Evidence map›Paper›PMID 34439870›Full record

ReviewBiomolecules2021

Chalcones: Synthetic Chemistry Follows Where Nature Leads.

Hiba A Jasim, Lutfun Nahar, Mohammad A Jasim, Sharon A Moore, Kenneth J Ritchie, Satyajit D Sarker

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
10.0field-weighted citation impact, top 1% of its field
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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 134 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Phytochemistry and Pharmacological Potential of the GenusPharmaceuticals (Basel, Switzerland) · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Nitrochalcones: Pharmacological Activities and Therapeutic Potential.International journal of molecular sciences · 2026
    Review
  13. Article
  14. Flavonoids as potential anti-asthmatic agents.Frontiers in immunology · 2026
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 3 countries.

Hiba A JasimCentre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK.ORCID 0000-0002-3637-3090
Lutfun NaharLaboratory of Growth Regulators, Institute of Experimental Botany ASCR & Palacký University, Šlechtitelů 27, 78371 Olomouc, Czech Republic.ORCID 0000-0002-1157-2405
Mohammad A JasimDepartment of Biology, College of Education for Women, University of Anbar, Al-Anbar 10081, Iraq.ORCID 0000-0003-0857-0676
Sharon A MooreFaculty of Science and Engineering, University of Wolverhampton, Wolverhampton WV1 1LY, UK.ORCID 0000-0003-0174-9606
Kenneth J RitchieCentre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK.
Satyajit D SarkerCentre for Natural Products Discovery (CNPD), School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, James Parsons Building, Byrom Street, Liverpool L3 3AF, UK.ORCID 0000-0003-4038-0514
Liverpool John Moores University · GBUniversity of Anbar · IQCzech Academy of Sciences, Institute of Experimental Botany · CZUniversity of Wolverhampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chalcones belong to the flavonoid class of phenolic compounds. They form one of the largest groups of bioactive natural products. The potential anticancer, anti-inflammatory, antimicrobial, antioxidant, and antiparasitic properties of naturally occurring chalcones, and their unique chemical structural features inspired the synthesis of numerous chalcone derivatives. In fact, structural features of chalcones are easy to construct from simple aromatic compounds, and it is convenient to perform structural modifications to generate functionalized chalcone derivatives. Many of these synthetic analogs were shown to possess similar bioactivities as their natural counterparts, but often with an enhanced potency and reduced toxicity. This review article aims to demonstrate how bioinspired synthesis of chalcone derivatives can potentially introduce a new chemical space for exploitation for new drug discovery, justifying the title of this article. However, the focus remains on critical appraisal of synthesized chalcones and their derivatives for their bioactivities, linking to their interactions at the biomolecular level where appropriate, and revealing their possible mechanisms of action.

Indexed as

Anti-Bacterial AgentsAnti-Inflammatory AgentsAntineoplastic AgentsAntioxidantsBiological ProductsChalconesCell LineDrug DiscoveryHumansStructure-Activity RelationshipAnti-Bacterial AgentsAnti-Inflammatory AgentsAntineoplastic AgentsAntioxidantsBiological ProductsChalconesanticancerantimicrobialbioactivitiesbiomolecular interactionschalconesmechanismsnatural productsphenolicssynthesis

Identifiers

PMID34439870
PMCPMC8392591
OpenAlexW3193295096

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.