Medicinally valuable
components derived from natural resources
are highly desirable as prospective alternatives to synthetic drugs
to treat fatal diseases, such as cancer and diabetes mellitus. Suaeda maritima (L.) Dumort (Amaranthaceae) (S. maritima) is a halophyte plant
that can thrive in saline environments and possesses excellent medicinal
properties. Hence, for the present investigation, S.
maritima has been chosen, and its phytochemical constituents
have been extracted utilizing various solvents, including hexane,
acetone, and methanol, and identified by GC-MS, LC-MS, and HPLC analyses.
The antioxidant activity of the compounds using DPPH, ABTS, and reducing
power assays demonstrated that all three extracts of S. maritima possessed significant radical scavenging
activity comparable to standard ascorbic acid with lower IC50 values (69.20–95.58 μg/mL). In addition, the evaluation
of antidiabetic activity by α-amylase inhibition and α-glucosidase
inhibition methods revealed that the acetone extract of S. maritima (SMAE) displayed equipotent activity
of standard acarbose with an IC50 of 32.6 μg/mL.
Advantageously, SMAE also exhibited better inhibition activity against
the growth of lung cancer cells with an IC50 of 78.19.
μg/mL and less toxicity on the noncancerous HUVEC cells with
a high IC50 of 300 μg/mL. In addition, the cancer
cell death mechanism via the apoptotic pathway induced by SMAE was
confirmed by DAPI staining and ROS analysis. The analysis of ADME
properties, including absorption, distribution, metabolism, and excretion,
witnessed that the physicochemical and druglikeness factors were best
catered by stigmasterol, γ-sitosterol, and vitamin E. Further,
the key phytochemicals identified from SMAE were docked with CtBP1
and SOX2 bound to importin-α target proteins associated with
carcinogenic pathways using Schrodinger software. The results showed
that the phytochemicals, scilicet, stigmasterol, γ-sitosterol,
octadecadienoic acid, and vitamin E, showed a good binding affinity
with Glide scores in the range −2.845–4.018 kcal/mol.
Overall, the findings support that the least investigated traditional
edible medicinal mangrove-related S. maritima is high in pharmacologically active constituents and might be one
of the finest sources of naturally derived molecules for drug development
and delivery systems.