Evidence map›Paper›PMID 36461627›Full record

ArticleChemistry, an Asian journal2023

9-Cyano-10-telluriumpyronin Derivatives as Red-light-activatable Raman Probes.

Minoru Kawatani, Spencer J Spratt, Hiroyoshi Fujioka, Jingwen Shou, Yoshihiro Misawa, Ryosuke Kojima, Yasuteru Urano, Yasuyuki Ozeki, Mako Kamiya

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Minoru KawataniDepartment of Life Science and Technology, Tokyo Institute of Technology, Kanagawa, 226-8501, Japan.ORCID http://orcid.org/0000-0002-0192-4366
Spencer J SprattDepartment of Electrical Engineering and Information Systems, The University of Tokyo, Tokyo, 113-8656, Japan.
Hiroyoshi FujiokaGraduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo, 113-0033, Japan.ORCID http://orcid.org/0000-0003-1904-0566
Jingwen ShouDepartment of Electrical Engineering and Information Systems, The University of Tokyo, Tokyo, 113-8656, Japan.ORCID http://orcid.org/0000-0003-4643-2119
Yoshihiro MisawaDepartment of Life Science and Technology, Tokyo Institute of Technology, Kanagawa, 226-8501, Japan.
Ryosuke KojimaGraduate School of Medicine, The University of Tokyo, Tokyo, 113-0033, Japan.ORCID http://orcid.org/0000-0002-3792-9222
Yasuteru UranoGraduate School of Medicine, The University of Tokyo, Tokyo, 113-0033, Japan.ORCID http://orcid.org/0000-0002-1220-6327
Yasuyuki OzekiDepartment of Electrical Engineering and Information Systems, The University of Tokyo, Tokyo, 113-8656, Japan.ORCID http://orcid.org/0000-0002-9004-0799
Mako KamiyaDepartment of Life Science and Technology, Tokyo Institute of Technology, Kanagawa, 226-8501, Japan.ORCID http://orcid.org/0000-0002-5592-1849

Funding

A. Advanced Research Networks JPMJCR1872Astellas Foundation for Research on Metabolic DisordersDaiichi Sankyo Foundation of Life ScienceJSPS KAKENHI JP19 J22546JSPS KAKENHI JP20H02650JSPS KAKENHI JP20H05725JSPS KAKENHI JPJSCCA20170007JSPS stipendMEXT JPMXS0118067246MEXT/JSPS KAKENHI JP19 K22242MEXT/JSPS KAKENHI JP20H05724MEXT/JSPS KAKENHI JP22H02193The Mitsubishi FoundationThe Naito Foundation
6 · The paper itself

Abstract

Photoactivatable fluorescence probes can track the dynamics of specific cells or biomolecules with high spatiotemporal resolution, but their broad absorption and emission peaks limit the number of wavelength windows that can be employed simultaneously. In contrast, the narrower peak width of Raman signals offers more scope for simultaneous discrimination of multiple targets, and therefore a palette of photoactivatable Raman probes would enable more comprehensive investigation of biological phenomena. Herein we report 9-cyano-10-telluriumpyronin (9CN-TeP) derivatives as photoactivatable Raman probes whose stimulated Raman scattering (SRS) intensity is enhanced by photooxidation of the tellurium atom. Modification to increase the stability of the oxidation product led to a julolidine-like derivative, 9CN-diMeJTeP, which is photo-oxidized at the tellurium atom by red light irradiation to afford a sufficiently stable oxidation product with strong electronic pre-resonance, resulting in a bathochromic shift of the absorption spectrum and increased SRS intensity.

Indexed as

LightTelluriumFluorescent DyesSpectrum Analysis, RamanFluorescent DyesTelluriumDyes/PigmentsPhotoactivationRaman spectroscopyStimulated Raman scatteringTellurium

Identifiers

PMID36461627
PMCPMC10107100

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.