Evidence map›Paper›PMID 24497731›Full record

ArticleBioinformation2013

Screening and design of anti-diabetic compounds sourced from the leaves of neem (Azadirachta indica).

Asma Jalil, Usman Ali Ashfaq, Samar Shahzadi, Ijaz Rasul, Shahid-Ur Rehman, Masaud Shah, Muhammad Rizwan Javed, Muhammad Shareef Masoud

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Bioinformation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Relevance of Indian traditional tisanes in the management of type 2 diabetes mellitus: A review.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
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  10. Article
4 · The record

Corrections and comments

  • Erratum issued
    Masoud, Muhammad Shareef [corrected to Javed, Muhammad Rizwan]
5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Asma JalilDepartment of Bioinformatics and Biotechnology, Government College University (GCU), Faisalabad, Pakistan.
Usman Ali AshfaqDepartment of Bioinformatics and Biotechnology, Government College University (GCU), Faisalabad, Pakistan.
Samar ShahzadiDepartment of Bioinformatics and Biotechnology, Government College University (GCU), Faisalabad, Pakistan.
Ijaz RasulDepartment of Bioinformatics and Biotechnology, Government College University (GCU), Faisalabad, Pakistan.
Shahid-Ur RehmanDepartment of Poultry Husbandry, University of Agriculture, Faisalabad, Pakistan.
Masaud ShahDepartment of Biochemistry, Abdul Wali Khan University, Mardan, Pakistan.
Muhammad Rizwan JavedDepartment of Bioinformatics and Biotechnology, Government College University (GCU), Faisalabad, Pakistan.
Muhammad Shareef MasoudDepartment of Bioinformatics and Biotechnology, Government College University (GCU), Faisalabad, Pakistan.
Government College University, Faisalabad · PKAbdul Wali Khan University Mardan · PKUniversity of Agriculture Faisalabad · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetes Mellitus is affecting people of all age groups worldwide. Many synthetic medicines available for type 2 diabetes mellitus in the market. However, there is a strong requirement for the development of better anti-diabetes compounds sourced especially from natural sources like medicinal plants. The extracts from the leaves of neem (Azadirachta indica) is traditionally known to have anti-diabetes properties. Therefore, there is an increased interest to identify potential compounds identified from neem leaf extracts showing predicted binding property with the known diabetes mellitus type 2 protein enzyme target phosphoenol-pyruvate carboxykinase(PEPCK). The structure data for compounds found in the leaf extract of neem was screened against PEPCK using molecular docking simulation and screening techniques. Results show that the compound 3-Deacetyl-3-cinnamoyl-azadirachtin possesses best binding properties with PEPCK. This observation finds application for further consideration in in vitro and in vivo validation.

Identifiers

PMID24497731
PMCPMC3910360
OpenAlexW2084856128

What OpenQuestion holds

Textmetadata
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.