Novel 1, 3-thiazole analogues with potent activity against breast cancer: A design, synthesis, in vitro, and in silico study

MG Salem, DMA El-Maaty, YIM El-Deen, BH Elesawy… - Molecules, 2022 - mdpi.com
Breast cancer is the most common cancer in women, responsible for over half a million
deaths in 2020. Almost 75% of FDA-approved drugs are mainly nitrogen-and sulfur …

Develo** our knowledge of the quinolone scaffold and its value to anticancer drug design

Y Singh, N Bhatia, A Biharee, S Kulkarni… - Expert Opinion on …, 2023 - Taylor & Francis
Introduction The quinolone scaffold is a bicyclic benzene-pyridinic ring scaffold with nitrogen
at the first position and a carbonyl group at the second or fourth position. It is endowed with a …

[HTML][HTML] A Review of Cinnamic Acid's Skeleton Modification: Features for Antibacterial-Agent-Guided Derivatives

RM Annuur, D Triana, T Ernawati, Y Murai, M Aswad… - Molecules, 2024 - mdpi.com
Antimicrobial resistance has emerged as a significant danger to global health, and the need
for more effective antimicrobial resistance (AMR) control has been highlighted. Cinnamic …

Design, synthesis, and characterization of cinnamic acid derivatives with two novel acrylohydrazones on HeLa and CHO-1 cancer cell lines: the experimental and …

AD Ogunlakin, MA Sonibare, OE Yeye, A Jabeen… - Chemistry Africa, 2024 - Springer
Purpose To investigate the effect of derivatives of cinnamic acid on the proliferation of CHO-
1 and HeLa cell lines. Methods Three Acrylohydrazones (7–9) derived from cinnamic acid …

Synthesis and anticancer evaluation of novel 7-aza-coumarine-3-carboxamides

AV Trifonov, AS Gazizov, AS Tapalova… - International Journal of …, 2023 - mdpi.com
Herein, we report the design and synthesis of novel 7-aza-coumarine-3-carboxamides via
scaffold-hop** strategy and evaluation of their in vitro anticancer activity. Additionally, the …

Design, synthesis and evaluation the bioactivities of novel 8‑methoxy-1-azacoumarin-3-carboxamide derivatives as anti-diabetic agents

M El Behery, IM El-Deen, MA El-Zend… - Journal of Molecular …, 2023 - Elsevier
In this study, a novel series of 8‑methoxy-2-oxo-1, 2-dihydroquinoline-3-carboxylic acid and
N-substituted 8‑methoxy-2-oxo-1, 2-dihydroquinoline-3-carboxamide derivatives 2–10 were …

In vitro anti-breast cancer study of hybrid cinnamic acid derivatives bearing 2-thiohydantoin moiety

DN Binjawhar, FA Al-Salmi, MA Alghamdi… - Future Medicinal …, 2024 - Taylor & Francis
Aim: To synthesize new hybrid cinnamic acids (10a, 10b and 11) and ester derivatives (7, 8
and 9) and investigate their anti-breast cancer activities. Materials & methods: Compounds 7 …

Anticancer Studies of Newly Synthesized Thiazole Derivatives: Synthesis, Characterization, Biological Activity, and Molecular Docking

FA Al-Salmi, AH Alrohaimi, ME Behery, W Megahed… - Crystals, 2023 - mdpi.com
Thiazole and its derivatives have received a lot of attention from researchers due to its wide
biological, pharmacological, and anticancer properties. A novel series of 2-[2-[4-Hydroxy-3 …

Study of Biological Activities and ADMET-Related Properties of Novel Chlorinated N-arylcinnamamides

T Strharsky, D Pindjakova, J Kos, L Vrablova… - International Journal of …, 2022 - mdpi.com
A series of eighteen 4-chlorocinnamanilides and eighteen 3, 4-dichlorocinnamanilides were
designed, prepared and characterized. All compounds were evaluated for their activity …

Cinnamamide derivatives with 4-hydroxypiperidine moiety enhance effect of doxorubicin to cancer cells and protect cardiomyocytes against drug-induced toxicity …

P Koczurkiewicz-Adamczyk, B Gąsiorkiewicz, K Piska… - Life Sciences, 2022 - Elsevier
Doxorubicin (DOX) is classified by World Health Organization (WHO) as an essential
medicine for cancer. However, its clinical application is limited due to resistance …