First synthesis for bis-spirothiazolidine derivatives as a novel heterocyclic framework and their biological activity

EM Flefel, WI El-Sofany, HM Awad… - Mini Reviews in …, 2020 - ingentaconnect.com
Background: Spirothiazolidines are versatile synthetic scaffold possessing wide spectrum of
biological interests involving potential anticancer activity. Objective: To report the first …

Recent developments on the synthesis and biological activities of fused pyrimidinone derivatives

P Seboletswe, P Awolade, P Singh - ChemMedChem, 2021 - Wiley Online Library
Heterocyclic compounds constitute a unique class of organic compounds endowed with a
wide range of synthetic and pharmaceutical applications. Pyrimidinones and their fused …

Novel fluorinated pyrazole-based heterocycles scaffold: cytotoxicity, in silico studies and molecular modelling targeting double mutant EGFR L858R/T790M as …

EA Fayed, NA Gohar, AH Bayoumi… - Medicinal Chemistry …, 2023 - Springer
Hepatocellular carcinoma (HCC), also known as hepatoma, is the most prevalent type of
primary liver cancer. It begins in the hepatocytes, the liver's major cell type. Cancer that …

Synthesis, molecular docking and in vitro screening of some newly synthesized triazolopyridine, pyridotriazine and pyridine–pyrazole hybrid derivatives

EM Flefel, WI El-Sofany, M El-Shahat, A Naqvi… - Molecules, 2018 - mdpi.com
A series of novel pyridine and fused pyridine derivatives have been prepared starting from 6-
(3, 4-dimethylphenyl)-2-hydrazinyl-4-(thiophen-2-yl)-pyridine-3-carbonitrile 1 which on …

Development of a novel series of anticancer and antidiabetic: Spirothiazolidines analogs

EM Flefel, WI El-Sofany, RAK Al-Harbi, M El-Shahat - Molecules, 2019 - mdpi.com
4-(4-Aminophenyl)-1-thia-4-azaspiro [4.5] decan-3-one 1 was prepared and allowed to react
with nitrogen nucleophiles to give the corresponding hydrazones 2–4. Further, compound 1 …

Design, synthesis, biological evaluation and molecular docking study of new pyrazolo [1, 5-a] pyrimidines as PIM kinase inhibitors and apoptosis inducers

FG Abdulrahman, R Sabour, SM Abd El-Gilil… - Journal of Molecular …, 2024 - Elsevier
This study involved designing and synthesizing new derivatives of pyrazolo [1, 5-a]
pyrimidine 5a-l, which were prepared via reaction of 4-Arylazo-1H-pyrazole-3, 5-diamines …

Microwave assists synthesis of spirothiazolidine derivatives to induce cervical cancer cell death-mediated apoptosis in vitro

WI El-Sofany, DAA Osman, AM Mahran… - Journal of Molecular …, 2023 - Elsevier
Herein, a new series of spirothiazolidine derivatives 1–14 are effectively produced using
microwave irradiation in a quick and efficient manner. IR, NMR, and mass spectra were used …

[PDF][PDF] Chemotherapeutic effect of Ulmus pumila leaves methanolic extract against N-methyl-N-nitrosourea-induced mammary carcinoma in female rats: An in vitro and …

AG Hussien, IH Borai, MM Said… - Journal of Applied …, 2019 - japsonline.com
Searching for a chemopreventive agent is an important approach for breast cancer
management. The aim of the study was to evaluate the chemopreventive potential of Ulmus …

New Facile synthesis of 2-alkylthiopyrimidin-4 (3H)-ones by tandem aza-Wittig reaction starting from the Baylis–Hillman adducts

J Xiong, X Wei, MW Ding - Synlett, 2017 - thieme-connect.com
Iminophosphoranes reacted with CS 2 at–5° C to produce the isothiocyanates, which were
treated with primary amine to give thioureas in 73–91% yields. The subsequent reaction of …

[PDF][PDF] 1, 3-Bis (4-chlorophenyl)-2, 3-epoxypropanone as synthons in synthesis of some interesting potential antimicrobial agents

AE Rashad, AH Shamroukh, MA El-Hashash… - Org. Chem. Indian …, 2013 - hakon-art.com
The usefulness of small ring heterocyclic compound has been clearly shown in recently
years [1-3]. Threemembered heterocycles are invested with a special allure that is derived …