Author(s): Sri Wahyuni Gayatri, Rosdiana Natzir, Rusdina Bte Ladju, Suryani As’ad, Nasrudin A. Mappaware, Brahmana Askandar

Email(s): sriwahyuni.gayatri@umi.ac.id , rosdiananatzir263@gmail.com

DOI: 10.52711/0974-360X.2026.00440   

Address: Sri Wahyuni Gayatri1,7*, Rosdiana Natzir2, Rusdina Bte Ladju3, Suryani As’ad4, Nasrudin A. Mappaware5, Brahmana Askandar6
1Doctoral Program, Faculty of Medicine, Universitas Hasanuddin, Makassar, Indonesia.
2Department of Biochemistry, Faculty of Medicine, Universitas Hasanuddin, Makassar, Indonesia.
3Department of Anatomic Pathology, Faculty of Medicine, Universitas Hasanuddin, Makassar, Indonesia.
4Departement of Nutrition, Faculty of Medicine, Universitas Hasanuddin, Makassar, Indonesia.
5Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Muslim Indonesia, Makassar, Indonesia.
6Department of Obstetrics and Gynecology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
7Department of Biochemistry, Faculty of Medicine, Universitas Muslim Indonesia, Makassar, Indonesia.
*Corresponding Author

Published In:   Volume - 19,      Issue - 7,     Year - 2026


ABSTRACT:
The nutraceutical properties of Ajwa dates exhibit significant potential in the management of various ailments, including inflammatory disorders, paralysis, neurological difficulties, and cognitive decline. Research indicates that Ajwa dates exhibit anti-inflammatory, anticancer, nephroprotective, hepatoprotective, and antioxidant characteristics. The therapeutic properties are likely due to the presence of phenolics, flavonoids, and glycosides. This study aims to evaluate the potential of the compound quercetin, isolated from Phoenix dactylifera L, through a molecular docking approach against the human protein isoform 14-3-3, which plays an important role in the development of cervical cancer. Two ligands were analysed: quercetin (2-thioindantoin) as the test ligand and the native compound of 2-thioindantoin. The docking results show that quercetin has a more complex and varied interaction pattern, involving hydrogen bonds, carbon-hydrogen bonds, alkyl interactions, and Van der Waals forces, which occur at active residues such as GLN:67, SER:63, ARG:60, and GLU:108. The binding energy of quercetin was recorded to be lower (?G = -5.6 kcal/mol) compared to the reference ligand (?G = -2.7 kcal/mol), indicating a stronger and more stable interaction with the target receptor (6ZFD). Thus, quercetin shows potential as a promising therapeutic agent for the treatment of cervical cancer through the mechanism of inhibiting the 14-3-3 protein isoform.


Cite this article:
Sri Wahyuni Gayatri, Rosdiana Natzir, Rusdina Bte Ladju, Suryani As’ad, Nasrudin A. Mappaware, Brahmana Askandar. Molecular Docking Analysis Quercetin of Phoenix dactylifera L activity, Against Human 14-3-3 Isoforms: A Promising Approach for Cervical Cancer Treatment. Research Journal of Pharmacy and Technology. 2026;19(7):3097-4. doi: 10.52711/0974-360X.2026.00440

Cite(Electronic):
Sri Wahyuni Gayatri, Rosdiana Natzir, Rusdina Bte Ladju, Suryani As’ad, Nasrudin A. Mappaware, Brahmana Askandar. Molecular Docking Analysis Quercetin of Phoenix dactylifera L activity, Against Human 14-3-3 Isoforms: A Promising Approach for Cervical Cancer Treatment. Research Journal of Pharmacy and Technology. 2026;19(7):3097-4. doi: 10.52711/0974-360X.2026.00440   Available on: https://rjptonline.org/AbstractView.aspx?PID=2026-19-7-27


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