JP7413346B2 - ピロロピラゾール誘導体 - Google Patents
ピロロピラゾール誘導体 Download PDFInfo
- Publication number
- JP7413346B2 JP7413346B2 JP2021503643A JP2021503643A JP7413346B2 JP 7413346 B2 JP7413346 B2 JP 7413346B2 JP 2021503643 A JP2021503643 A JP 2021503643A JP 2021503643 A JP2021503643 A JP 2021503643A JP 7413346 B2 JP7413346 B2 JP 7413346B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- phenyl
- trifluoromethyl
- cancer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2019040649 | 2019-03-06 | ||
| JP2019040649 | 2019-03-06 | ||
| PCT/JP2020/009357 WO2020179859A1 (ja) | 2019-03-06 | 2020-03-05 | ピロロピラゾール誘導体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPWO2020179859A1 JPWO2020179859A1 (enExample) | 2020-09-10 |
| JPWO2020179859A5 JPWO2020179859A5 (enExample) | 2022-11-11 |
| JP7413346B2 true JP7413346B2 (ja) | 2024-01-15 |
Family
ID=72338358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021503643A Active JP7413346B2 (ja) | 2019-03-06 | 2020-03-05 | ピロロピラゾール誘導体 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US12240855B2 (enExample) |
| EP (1) | EP3936192B1 (enExample) |
| JP (1) | JP7413346B2 (enExample) |
| KR (1) | KR20210135521A (enExample) |
| CN (1) | CN113543852A (enExample) |
| TW (1) | TW202100526A (enExample) |
| WO (1) | WO2020179859A1 (enExample) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2022080305A1 (ja) * | 2020-10-13 | 2022-04-21 | 第一三共株式会社 | 抗ptdss2抗体 |
| CN114426466B (zh) * | 2020-10-29 | 2023-11-21 | 江苏和成新材料有限公司 | 一种醇羟基供体与活性氢供体进行光延反应的方法 |
| US12350241B1 (en) | 2024-04-29 | 2025-07-08 | Imam Mohammad Ibn Saud Islamic University | Method for inhibiting proliferation of cancer cells |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012046030A2 (en) | 2010-10-07 | 2012-04-12 | Riotech Pharmaceuticals Ltd | Phosphodiesterase inhibitors |
| CN104876936A (zh) | 2015-05-25 | 2015-09-02 | 中国人民解放军第二军医大学 | 吡咯酮并吡唑类化合物的制备及作为药物的用途 |
| WO2016148115A1 (ja) | 2015-03-16 | 2016-09-22 | 第一三共株式会社 | ホスファチジルセリンシンターゼ1阻害剤への応答性を予測する方法 |
Family Cites Families (101)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0395144A (ja) | 1989-08-04 | 1991-04-19 | Ono Pharmaceut Co Ltd | アミノフェノール誘導体の製造方法 |
| JPH1129540A (ja) | 1997-07-04 | 1999-02-02 | Showa Kako Kk | エステル誘導体の製造方法 |
| AU2852199A (en) | 1998-03-23 | 1999-10-18 | Asahi Kasei Kogyo Kabushiki Kaisha | Benzothiazolone-7-sulfonamide derivatives |
| US6316474B1 (en) | 1999-10-29 | 2001-11-13 | Merck & Co., Inc. | 2-benzyl and 2-heteroaryl benzimidazole NMDA/NR2B antagonists |
| HN2001000008A (es) | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo |
| GB0007884D0 (en) | 2000-03-31 | 2000-05-17 | Pfizer Ltd | Diphenyl ether compounds useful in therapy |
| JP2004507523A (ja) | 2000-08-31 | 2004-03-11 | ファイザー・インク | 選択的セロトニン再取込み阻害剤としてのフェノキシベンジルアミン誘導体 |
| DE60230591D1 (de) | 2001-02-26 | 2009-02-12 | Kissei Pharmaceutical | Glykopyranosyloxypyrazolderivate und deren medizinische verwendung |
| CA2442114C (en) | 2001-03-29 | 2011-06-21 | Eli Lilly And Company | N-(2-arylethyl)benzylamines as antagonists of the 5-ht6 receptor |
| GB0109103D0 (en) | 2001-04-11 | 2001-05-30 | Pfizer Ltd | Novel compounds |
| JP2003321406A (ja) | 2002-04-30 | 2003-11-11 | Mitsubishi Gas Chem Co Inc | 高純度フルオロアルキルベンゼン誘導体及びその製造法 |
| US20040132708A1 (en) | 2002-05-01 | 2004-07-08 | Wyeth | Process for preparing 6-alkylidene penem derivatives |
| US20050104233A1 (en) | 2002-05-31 | 2005-05-19 | Shinji Kato | Method of substituent introduction through halogen-metal exchange reaction |
| KR101150449B1 (ko) | 2002-08-21 | 2012-06-01 | 베링거 잉겔하임 파르마 게엠베하 운트 코 카게 | 8-[3-아미노-피페리딘-1-일]-크산틴, 이의 제조방법 및 이를 포함하는 약제학적 조성물 |
| US20040110802A1 (en) | 2002-08-23 | 2004-06-10 | Atli Thorarensen | Antibacterial benzoic acid derivatives |
| CA2495939A1 (en) | 2002-09-04 | 2004-03-18 | Merck Frosst Canada & Co./Merck Frosst Canada & Cie | Cathepsin cysteine protease inhibitors |
| US7256218B2 (en) | 2002-11-22 | 2007-08-14 | Jacobus Pharmaceutical Company, Inc. | Biguanide and dihydrotriazine derivatives |
| TW200615273A (en) | 2004-11-10 | 2006-05-16 | Nicholas Piramal India Ltd | Fused tricyclic compounds as inhibitors of tumor necrosis factor-alpha |
| ATE477254T1 (de) | 2004-12-20 | 2010-08-15 | Genentech Inc | Pyrrolidine als inhibitoren von iap |
| JP4794873B2 (ja) | 2005-03-03 | 2011-10-19 | 富士フイルムファインケミカルズ株式会社 | ハロゲン−リチウム交換反応を用いる有機化合物の製造法 |
| AU2006227778A1 (en) | 2005-03-16 | 2006-09-28 | Janssen Pharmaceutica N.V. | Novel thiophene sulfoximines for treating complement-mediated diseases and conditions |
| TW200716104A (en) | 2005-06-01 | 2007-05-01 | Wyeth Corp | Tricyclic 6-alkylidene-penems as class-D β -lactamases inhibitors |
| NZ564696A (en) | 2005-06-10 | 2011-05-27 | Boehringer Ingelheim Int | Glucocorticoid, indazole, mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| US20090069385A1 (en) | 2005-07-20 | 2009-03-12 | Meinke Peter T | Antidiabetic Oxazolidinediones and Thiazolidinediones |
| JP2009504769A (ja) | 2005-08-16 | 2009-02-05 | ジェンザイム・コーポレーション | ケモカイン受容体結合化合物 |
| CN101331120A (zh) | 2005-10-13 | 2008-12-24 | 史密丝克莱恩比彻姆公司 | 作为阿片样物质受体调节剂的酚醚化合物 |
| AU2006316620B2 (en) | 2005-11-21 | 2011-03-03 | Amgen Inc. | Beta-secretase modulators and methods of use |
| KR20080080410A (ko) | 2006-01-27 | 2008-09-03 | 에프. 호프만-라 로슈 아게 | 이미다졸린 유도체의 치환된 2-이미다졸의 용도 |
| US7745477B2 (en) | 2006-02-07 | 2010-06-29 | Hoffman-La Roche Inc. | Heteroaryl and benzyl amide compounds |
| CA2644368A1 (en) | 2006-03-10 | 2007-09-20 | Ono Pharmaceutical Co., Ltd. | Nitrogenated heterocyclic derivative, and pharmaceutical agent comprising the derivative as active ingredient |
| US20100292266A1 (en) | 2006-05-26 | 2010-11-18 | Richard Apodaca | Oxazolyl Piperidine Modulators of Fatty Acid Amide Hydrolase |
| ATE520651T1 (de) | 2006-10-23 | 2011-09-15 | Pfizer | Substituierte phenylmethylbicyclocarbonsäureamidverbindungen |
| AU2007326395B2 (en) | 2006-12-01 | 2012-10-11 | Msd K.K. | Novel phenyl-isoxazol-3-ol derivative |
| RU2009126767A (ru) | 2006-12-14 | 2011-01-20 | Тайсо Фармасьютикал Ко., Лтд. (Jp) | Производное 1-фенил-1-тио-d-глюцитола |
| CN101679246A (zh) | 2007-03-30 | 2010-03-24 | 盐野义制药株式会社 | 新型吡咯啉酮衍生物以及包含其的药物组合物 |
| US20090227560A1 (en) | 2007-04-27 | 2009-09-10 | Takanobu Kuroita | Substituted imidazole compound and use thereof |
| TW200841879A (en) | 2007-04-27 | 2008-11-01 | Eisai R&D Man Co Ltd | Pyridine derivatives substituted by heterocyclic ring and phosphonoamino group, and anti-fungal agent containing same |
| WO2008147544A1 (en) | 2007-05-25 | 2008-12-04 | Amgen Inc. | Substituted hydroxyethyl amine compounds as beta-secretase modulators and methods of use |
| WO2009004430A1 (en) | 2007-06-29 | 2009-01-08 | Pfizer Inc. | N-benzyl oxazolidinones and related heterocycleic compounds as potentiators of glutamate receptors |
| WO2009051956A2 (en) | 2007-10-16 | 2009-04-23 | E. I. Du Pont De Nemours And Company | Pyrazole-substituted isoxazoline insecticides |
| WO2009058921A1 (en) | 2007-10-31 | 2009-05-07 | Smithkline Beecham Corporation | Ccr5 antagonists as therapeutic agents |
| JP2009120553A (ja) | 2007-11-16 | 2009-06-04 | Taisho Pharmaceutical Co Ltd | C−フェニルグルシト−ル化合物を有効成分とする糖尿病治療剤 |
| DE502008003324D1 (de) | 2007-11-30 | 2011-06-01 | Bayer Schering Pharma Ag | Heteroaryl-substituierte piperidine |
| US8134001B2 (en) | 2007-12-14 | 2012-03-13 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| JP2009155212A (ja) | 2007-12-25 | 2009-07-16 | Taisho Pharmaceutical Co Ltd | C−フェニル1−チオグルシト−ル化合物を有効成分とする糖尿病治療剤 |
| CA2714743C (en) | 2008-02-19 | 2017-01-17 | Janssen Pharmaceutica N.V. | Aryl-hydroxyethylamino-pyrimidines and triazines as modulators of fatty acid amide hydrolase |
| EP2187893A4 (en) | 2008-03-06 | 2012-02-22 | Anacor Pharmaceuticals Inc | SMALL BORON-CONTAINING MOLECULES AS ANTI-INFLAMMATORY AGENTS |
| US8633245B2 (en) | 2008-04-11 | 2014-01-21 | Institute Of Medicinal Molecular Design, Inc. | PAI-1 inhibitor |
| KR20100132073A (ko) | 2008-04-11 | 2010-12-16 | 가부시키가이샤 이야쿠 분지 셋케이 겐쿠쇼 | Pai―1 저해제 |
| US20110053949A1 (en) | 2008-04-17 | 2011-03-03 | Pfizer Inc. | 4-[3-(aryloxy)benzylidene]-3-methyl piperidine aryl carboxamide compounds useful as faah inhibitors |
| CA2720654A1 (en) | 2008-04-22 | 2009-10-29 | Merck Frosst Canada Ltd. | Novel substituted heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| SI2297106T1 (sl) | 2008-05-27 | 2014-09-30 | Astrazeneca Ab | Fenoksipiridinilamid derivati in njih uporaba pri zdravljenju PDE4 posredovanih bolezenskih stanj |
| US8153634B2 (en) | 2008-05-29 | 2012-04-10 | Kowa Company, Ltd. | Carbinol derivatives having cyclic linker |
| WO2010003120A2 (en) | 2008-07-03 | 2010-01-07 | Amira Pharmaceuticals, Inc. | Antagonists of prostaglandin d2 receptors |
| US8481532B2 (en) | 2008-07-09 | 2013-07-09 | Envivo Pharmaceuticals, Inc. | PDE-10 inhibitors |
| WO2010021680A2 (en) | 2008-08-19 | 2010-02-25 | Vitae Pharmaceuticals, Inc. | Inhibitors of beta-secretase |
| WO2010035727A1 (ja) | 2008-09-25 | 2010-04-01 | 塩野義製薬株式会社 | 新規ピロリノン誘導体およびそれを含有する医薬組成物 |
| WO2010123599A2 (en) | 2009-01-23 | 2010-10-28 | The Board Of Trustees Of The University Of Illinois | Anti-bacterial compositions and methods including targeting virulence factors of staphylococcus aureus |
| WO2010093704A1 (en) | 2009-02-10 | 2010-08-19 | Abbott Laboratories | Agonists and antagonists of the s1p5 receptor, and methods of uses thereof |
| WO2010115736A2 (en) | 2009-04-02 | 2010-10-14 | Merck Serono S.A. | Dihydroorotate dehydrogenase inhibitors |
| RU2549547C2 (ru) | 2009-04-22 | 2015-04-27 | Янссен Фармацевтика Нв | Азетидинилдиамиды в качестве ингибиторов моноацилглицерин-липазы |
| WO2011022348A1 (en) | 2009-08-18 | 2011-02-24 | Janssen Pharmaceutica Nv | Ethylene diamine modulators of fatty acid amide hydrolase |
| WO2011023753A1 (en) | 2009-08-27 | 2011-03-03 | Glaxo Group Limited | Benzoxazine derivatives as glycine transport inhibitors |
| TW201139406A (en) | 2010-01-14 | 2011-11-16 | Glaxo Group Ltd | Voltage-gated sodium channel blockers |
| US8785634B2 (en) | 2010-04-26 | 2014-07-22 | Merck Sharp & Dohme Corp | Spiropiperidine prolylcarboxypeptidase inhibitors |
| DE102010030688A1 (de) | 2010-06-30 | 2012-01-05 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Dicyanopyridine und ihre Verwendung |
| RU2535671C1 (ru) | 2010-10-18 | 2014-12-20 | Раквалиа Фарма Инк. | Производные ариламидов в качестве блокаторов ttx-s |
| KR20130140020A (ko) | 2010-10-22 | 2013-12-23 | 얀센 파마슈티카 엔.브이. | 모노아실글리세롤 리파아제 억제제로서의 아미노-피롤리딘-아제티딘 다이아미드 |
| TWI396678B (zh) | 2010-12-07 | 2013-05-21 | Nat Univ Tsing Hua | 二級醇製備方法 |
| WO2012093174A1 (en) | 2011-01-07 | 2012-07-12 | Vivalis | 1-(6-membered azo-heterocyclic)-2,5-dihydro-1h-pyrrol-2-one derivatives as anti-hepatitis c virus, the pharmaceutical composition thereof and their therapeutic use |
| US8592426B2 (en) | 2011-01-24 | 2013-11-26 | Hoffmann—La Roche Inc. | Aryl-benzocycloalkyl amide derivatives |
| FR2973487B1 (fr) | 2011-03-31 | 2018-01-26 | L'air Liquide, Societe Anonyme Pour L'etude Et L'exploitation Des Procedes Georges Claude | Procede et appareil de production d'un gaz de l'air sous pression par distillation cryogenique |
| US9051333B2 (en) | 2011-04-15 | 2015-06-09 | Otsuka Pharmaceutical Co., Ltd. | 6,7-dihydroimidazo [2,1-b] [1,3]oxazine bactericides |
| EP2520556A1 (en) | 2011-05-03 | 2012-11-07 | Bayer Pharma Aktiengesellschaft | Radiolabeled amino acids for diagnostic imaging |
| GB201113689D0 (en) | 2011-08-09 | 2011-09-21 | Amakem Nv | Novel PDE4 inhibitors |
| WO2013038374A1 (en) | 2011-09-16 | 2013-03-21 | Actelion Pharmaceuticals Ltd | Process for manufacturing a synthetic intermediate |
| GB201118334D0 (en) | 2011-10-24 | 2011-12-07 | Biotica Tech Ltd | Novel dosage form |
| WO2013067302A1 (en) | 2011-11-04 | 2013-05-10 | Glaxosmithkline Intellectual Property (No. 2) Limited | Method of treatment |
| WO2013075083A1 (en) | 2011-11-18 | 2013-05-23 | Constellation Pharmaceuticals | Modulators of methyl modifying enzymes, compositions and uses thereof |
| US8791091B2 (en) | 2011-12-02 | 2014-07-29 | Bristol-Myers Squibb Company | Aryl dihydropyridinone and piperidinone MGAT2 inhibitors |
| ES2645984T3 (es) | 2012-04-25 | 2017-12-11 | Raqualia Pharma Inc | Derivados de pirrolopiridinona como bloqueadores de TTX-S |
| US8975398B2 (en) | 2012-05-11 | 2015-03-10 | Abbvie Inc. | NAMPT inhibitors |
| TWI585088B (zh) | 2012-06-04 | 2017-06-01 | 第一三共股份有限公司 | 作爲激酶抑制劑之咪唑并[1,2-b]嗒衍生物 |
| AU2013297601B2 (en) | 2012-07-30 | 2017-02-16 | Taisho Pharmaceutical Co., Ltd. | Partially saturated nitrogen-containing heterocyclic compound |
| BR112015009738A8 (pt) | 2012-10-31 | 2019-09-17 | Raqualia Pharma Inc | composto , uso do referido composto no tratamento de uma condição ou distúrbio em que bloqueadores de canal ttx-s, composição farmacêutica contendo o referido composto e processo para preparar a referida composição |
| JP2016028016A (ja) | 2012-12-12 | 2016-02-25 | 大日本住友製薬株式会社 | オキサジアゾール誘導体とその医薬用途 |
| US9834521B2 (en) | 2013-03-15 | 2017-12-05 | Ariad Pharmaceuticals, Inc. | Choline kinase inhibitors |
| CN105431427B (zh) | 2013-07-10 | 2017-12-08 | 明治制果药业株式会社 | 新型pde4 抑制剂 |
| EP2905282A1 (en) | 2014-02-05 | 2015-08-12 | AXXAM S.p.A. | Substituted thiazole or oxazole as P2X7 receptor antagonists |
| WO2015150957A1 (en) | 2014-04-01 | 2015-10-08 | Pfizer Inc. | Chromene and 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones as gamma-secretase modulators |
| CN106231901A (zh) | 2014-04-15 | 2016-12-14 | 美国陶氏益农公司 | 作为杀真菌剂的金属酶抑制剂化合物 |
| WO2016019588A1 (en) | 2014-08-08 | 2016-02-11 | The Broad Institute, Inc. | Oxacazone compounds to treat clostridium difficile |
| US20170210695A1 (en) | 2014-10-08 | 2017-07-27 | Dow Global Technologies Llc | Method for coupling a first compound to a second compound |
| US9980945B2 (en) | 2015-01-13 | 2018-05-29 | Vanderbilt University | Benzoisoxazole-substituted compounds as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
| CN105837576B (zh) | 2015-01-14 | 2019-03-26 | 湖北生物医药产业技术研究院有限公司 | Btk抑制剂 |
| AU2016246410B2 (en) | 2015-04-10 | 2020-11-05 | Fmc Corporation | Substituted cyclic amides as herbicides |
| US9795140B2 (en) | 2015-04-17 | 2017-10-24 | Dow Agrosciences Llc | Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto |
| CA2988391C (en) | 2015-10-19 | 2023-05-09 | Latvian Institute Of Organic Synthesis | Substituted aminoalkylazoles as malarial aspartic protease inhibitors |
| AU2017226004B2 (en) | 2016-03-01 | 2021-07-22 | Propellon Therapeutics Inc. | Inhibitors of WDR5 protein-protein binding |
| WO2017197555A1 (en) | 2016-05-16 | 2017-11-23 | Merck Sharp & Dohme Corp. | Fused pyrazine derivatives useful as soluble guanylate cyclase stimulators |
| JP7071383B2 (ja) | 2016-11-08 | 2022-05-18 | キャンサー・リサーチ・テクノロジー・リミテッド | cdc7阻害剤としてのピリミジノン誘導体 |
-
2020
- 2020-03-05 WO PCT/JP2020/009357 patent/WO2020179859A1/ja not_active Ceased
- 2020-03-05 TW TW109107195A patent/TW202100526A/zh unknown
- 2020-03-05 EP EP20765620.8A patent/EP3936192B1/en active Active
- 2020-03-05 US US17/436,500 patent/US12240855B2/en active Active
- 2020-03-05 JP JP2021503643A patent/JP7413346B2/ja active Active
- 2020-03-05 KR KR1020217029321A patent/KR20210135521A/ko not_active Withdrawn
- 2020-03-05 CN CN202080018933.7A patent/CN113543852A/zh active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012046030A2 (en) | 2010-10-07 | 2012-04-12 | Riotech Pharmaceuticals Ltd | Phosphodiesterase inhibitors |
| WO2016148115A1 (ja) | 2015-03-16 | 2016-09-22 | 第一三共株式会社 | ホスファチジルセリンシンターゼ1阻害剤への応答性を予測する方法 |
| CN104876936A (zh) | 2015-05-25 | 2015-09-02 | 中国人民解放军第二军医大学 | 吡咯酮并吡唑类化合物的制备及作为药物的用途 |
Non-Patent Citations (2)
| Title |
|---|
| MANGIATORDI, G. F. et al.,Novel chemotypes targeting tubulin at the colchicine binding site and unbiasing P-glycoprotein,European Journal of Medicinal Chemistry,2017年,139,pp. 792-803,DOI 10.1016/j.ejmech.2017.07.037 |
| ZHOU, D. et al.,Small molecules inhibit ex vivo tumor growth in bone,Bioorganic & Medicinal Chemistry,2018年,26(23-24),pp. 6128-6134,DOI 10.1016/j.bmc.2018.11.025 |
Also Published As
| Publication number | Publication date |
|---|---|
| US12240855B2 (en) | 2025-03-04 |
| EP3936192A1 (en) | 2022-01-12 |
| JPWO2020179859A1 (enExample) | 2020-09-10 |
| CN113543852A (zh) | 2021-10-22 |
| EP3936192B1 (en) | 2025-04-09 |
| US20220185815A1 (en) | 2022-06-16 |
| EP3936192A4 (en) | 2022-11-16 |
| KR20210135521A (ko) | 2021-11-15 |
| WO2020179859A1 (ja) | 2020-09-10 |
| TW202100526A (zh) | 2021-01-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US12077530B2 (en) | Chemical compounds | |
| AU2018211495B2 (en) | Estrogen receptor modulators | |
| JP7413346B2 (ja) | ピロロピラゾール誘導体 | |
| HK40061019A (en) | Pyrrolopyrazole derivative | |
| CA3050337C (en) | 1,3,4,9-tetrahydro-2h-pyrido[3,4-b]indole compounds as estrogen receptor modulators | |
| HK40026812A (en) | 6,7,8,9-tetrahydro-3h-pyrazolo[4,3-f]isoquinoline derivatives useful in the treatment of cancer | |
| HK40007252A (en) | Estrogen receptor modulators | |
| HK40007252B (en) | Estrogen receptor modulators | |
| EA038160B1 (ru) | Модуляторы рецептора эстрогена | |
| HK40002601B (en) | 6,7,8,9-tetrahydro-3h-pyrazolo[4,3-f]isoquinoline derivative useful in the treatment of cancer | |
| HK40002601A (en) | 6,7,8,9-tetrahydro-3h-pyrazolo[4,3-f]isoquinoline derivative useful in the treatment of cancer | |
| EA037533B1 (ru) | 6,7,8,9-ТЕТРАГИДРО-3H-ПИРАЗОЛО[4,3-f]ИЗОХИНОЛИНОВЫЕ ПРОИЗВОДНЫЕ, ПРИМЕНИМЫЕ В ЛЕЧЕНИИ РАКА |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A821 Effective date: 20210521 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20221101 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20221101 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20231211 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20231227 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 7413346 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |