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<title>Journal Of Tropical Pharmacy and Cemistry Vol 8 No 2 (2024)</title>
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<place><placeTerm type="text">Samarinda</placeTerm></place>
<publisher>Universitas Mulawarman</publisher>
<dateIssued>2024</dateIssued>
<issuance>monographic</issuance>
<edition>Vol 8 No 2 (2024)</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<form authority="gmd">Karya Tulis Ilmiah</form>
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<note>Abstract
The immune system of humans is impacted by many drugs. Chemicals that have a gender-bending
impact on boys, were synthesized, their use spread, and as a consequence, they entered the ecology,
the food chain, and eventually ended up in blood or human breast milk. Due to the use of benzene in
both industry and medicine, chemicals with benzene rings are among the most problematic. The
generation of benzene metabolites that produce superoxide, the phenoxy radical, and benzene-drug
binding are only a few of the processes by which benzene and its derivatives cause harm. Benzene
metabolites are distinct from chemical metabolites apart from benzene, which is lipophilic in nature
and binds to cellular membranes, in that they bind to the intracellular plasma membrane where they
produce degenerative alterations. Many diseases are associated with degenerative alterations in the
mitochondria that culminate in mitochondrial dysfunction. Herein, twenty benzene derivatives (BDs)
have been studied in terms of their biological and physiochemical properties, and the compounds have
also been investigated using quantum mechanical computations. Binding affinities and behaviors of all
BDs have been investigated using molecular docking and nonbonding interactions on 3D crystal
structures of human receptor proteins serum albumin (1AO6), free native cellulase CEL48F (1G9G),
and human D-amino acid oxidase mutant (P219L) complexed with benzoate (6KBP). Geometry as well
as thermochemical data support the stability of all structures. All derivatives were predicted by ADMET
to have improved pharmacokinetic properties and less acute oral toxicity.

Keywords: Benzene derivatives (BDs), Density functional theory, Thermochemistry, Molecular docking, and toxicology.</note>
<subject authority=""><topic>Density functional theory</topic></subject>
<subject authority=""><topic>Benzene derivatives</topic></subject>
<subject authority=""><topic>toxicology</topic></subject>
<subject authority=""><topic>Thermochemistry</topic></subject>
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