JP2020504754A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2020504754A5 JP2020504754A5 JP2019535843A JP2019535843A JP2020504754A5 JP 2020504754 A5 JP2020504754 A5 JP 2020504754A5 JP 2019535843 A JP2019535843 A JP 2019535843A JP 2019535843 A JP2019535843 A JP 2019535843A JP 2020504754 A5 JP2020504754 A5 JP 2020504754A5
- Authority
- JP
- Japan
- Prior art keywords
- carboxamide
- group
- amino
- ethyl
- oxoethyl
- 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
Links
- CQUNASYKUVRVAK-UHFFFAOYSA-N CC(CCOCCOCCOCCOCCNC)=O Chemical compound CC(CCOCCOCCOCCOCCNC)=O CQUNASYKUVRVAK-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662439600P | 2016-12-28 | 2016-12-28 | |
| US62/439,600 | 2016-12-28 | ||
| PCT/US2017/068686 WO2018125992A1 (en) | 2016-12-28 | 2017-12-28 | Functionalized nanoluc inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020504754A JP2020504754A (ja) | 2020-02-13 |
| JP2020504754A5 true JP2020504754A5 (enExample) | 2021-02-12 |
| JP7161475B2 JP7161475B2 (ja) | 2022-10-26 |
Family
ID=61007855
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019535843A Active JP7161475B2 (ja) | 2016-12-28 | 2017-12-28 | 官能化nanoluc阻害剤 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US10815247B2 (enExample) |
| EP (1) | EP3562823B1 (enExample) |
| JP (1) | JP7161475B2 (enExample) |
| WO (1) | WO2018125992A1 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3313846B1 (en) | 2015-06-25 | 2020-05-06 | Promega Corporation | Thienopyrrole compounds and uses thereof as inhibitors of oplophorus-derived luciferases |
| JP7161475B2 (ja) | 2016-12-28 | 2022-10-26 | プロメガ コーポレイション | 官能化nanoluc阻害剤 |
| US12181452B2 (en) | 2017-09-18 | 2024-12-31 | Waters Technologies Corporation | Use of vapor deposition coated flow paths for improved chromatography of metal interacting analytes |
| US12180581B2 (en) | 2017-09-18 | 2024-12-31 | Waters Technologies Corporation | Use of vapor deposition coated flow paths for improved chromatography of metal interacting analytes |
| US11709155B2 (en) | 2017-09-18 | 2023-07-25 | Waters Technologies Corporation | Use of vapor deposition coated flow paths for improved chromatography of metal interacting analytes |
| US11709156B2 (en) | 2017-09-18 | 2023-07-25 | Waters Technologies Corporation | Use of vapor deposition coated flow paths for improved analytical analysis |
| EP4140991B1 (en) * | 2018-06-01 | 2024-05-15 | Promega Corporation | Inhibitors of oplophorus luciferase-derived bioluminescent complexes |
| JP7653351B2 (ja) | 2018-08-23 | 2025-03-28 | プロメガ コーポレイション | セレンテラジン類似体 |
| TWI815954B (zh) | 2018-08-27 | 2023-09-21 | 日商住友製藥股份有限公司 | 光學活性氮雜雙環衍生物 |
| CN111848657B (zh) * | 2019-04-24 | 2021-12-31 | 中国科学院上海药物研究所 | 靶向酪氨酸激酶识别的可逆性荧光化合物及其制备方法和应用 |
| US11918936B2 (en) | 2020-01-17 | 2024-03-05 | Waters Technologies Corporation | Performance and dynamic range for oligonucleotide bioanalysis through reduction of non specific binding |
| WO2022064447A1 (en) | 2020-09-24 | 2022-03-31 | Waters Technologies Corporation | Chromatographic hardware improvements for the separation of reactive molecules |
| CN120051474A (zh) | 2022-10-14 | 2025-05-27 | 普罗美加公司 | 腔肠素类似物 |
| CN117451696A (zh) * | 2023-10-26 | 2024-01-26 | 重庆大学 | 多维时间分辨bret阵列传感器及其应用 |
| US20250206747A1 (en) | 2023-12-20 | 2025-06-26 | Promega Corporation | Coelenterazine analogues |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3828535A1 (de) | 1988-08-23 | 1990-03-08 | Basf Ag | Benzimidazol-2-carbonsaeureanilide, ihre verwendung als lichtschutzmittel fuer organisches material und mit diesen aniliden stabilisiertes organisches material |
| US5283179A (en) | 1990-09-10 | 1994-02-01 | Promega Corporation | Luciferase assay method |
| ES2122555T3 (es) * | 1994-02-22 | 1998-12-16 | Merrell Pharma Inc | Nuevos derivados indolicos utiles para tratar neoplasmas y trastornos relacionados con estrogenos. |
| US7268229B2 (en) | 2001-11-02 | 2007-09-11 | Promega Corporation | Compounds to co-localize luminophores with luminescent proteins |
| EP1314733A1 (en) | 2001-11-22 | 2003-05-28 | Aventis Pharma Deutschland GmbH | Indole-2-carboxamides as factor Xa inhibitors |
| MXPA06013250A (es) | 2004-05-14 | 2007-02-28 | Abbott Lab | Inhibidores de quinasa como agentes terapeuticos. |
| FR2897061B1 (fr) | 2006-02-03 | 2010-09-03 | Sanofi Aventis | Derives de n-heteroaryl-carboxamides tricycliques contenant un motif benzimidazole, leur preparation et leur application en therapeutique. |
| US20080248511A1 (en) | 2007-03-26 | 2008-10-09 | Promega Corporation | Methods to quench light from optical reactions |
| US8163910B2 (en) | 2007-10-03 | 2012-04-24 | Elitech Holding B.V. | Amide-substituted xanthene dyes |
| WO2010051048A1 (en) | 2008-02-20 | 2010-05-06 | The Wistar Institute | Microrna modulators and method for identifying and using the same |
| WO2010118208A1 (en) | 2009-04-09 | 2010-10-14 | Exelixis, Inc. | Benzoxazepin-4- (5h) -yl derivatives and their use to treat cancer |
| ES2795287T3 (es) | 2009-05-01 | 2020-11-23 | Promega Corp | Luciferasas de Oplophorus sintéticas con mayor emisión de luz |
| WO2011100359A1 (en) | 2010-02-09 | 2011-08-18 | Ironwood Pharmaceuticals, Inc. | Cannabinoid agonists |
| CN103443121B (zh) | 2010-11-02 | 2016-04-20 | 普罗梅加公司 | 新型腔肠素底物及其使用方法 |
| CA2815381C (en) | 2010-11-02 | 2019-03-19 | Promega Corporation | Coelenterazine derivatives and methods of using same |
| US9273343B2 (en) | 2011-09-02 | 2016-03-01 | Promega Corporation | Compounds and methods for assaying redox state of metabolically active cells and methods for measuring NAD(P)/NAD(P)H |
| EP2900833B1 (en) | 2012-09-26 | 2018-05-30 | Promega Corporation | Real-time monitoring |
| WO2015067302A1 (en) | 2013-11-05 | 2015-05-14 | Ecole Polytechnique Federale De Lausanne (Epfl) | Sensor molecules and uses thereof |
| US9790537B2 (en) * | 2014-01-29 | 2017-10-17 | Promega Corporation | Quinone-masked probes as labeling reagents for cell uptake measurements |
| EP3099691B1 (en) | 2014-01-29 | 2019-11-20 | Promega Corporation | Pro-substrates for live cell applications |
| JP6876002B2 (ja) | 2015-06-05 | 2021-05-26 | プロメガ コーポレイションPromega Corporation | 機能的要素を共有結合により係留させるための細胞透過性、細胞適合性、かつ開裂可能であるリンカー |
| EP3313846B1 (en) | 2015-06-25 | 2020-05-06 | Promega Corporation | Thienopyrrole compounds and uses thereof as inhibitors of oplophorus-derived luciferases |
| JP7161475B2 (ja) | 2016-12-28 | 2022-10-26 | プロメガ コーポレイション | 官能化nanoluc阻害剤 |
-
2017
- 2017-12-28 JP JP2019535843A patent/JP7161475B2/ja active Active
- 2017-12-28 WO PCT/US2017/068686 patent/WO2018125992A1/en not_active Ceased
- 2017-12-28 US US15/856,302 patent/US10815247B2/en active Active
- 2017-12-28 EP EP17832700.3A patent/EP3562823B1/en active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20190169158A1 (en) | Small Molecule Activators of Parkin Enzyme Function | |
| US10745393B2 (en) | Small molecular probes, processes and use thereof | |
| US20110065734A1 (en) | Novel bifunctional compounds which inhibit protein kinases and histone deacetylases | |
| JP7161475B2 (ja) | 官能化nanoluc阻害剤 | |
| JP6862368B2 (ja) | チエノピロール化合物、及びそのOplophorus由来ルシフェラーゼの阻害剤としての使用 | |
| JP2018524334A5 (enExample) | ||
| JP2017506622A5 (enExample) | ||
| PE20091849A1 (es) | Compuestos y composiciones como inhibidores de cinasa | |
| JP7850460B2 (ja) | ヘテロ環式カリンringユビキチンリガーゼ化合物及びその使用 | |
| CN107428690A (zh) | 可用于治疗癌症的突变idh1抑制剂 | |
| Heinrich et al. | Identification of methionine aminopeptidase-2 (MetAP-2) inhibitor M8891: a clinical compound for the treatment of cancer | |
| JP2019508496A (ja) | 癌の治療法のためのtaf1阻害剤 | |
| Roecker et al. | Kinesin spindle protein (KSP) inhibitors. Part 8: Design and synthesis of 1, 4-diaryl-4, 5-dihydropyrazoles as potent inhibitors of the mitotic kinesin KSP | |
| US20230147145A1 (en) | Novel tunable photoactivatable silicon rhodamine fluorophores | |
| Aristova et al. | Monomethine cyanine probes for visualization of cellular RNA by fluorescence microscopy | |
| WO2011041655A1 (en) | Quinazolin-4-amine derivatives; and methods of use | |
| CN109896997A (zh) | N-酰基苯胺类c-Met激酶抑制剂的制备方法及其用途 | |
| JP6933702B2 (ja) | Bcl−3阻害剤としての2−ベンゾイルアミノベンズアミド誘導体 | |
| Sardon et al. | Development and biological evaluation of a novel aurora A kinase inhibitor | |
| War et al. | Synthesis and DNA‐binding study of imidazole linked thiazolidinone derivatives | |
| Hamed et al. | 6‐Aryl and Heterocycle Quinazoline Derivatives as Potent EGFR Inhibitors with Improved Activity toward Gefitinib‐Sensitive and‐Resistant Tumor Cell Lines | |
| CA2805658C (en) | Combination therapy with mdm2 and egfr inhibitors | |
| WO2008157407A2 (en) | Thiadiazole, oxadiazole and triazole derivatives for treating leukemia | |
| Pinson et al. | Synthesis and pharmacological evaluation of 4-iminothiazolidinones for inhibition of PI3 kinase | |
| Zhou et al. | Small molecules inhibit STAT3 activation, autophagy, and cancer cell anchorage-independent growth |