Evidence map›Paper›PMID 42397482›Full record

ArticlePhotochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology2026

Synthesis of tetrazole based donor-acceptor type fluorescent molecules and their interaction with transport protein bovine serum albumin.

Souvik Santra, Atanu Panja, Nikhil Guchhait

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Article in Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Souvik SantraDepartment of Chemistry, University of Calcutta, 92, A.P.C. Road, Kolkata, 700009, India.
Atanu PanjaDepartment of Chemistry, University of Calcutta, 92, A.P.C. Road, Kolkata, 700009, India.
Nikhil GuchhaitDepartment of Chemistry, University of Calcutta, 92, A.P.C. Road, Kolkata, 700009, India. nguchhait@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tetrazole derivatives are profoundly used in pharmaceutical and agricultural chemistry as their bioactivity is governed by the possible strong interaction with protein molecules. For this purpose, two tetrazole based donor-acceptor type fluorophores N, N-diphenyl-4-(1 H-tetrazol-5-yl)aniline (DPTA) and N-(4-(1 H-tetrazol-5-yl)phenyl)-N-(naphthalen-2-yl)naphthalen-2-amine (TPNNA) were synthesised and their detailed photophysical behaviour were explored using absorption, emission and fluorescence lifetime measurement in different polar medium. Structurally TPNNA is expected to be more non-polar than DPTA due to the presence of more hydrophobic units in the donor part. Both molecules show local and a polarity dependent charge transfer emission. Upon interaction with transport protein Bovine serum albumin (BSA), both molecules show a significant change in their emission behaviour, where DPTA shows a ratiometric change in the emission spectra and TPNNA shows a rapid blue shift (~ 38 nm) in the emission spectra. Stronger binding interaction of TPNNA than DPTA with BSA is reflected by the calculated binding constants of 1.25 × 10

Indexed as

Fluorescent DyesSerum Albumin, BovineTetrazolesAnimalsCattleMolecular Docking SimulationMolecular StructureProtein BindingSpectrometry, FluorescenceFluorescent DyesSerum Albumin, BovineTetrazolesBovine serum albuminFluorescenceInteractionMolecular dockingTetrazole derivatives

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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 Socratic graph.