EventsThe 28th International Electronic Conference on Synthetic Organic Chemistry
Published
with-doi10.3390/ecsoc-28-20225 (registering DOI)
This submission belongs to the session S5. Computational Chemistry of the event The 28th International Electronic Conference on Synthetic Organic Chemistry
Published date
14 Nov, 2024
Academic Editor
author-avatarJulio A. Seijas
Citation
nourelhouda bendjeffel, Discovery of Amaranthin as a Promising Drug Target for Vascular Endothelial Growth Factor (VEGF) Therapy, in Proceedings of The 28th International Electronic Conference on Synthetic Organic Chemistry, 15 November–30 November 2024, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-28-20225
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Discovery of Amaranthin as a Promising Drug Target for Vascular Endothelial Growth Factor (VEGF) Therapy

1. biology department of Tlemcen University, 13000, Tlemcen, Algeria, Algeria
Abstract

Background: Angiogenesis plays a major role in the process of tumour genesis through its capacity to acquire sustenance in the form of nutrients and oxygen. Hence, defining as one of the hallmarks of cancer. Vascular endothelial growth factor (VEGF) is a major regulator of angiogenesis both under normal conditions and in disease state, numerous studies has been shown that targeting VEGF has become the most prominent approach to stop tumour growth. Recently, amaranth has become an area of increasing scientific. This is due to its valuable biological properties, and wide pharmacological activity. Therefore it is of interest to study the molecular docking analysis of VEGF with amaranthin compounds as drug target discovery.

Material and methods: A molecular docking study were conclude using autodock vina briefly the VEGF 3D structure was retrieve from protein data bank under the code of 2PVF, Amaranthin were retrieve from PUBCHEM (CID 6325284) both the protein and ligand were prepare using MGLTools then dock using autodick vina (V. 4.0).

Results: the molecular docking results were vizualizate using pymol software ,our results shown that the binding affinity was - 6.8 kcal/mol. Analysis of the docking results showed that selected compound interact with VEGF protein via H bond interactions.

Conclusion: Natural products provide a promising opportunity to discover new compounds that can utilize as drugs given their chemical structure diversity. Of note Amaranthin shown an interesting drug target for targeting VEGF need further studies.

Keywords
VEGF
Amaranthin
molecular docking
Manuscript
In Silico Evaluation of Novel 2-Pyrazoline Carboxamide Derivatives as Potential Protease Inhibitors Against Plasmodium Parasites
MULTITARGET IN SILICO EVALUATION OF NEW 2-PYRAZOLINES AS POTENTIAL ANTIMICROBIAL AGENTS