Recent advances in biological active sulfonamide based hybrid compounds part B: Two-component sulfonamide hybrids

S Ghomashi, R Ghomashi, H Aghaei… - Current Medicinal …, 2023 - ingentaconnect.com
Sulfonamide compounds, also known as sulfa drugs, are a significant class of synthetic
bacteriostatic antimicrobials and were the primary source of therapy against bacterial …

Fluorinated aliphatic diazirines: preparation, characterization, and model photolabeling studies

Y Kornii, O Shablykin, T Tarasiuk… - The Journal of …, 2022 - ACS Publications
The previously unknown difluoromethyl diazirines and the previously neglected
trifluoromethyl-aliphatic diazirines were synthesized and characterized. Model photolabeling …

Synthesis, anticancer evaluation and molecular docking studies of new heterocycles linked to sulfonamide moiety as novel human topoisomerase types I and II …

AH Halawa, WE Elgammal, SM Hassan, AH Hassan… - Bioorganic …, 2020 - Elsevier
A series of heterocyclic compounds with a sulfonamide moiety were synthesized from
reaction of enaminone 4 with active methylene compounds, glycine derivatives, 1, 4 …

Anti-liver and anti-breast cancer activities of 2-thioxo-4-imidazolidinone derivatives

LA AbdulJabar, AAA Al-Shawi, DZ Mutlaq - Medicinal Chemistry Research, 2021 - Springer
MTT assay and flow cytometry analysis were used to examine the anti-liver (HepG2) and
anti-breast cancer (MCF-7) activities of twelve compounds derived from 2-thioxo-4 …

In Silico, in Vitro and in Vivo Study of Substituted Imidazolidinone Sulfonamides as Antibacterial Agents

D Hodyna, V Kovalishyn, M Kachaeva… - Chemistry & …, 2023 - Wiley Online Library
New substituted imidazolidinone sulfonamides have been developed using a rational drug
design strategy. Predictive QSAR models for the search of new antibacterials were created …

In vitro activity of novel 4-iminohydantoin sulfamide derivatives against human cytomegalovirus

V Zhirnov, O Shablykin, S Chumachenko, Y Kornii… - Chemical Papers, 2024 - Springer
Here, we describe machine learning models, predicted ADMET properties, and analysis in
vitro activity of selected 4-iminohydantoin sulfamide derivatives with different N-substitution …

New 2‐Oxoimidazolidine Derivatives: Design, Synthesis and Evaluation of Anti‐BK Virus Activities in Vitro

Y Kornii, S Chumachenko, O Shablykin… - Chemistry & …, 2019 - Wiley Online Library
A series of novel 2‐oxoimidazolidine derivatives were synthesized and their antiviral
activities against BK human polyomavirus type 1 (BKPyV) were evaluated in vitro. Bioassays …

New 4-iminohydantoin sulfamide derivatives with antiviral and anticancer activity

YE Kornii, V Shablykin, OV Shablykina… - Ukrainica …, 2021 - bioorganica.com.ua
A number of sulfamides were obtained by reaction interaction of (5-(dichloromethylene)-2-
oxoimidazolidin-4-ylidene) sulfamoyl chloride with anilines, benzylamines, Boc-protected …

[PDF][PDF] Design and Biological Evaluation of 4-Iminohydantoin Sulfamides as New Anti-Acinetobacter baumannii Agents

D Hodyna, V Kovalishyn, I Semenyuta, M Kachaeva… - 2023 - researchgate.net
With the emergence of multidrug-resistant bacterial strains, there is an urgent need to find
antibacterial agents directed at alternative molecular targets. A series of 4-iminohydantoin …

Fluorinated Aliphatic Diazirines: Preparation, Characterization, and Photolabeling Studies

U Kornii, O Shablykin, T Tarasiuk, O Stepaniuk… - 2022 - chemrxiv.org
The previously unknown difluoromethyl-and the previously neglected trifluoromethyl-
aliphatic diazirines were synthesized and characterized. Model photolabeling experiments …