Evidence map›Paper›PMID 29323683›Full record

ArticleChemical communications (Cambridge, England)2018

Ru(ii) polypyridyl complexes as photocages for bioactive compounds containing nitriles and aromatic heterocycles.

Ao Li, Claudia Turro, Jeremy J Kodanko

Abstract read
In one paragraph

Article in Chemical communications (Cambridge, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. UV photo-uncaging of Ru(II)-polypyridyl bioconjugates in high vacuum.Physical chemistry chemical physics : PCCP · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. RuBi-Ruxolitinib: A Photoreleasable Antitumor JAK Inhibitor.Journal of the American Chemical Society · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Not AllInorganic chemistry · 2022
    Article
  14. Article
  15. Article
  16. Using photocaging for fast time-resolved structural biology studies.Acta crystallographica. Section D, Structural biology · 2021
    Review
  17. Review
  18. Ruthenium-based PACT agents based on bisquinoline chelates: synthesis, photochemistry, and cytotoxicity.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2021
    Article
  19. Article
  20. Review
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

3 authors.

Ao LiDepartment of Chemistry, Wayne State University, 5101 Cass Ave, Detroit, Michigan 48202, USA. jkodanko@chem.wayne.edu.
Claudia Turro
Jeremy J Kodanko

Funding

Light Activation of Enzyme InhibitionR01EB016072 · NIBIB · WAYNE STATE UNIVERSITY · PI KODANKO, JEREMY · 2013 to 2016
$1.5M
Structure and Function of Cytochrome P450 17A1R01GM102505 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI AUBE, JEFFREY, SCOTT, EMILY E · 2012 to 2015
$1.2M
NIBIB NIH HHS R01 EB016072NIGMS NIH HHS R01 GM102505
6 · The paper itself

Abstract

Photocaging allows for precise spatiotemporal control over the release of biologically active compounds with light. Most photocaged molecules employ organic photolabile protecting groups; however, biologically active compounds often contain functionalities such as nitriles and aromatic heterocycles that cannot be caged with organic groups. Despite their prevalence, only a few studies have reported successful caging of nitriles and aromatic heterocycles. Recently, Ru(ii)-based photocaging has emerged as a powerful method for the release of bioactive molecules containing these functional groups, in many cases providing high levels of spatial and temporal control over biological activity. This Feature Article discusses recent developments in applying Ru(ii)-based photocaging towards biological problems. Our groups designed and synthesized Ru(ii)-based platforms for the photoinduced delivery of cysteine protease and cytochrome P450 inhibitors in order to achieve selective control over enzyme inhibition. We also reported Ru(ii) photocaging groups derived from higher-denticity ancillary ligands that possess photophysical and photochemical properties distinct from more traditional Ru(ii)-based caging groups. In addition, for the first time, we are able to rapidly synthesize and screen Ru(ii) polypyridyl complexes that elicit desired properties by solid-phase synthesis. Finally, our work also defined steric and orbital mixing effects that are important factors in controlling photoinduced ligand exchange.

Indexed as

Drug LiberationCathepsinsCell Line, TumorCoordination ComplexesCysteine Proteinase InhibitorsCytochrome P-450 Enzyme InhibitorsHumansLightMolecular StructureNitrilesPyridinesRutheniumSteroid 17-alpha-HydroxylaseCathepsinsCoordination ComplexesCYP17A1 protein, humanCysteine Proteinase InhibitorsCytochrome P-450 Enzyme InhibitorsNitrilesPyridinesRutheniumSteroid 17-alpha-Hydroxylase

Identifiers

PMID29323683
PMCPMC5904840

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Registered trials

None linked

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.