JP2014534261A5 - - Google Patents

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Publication number
JP2014534261A5
JP2014534261A5 JP2014543546A JP2014543546A JP2014534261A5 JP 2014534261 A5 JP2014534261 A5 JP 2014534261A5 JP 2014543546 A JP2014543546 A JP 2014543546A JP 2014543546 A JP2014543546 A JP 2014543546A JP 2014534261 A5 JP2014534261 A5 JP 2014534261A5
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Japan
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alkyl
independently
aryl
heteroaryl
ring
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JP2014543546A
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English (en)
Japanese (ja)
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JP2014534261A (ja
JP6522339B2 (ja
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Priority claimed from PCT/US2012/066139 external-priority patent/WO2013078244A1/en
Publication of JP2014534261A publication Critical patent/JP2014534261A/ja
Publication of JP2014534261A5 publication Critical patent/JP2014534261A5/ja
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JP2014543546A 2011-11-21 2012-11-20 カルボキシxローダミン類似体 Active JP6522339B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161562021P 2011-11-21 2011-11-21
US61/562,021 2011-11-21
PCT/US2012/066139 WO2013078244A1 (en) 2011-11-21 2012-11-20 Carboxy x rhodamine analogs

Related Child Applications (2)

Application Number Title Priority Date Filing Date
JP2017183422A Division JP6574821B2 (ja) 2011-11-21 2017-09-25 カルボキシxローダミン類似体
JP2018213096A Division JP7227741B2 (ja) 2011-11-21 2018-11-13 カルボキシxローダミン類似体

Publications (3)

Publication Number Publication Date
JP2014534261A JP2014534261A (ja) 2014-12-18
JP2014534261A5 true JP2014534261A5 (enExample) 2017-11-16
JP6522339B2 JP6522339B2 (ja) 2019-05-29

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Family Applications (4)

Application Number Title Priority Date Filing Date
JP2014543546A Active JP6522339B2 (ja) 2011-11-21 2012-11-20 カルボキシxローダミン類似体
JP2017183422A Active JP6574821B2 (ja) 2011-11-21 2017-09-25 カルボキシxローダミン類似体
JP2018213096A Active JP7227741B2 (ja) 2011-11-21 2018-11-13 カルボキシxローダミン類似体
JP2020209163A Pending JP2021063089A (ja) 2011-11-21 2020-12-17 カルボキシxローダミン類似体

Family Applications After (3)

Application Number Title Priority Date Filing Date
JP2017183422A Active JP6574821B2 (ja) 2011-11-21 2017-09-25 カルボキシxローダミン類似体
JP2018213096A Active JP7227741B2 (ja) 2011-11-21 2018-11-13 カルボキシxローダミン類似体
JP2020209163A Pending JP2021063089A (ja) 2011-11-21 2020-12-17 カルボキシxローダミン類似体

Country Status (4)

Country Link
US (3) US9056885B2 (enExample)
EP (1) EP2782916B1 (enExample)
JP (4) JP6522339B2 (enExample)
WO (1) WO2013078244A1 (enExample)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2626703B1 (en) * 2008-03-27 2017-05-03 Promega Corporation Protein labeling with cyanobenzothiazole conjugates
WO2013078244A1 (en) * 2011-11-21 2013-05-30 Promega Corporation Carboxy x rhodamine analogs
EP2900833B1 (en) * 2012-09-26 2018-05-30 Promega Corporation Real-time monitoring
US10067149B2 (en) 2012-12-12 2018-09-04 Promega Corporation Recognition of cellular target binding by a bioactive agent using intracellular bioluminescence resonance energy transfer
US10024862B2 (en) * 2012-12-12 2018-07-17 Promega Corporation Recognition of cellular target binding by a bioactive agent using intracellular bioluminescence resonance energy transfer
US11072812B2 (en) 2013-03-15 2021-07-27 Promega Corporation Substrates for covalent tethering of proteins to functional groups or solid surfaces
WO2014152298A1 (en) 2013-03-15 2014-09-25 Promega Corporation New silicon and germanium dyes for use in genetic identity
WO2014145458A1 (en) 2013-03-15 2014-09-18 Arizona Board Of Regents On Behalf Of Arizona State University Nucleic acid-tagged compositions and methods for multiplexed protein-protein interaction profiling
EP3502693A1 (en) * 2014-05-16 2019-06-26 Life Technologies Corporation Cell tracking reagents and their methods of use
JP6802841B2 (ja) 2015-10-02 2020-12-23 プロメガ コーポレイションPromega Corporation ローダミン色素の合成方法
JP7200102B2 (ja) * 2016-11-01 2023-01-06 プロメガ コーポレイション エネルギー受容体に係留されたセレンテラジン類縁体
EP3548492B1 (en) 2016-12-01 2023-07-05 Promega Corporation Cell impermeable coelenterazine analogues
JP7161760B2 (ja) 2017-02-03 2022-10-27 国立大学法人東北大学 複素環化合物
EP3788048A1 (en) 2018-05-01 2021-03-10 Promega Corporation Coelenterazine compounds as nanoluc suicide substrates
WO2019232225A1 (en) 2018-05-30 2019-12-05 Promega Corporation Broad-spectrum kinase binding agents
EP3807419A4 (en) 2018-06-12 2022-09-07 Promega Corporation MULTIPLE LUCIFERASE
WO2020113036A2 (en) 2018-11-28 2020-06-04 Promega Corporation Reactive peptide labeling
KR20210104125A (ko) * 2018-12-20 2021-08-24 라이프 테크놀로지스 코포레이션 비대칭 로다민 염료 및 생물학적 분석에서의 그 용도
US11913944B2 (en) 2019-03-20 2024-02-27 Promega Corporation Photoaffinity probes
IL293204B1 (en) 2019-11-27 2026-08-01 Promega Corp Multipartite luciferase peptides and polypeptides
WO2021119149A1 (en) 2019-12-10 2021-06-17 Promega Corporation Compositions and methods for bioluminescent detection using multifunctional probes
WO2022047186A1 (en) 2020-08-28 2022-03-03 Promega Corporation Target engagement assay for ras proteins
US20220195518A1 (en) * 2020-12-22 2022-06-23 Illumina Cambridge Limited Methods and compositions for nucleic acid sequencing
EP4337646A4 (en) 2021-05-13 2025-05-21 Promega Corporation BIOLUMINESCENT DETECTION OF DNA SYNTHESIS
WO2024263837A2 (en) * 2023-06-22 2024-12-26 Promega Corporation Compounds and methods of use thereof for assessing target engagement for dna polymerase theta

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES258418A1 (es) * 1959-05-28 1960-11-16 Geigy Ag J R Procedimiento para la prepaarcion de nuevos derivados de iminodibencilo
US5171534A (en) 1984-01-16 1992-12-15 California Institute Of Technology Automated DNA sequencing technique
CA1340806C (en) 1986-07-02 1999-11-02 James Merrill Prober Method, system and reagents for dna sequencing
US4900686A (en) 1987-04-02 1990-02-13 Polaroid Corporation Fluorescent conjugates and biological diagnostic assay
US4965349A (en) * 1987-12-24 1990-10-23 Applied Biosystems, Inc. Method of synthesizing oligonucleotides labeled with ammonia-labile groups on solid phase supports
US4997928A (en) 1988-09-15 1991-03-05 E. I. Du Pont De Nemours And Company Fluorescent reagents for the preparation of 5'-tagged oligonucleotides
US5304644A (en) * 1992-04-15 1994-04-19 G. D. Searle & Co. 1-,2-,3-,4-,5-,6-,7-,8- and/or 9 substituted dibenzoxazepine compounds, pharmaceutical compositions and methods for treating pain
DE69324494T2 (de) 1992-09-03 1999-09-23 The Perkin-Elmer Corp., Foster City 4,7-dichlorofluoroszein-farbestoffe als molekulare sonden
US5658751A (en) 1993-04-13 1997-08-19 Molecular Probes, Inc. Substituted unsymmetrical cyanine dyes with selected permeability
US6080852A (en) * 1996-06-27 2000-06-27 The Perkin-Elmer Corporation 4,7-dichlororhodamine dyes
US5936087A (en) * 1997-11-25 1999-08-10 The Perkin-Elmer Corporation Dibenzorhodamine dyes
US6583168B1 (en) 1997-11-25 2003-06-24 Applera Corporation Sulfonated diarylrhodamine dyes
WO2000007992A1 (en) * 1998-08-04 2000-02-17 Toray Industries, Inc. Fused benzene heterocycle derivatives and utilization thereof
US6403860B1 (en) 1999-03-25 2002-06-11 Pioneer Hi-Bred International, Inc. Ku80 homologue and uses thereof
US6248884B1 (en) * 1999-06-03 2001-06-19 The Perkin-Elmer Corporation Extended rhodamine compounds useful as fluorescent labels
WO2003034987A2 (en) 2001-10-19 2003-05-01 Merck & Co., Inc. Androgen receptor modulators and methods of use thereof
TW200305423A (en) 2002-02-14 2003-11-01 Ono Pharmaceutical Co N-carbamoyl nitrogen-containing condensed ring compound and medicament containing same as active ingredient
KR20050109934A (ko) 2003-01-31 2005-11-22 프로메가 코포레이션 관능기의 단백질로의 공유 테더링
CA2526579A1 (en) 2003-05-23 2004-12-02 Epfl-Ecole Polytechnique Federale De Lausanne Methods for protein labeling based on acyl carrier protein
US7667024B2 (en) 2003-11-19 2010-02-23 Allelogic Biosciences Corp. Oligonucleotides labeled with a plurality of fluorophores
EP1882688A1 (en) 2006-07-25 2008-01-30 EPFL Ecole Polytechnique Fédérale de Lausanne Labelling of fusion proteins with synthetic probes
CN101184082B (zh) 2006-11-17 2011-04-20 华为技术有限公司 群组用户注册方法、状态更新方法、处理装置、ims网络实体和通信系统
EP2626703B1 (en) 2008-03-27 2017-05-03 Promega Corporation Protein labeling with cyanobenzothiazole conjugates
EP2298731A4 (en) 2008-06-25 2011-09-21 Takeda Pharmaceutical AMIDE COMPOUND
ES2795287T3 (es) 2009-05-01 2020-11-23 Promega Corp Luciferasas de Oplophorus sintéticas con mayor emisión de luz
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
WO2013078244A1 (en) 2011-11-21 2013-05-30 Promega Corporation Carboxy x rhodamine analogs
CN104853767B (zh) * 2012-12-12 2017-04-05 普洛麦格公司 用于捕获生物活性剂的细胞标靶的组合物和方法

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