Evidence map›Paper›PMID 42855938›Full record

ArticleChemistry & biodiversity2026

Phytochemical Fingerprinting of Sanchezia nobilis Hook. F. Leaf Extract and Evaluation of Anxiolytic, Cytotoxic, and Antioxidant Activities In Vivo, In Vitro, and In Silico.

Progga Paramita Paul, Musfiqur Rahman Sakib, Pritam Kundu, Dabashis Chakraborty, Tasnim Fatema, Shahriar Hossen, Ahsan Abid, Trina Mitra, Manik Chandra Shill, Utpal Kumar Karmakar

Abstract read
In one paragraph

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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Progga Paramita Paul *Pharmacy Discipline, Life Sciences School, Khulna University, Khulna, Bangladesh.
Musfiqur Rahman Sakib *Department of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Pritam KunduPharmacy Discipline, Life Sciences School, Khulna University, Khulna, Bangladesh.
Dabashis ChakrabortyDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.ORCID https://orcid.org/0009-0003-9143-9499
Tasnim FatemaDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.
Shahriar HossenPharmacy Discipline, Life Sciences School, Khulna University, Khulna, Bangladesh.ORCID https://orcid.org/0009-0006-8957-0350
Ahsan AbidDepartment of Pharmacy, Jashore University of Science and Technology, Jashore, Bangladesh.ORCID https://orcid.org/0000-0003-3839-2145
Trina MitraDepartment of Pharmacy, Jashore University of Science and Technology, Jashore, Bangladesh.ORCID https://orcid.org/0000-0001-7979-9852
Manik Chandra ShillDepartment of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.ORCID https://orcid.org/0000-0002-0946-3816
Utpal Kumar KarmakarPharmacy Discipline, Life Sciences School, Khulna University, Khulna, Bangladesh.ORCID https://orcid.org/0000-0002-5243-0163

Funding

GARE LS20201523Ministry of Education, Government of the People's Republic of Bangladesh
6 · The paper itself

Abstract

Present studies emphasize the pharmacological, toxicological, and molecular simulation studies of the potent phytoconstituents in the Sanchezia nobilis leaf extract (SNE) and its nonpolar and polar fractions. We identified 27 phytoconstituents in SNE using Gas Chromatography Mass Spectrometry (GC-MS), where aniline, dibutyl phthalate, and isoquinoline are noteworthy. Anxiolytic assessments by hole board test (HBT) and elevated plus maze test (EPMT) demonstrated dose-dependent effects of nonpolar and polar fractions of SNE. Both fractions also exhibited minimal cytotoxicity in brine shrimp lethality test. SNE crude extract demonstrated good antioxidant properties. In silico analysis revealed promising binding affinities of aniline and isoquinoline with target protein molecules responsible for anxiolytic and antidepressive effects. Molecular dynamics (MD) modelling and quantitative chemical-based DFT approaches confirmed satisfactory pharmacokinetics (PK) and toxicity profiles for the selected medications. HOMO-LUMO analysis highlighted the remarkable features of the chosen components. MD studies also supported aniline and isoquinoline as potential candidates requiring further pharmacological validation due to their interactions with chimeric alpha1GABA

Indexed as

Anti-Anxiety AgentsAntioxidantsPhytochemicalsPlant ExtractsAnimalsArtemiaCell SurvivalDose-Response Relationship, DrugMiceMolecular Dynamics SimulationPlant LeavesStructure-Activity RelationshipAnti-Anxiety AgentsAntioxidantsPhytochemicalsPlant Extractsanxiolytic activitydrug discoveryGABAA receptorGC‐MS fingerprintphytochemicalsSanchezia nobilis

Identifiers

PMID42855938
PMCPMC13653134

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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.