World Journal of
Pharmaceutical and Life Sciences

( An ISO 9001:2015 Certified International Journal )

An International Peer Reviewed Journal for Pharmaceutical and Life Sciences
An Official Publication of Society for Advance Healthcare Research (Reg. No. : 01/01/01/31674/16)
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Abstract

PHARMACOKINETICS AND TOXICITY PROFILING OF NOVEL NITROGEN HETEROCYCLIC SMALL MOLECULES USING DEEP-PK IN SILICO TOOLS

Mahesh Parit*, Siddaram Bagalkote, Akshaykumar S. N.

ABSTRACT

Nitrogen-containing heterocyclic compounds, especially pyridine derivatives, represent a pivotal class of
molecules with extensive pharmacological and therapeutic potential. Pyridine, a planar aromatic heterocycle
analogous to benzene but substituted with a nitrogen atom, serves as a fundamental scaffold in drug design due to
its versatile chemical properties. This report highlights the synthesis, pharmacokinetic evaluation, and
antimicrobial efficacy of novel small molecules that incorporate hybrid structures of pyridine, piperidine,
benzimidazole, and pyrazole moieties. These hybrids exhibit diverse biological activities including antibacterial,
anti-inflammatory, anticancer, and antiviral effects, making them promising candidates for pharmaceutical
development. Through computational in silico approaches, the pharmacokinetics and toxicity profiles of these
molecules were predicted, focusing on absorption, distribution, metabolism, excretion, and toxicity (ADMET)
parameters. The selected compounds demonstrate favorable drug-like properties consistent with Lipinski’s rule of
five, including optimal molecular weight, lipophilicity, and hydrogen bonding capacity, predicting good oral
bioavailability and membrane permeability. Metabolic pathway predictions indicate probable interactions with key
enzymes like CYP isoforms and drug transporters, suggesting paths for further optimization. Toxicity assessments
reveal safety in genetic and environmental endpoints but indicate potential risks for liver injury and respiratory
effects, highlighting the need for in vivo validation. This study underscores the importance of integrating synthetic
chemistry with computational pharmacokinetics to streamline the discovery of bioactive heterocycles. The novel
hybrids presented provide a foundation for developing safe, effective therapeutic agents targeting infectious
diseases, cancer, and inflammatory disorders.

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