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Senthamaraikannan Kabilan

Researcher at Annamalai University

Publications -  145
Citations -  2025

Senthamaraikannan Kabilan is an academic researcher from Annamalai University. The author has contributed to research in topics: Antibacterial activity & Antimicrobial. The author has an hindex of 22, co-authored 141 publications receiving 1624 citations. Previous affiliations of Senthamaraikannan Kabilan include Instituto Superior de Engenharia de Lisboa.

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Characterization of β-Cryptoxanthin and Other Carotenoid Derivatives from Rhodotorula taiwanensis, A Novel Yeast Isolated from Traditional Starter Culture of Assam.

TL;DR: The present investigation was intended to characterize pigments for the first time from Rhodotorula taiwanensis yeast isolated from the ethic fermentation starter culture source meant to evaluate its carotenoid contents for beneficial applications.
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Screening and Toxicity Risk Assessment of Selected Compounds to Target Cancer using QSAR and Pharmacophore Modelling

TL;DR: From the results the compound 7 (Zinc-69489055) was found to be safe to use as a drug and hence, the compound could be further redesigned, synthesized to target cancer.
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Synthesis, stereochemistry and in vitro antimicrobial evaluation of novel 2-[(2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-ylidene)hydrazono]-4-phenyl-2,3-dihydrothiazoles

TL;DR: The results show that 3e against Escherichia coli and Cryptococcus neoformans3i against Bacillus Subtilis, 3b against Aspergillus flavus, and 3k against Rhizopus sp.
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Synthesis, Stereochemistry and Antimicrobial Studies of Novel Oxime Ethers of Aza/Diazabicycles.

TL;DR: Two series of bicyclic oxime ethers viz, 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-one O-benzyloximes 13-24 and 2, 4,6,8-tetraaryl-3,7-diazabicycleclo [3.2.3] nonan-nine-one oxime oximes 31-36 were synthesized and stereochemistry was established by their spectral (1D and 2D NMR) and crystal
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Spectral characterization and crystal structure of tetrahydropyran-4-one thiosemicarbazones

TL;DR: In this paper, the properties of compound 3 and 4 were characterized using FT-IR, 1H NMR, 13C NMR and NOESY spectroscopy and X-ray single-crystal diffraction analysis.