Evidence map›Paper›PMID 33225826›Full record

ArticleJournal of biomolecular structure & dynamics2022

Cordycepin: a bioactive metabolite of C

Akalesh Kumar Verma

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Journal of biomolecular structure & dynamics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00709215 (A Phase I/II Study of Cordycepin Plus Pentostatin in Patients With Refractory TdT-Positive Leukemia), which is not on this map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 4% 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.

NCT00709215 phase1 / phase2unknown statusnot on this map

A Phase I/II Study of Cordycepin Plus Pentostatin in Patients With Refractory TdT-Positive Leukemia

TypeinterventionalSponsorOncoVista, Inc.Ran2008 to 2010Enrolled44ConditionsRefractory TdT-Positive LeukemiaArmsCordycepin plus Pentostatin
3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Anti-Inflammatory Mechanisms and Translational Relevance ofJournal of inflammation research · 2026
    Review
  4. Article
  5. Effects of cottonseed powder and perilla oil on cordycepin production from Cordyceps militaris in liquid culture.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2025
    Article
  6. Article
  7. The GenusLife (Basel, Switzerland) · 2025
    Review
  8. Exploring the Therapeutic Potential ofJournal of microbiology and biotechnology · 2025
    Article
  9. Article
  10. Article
  11. Core microbes inMicrobiology spectrum · 2024
    Article
  12. A novel complementary pathway of cordycepin biosynthesis in Cordyceps militaris.International microbiology : the official journal of the Spanish Society for Microbiology · 2024
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

1 author at 1 institution in 1 country.

Akalesh Kumar VermaDepartment of Zoology, Cell and Biochemical Technology Laboratory, Cotton University, Guwahati, India.ORCID 0000-0001-8176-5694
Cotton University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spike protein and main proteases of SARS-CoV-2 have been identified as potential therapeutic targets and their inhibition may lead to the reticence of viral entry and replication in the host body. Despite several efforts; till now no specific drugs are available to treat SARS-CoV-2. Considering all these challenges, the main objective of the present study was to establish therapeutic potential of cordycepin against COVID-19 as a conventional therapeutic strategy. In the present study; molecular interaction study was performed to assess potential binding affinity of cordycepin with SARS-CoV-2 target proteins using computational approach. Additionally, network pharmacology was used to understand cordycepin-protein interactions and their associated pathways in human body. Cordycepin is under clinical trial (NCT00709215) and possesses structural similarity with adenosine except that, it lacks a 3' hydroxyl group in its ribose moiety and hence it served as a poly(A) polymerase inhibitor and terminate premature protein synthesis. Additionally, it is known that functional RNAs of SARS-CoV-2 genome are highly 3'-plyadenylated and leading to synthesis of all viral proteins and if cordycepin can destabilize SARS-CoV-2 RNAs by inhibiting polyadenylation process then it may step forward in terms of inhibition of viral replication and multiplication in the host. Moreover, cordycepin showed strong binding affinity with SARS-CoV-2 spike protein (-145.3) and main proteases (-180.5) that further corroborate therapeutic potential against COVID-19. Since cordycepin has both pre-clinical and clinical information about antiviral activities, therefore; it is suggested to the world community to undertake repurposing cordycepin to test efficacy and safety for the treatment of COVID-19.

Indexed as

CordycepsCOVID-19 Drug TreatmentAntiviral AgentsClinical Trials as TopicDeoxyadenosinesHumansPeptide HydrolasesPolyadenylationSARS-CoV-2Spike Glycoprotein, CoronavirusAntiviral AgentscordycepinDeoxyadenosinesPeptide HydrolasesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-22019nCovCoronavirusmain proteasesSARS-CoV-2spike protein

Identifiers

PMID33225826
PMCPMC7754931
OpenAlexW3109959395

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.