Search bioRxiv⌕ Search

Biology subjects

Selvam, A. A. A.

Publications and source records attributed to Selvam, A. A. A..

2 recordsLinked to original sources

Extraction, Characterization, and Toxicological Assessment of Chemicals from Thermal Bill Paper: An In-Silico ADME and Daphnia pulex Study

The current study provides a comprehensive analysis of the chemical composition of thermal bill paper, revealing the presence of hazardous chemical compounds such as Bisphenol S (BPS) and Diphenyl Sulfone (DPS). The extraction process using ethyl acetate as the solvent effectively isolated these compounds, as evidenced by Thin Layer Chromatography (TLC) results, which displayed distinct spots corresponding to the compounds of interest. Fourier Transform Infrared (FTIR) spectroscopy confirmed the presence of characteristic functional groups, while High-Resolution Mass Spectrometry (HR-MS) identified molecular weights consistent with BPS and DPS. In-silico analysis using the SwissADME web tool provided insights into the pharmacokinetic properties of these compounds, with bioavailability radar plots indicating optimal absorption ranges, except for a low degree of saturation. The BOILED-Egg model predicted that BPS is likely to be absorbed by the gastrointestinal tract, while DPS may cross the blood-brain barrier, raising potential concerns about its impact on the central nervous system. Toxicity studies conducted with Daphnia pulex showed significant toxicity at higher concentrations, supporting the idea that the presence of BPS and DPS in thermal bill paper poses a risk to human health and the environment. These findings underscore the need for increased regulation and the exploration of safer alternatives.

biochemistry↗

Three-Dimensional Quantitative Structure-Activity Relationships and Molecular Dynamic Simulations Studies to Discover Aurora Kinase-B Inhibitors

The serine-threonine kinase gene Aurora-B kinase plays a critical role in spindle assembly, chromosome alignment, mitotic checkpoint activation, and cytokinesis. The overexpression of Aurora-B causes errors in cell division and multinucleation in centrosome numbers leads to cancer. Three-dimensional Quantitative Structure-Activity Relationship studies were conducted on known inhibitors to find valid pharmacophore hypotheses. The five features hypothesis AADRR with better parameters using partial least square analysis has been selected for virtual screening. Molecular docking was applied to find the binding mode interactions of ligands with the Aurora-B binding pocket. Lys 106, Ala 157, Glu 161, and Phe 219 were identified as crucial residues that formed several interactions with the ligands which are essential for Aurora-B inhibition. After the different levels of screening, five compounds from the National Cancer Institute database were acknowledged as novel inhibitors of Aurora-B. The active site interactions of the protein-ligand complex were examined by molecular dynamics simulation studies. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=72 SRC="FIGDIR/small/605534v1_ufig1.gif" ALT="Figure 1"> View larger version (29K): org.highwire.dtl.DTLVardef@b58431org.highwire.dtl.DTLVardef@f9ae5aorg.highwire.dtl.DTLVardef@25c55forg.highwire.dtl.DTLVardef@1c0ffd9_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioinformatics↗