Evidence map›Paper›PMID 42801761›Full record

ArticleChemistry & biodiversity2026

Antifungal Activity of Hedychium spicatum Essential Oil Against Candidemia-Causing Candida tropicalis and Candida parapsilosis: In Vitro Evaluation and Computational Identification of Cis-γ-Bisabolene as a Putative CYP51-Binding Constituent.

Preeti Verma, Devesh Singh Baral, Rakesh Verma

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Article in Chemistry & biodiversity, 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Preeti VermaDepartment of Chemistry, PG College Kapkot, SSJ University, Almora, Uttarakhand, India.ORCID https://orcid.org/0009-0004-5499-7683
Devesh Singh BaralDepartment of Zoology, SSJ University, L.S.M. Campus, Pithoragarh, Uttarakhand, India.ORCID https://orcid.org/0009-0005-6149-8986
Rakesh VermaDepartment of Zoology, SSJ University, L.S.M. Campus, Pithoragarh, Uttarakhand, India.ORCID https://orcid.org/0009-0002-2891-419X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Candidiasis is caused by Candida parapsilosis and Candida tropicalis emerges due to antifungal resistance and limited therapies. We aim to assess the antifungal activity of Hedychium spicatum essential oil (HSEO), followed by computational analyses to identify potential lead phytochemicals, targeting lanosterol 14α-demethylase (CYP51), a key enzyme in ergosterol biosynthesis. GC-MS identified 29 phytoconstituents, with τ-cadinol (17.94%) as the major component. Disc diffusion demonstrated concentration-dependent antifungal activity against C. parapsilosis and C. tropicalis, with inhibition zones of 11.00 ± 0.53 and 10.40 ± 0.36 mm, respectively, at 100% (v/v). Homology models of CYP51 exhibited structural reliability based on Ramachandran and validation metrics. Molecular docking identified cis-γ-bisabolene with the lowest binding energies (-7.6 and -7.9 kcal/mol) against haem-free CYP51 models of C. parapsilosis and C. tropicalis, respectively, through hydrophobic interactions. ADMET predictions indicated favorable oral absorption, Lipinski compliance, minimal CYP450 inhibition risk, and no hepatotoxicity or mutagenicity. MD simulations confirmed stable complexes using RMSD, RMSF, Rg, and SASA profiles. MM-PBSA showed favorable binding energies of -6.02 and -8.05 kJ/mol compared to fluconazole (0.98 and 0.66 kJ/mol). DFT showed comparable HOMO-LUMO gaps (6.216 and 6.176 eV) and global hardness (3.108 and 3.088 eV). Overall, HSEO shows promising antifungal potential, with cis-γ-bisabolene as a lead candidate.

Indexed as

Antifungal AgentsCandida parapsilosisCandida tropicalisOils, VolatileSesquiterpenesSterol 14-DemethylaseCandidemiaDose-Response Relationship, DrugMicrobial Sensitivity TestsMolecular Docking SimulationMonocyclic SesquiterpenesStructure-Activity RelationshipAntifungal AgentsMonocyclic SesquiterpenesOils, VolatileSesquiterpenesSterol 14-DemethylaseCYP51 inhibitionergosterol biosynthesis pathwayessential oilHedychium spicatumzone of inhibition

Identifiers

PMID42801761
PMCPMC13616462

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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.