Experimental and computational evaluation of dinaphthodiospyrol F and dinaphthodiospyrol G from <i>Diospyros lotus</i> L. as ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) inhibitors
By hydrolysing 2',3'-cyclic GMP-AMP dinucleotide (2',3'-cGAMP), ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) regulates downstream pathways related to cancer progression and immunomodulation. Thus, it represents an attractive target for the discovery of novel ligands. We here disclose the activity of Dinaphthodiospyrol F and dinaphthodiospyrol G, two dimeric naphthoquinones extracted from <i>Diospyros lotus</i> L. as ENPP1 inhibitors by means of computational and <i>in vitro</i> techniques. Our study showed that the two molecules inhibit ENPP1 with a potency similar to that of the positive control (disodium EDTA), suggesting their possible use as new natural scaffolds in the development of optimised derivatives.
Authors
- Zuneera Akram (ORCID: https://orcid.org/0000-0002-9884-0520)
- Giovanni Ribaudo (ORCID: https://orcid.org/0000-0003-3679-5530)
- Omar Bahattab (ORCID: https://orcid.org/0000-0003-3584-6674)
- Muhammad Saleem
- Abdur Rauf
- Yahya S. Al-Awthan
Institutions
- Baqai Medical University (PK)
- Brescia University (US)
- Ghazi University (PK)
- Berlin Center for Genomics in Biodiversity Research (DE)
- University of Swabi (PK)
- University of Tabuk (SA)
- University of Brescia (IT)
Publication Details
- Journal
- Natural Product Research
- Published
- 2026-02-22
- DOI
- https://doi.org/10.1080/14786419.2026.2633710
- Primary Topic
- Sphingolipid Metabolism and Signaling
- Type
- article
- Field-Weighted Citation Impact
- 0.00