JP2018515525A5 - - Google Patents
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- JP2018515525A5 JP2018515525A5 JP2017559003A JP2017559003A JP2018515525A5 JP 2018515525 A5 JP2018515525 A5 JP 2018515525A5 JP 2017559003 A JP2017559003 A JP 2017559003A JP 2017559003 A JP2017559003 A JP 2017559003A JP 2018515525 A5 JP2018515525 A5 JP 2018515525A5
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- JP
- Japan
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Links
- 0 CC(C)c1c(*)nn[n]1 Chemical compound CC(C)c1c(*)nn[n]1 0.000 description 25
- JPDPRXXLFYTTRV-UHFFFAOYSA-N CC(C)c1c(C)[o]nc1C Chemical compound CC(C)c1c(C)[o]nc1C JPDPRXXLFYTTRV-UHFFFAOYSA-N 0.000 description 4
- VTYLNNZBVOSGTA-UHFFFAOYSA-N CC(C)c([n](C)nn1)c1OC Chemical compound CC(C)c([n](C)nn1)c1OC VTYLNNZBVOSGTA-UHFFFAOYSA-N 0.000 description 3
- DWVFSQVBDSMYJA-UHFFFAOYSA-N CC(C)c([nH]nn1)c1OC Chemical compound CC(C)c([nH]nn1)c1OC DWVFSQVBDSMYJA-UHFFFAOYSA-N 0.000 description 2
- FMSYGTJKIDOBPH-UHFFFAOYSA-N CCc1c(C(C)C)[nH]nn1 Chemical compound CCc1c(C(C)C)[nH]nn1 FMSYGTJKIDOBPH-UHFFFAOYSA-N 0.000 description 2
- MRFNWSQNINZIIA-UHFFFAOYSA-O CC(C)C1=C(C)N(C)N[NH2+]1 Chemical compound CC(C)C1=C(C)N(C)N[NH2+]1 MRFNWSQNINZIIA-UHFFFAOYSA-O 0.000 description 1
- VSNWPYLQRCUJJC-UHFFFAOYSA-O CC(C)C1=C(C)N=N[NH2+]1 Chemical compound CC(C)C1=C(C)N=N[NH2+]1 VSNWPYLQRCUJJC-UHFFFAOYSA-O 0.000 description 1
- MMTJVWTXKUNWCZ-UHFFFAOYSA-N CC(C)c1c(C)nn[n]1C Chemical compound CC(C)c1c(C)nn[n]1C MMTJVWTXKUNWCZ-UHFFFAOYSA-N 0.000 description 1
- UJKAFNFFPBCHLA-UHFFFAOYSA-N CCC1=C(C(C)C)NNN1C Chemical compound CCC1=C(C(C)C)NNN1C UJKAFNFFPBCHLA-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562159991P | 2015-05-12 | 2015-05-12 | |
| US62/159,991 | 2015-05-12 | ||
| US15/150,492 | 2016-05-10 | ||
| US15/150,492 US9725449B2 (en) | 2015-05-12 | 2016-05-10 | Tricyclic compounds as anticancer agents |
| PCT/US2016/031707 WO2016183118A1 (en) | 2015-05-12 | 2016-05-11 | Tricyclic compounds as anticancer agents |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018515525A JP2018515525A (ja) | 2018-06-14 |
| JP2018515525A5 true JP2018515525A5 (2) | 2019-06-13 |
| JP6843767B2 JP6843767B2 (ja) | 2021-03-17 |
Family
ID=56117957
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017559003A Active JP6843767B2 (ja) | 2015-05-12 | 2016-05-11 | 抗がん剤としての三環式化合物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9725449B2 (2) |
| EP (1) | EP3294739B1 (2) |
| JP (1) | JP6843767B2 (2) |
| CN (1) | CN107709322B (2) |
| ES (1) | ES2746131T3 (2) |
| TW (1) | TW201713657A (2) |
| UY (1) | UY36677A (2) |
| WO (1) | WO2016183118A1 (2) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102238012B1 (ko) * | 2016-01-20 | 2021-04-09 | 닝보 웬다 파르마 테크놀로지 엘티디 | 브로모도메인 억제제인 카르볼린 유도체 |
| CN108770356A (zh) * | 2016-02-05 | 2018-11-06 | 正大天晴药业集团股份有限公司 | 溴区结构域蛋白抑制剂的三环类化合物及其制备、药物组合物和用途 |
| BR102018007822A2 (pt) | 2017-04-20 | 2018-11-06 | Gilead Sciences, Inc. | composto, métodos para inibir pd-1, pd-l1 e/ou interação de pd-1/pd-l1 e para tratamento de câncer, composição farmacêutica, e, kit para tratamento de ou prevenção de câncer ou uma doença ou condição |
| CN111356695B (zh) * | 2017-10-27 | 2022-12-30 | 北京加科思新药研发有限公司 | 新的三环化合物 |
| TWI707849B (zh) | 2018-02-13 | 2020-10-21 | 美商基利科學股份有限公司 | Pd‐1/pd‐l1抑制劑 |
| SG11202012819YA (en) * | 2018-06-25 | 2021-01-28 | Jacobio Pharmaceuticals Co Ltd | Tricyclic compounds |
| EP3820572B1 (en) | 2018-07-13 | 2023-08-16 | Gilead Sciences, Inc. | Pd-1/pd-l1 inhibitors |
| WO2020200284A1 (zh) * | 2019-04-04 | 2020-10-08 | 上海华汇拓医药科技有限公司 | 三环类化合物制备方法及其在医药领域的应用 |
| US10947253B2 (en) | 2019-08-05 | 2021-03-16 | Ankh Life Sciences Limited | Fused polycyclic dimers |
| EP4051663B1 (en) * | 2019-10-30 | 2024-02-21 | Janssen Sciences Ireland Unlimited Company | Synthesis of 3-nitro-n-(2,2,2-trifluoroethyl)-4-pyridinamine |
| US12129265B2 (en) | 2020-07-21 | 2024-10-29 | Ankh Life Sciences Limited | Therapeutic agents and uses thereof |
| CA3206066A1 (en) * | 2021-01-22 | 2022-07-28 | Jingrui Biopharma Co., Ltd. | Tricyclic compounds as anticancer agents |
| WO2024099441A1 (en) * | 2022-11-11 | 2024-05-16 | Jingrui Biopharma (Shandong) Co., Ltd. | Bromodomain and extra-terminal (bet) protein degrader |
| US12173005B1 (en) | 2023-12-21 | 2024-12-24 | King Faisal University | Pyrimido[1′,6′:1,5]pyrazolo[4,3-b][1,7]naphthyridine compounds as CK2 inhibitors |
Family Cites Families (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE504828C2 (sv) | 1990-04-11 | 1997-05-12 | Sandvik Ab | Hammaranordning där kolv och borrkrona har omvänd design relativt varandra vad gäller impedans |
| TWI309240B (en) | 2004-09-17 | 2009-05-01 | Hoffmann La Roche | Anti-ox40l antibodies |
| AU2006230099B2 (en) | 2005-03-25 | 2012-04-19 | Gitr, Inc. | GITR binding molecules and uses therefor |
| PL1879573T3 (pl) | 2005-05-10 | 2013-05-31 | Incyte Holdings Corp | Modulatory 2,3-dioksygenazy indoloaminy i sposoby ich zastosowania |
| CN104356236B (zh) | 2005-07-01 | 2020-07-03 | E.R.施贵宝&圣斯有限责任公司 | 抗程序性死亡配体1(pd-l1)的人单克隆抗体 |
| CA2634198C (en) | 2005-12-20 | 2014-06-03 | Incyte Corporation | N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase |
| US7696166B2 (en) | 2006-03-28 | 2010-04-13 | Albany Molecular Research, Inc. | Use of cyclosporin alkyne/alkene analogues for preventing or treating viral-induced disorders |
| CL2007002650A1 (es) | 2006-09-19 | 2008-02-08 | Incyte Corp | Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras. |
| ES2444574T3 (es) | 2006-09-19 | 2014-02-25 | Incyte Corporation | N-hidroxiamidinoheterociclos como moduladores de la indolamina 2,3-dioxigenasa |
| EP1987839A1 (en) | 2007-04-30 | 2008-11-05 | I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale | Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease |
| ES2776406T3 (es) | 2007-07-12 | 2020-07-30 | Gitr Inc | Terapias de combinación que emplean moléculas de enlazamiento a GITR |
| EP2044949A1 (en) | 2007-10-05 | 2009-04-08 | Immutep | Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response |
| 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 |
| BRPI0821209A2 (pt) * | 2007-12-19 | 2019-09-24 | Amgen Inc | composto, composição farmacêutica, métodos de tratar câncer, para reduzir o tamanho de tumor, para tratar distúrbios, e para reduzir metástase em um tumor. |
| AR072999A1 (es) | 2008-08-11 | 2010-10-06 | Medarex Inc | Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos |
| AU2009333580B2 (en) | 2008-12-09 | 2016-07-07 | Genentech, Inc. | Anti-PD-L1 antibodies and their use to enhance T-cell function |
| CA2743028A1 (en) | 2008-12-18 | 2010-07-15 | E. I. Dupont De Nemours And Company | Powder coating composition with new pigment |
| EP2473531A4 (en) | 2009-09-03 | 2013-05-01 | Merck Sharp & Dohme | Anti-gitr antibodies |
| US8722720B2 (en) | 2009-10-28 | 2014-05-13 | Newlink Genetics Corporation | Imidazole derivatives as IDO inhibitors |
| PH12012500881A1 (en) | 2009-12-10 | 2017-07-26 | Hoffmann La Roche | Antibodies binding preferentially human csf1r extracellular domain 4 and their use |
| JP5998060B2 (ja) | 2010-03-04 | 2016-09-28 | マクロジェニクス，インコーポレーテッド | Ｂ７−ｈ３と反応性のある抗体、その免疫学的に活性なフラグメントおよびその使用 |
| CN102918061B (zh) | 2010-03-05 | 2016-06-08 | 霍夫曼-拉罗奇有限公司 | 针对人csf-1r的抗体及其用途 |
| CA2789076C (en) | 2010-03-05 | 2017-11-21 | F. Hoffmann-La Roche Ag | Antibodies against human colony stimulating factor-1 receptor and uses thereof |
| MX378336B (es) | 2010-05-04 | 2025-03-10 | Five Prime Therapeutics Inc | Anticuerpos que se unen a factor estimulante de colonias 1 (csf1r). |
| PT2614082T (pt) | 2010-09-09 | 2018-12-03 | Pfizer | Moléculas de ligação a 4-1bb |
| US8580399B2 (en) | 2011-04-08 | 2013-11-12 | Universal Display Corporation | Substituted oligoazacarbazoles for light emitting diodes |
| NO2694640T3 (2) | 2011-04-15 | 2018-03-17 | ||
| KR101970025B1 (ko) | 2011-04-20 | 2019-04-17 | 메디뮨 엘엘씨 | Ｂ7-ｈ1 및 ｐｄ-1과 결합하는 항체 및 다른 분자들 |
| JP6012611B2 (ja) | 2011-09-28 | 2016-10-25 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子 |
| HRP20201595T1 (hr) | 2011-11-28 | 2020-12-11 | Merck Patent Gmbh | Anti-pd-l1 protutijela i njihova uporaba |
| BR112014012624A2 (pt) | 2011-12-15 | 2018-10-09 | F Hoffmann-La Roche Ag | anticorpos, composição farmacêutica, ácido nucleico, vetores de expressão, célula hospedeira, método para a produção de um anticorpo recombinante e uso do anticorpo |
| RU2014136332A (ru) | 2012-02-06 | 2016-03-27 | Дженентек, Инк. | Композиции и способы применения ингибиторов csf1r |
| AR090263A1 (es) | 2012-03-08 | 2014-10-29 | Hoffmann La Roche | Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma |
| EP2847220A1 (en) | 2012-05-11 | 2015-03-18 | Five Prime Therapeutics, Inc. | Methods of treating conditions with antibodies that bind colony stimulating factor 1 receptor (csf1r) |
| AR091649A1 (es) | 2012-07-02 | 2015-02-18 | Bristol Myers Squibb Co | Optimizacion de anticuerpos que se fijan al gen de activacion de linfocitos 3 (lag-3) y sus usos |
| CN107759690A (zh) | 2012-08-31 | 2018-03-06 | 戊瑞治疗有限公司 | 用结合群落刺激因子1受体(csf1r)的抗体治疗病状的方法 |
| UA115576C2 (uk) | 2012-12-06 | 2017-11-27 | Байєр Фарма Акцієнгезелльшафт | Похідні бензимідазолу як антагоністи ер4 |
| CN105189488B (zh) | 2013-02-27 | 2018-07-24 | 百时美施贵宝公司 | 用作溴区结构域抑制剂的咔唑化合物 |
| US9492460B2 (en) | 2013-02-27 | 2016-11-15 | Bristol-Myers Squibb Company | Carbazole compounds useful as bromodomain inhibitors |
| EP2970312B1 (en) | 2013-03-11 | 2017-11-15 | The Regents of The University of Michigan | Bet bromodomain inhibitors and therapeutic methods using the same |
| ES2857848T3 (es) | 2013-12-24 | 2021-09-29 | Bristol Myers Squibb Co | Compuestos tricíclicos como agentes antineoplásicos |
| US9458156B2 (en) | 2014-12-23 | 2016-10-04 | Bristol-Myers Squibb Company | Tricyclic compounds as anticancer agents |
| WO2015110263A1 (en) | 2014-01-21 | 2015-07-30 | Ac Immune Sa | Carbazole and carboline compounds for use in the diagnosis, treatment, alleviation or prevention of disorders associated with amyloid or amyolid-like proteins |
| US9580430B2 (en) | 2014-02-28 | 2017-02-28 | The Regents Of The University Of Michigan | 9H-pyrimido[4,5-B]indoles and related analogs as BET bromodomain inhibitors |
-
2016
- 2016-05-10 US US15/150,492 patent/US9725449B2/en active Active
- 2016-05-11 UY UY0001036677A patent/UY36677A/es unknown
- 2016-05-11 TW TW105114608A patent/TW201713657A/zh unknown
- 2016-05-11 WO PCT/US2016/031707 patent/WO2016183118A1/en not_active Ceased
- 2016-05-11 JP JP2017559003A patent/JP6843767B2/ja active Active
- 2016-05-11 CN CN201680039269.8A patent/CN107709322B/zh active Active
- 2016-05-11 ES ES16728765T patent/ES2746131T3/es active Active
- 2016-05-11 EP EP16728765.5A patent/EP3294739B1/en active Active
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