Add like
Add dislike
Add to saved papers

Evaluation of Hymenodictyon excelsum Phytochemical's Therapeutic Value Against Prostate Cancer by Molecular Docking Study.

BACKGROUND: Hymenodictyon excelsum is a medicinal plant traditionally used for tumor treatment as it contains phytochemicals of anthraquinone and coumarin class.

OBJECTIVES: The aim of the present study was to unfold the therapeutic value of selected phytocompounds of Hymenodictyon excelsum in prostate cancer.

MATERIALS AND METHODS: Eight phytochemicals were selected based on the literature search including anthragallol, damnacanthal, esculin, lucidin, morindone, nordamnacanthal, rubiadin, and soranjidiol while dihydrotestosterone was considered as the control. Human androgen receptor (AR) ligand binding domain (PDB id: 1e3g) was selected as the receptor for subsequent computational docking study. First, the selected phytocompounds were screened for their drug likeness and safety profile. Molegro Virtual Docker (MVD) was subjected only to drug-like and safe phytocompounds for the computational docking study.

RESULTS: Except for anthragallol, nordamnacanthal and rubiadin, all the ligands were drug-like and safe. Results of the docking study suggest a favorable binding of esculin to the receptor with respect to dihydrotestosterone. Analysis of docking pattern revealed a nearly similar ligand-receptor interaction for both dihydrotestosterone and esculin.

CONCLUSIONS: The anthraquinone and coumarin principles of H. excelsum have an anti-prostate cancer effect that has been proposed to be exerted by antagonistic effects on AR.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app