Towards alternative treatment for type 2 diabetes: An in silico analysis of sponge-derived marine bioactive compounds on PTP1B and DPP-4

Clicks: 4
ID: 285041
2022
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Steady

Ranked #455 of 3,757 articles by views in Malay Journal

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 3,757 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Type 2 Diabetes is a medical condition involving pathophysiological manifestations of atypical blood glucose levels due to impaired insulin receptor sensitivity. Factors such as genetic makeup and lifestyle predispose individuals to develop such a chronic disease. As the number of Type 2 Diabetes cases increases each year, there is a proportional necessity to design and develop drugs that are competent with respect to the existing market. Marine-derived compounds, specifically that of sponge origin hold great potential due to their biological and chemical diversity. In this study, 50 of them were examined for their bioactivity towards Type 2 Diabetes targets, Dipeptidyl Peptidase-4 (DPP-4) and Protein Tyrosine Phosphatase 1B (PTP1B). The compounds were subjected to a number of in silico analyses starting with molecular docking to assess and rank them based on the lowest binding free energy scores. From there, the top 10 compounds for each drug target were subjected to ADMET profiling and interaction analyses to characterize drug-likeness and determine participating residues within the binding pocket. Cumulatively, the results obtained from the aforementioned analyses narrowed down to (S)-6’-debromohamacanthin B (DB1) as a potential multi-target inhibitor towards DPP-4 and PTP1B. Validity of such a claim was confirmed through molecular dynamics simulations.
Reference Key
persistent_1760654452_68f174741fc51 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors San Juan, Maria Angela D.
Journal Malay Journal
Year 2022
DOI
DOI not found
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.