JP2018525430A5 - - Google Patents

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Publication number
JP2018525430A5
JP2018525430A5 JP2018511057A JP2018511057A JP2018525430A5 JP 2018525430 A5 JP2018525430 A5 JP 2018525430A5 JP 2018511057 A JP2018511057 A JP 2018511057A JP 2018511057 A JP2018511057 A JP 2018511057A JP 2018525430 A5 JP2018525430 A5 JP 2018525430A5
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Japan
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aryl
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JP2018511057A
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English (en)
Japanese (ja)
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JP2018525430A (ja
JP7334041B2 (ja
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Priority claimed from PCT/NZ2016/050135 external-priority patent/WO2017034420A1/en
Publication of JP2018525430A publication Critical patent/JP2018525430A/ja
Publication of JP2018525430A5 publication Critical patent/JP2018525430A5/ja
Priority to JP2021182007A priority Critical patent/JP2022033753A/ja
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Publication of JP7334041B2 publication Critical patent/JP7334041B2/ja
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JP2018511057A 2015-08-27 2016-08-25 トリプトファンジオキシゲナーゼ(ido1及びtdo)の阻害剤及び治療におけるその使用 Active JP7334041B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2021182007A JP2022033753A (ja) 2015-08-27 2021-11-08 トリプトファンジオキシゲナーゼ(ido1及びtdo)の阻害剤及び治療におけるその使用

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
NZ711514 2015-08-27
NZ71151415 2015-08-27
PCT/NZ2016/050135 WO2017034420A1 (en) 2015-08-27 2016-08-25 Inhibitors of tryptophan dioxygenases (ido1 and tdo) and their use in therapy

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2021182007A Division JP2022033753A (ja) 2015-08-27 2021-11-08 トリプトファンジオキシゲナーゼ(ido1及びtdo)の阻害剤及び治療におけるその使用

Publications (3)

Publication Number Publication Date
JP2018525430A JP2018525430A (ja) 2018-09-06
JP2018525430A5 true JP2018525430A5 (https=) 2019-10-10
JP7334041B2 JP7334041B2 (ja) 2023-08-28

Family

ID=58100623

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2018511057A Active JP7334041B2 (ja) 2015-08-27 2016-08-25 トリプトファンジオキシゲナーゼ(ido1及びtdo)の阻害剤及び治療におけるその使用
JP2021182007A Pending JP2022033753A (ja) 2015-08-27 2021-11-08 トリプトファンジオキシゲナーゼ(ido1及びtdo)の阻害剤及び治療におけるその使用

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2021182007A Pending JP2022033753A (ja) 2015-08-27 2021-11-08 トリプトファンジオキシゲナーゼ(ido1及びtdo)の阻害剤及び治療におけるその使用

Country Status (9)

Country Link
US (2) US11414428B2 (https=)
EP (1) EP3350188B1 (https=)
JP (2) JP7334041B2 (https=)
KR (1) KR20180048798A (https=)
CN (1) CN108349997B (https=)
AU (2) AU2016312848A1 (https=)
CA (1) CA2996681C (https=)
WO (1) WO2017034420A1 (https=)
ZA (1) ZA201800787B (https=)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2996681C (en) * 2015-08-27 2024-04-09 Auckland Uniservices Limited Inhibitors of tryptophan dioxygenases (ido1 and tdo) and their use in therapy
WO2018223969A1 (zh) * 2017-06-05 2018-12-13 复旦大学 N-苄基色胺酮类衍生物作为色氨酸双加氧酶(tdo)抑制剂的用途
GB201809050D0 (en) 2018-06-01 2018-07-18 E Therapeutics Plc Modulators of tryptophan catabolism
CN112823036B (zh) * 2018-07-03 2024-11-08 艾福姆德尤股份有限公司 用于治疗与sting活性有关的疾病的化合物和组合物
TW202235073A (zh) 2021-01-08 2022-09-16 美商Ifm Due有限公司 用於治療與sting活性相關的病狀之化合物及組合物
WO2022184930A2 (en) 2021-03-05 2022-09-09 Universität Basel Compositions for the treatment of ebv associated diseases or conditions
EP4052705A1 (en) 2021-03-05 2022-09-07 Universität Basel Vizerektorat Forschung Compositions for the treatment of ebv associated diseases or conditions
JP2025507981A (ja) 2022-03-04 2025-03-21 アンティド セラピューティクス インターナショナル ソシエテ ア レスポンサビリテ リミティー トリプトファンジオキシゲナーゼ(ido1及びtdo)の二重阻害剤と療法におけるそれらの使用

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2001255410A1 (en) 2000-04-14 2001-10-30 Corvas International, Inc. Substituted hydrazinyl heteroaromatic inhibitors of thrombin
US20070197610A1 (en) 2004-03-16 2007-08-23 Janssen Pharmaceutica N.V. Benzisoxazoles
TW200633990A (en) 2004-11-18 2006-10-01 Takeda Pharmaceuticals Co Amide compound
DE102005018389A1 (de) 2005-04-20 2006-10-26 Sanofi-Aventis Deutschland Gmbh Azolderivate als Inhibitoren von Lipasen und Phospholipasen
DE102005038947A1 (de) * 2005-05-18 2006-11-30 Grünenthal GmbH Substituierte Benzo[d]isoxazol-3-yl-amin-Verbindungen und deren Verwendung in Arzneimitteln
DE102005026194A1 (de) 2005-06-06 2006-12-07 Grünenthal GmbH Substituierte N-Benzo[d]isoxazol-3-yl-amin-Derivate und deren Verwendung zur Herstellung von Arzneimitteln
JP5583592B2 (ja) 2007-11-30 2014-09-03 ニューリンク ジェネティクス コーポレイション Ido阻害剤
US8461159B2 (en) 2008-11-25 2013-06-11 Jannsen Pharmaceutica BV Heteroaryl-substituted urea modulators of fatty acid amide hydrolase
US8598356B2 (en) * 2008-11-25 2013-12-03 Janssen Pharmaceutica Nv Heteroaryl-substituted urea modulators of fatty acid amide hydrolase
BRPI1009428A2 (pt) 2009-03-10 2016-03-01 Gruenenthal Gmbh 3-aminoisoxazolopiridina substituída como moduladores de kcnq2/3
WO2011100614A1 (en) 2010-02-11 2011-08-18 Vanderbilt University BENZISOXAZOLES AND AZABENZISOXAZOLES AS mgluR4 ALLOSTERIC POTENTIATORS, COMPOSITIONS, AND METHODS OF TREATING NEUROLOGICAL DYSFUNCTION
PL2595995T3 (pl) 2010-07-22 2016-05-31 Basf Se Chwastobójcze izoksazolo[5,4-b]pirydyny
JP2015504889A (ja) 2012-01-12 2015-02-16 ビーエーエスエフ ソシエタス・ヨーロピアBasf Se 除草性イソオキサゾロ[5,4−b]ピリジン
PL220630B1 (pl) 2012-12-28 2015-11-30 Inst Immunologii I Terapii Doświadczalnej Pan Nowe sulfonamidowe pochodne izoksazolo[5,4-b]pirydyny o aktywności przeciwbakteryjnej, sposób ich wytwarzania oraz nowe zastosowanie 3-aminoizoksazolo[5,4-b]pirydyny
CN105209449B (zh) 2013-03-14 2019-02-01 库拉德夫制药私人有限公司 犬尿氨酸途径的抑制剂
WO2015082499A2 (en) 2013-12-03 2015-06-11 Iomet Pharma Ltd Pharmaceutical compound
AU2015302908B2 (en) * 2014-08-13 2020-02-13 Auckland Uniservices Limited Inhibitors of tryptophan dioxygenases (IDO1 and TDO) and their use in therapy
CA2996681C (en) * 2015-08-27 2024-04-09 Auckland Uniservices Limited Inhibitors of tryptophan dioxygenases (ido1 and tdo) and their use in therapy
RU2619120C1 (ru) 2016-06-06 2017-05-12 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Кубанский государственный аграрный университет" 5-Хлор-3-(3-хлорфенилкарбоксамидо)-4,6-диметилизоксазоло[5,4-b]пиридин в качестве антидота 2,4-Д на подсолнечнике

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