JP2018524403A5 - - Google Patents

Download PDF

Info

Publication number
JP2018524403A5
JP2018524403A5 JP2018520047A JP2018520047A JP2018524403A5 JP 2018524403 A5 JP2018524403 A5 JP 2018524403A5 JP 2018520047 A JP2018520047 A JP 2018520047A JP 2018520047 A JP2018520047 A JP 2018520047A JP 2018524403 A5 JP2018524403 A5 JP 2018524403A5
Authority
JP
Japan
Prior art keywords
optionally substituted
alkyl
membered
substituted
compound according
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.)
Granted
Application number
JP2018520047A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018524403A (ja
JP6836589B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IB2016/054091 external-priority patent/WO2017006282A1/en
Publication of JP2018524403A publication Critical patent/JP2018524403A/ja
Publication of JP2018524403A5 publication Critical patent/JP2018524403A5/ja
Application granted granted Critical
Publication of JP6836589B2 publication Critical patent/JP6836589B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2018520047A 2015-07-08 2016-07-07 ヒダントインを含むデオキシウリジントリホスファターゼ阻害剤 Active JP6836589B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN740/KOL/2015 2015-07-08
IN740KO2015 2015-07-08
PCT/IB2016/054091 WO2017006282A1 (en) 2015-07-08 2016-07-07 Hydantoin containing deoxyuridine triphosphatase inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2020170594A Division JP7071044B2 (ja) 2015-07-08 2020-10-08 ヒダントインを含むデオキシウリジントリホスファターゼ阻害剤

Publications (3)

Publication Number Publication Date
JP2018524403A JP2018524403A (ja) 2018-08-30
JP2018524403A5 true JP2018524403A5 (cg-RX-API-DMAC7.html) 2019-08-22
JP6836589B2 JP6836589B2 (ja) 2021-03-03

Family

ID=56740270

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2018520047A Active JP6836589B2 (ja) 2015-07-08 2016-07-07 ヒダントインを含むデオキシウリジントリホスファターゼ阻害剤
JP2020170594A Active JP7071044B2 (ja) 2015-07-08 2020-10-08 ヒダントインを含むデオキシウリジントリホスファターゼ阻害剤

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2020170594A Active JP7071044B2 (ja) 2015-07-08 2020-10-08 ヒダントインを含むデオキシウリジントリホスファターゼ阻害剤

Country Status (16)

Country Link
US (6) US10570098B2 (cg-RX-API-DMAC7.html)
EP (1) EP3319939B1 (cg-RX-API-DMAC7.html)
JP (2) JP6836589B2 (cg-RX-API-DMAC7.html)
CN (1) CN107922330A (cg-RX-API-DMAC7.html)
AU (1) AU2016290987C1 (cg-RX-API-DMAC7.html)
CA (1) CA2991468C (cg-RX-API-DMAC7.html)
DK (1) DK3319939T3 (cg-RX-API-DMAC7.html)
EA (1) EA037990B1 (cg-RX-API-DMAC7.html)
ES (1) ES3016670T3 (cg-RX-API-DMAC7.html)
FI (1) FI3319939T3 (cg-RX-API-DMAC7.html)
HU (1) HUE070225T2 (cg-RX-API-DMAC7.html)
IL (1) IL256221B (cg-RX-API-DMAC7.html)
PL (1) PL3319939T3 (cg-RX-API-DMAC7.html)
PT (1) PT3319939T (cg-RX-API-DMAC7.html)
SI (1) SI3319939T1 (cg-RX-API-DMAC7.html)
WO (1) WO2017006282A1 (cg-RX-API-DMAC7.html)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6450323B2 (ja) 2013-01-07 2019-01-09 ユニバーシティ オブ サザン カリフォルニア デオキシウリジントリホスファターゼ阻害剤
WO2015103489A1 (en) 2014-01-03 2015-07-09 University Of Southern California Heteroatom containing deoxyuridine triphosphatase inhibitors
WO2017006271A1 (en) 2015-07-08 2017-01-12 University Of Southern California Deoxyuridine triphosphatase inhibitors containing amino sulfonyl linkage
HUE070225T2 (hu) 2015-07-08 2025-05-28 Cv6 Therapeutics Ni Ltd Hidantoint tartalmazó dezoxiuridin-trifoszfatáz gátlók
WO2017006270A1 (en) 2015-07-08 2017-01-12 University Of Southern California Deoxyuridine triphosphatase inhibitors
WO2017006283A1 (en) 2015-07-08 2017-01-12 Cv6 Therapeutics (Ni) Limited Deoxyuridine triphosphatase inhibitors containing cyclopropano linkage
JP7022702B2 (ja) 2016-05-23 2022-02-18 エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト 第二級アミド基を有するベンズアゼピンジカルボキサミド化合物
CN109153648B (zh) 2016-05-23 2022-07-22 豪夫迈·罗氏有限公司 具有叔酰胺官能团的苯并氮杂卓二甲酰胺化合物
EP3468963B1 (en) 2016-06-12 2021-10-27 F. Hoffmann-La Roche AG Dihydropyrimidinyl benzazepine carboxamide compounds
WO2018098206A1 (en) * 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Hydantoin containing deoxyuridine triphosphatase inhibitors
US11174271B2 (en) 2016-11-23 2021-11-16 Cv6 Therapeutics (Ni) Limited 6-membered uracil isosteres
WO2018098209A1 (en) * 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Amino sulfonyl compounds
WO2018098207A1 (en) * 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Hydantoin containing deoxyuridine triphosphatase inhibitors
WO2018098208A1 (en) * 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Nitrogen ring linked deoxyuridine triphosphatase inhibitors
WO2018128720A1 (en) 2017-01-05 2018-07-12 Cv6 Therapeutics (Ni) Limited Uracil containing compounds
BR112022026247A2 (pt) * 2020-06-26 2023-01-17 Cv6 Therapeutics Ni Ltd Método para aumentar a eficácia terapêutica de um agente de imunoterapia, método de tratamento de câncer e método de inibição do crescimento de uma célula de câncer
CN116323623B (zh) 2020-09-18 2025-09-26 拜耳公司 作为SOS1抑制剂的吡啶并[2,3-d]嘧啶-4-胺
EP4074317A1 (en) 2021-04-14 2022-10-19 Bayer AG Phosphorus derivatives as novel sos1 inhibitors
WO2023111996A1 (en) 2021-12-17 2023-06-22 Reglagene Holding, Inc. Compositions and methods of making and using small molecules in the treatment of cancer
US12215102B2 (en) 2023-02-28 2025-02-04 Reglagene, Inc. Compositions and methods for making and using small molecules for tubulin-targeted therapy in the treatment of cancers and related conditions
WO2025202022A1 (en) 2024-03-27 2025-10-02 Bayer Aktiengesellschaft Anticancer macrocyclic quinazoline-based inhibitors of the ineraction between ras and sos1

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US100720A (en) * 1870-03-15 Improve ment in cultivators
JPS4829785B1 (cg-RX-API-DMAC7.html) 1970-03-26 1973-09-13
BE787766A (fr) 1971-08-21 1973-02-19 Merck Patent Gmbh Imides d'acide glutarique et leur procede de preparation
US4063019A (en) * 1976-03-30 1977-12-13 E. R. Squibb & Sons, Inc. [[[(2,4-Dioxo-1-imidazolidinyl)amino]carbonyl]amino]-acetylcephalosporin derivatives
US4038271A (en) 1976-11-08 1977-07-26 E. R. Squibb & Sons, Inc. [[[(2,4-Dioxo-1-imidazolidinyl)amino]-carbonyl]amino]acetylpenicillin derivatives
US4304715A (en) * 1979-06-08 1981-12-08 Derek Hudson Enkephalin analogues
DE3027596A1 (de) 1980-07-21 1982-02-18 Bayer Ag, 5090 Leverkusen Triazolidin-3,5-dion-oxyalkylverbindungen und verfahren zu ihrer herstellung
JPS5839672A (ja) 1981-09-03 1983-03-08 Chugai Pharmaceut Co Ltd ウラシル誘導体
JPS60243017A (ja) 1984-05-16 1985-12-03 Kyowa Hakko Kogyo Co Ltd 抗けいれん組成物
JPH0674251B2 (ja) 1986-02-07 1994-09-21 全薬工業株式▲会▼社 ビス−ジオキソピペラジン誘導体
JPS63101361A (ja) 1986-09-08 1988-05-06 ブリティッシュ・テクノロジー・グループ・リミテッド ジオキソピペリジン誘導体を含有する不安解消組成物
FR2644786B1 (fr) 1989-03-21 1993-12-31 Adir Cie Nouveaux derives fluoro-4 benzoiques, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent
US5463063A (en) 1993-07-02 1995-10-31 Celgene Corporation Ring closure of N-phthaloylglutamines
US5599796A (en) 1993-12-02 1997-02-04 Emory University Treatment of urogenital cancer with boron neutron capture therapy
WO1996016079A2 (en) 1994-11-24 1996-05-30 Takeda Chemical Industries, Ltd Alpha-ketoamide derivatives as cathepsin l inhibitor
US5962246A (en) 1996-03-29 1999-10-05 The University Of Medicine And Dentistry Of New Jersey dUTPase, its isoforms, and diagnostic and other uses
JPH09286786A (ja) 1996-04-18 1997-11-04 Nippon Paper Ind Co Ltd ピリミジン誘導体及びその抗腫瘍剤としての用途
DK0927168T3 (da) * 1996-08-28 2003-03-10 Procter & Gamble 1,3-diheterocykliske metalloproteaseinhibitorer
DE19756212A1 (de) * 1997-12-17 1999-07-01 Klinge Co Chem Pharm Fab Neue, mit einem cyclischen Imid substituierte Pyridylalkan-, alken- und -alkincarbonsäureamide
JP4524039B2 (ja) 1997-12-18 2010-08-11 ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド Srcファミリーsh2ドメインインヒビターとしてのピリドン
CA2366264A1 (en) 1999-04-02 2000-10-12 Bristol-Myers Squibb Company Novel amide derivatives as inhibitors of matrix metalloproteinases, tnf-.alpha., and aggrecanase
DE10002509A1 (de) 2000-01-21 2001-07-26 Gruenenthal Gmbh Substituierte Glutarimide
RU2003127732A (ru) 2001-03-15 2005-03-20 Астразенека Аб (Se) Ингибиторы металлопротеиназ
JP2002284686A (ja) 2001-03-28 2002-10-03 Sankyo Co Ltd スルホンアミド化合物を含有する医薬組成物
CA2444148A1 (en) 2001-04-11 2002-10-24 Queen's University At Kingston Pyrimidine compounds as anti-ictogenic and/or anti-epileptogenic agents
US6822097B1 (en) 2002-02-07 2004-11-23 Amgen, Inc. Compounds and methods of uses
AU2003249812A1 (en) 2002-07-18 2004-02-09 Queen's University At Kingston Dihydrouracil compounds as anti-ictogenic or anti-epileptogenic agents
US7125865B2 (en) 2002-07-25 2006-10-24 Merck & Co., Inc. Therapeutic compounds for treating dyslipidemic conditions
GB0221246D0 (en) 2002-09-13 2002-10-23 Astrazeneca Ab Compounds
CA2523118C (en) 2003-04-21 2013-06-04 Rgb Networks, Inc. Wideband multi-channel quadrature amplitude modulation of cable television signals
GB0400290D0 (en) 2004-01-08 2004-02-11 Medivir Ab dUTPase inhibitors
ATE503746T1 (de) * 2004-08-03 2011-04-15 Chugai Pharmaceutical Co Ltd Neue imidazolidinderivate
CA2590939C (en) * 2004-12-17 2011-10-18 Amgen Inc. Aminopyrimidine compounds and methods of use
EP1848433A2 (en) 2005-01-25 2007-10-31 Celgene Corporation Methods and compositions using 4-amino-2-(3-methyl-2,6-dioxopiperidin-3-yl)-isoindole-1-3-dione
WO2006135763A2 (en) 2005-06-09 2006-12-21 The Johns Hopkins University Inhibitors of dna repair enzymes and methods of use thereof
US8693525B2 (en) 2006-07-14 2014-04-08 Qualcomm Incorporated Multi-carrier transmitter for wireless communication
EP2044037A2 (en) 2006-07-24 2009-04-08 Gilead Sciences, Inc. Hiv reverse transcriptase inhibitors
EP1939186A1 (en) 2006-12-22 2008-07-02 Sulfidris S.r.l. 5-Fluorouracil derivatives and their use for the treatment of cancer
US20090052556A1 (en) 2007-08-23 2009-02-26 Fernandez Andrew D Frequency interleaving method for wideband signal generation
NZ585789A (en) * 2007-12-10 2012-03-30 Novartis Ag Pyrazine-2-carboxamide derivatives to treat diseases mediated by blockade of the epithelial sodium channel
TWI466871B (zh) 2008-06-03 2015-01-01 Taiho Pharmaceutical Co Ltd 具羥尿苷三磷酸酶抑制活性之新穎尿嘧啶化合物或其鹽
WO2010025308A2 (en) 2008-08-27 2010-03-04 Universtiy Of Southern California Inhibitors of dutpase
JP2011231015A (ja) 2008-08-29 2011-11-17 Taiho Yakuhin Kogyo Kk 含窒素複素環を有する新規ウラシル化合物又はその塩
CN102333788A (zh) 2009-02-19 2012-01-25 诺沃—诺迪斯克有限公司 因子viii的修饰
FR2944524B1 (fr) * 2009-04-17 2012-11-30 Ipsen Pharma Sas Derives d'imidazolidine-2,4-dione et leur utilisation comme medicament
US8115662B2 (en) 2009-06-24 2012-02-14 Intersil Americas Inc. Sampler linearity by simultaneous derivative sampling
US8912329B2 (en) 2009-06-25 2014-12-16 BioVersys AG Composition for treatment of tuberculosis
JP2013032293A (ja) * 2009-11-30 2013-02-14 Taiho Yakuhin Kogyo Kk ヒトdUTPase阻害活性を有する5−フルオロウラシル化合物又はその塩
RU2548913C2 (ru) 2009-11-30 2015-04-20 Тайхо Фармасьютикал Ко., Лтд. Усилитель действия противоопухолевого средства
JP2011111433A (ja) * 2009-11-30 2011-06-09 Taiho Yakuhin Kogyo Kk ウレイド構造を有するウラシル化合物又はその塩
JP2013047189A (ja) * 2009-12-25 2013-03-07 Kyorin Pharmaceutical Co Ltd 新規パラバン酸誘導体及びそれらを有効成分とする医薬
GB201020032D0 (en) 2010-11-25 2011-01-12 Sigmoid Pharma Ltd Composition
ES2899000T3 (es) * 2011-07-18 2022-03-09 Merck Patent Gmbh Benzamidas
PE20141361A1 (es) 2011-11-15 2014-10-13 Takeda Pharmaceutical Compuesto heterociclico dihidroxi aromatico
US9030340B1 (en) 2012-09-05 2015-05-12 IQ-Analog Corporation N-path interleaving analog-to-digital converter (ADC) with background calibration
JP6450323B2 (ja) 2013-01-07 2019-01-09 ユニバーシティ オブ サザン カリフォルニア デオキシウリジントリホスファターゼ阻害剤
CN103435606A (zh) * 2013-08-22 2013-12-11 中国药科大学 CDK2与GSK3β双重抑制剂及用途
WO2015103489A1 (en) 2014-01-03 2015-07-09 University Of Southern California Heteroatom containing deoxyuridine triphosphatase inhibitors
US9525940B1 (en) 2014-03-05 2016-12-20 Cirrus Logic, Inc. Multi-path analog front end and analog-to-digital converter for a signal processing system
WO2015142001A2 (ko) 2014-03-21 2015-09-24 충남대학교산학협력단 강심 활성을 갖는 화합물 및 이를 함유하는 심부전 예방 또는 치료용 약학적 조성물
US20180110780A1 (en) 2015-04-30 2018-04-26 Taiho Pharmaceutical Co., Ltd. Agent for alleviating side effect of antitumor drug
US10259792B2 (en) 2015-05-01 2019-04-16 Taiho Pharmaceutical Co., Ltd. Crystal of uracil compound
HUE070225T2 (hu) 2015-07-08 2025-05-28 Cv6 Therapeutics Ni Ltd Hidantoint tartalmazó dezoxiuridin-trifoszfatáz gátlók
WO2017006283A1 (en) 2015-07-08 2017-01-12 Cv6 Therapeutics (Ni) Limited Deoxyuridine triphosphatase inhibitors containing cyclopropano linkage
WO2017006271A1 (en) 2015-07-08 2017-01-12 University Of Southern California Deoxyuridine triphosphatase inhibitors containing amino sulfonyl linkage
WO2017006270A1 (en) 2015-07-08 2017-01-12 University Of Southern California Deoxyuridine triphosphatase inhibitors
MA43590A (fr) 2016-01-08 2018-11-14 Taiho Pharmaceutical Co Ltd Agent antitumoral contenant un immunomodulateur et un amplificateur d'effet antitumoral
WO2018098209A1 (en) 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Amino sulfonyl compounds
WO2018098206A1 (en) 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Hydantoin containing deoxyuridine triphosphatase inhibitors
WO2018098208A1 (en) 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Nitrogen ring linked deoxyuridine triphosphatase inhibitors
US11174271B2 (en) 2016-11-23 2021-11-16 Cv6 Therapeutics (Ni) Limited 6-membered uracil isosteres
WO2018098207A1 (en) 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Hydantoin containing deoxyuridine triphosphatase inhibitors
WO2018128720A1 (en) 2017-01-05 2018-07-12 Cv6 Therapeutics (Ni) Limited Uracil containing compounds

Similar Documents

Publication Publication Date Title
JP2018524403A5 (cg-RX-API-DMAC7.html)
JP6806562B2 (ja) eIF2α経路の調節因子
RU2768827C2 (ru) Модуляторы хемокинового рецептора и их применение
RU2581834C1 (ru) Новое пиперидиновое соединение или его соль
US20220193242A1 (en) Immunophilin-dependent inhibitors and uses thereof
JP2022141811A5 (cg-RX-API-DMAC7.html)
IL277783B2 (en) Shp2 inhibitor compositions, methods for treating cancer and methods for identifying a subject with shp2 mutations
PT1940789E (pt) Métodos e compostos para preparar análogos cc-1065
JP2020517616A5 (cg-RX-API-DMAC7.html)
JP2008535902A5 (cg-RX-API-DMAC7.html)
JP2016053042A5 (cg-RX-API-DMAC7.html)
EP4473980A3 (en) Labeled inhibitors of prostate specific membrane antigen (psma), their use as imaging agents and pharmaceutical agents for the treatment of psma-expressing cancers
CN107001331A (zh) 作为bub1抑制剂的苄基取代的吲唑
RU2020102453A (ru) Фармацевтические композиции
EP3411046B1 (en) Rapaglutins, novel inhibitors of glut and use thereof
KR20210029165A (ko) 비아릴에테르형 퀴나졸린 유도체
JP2017535514A (ja) Bub1キナーゼ阻害薬としてのベンジル置換インダゾール類
JP2017502967A5 (cg-RX-API-DMAC7.html)
JP2017516859A (ja) 1,3,4−チアジアゾール化合物および癌を治療する際のその使用
JPWO2020028608A5 (cg-RX-API-DMAC7.html)
RU2017109355A (ru) Гетероциклические соединения и их применение
ES2759940T3 (es) Compuestos de 1,3,4-tiadiazol y su uso para tratar el cáncer
JP2017137323A (ja) 新規抗がん剤
EP4032890A1 (en) Heterocyclic amide compound, pharmaceutically acceptable salt thereof, and preparation method therefor and use thereof
US11739121B2 (en) EPHA2 agonists and uses thereof