A review of recent synthetic strategies and biological activities of isoxazole

CP Pandhurnekar, HC Pandhurnekar… - Journal of …, 2023 - Wiley Online Library
Among different heterocyclic compounds, isoxazole and their analogues are very important
classes of heterocyclic compounds as they display an extensive range of biological actions …

Novel 3-(pyrazol-4-yl)-2-(1H-indole-3-carbonyl)acrylonitrile derivatives induce intrinsic and extrinsic apoptotic death mediated P53 in HCT116 colon carcinoma

MF Mohamed, NS Ibrahim, AA Saddiq… - Scientific Reports, 2023 - nature.com
A novel series of α-cyano indolylchalcones was prepared, and their chemical structures
were confirmed based on the different spectral data. Among them, compound 7f was …

Design, Synthesis, In silico and In Vitro Anticancer Activity of Novel Bis‐Furanyl‐Chalcone Derivatives Linked through Alkyl Spacers

EM Fathi, FM Sroor, KF Mahrous… - …, 2021 - Wiley Online Library
A novel series of bis (furan‐based chalcone) derivatives linked to aliphatic linkers, with the
furan units at the A‐or B‐rings, were synthesized and evaluated as anticancer agents …

Novel 2‐cyanoacrylamido‐4,5,6,7‐tetrahydrobenzo[b]thiophene derivatives as potent anticancer agents

FM Sroor, MM Aboelenin, KF Mahrous… - Archiv der …, 2020 - Wiley Online Library
Abstract Ethyl 2‐acrylamido‐4, 5, 6, 7‐tetrahydrobenzo [b] thiophene‐3‐carboxylate as well
as its corresponding bis‐derivatives, 5–10, with aliphatic linkers were synthesized, fully …

Novel Tetrahydro-[1,2,4]triazolo[3,4-a]isoquinoline Chalcones Suppress Breast Carcinoma through Cell Cycle Arrests and Apoptosis

MIM Darwish, AM Moustafa, AM Youssef, M Mansour… - Molecules, 2023 - mdpi.com
Chalcones are interesting anticancer drug candidates which have attracted much interest
due to their unique structure and their extensive biological activity. Various functional …

Impact of trifluoromethyl and sulfonyl groups on the biological activity of novel aryl-urea derivatives: synthesis, in-vitro, in-silico and SAR studies

FM Sroor, KF Mahrous, HAMA El-Kader, AM Othman… - Scientific Reports, 2023 - nature.com
We designed and prepared a novel series of urea derivatives with/without sulfonyl group in
their structures to investigate the impact of the sulfonyl group on the biological activity of the …

Synthesis, antimicrobial, anti-cancer and in silico studies of new urea derivatives

FM Sroor, AM Othman, MA Tantawy, KF Mahrous… - Bioorganic …, 2021 - Elsevier
The reaction of an alkyl or aryl isocyanates with some primary amines in acetonitrile at room
temperature afforded the corresponding alkyl-and aryl-urea derivatives. All the prepared …

Thiazole and Related Heterocyclic Systems as Anticancer Agents: A Review on Synthetic Strategies, Mechanisms of Action and SAR Studies

K Kaur, V Jaitak - Current medicinal chemistry, 2022 - ingentaconnect.com
Background: Cancer is the second leading cause of death worldwide. Many anticancer
drugs are commercially available, but lack of selectivity, target specificity, cytotoxicity, and …

[HTML][HTML] Anticancer and antimicrobial activities of new thiazolyl-urea derivatives: gene expression, DNA damage, DNA fragmentation and SAR studies

FM Sroor, AM Othman, MM Aboelenin… - Medicinal Chemistry …, 2022 - Springer
The drug resistance became the major challenge in the antimicrobial and anticancer drugs
therapy. Therefore, there is an urgent need to looking for new types of antimicrobial and …

Design, synthesis, and mechanism of antiviral acylurea derivatives containing a trifluoromethylpyridine moiety

S Guo, W Zhao, Y Wang, W Zhang… - Journal of Agricultural …, 2021 - ACS Publications
Novel acylurea derivatives 7a–7ab were designed and synthesized by linking the active
substructures trifluoromethylpyridine and anthranilic diamide via an acylurea bridge. Most of …