2016-09-29 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. New toll-like receptor 9 antagonists
JP2020529436A (ja) 2017-08-04 2020-10-08 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company [1,2,4]トリアゾロ[4,3−a]ピリジニル置換のインドール化合物
JP2021503004A (ja) 2017-11-14 2021-02-04 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 置換インドール化合物
JP6995067B2 (ja) 2016-06-29 2022-01-14 ブリストル-マイヤーズ スクイブ カンパニー [1,2,4]トリアゾロ[1,5-a]ピリジニル置換インドール化合物
JP6995109B2 (ja) 2016-07-30 2022-01-14 ブリストル-マイヤーズ スクイブ カンパニー ジメトキシフェニル置換インドール化合物
JP7028861B2 (ja) 2016-09-09 2022-03-02 ブリストル-マイヤーズ スクイブ カンパニー ピリジル置換のインドール化合物
JP7104775B2 (ja) 2017-08-04 2022-07-21 ブリストル-マイヤーズ スクイブ カンパニー Tlr7/8/9の阻害剤として有用な置換インドール化合物

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6187777B1 (en) 1998-02-06 2001-02-13 Amgen Inc. Compounds and methods which modulate feeding behavior and related diseases
HUP0104987A3 (en) 1998-12-18 2002-09-30 Axys Pharmaceuticals Inc South Benzimidazole or indole derivatives protease inhibitors, and pharmaceutical compositions containing them
AU2003239508A1 (en) * 2002-05-21 2003-12-12 Bristol-Myers Squibb Company Indole compounds useful as impdh inhibitors
MXPA05013922A (es) 2003-06-20 2006-02-24 Coley Pharm Group Inc Antagonistas de receptor tipo toll de molecula pequena.
ZA200701235B (en) * 2004-07-14 2009-10-28 Ptc Therapeutics Inc Methods for treating hepatitis C
WO2007115306A2 (en) 2006-04-04 2007-10-11 Myriad Genetics, Inc. Compounds for diseases and disorders
DE102006033109A1 (de) 2006-07-18 2008-01-31 Grünenthal GmbH Substituierte Heteroaryl-Derivate
US8027888B2 (en) 2006-08-31 2011-09-27 Experian Interactive Innovation Center, Llc Online credit card prescreen systems and methods
WO2008065198A1 (en) 2006-12-01 2008-06-05 Galapagos N.V. Triazolopyridine compounds useful for the treatment of degenerative & inflammatory diseases
WO2008152471A1 (en) 2007-06-12 2008-12-18 Coley Pharmaceutical Group, Inc. Quinazoline derivative useful as toll-like receptor antagonist
WO2009030996A1 (en) 2007-09-05 2009-03-12 Coley Pharmaceutical Group, Inc. Triazole compounds as toll-like receptor (tlr) agonists
CA2738929A1 (en) 2008-10-17 2010-04-22 Boehringer Ingelheim International Gmbh Heteroaryl substituted indole compounds useful as mmp-13 inhibitors
TWI462920B (zh) 2009-06-26 2014-12-01 葛萊伯格有限公司 用於治療退化性及發炎疾病之新穎化合物
NO2453895T3 (https=) 2009-07-16 2018-10-20
BR112012006630A2 (pt) 2009-09-24 2016-05-03 Hoffmann La Roche derivados em indol como moduladores dos canais de cálcio ativados para liberação de cálcio (crac)
US20110098311A1 (en) 2009-10-22 2011-04-28 Vertex Pharmaceuticals Incorported Compositions for treatment of cystic fibrosis and other chronic diseases
WO2012054862A2 (en) 2010-10-21 2012-04-26 The Brigham And Women's Hospital, Inc. Agents, compositions, and methods for treating pruritis and related skin conditions
DK2663555T3 (en) 2011-01-12 2017-03-27 Ventirx Pharmaceuticals Inc SUBSTITUTED BENZOAZEPINS AS MODULATORS OF TOLL-LIKE RECEPTORS
EP3208263A1 (en) 2011-01-12 2017-08-23 VentiRx Pharmaceuticals, Inc. Substituted benzoazepines as toll-like receptor modulators
CA2837227C (en) 2011-06-01 2022-05-10 Janus Biotherapeutics, Inc. Novel immune system modulators
WO2012167053A1 (en) 2011-06-01 2012-12-06 Janus Biotherapeutics, Inc. Novel immune system modulators
CA2836487A1 (en) 2011-06-09 2012-12-13 Rhizen Pharmaceuticals Sa Novel compounds as modulators of gpr-119
TWI567079B (zh) 2011-07-15 2017-01-21 健生醫藥公司 作為伽瑪分泌酶調節劑之新穎的經取代的吲哚衍生物
CA2850932A1 (en) 2011-10-04 2013-04-11 Janus Biotherapeutics, Inc. Novel imidazole quinoline-based immune system modulators
JP6184423B2 (ja) 2012-05-18 2017-08-23 大日本住友製薬株式会社 カルボン酸化合物
EP2738172A1 (en) 2012-11-28 2014-06-04 Almirall, S.A. New bicyclic compounds as crac channel modulators
SG10202103278TA (en) 2013-10-14 2021-04-29 Eisai R&D Man Co Ltd Selectively substituted quinoline compounds
EP3080124A1 (en) 2013-12-13 2016-10-19 Takeda Pharmaceutical Company Limited Pyrrolo[3,2-c]pyridine derivatives as tlr inhibitors
HRP20210927T1 (hr) 2014-08-15 2021-09-03 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Spojevi pirolopirimidina koje se koriste kao agonist tlr7
EP3183251A4 (en) 2014-08-22 2017-12-27 Janus Biotherapeutics, Inc. Novel n2, n4, n7, 6-tetrasubstituted pteridine-2,4,7-triamine and 2, 4, 6, 7-tetrasubstituted pteridine compounds and methods of synthesis and use thereof

Patent Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003512369A (ja) 1999-10-19 2003-04-02 メルク エンド カムパニー インコーポレーテッド チロシンキナーゼ阻害剤
JP2005524621A (ja) 2002-01-07 2005-08-18 エーザイ株式会社 デアザプリンおよびそれらの用途
JP2006526654A (ja) 2003-06-05 2006-11-24 メルク エンド カムパニー インコーポレーテッド 置換インドールおよび置換インドールの調製方法
JP2008534439A (ja) 2005-01-28 2008-08-28 メルク エンド カムパニー インコーポレーテッド チェックポイントキナーゼの阻害剤
WO2006113458A1 (en) 2005-04-15 2006-10-26 Bristol-Myers Squibb Company Heterocyclic inhibitors of protein arginine methyl transferases
JP2009526766A (ja) 2006-02-03 2009-07-23 メルク シャープ エンド ドーム リミテッド アルツハイマー病の治療のためのインダゾール誘導体
WO2009042092A1 (en) 2007-09-25 2009-04-02 Merck & Co., Inc. 2-aryl or heteroaryl indole derivatives
JP2012504133A (ja) 2008-09-26 2012-02-16 エーザイ・アール・アンド・ディー・マネジメント株式会社 ベンゾオキサゾール化合物および使用方法
JP2015523981A (ja) 2012-05-31 2015-08-20 エーザイ・アール・アンド・ディー・マネジメント株式会社 テトラヒドロピラゾロピリミジン化合物
WO2016151085A1 (en) 2015-03-24 2016-09-29 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. New toll-like receptor 9 antagonists
JP6995067B2 (ja) 2016-06-29 2022-01-14 ブリストル-マイヤーズ スクイブ カンパニー [1,2,4]トリアゾロ[1,5-a]ピリジニル置換インドール化合物
JP6995109B2 (ja) 2016-07-30 2022-01-14 ブリストル-マイヤーズ スクイブ カンパニー ジメトキシフェニル置換インドール化合物
JP7028861B2 (ja) 2016-09-09 2022-03-02 ブリストル-マイヤーズ スクイブ カンパニー ピリジル置換のインドール化合物
JP2020529436A (ja) 2017-08-04 2020-10-08 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company [1,2,4]トリアゾロ[4,3−a]ピリジニル置換のインドール化合物
JP7104775B2 (ja) 2017-08-04 2022-07-21 ブリストル-マイヤーズ スクイブ カンパニー Tlr7/8/9の阻害剤として有用な置換インドール化合物
JP2021503004A (ja) 2017-11-14 2021-02-04 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 置換インドール化合物

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Bioorganic & Medicinal Chemistry Letters,2006年,Vol.16, No.22,pp.5907-5912

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022532145A (ja) * 2019-05-09 2022-07-13 ブリストル-マイヤーズ スクイブ カンパニー 置換ベンズイミダゾロン化合物
JP7621275B2 (ja) 2019-05-09 2025-01-24 ブリストル-マイヤーズ スクイブ カンパニー 置換ベンズイミダゾロン化合物

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