Publications by authors named "Nagla Mohamed"

Background: Sesquiterpene lactones having α-methylene-γ-lactone moiety are promising natural metabolites showing various biological activity. One of the major metabolites isolated from Pulicaria undulata, 2α-hydroxyalantolactone (PU-1), has not been investigated in detail yet. Multidrug resistance (MDR) represents a major obstacle for cancer chemotherapy and the capability of novel natural products to overcoming MDR is of great interest.

View Article and Find Full Text PDF

In the present study, nanocomposite ultrafiltration membranes were prepared by incorporating nanotubes clay halloysite (HNTs) into polysulfone (PSF) and PSF/polyvinylpyrrolidone (PVP) dope solutions followed by membrane casting using phase inversion method. Characterization of HNTs were conducted using scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and thermogravimetric (TGA) analysis. The pore structure, morphology, hydrophilicity and mechanical properties of the composite membranes were characterized by using SEM, water contact angle (WCA) measurements, and dynamic mechanical analysis.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates how certain agents (LPA, PMA, A23187) trigger the exposure of phosphatidylserine (PS) on red blood cells (RBCs) by exploring three key mechanisms: scramblase activation, PKCα activation, and lipid flip flop.
  • Researchers used flow cytometry and specific inhibitors to assess the impact on PS exposure and intracellular calcium levels after RBC treatment.
  • Findings indicate that inhibiting scramblase and PKCα significantly reduces PS exposure, with the effect being stronger when both pathways are inhibited; also, blocking the Gardos channel similarly lowers PS exposure across all treatments.
View Article and Find Full Text PDF

Here, we describe the synthesis, bioactivity screening, and structure-activity relationships of various synthetic triterpenoids prepared from the cork processing byproducts friedelin (1) and 3-hydroxyfriedel-3-en-2-one (2) via oxidative procedures. The synthesis of compounds 2alpha-trimethylsiloxyfriedelan-3-one (17), friedelin-2,3-lactone (18), friedelin-3-oxime (19), and friedelin-3,4-lactam (20) is also described. We have studied the insecticidal and phytotoxic potential of these compounds, their selective cytotoxic effects on insect and mammalian cells, and their antiparasitic effects.

View Article and Find Full Text PDF