JPWO2020179859A1 - - Google Patents
Info
- Publication number
- JPWO2020179859A1 JPWO2020179859A1 JP2021503643A JP2021503643A JPWO2020179859A1 JP WO2020179859 A1 JPWO2020179859 A1 JP WO2020179859A1 JP 2021503643 A JP2021503643 A JP 2021503643A JP 2021503643 A JP2021503643 A JP 2021503643A JP WO2020179859 A1 JPWO2020179859 A1 JP WO2020179859A1
- Authority
- JP
- Japan
- 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.)
- Granted
Links
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 true JPWO2020179859A1 (https=) | 2020-09-10 |
| JPWO2020179859A5 JPWO2020179859A5 (https=) | 2022-11-11 |
| JP7413346B2 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 (https=) |
| EP (1) | EP3936192B1 (https=) |
| JP (1) | JP7413346B2 (https=) |
| KR (1) | KR20210135521A (https=) |
| CN (1) | CN113543852A (https=) |
| TW (1) | TW202100526A (https=) |
| WO (1) | WO2020179859A1 (https=) |
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 |
| WO1999048880A1 (en) | 1998-03-23 | 1999-09-30 | 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 |
| MXPA03001848A (es) | 2000-08-31 | 2003-06-04 | Pfizer | Derivados de fenoxibencilamina como inhibidores de la reabsorcion de serotonina. |
| US7087579B2 (en) | 2001-02-26 | 2006-08-08 | Kissei Pharmaceutical Co., Ltd. | Glucopyranosyloxypyrazole derivatives and medicinal use thereof |
| DK1859798T3 (en) | 2001-03-29 | 2016-03-21 | Lilly Co Eli | N- (2-arylethyl) -BENZYLAMINER as antagonists of 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 |
| AU2003235447A1 (en) | 2002-05-31 | 2003-12-19 | Banyu Pharmaceutical Co., Ltd. | Method of substituent introduction through halogen-metal exchange reaction |
| ES2339112T3 (es) | 2002-08-21 | 2010-05-17 | BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG | 8-(3-amino-piperidin-1-il)-xantinas,su preparacion y su uso como medicamentos. |
| US20040110802A1 (en) | 2002-08-23 | 2004-06-10 | Atli Thorarensen | Antibacterial benzoic acid derivatives |
| EP1537074B1 (en) | 2002-09-04 | 2019-02-27 | Merck Canada Inc. | 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 |
| DK1836201T4 (da) | 2004-12-20 | 2013-11-11 | Genentech Inc | Pyrrolidininhibitorer af 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 |
| KR20080002832A (ko) | 2005-03-16 | 2008-01-04 | 얀센 파마슈티카 엔.브이. | 보체 매개성 질병 및 이상을 치료하기 위한 신규한 티오펜설폭시민 |
| TW200716104A (en) | 2005-06-01 | 2007-05-01 | Wyeth Corp | Tricyclic 6-alkylidene-penems as class-D β -lactamases inhibitors |
| EP1893588A1 (en) | 2005-06-10 | 2008-03-05 | Boehringer Ingelheim International GmbH | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| JP2009502783A (ja) | 2005-07-20 | 2009-01-29 | メルク エンド カムパニー インコーポレーテッド | 抗糖尿病性オキサゾリジンジオン及びチアゾリジンジオン |
| CA2619881A1 (en) | 2005-08-16 | 2007-02-22 | Genzyme Corporation | Chemokine receptor binding compounds |
| WO2007047397A2 (en) | 2005-10-13 | 2007-04-26 | Smithkline Beecham Corporation | Phenol ethers as modulators of the opioid receptors |
| WO2007061670A1 (en) | 2005-11-21 | 2007-05-31 | Amgen Inc. | Beta-secretase modulators and methods of use |
| CA2637312A1 (en) | 2006-01-27 | 2007-08-02 | F. Hoffmann-La Roche Ag | Use of substituted 2-imidazole of imidazoline derivatives |
| 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 |
| WO2007140005A2 (en) | 2006-05-26 | 2007-12-06 | Janssen Pharmaceutica N.V. | 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 |
| WO2008072726A1 (ja) | 2006-12-14 | 2008-06-19 | Taisho Pharmaceutical Co., Ltd. | 1-フェニル 1-チオ-d-グルシト-ル誘導体 |
| TW200843739A (en) | 2007-03-30 | 2008-11-16 | Shionogi & Co | Novel pyrrolinone derivative and composition containing the same |
| 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 |
| US20090227560A1 (en) | 2007-04-27 | 2009-09-10 | Takanobu Kuroita | Substituted imidazole compound and use thereof |
| 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 |
| CN101932577B (zh) | 2007-11-30 | 2013-07-17 | 拜耳知识产权有限责任公司 | 杂芳基取代的哌啶 |
| 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 |
| WO2009111676A2 (en) | 2008-03-06 | 2009-09-11 | Anacor Pharmaceuticals, Inc | Boron-containing small molecules as anti-inflammatory agents |
| EP2254415B1 (en) | 2008-02-19 | 2013-01-23 | Janssen Pharmaceutica, N.V. | Aryl-hydroxyethylamino-pyrimidines and triazines as modulators of fatty acid amide hydrolase |
| US8633245B2 (en) | 2008-04-11 | 2014-01-21 | Institute Of Medicinal Molecular Design, Inc. | PAI-1 inhibitor |
| EP2272817A4 (en) | 2008-04-11 | 2011-12-14 | Inst Med Molecular Design Inc | PAI-1 INHIBITORS |
| US20110053949A1 (en) | 2008-04-17 | 2011-03-03 | Pfizer Inc. | 4-[3-(aryloxy)benzylidene]-3-methyl piperidine aryl carboxamide compounds useful as faah inhibitors |
| WO2009129625A1 (en) | 2008-04-22 | 2009-10-29 | Merck Frosst Canada Ltd. | Novel substituted heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| MX2010012492A (es) | 2008-05-27 | 2010-12-21 | Astrazeneca Ab | Derivados de fenoxipiridinilamida y su uso en el tratamiento de estados de enfermedad mediados por fosfodiesterasa 4. |
| AU2009252615B2 (en) | 2008-05-29 | 2013-08-15 | Kowa Company, Ltd. | Substituted carbinol compound having cyclic linker |
| US8071807B2 (en) | 2008-07-03 | 2011-12-06 | Panmira Pharmaceuticals, Llc | Antagonists of prostaglandin D2 receptors |
| EP2318410A2 (en) | 2008-07-09 | 2011-05-11 | Envivo Pharmaceuticals, Inc. | New small-molecule pde-10 inhibitors |
| WO2010021680A2 (en) | 2008-08-19 | 2010-02-25 | Vitae Pharmaceuticals, Inc. | Inhibitors of beta-secretase |
| TW201016702A (en) | 2008-09-25 | 2010-05-01 | Shionogi & Co | Novel pyrrolinone derivative and pharmaceutical composition comprising the same |
| 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 |
| PE20120578A1 (es) | 2009-02-10 | 2012-06-17 | Abbott Lab | Agonistas y antagonistas del receptor de s1p5, y metodos de uso de los mismos |
| MY159575A (en) | 2009-04-02 | 2017-01-13 | Merck Serono Sa | Dihydroorotate dehydrogenase inhibitors |
| JP2012524800A (ja) | 2009-04-22 | 2012-10-18 | 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 | モノアシルグリセロールリパーゼ阻害剤としてのアゼチジニルジアミド |
| US8906914B2 (en) | 2009-08-18 | 2014-12-09 | Janssen Pharmaceutica Nv | Ethylene diamine modulators of fatty acid 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 |
| WO2011137024A1 (en) | 2010-04-26 | 2011-11-03 | Merck Sharp & Dohme Corp. | Novel spiropiperidine prolylcarboxypeptidase inhibitors |
| DE102010030688A1 (de) | 2010-06-30 | 2012-01-05 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Dicyanopyridine und ihre Verwendung |
| CN103249721B (zh) | 2010-10-18 | 2016-10-12 | 拉夸里亚创药株式会社 | 作为ttx-s阻滞剂的芳胺衍生物 |
| BR112013009828A2 (pt) | 2010-10-22 | 2016-07-26 | Janssen Pharmaceutica Nv | diamidas de amino-pirrolidina-azetidina como inibidores de monoacilglicerol lipase |
| 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 |
| AR087875A1 (es) | 2011-09-16 | 2014-04-23 | Actelion Pharmaceuticals Ltd | Proceso para la elaboracion de derivados de piridazina como intermediarios de sintesis de antibioticos |
| 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 |
| EP2780014A4 (en) | 2011-11-18 | 2015-07-01 | Constellation Pharmaceuticals Inc | 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 |
| MX360323B (es) | 2012-04-25 | 2018-10-29 | Raqualia Pharma Inc | Derivados de pirrolopiridinona como bloqueadores de ttx-s. |
| AR091023A1 (es) | 2012-05-11 | 2014-12-30 | Abbvie Inc | Inhibidores del nampt |
| 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 |
| TWI583670B (zh) | 2012-07-30 | 2017-05-21 | 大正製藥股份有限公司 | Partially saturated nitrogenous heterocyclic compounds |
| ES2661585T3 (es) | 2012-10-31 | 2018-04-02 | Raqualia Pharma Inc | Derivados de pirazolopiridina como bloqueadores de TTX-S |
| 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 |
| KR102214222B1 (ko) | 2013-07-10 | 2021-02-08 | 메이지 세이카 파루마 가부시키가이샤 | 신규 pde4 저해제 |
| EP2905282A1 (en) | 2014-02-05 | 2015-08-12 | AXXAM S.p.A. | Substituted thiazole or oxazole as P2X7 receptor antagonists |
| AP2016009465A0 (en) | 2014-04-01 | 2016-09-30 | Pfizer | Chromene and 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones as gamma-secretase modulators |
| WO2015160665A1 (en) | 2014-04-15 | 2015-10-22 | Dow Agrosciences Llc | Metalloenzyme inhibitor compounds as fungicides |
| WO2016019588A1 (en) | 2014-08-08 | 2016-02-11 | The Broad Institute, Inc. | Oxacazone compounds to treat clostridium difficile |
| EP3204351A1 (en) | 2014-10-08 | 2017-08-16 | Dow Global Technologies LLC | Method for coupling a fluorosulfonate compound with an amine compound |
| WO2016115282A1 (en) | 2015-01-13 | 2016-07-21 | 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 |
| EP3280709B1 (en) | 2015-04-10 | 2021-05-26 | FMC Corporation | Substituted cyclic amides as herbicides |
| ES2735924T3 (es) | 2015-04-17 | 2019-12-20 | Dow Agrosciences Llc | Moléculas que tienen utilidad plaguicida e intermediarios, composiciones y procesos, relacionados con ellas |
| WO2017069601A1 (en) | 2015-10-19 | 2017-04-27 | Latvian Institute Of Organic Synthesis | Substituted aminoalkylazoles as malarial aspartic protease inhibitors |
| US11319299B2 (en) | 2016-03-01 | 2022-05-03 | Propellon Therapeutics Inc. | Substituted carboxamides as 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 |
| EP3538523B1 (en) | 2016-11-08 | 2021-05-19 | Cancer Research Technology Limited | Pyrimidinone derivatives as cdc7 inhibitors |
-
2020
- 2020-03-05 WO PCT/JP2020/009357 patent/WO2020179859A1/ja not_active Ceased
- 2020-03-05 JP JP2021503643A patent/JP7413346B2/ja active Active
- 2020-03-05 TW TW109107195A patent/TW202100526A/zh unknown
- 2020-03-05 CN CN202080018933.7A patent/CN113543852A/zh active Pending
- 2020-03-05 KR KR1020217029321A patent/KR20210135521A/ko not_active Withdrawn
- 2020-03-05 US US17/436,500 patent/US12240855B2/en active Active
- 2020-03-05 EP EP20765620.8A patent/EP3936192B1/en active Active
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, vol. 139, JPN6020016114, 2017, pages 792 - 803, ISSN: 0005215321 * |
| ZHOU, D. ET AL.: "Small molecules inhibit ex vivo tumor growth in bone", BIOORGANIC & MEDICINAL CHEMISTRY, vol. 26(23-24), JPN6020016111, 2018, pages 6128 - 6134, ISSN: 0005215320 * |
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| EP3936192A1 (en) | 2022-01-12 |
| US20220185815A1 (en) | 2022-06-16 |
| KR20210135521A (ko) | 2021-11-15 |
| TW202100526A (zh) | 2021-01-01 |
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| EP3936192B1 (en) | 2025-04-09 |
| WO2020179859A1 (ja) | 2020-09-10 |
| CN113543852A (zh) | 2021-10-22 |
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