ArticleInternational journal of molecular sciences2026
Rational Design of Conjugated Phenylpropanoid-Polyene Hybrids: Density Functional Theory Insights into Antiradical and Optical Properties.
Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A structural analysis of phenylpropanoids demonstrates that the benzene ring and the propenoic fragment act as two largely independent π-electron systems. This distinctive feature provides a theoretical basis for the rational design of novel compounds obtained through the structural integration of phenylpropanoids with polyene aldehydes and acids. These classes may be combined by elongating the carbon backbone via iterative vinyl group extension, thereby generating an expanded conjugated double-bond system. Alternatively, the structure of polyene aldehydes may be modified by replacing the unreactive methyl group with a benzene ring bearing suitable functional substituents. DFT computational studies performed at the B3LYP/QZVP level of theory indicate that the designed analogs predominantly scavenge radicals through the sequential proton loss electron transfer (SPLET) mechanism in aqueous environments. This pathway involves the initial deprotonation of carboxyl, aldehyde, or phenolic groups, with the hydroxyl moiety exhibiting the greatest propensity for proton dissociation. Carbon chain extension exerts only a minor influence on proton affinity (PA) values but significantly affects electron transfer enthalpy (ETE) parameters. Consequently, increasing the number of conjugated double bonds enhances activation of the second step of the SPLET mechanism, thereby improving overall radical-scavenging activity. Comparison of the calculated chemical reactivity parameters substantiates the conclusions drawn from the thermodynamic analysis. A pronounced enhancement in the reactivity of the modeled compounds, relative to the parent constituents, is observed. Time-dependent density functional theory (TD-DFT) calculations further predict absorption in the visible region, indicating potential applications of the modeled compounds as radical-scavenging dyes in food, pharmaceutical, cosmetic, and dietary supplement formulations.
Indexed as
Identifiers
What Socratic holds
Registered trials
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.